NP-MRD: Showing NP-Card for Embellicine C (NP0331528)

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Record Information

Version

2.0

Created at

2023-03-08 00:19:11 UTC

Updated at

2024-09-03 04:16:02 UTC

NP-MRD ID

NP0331528

Natural Product DOI

https://doi.org/10.57994/0501

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Embellicine C

Description

Corynoxine belongs to the class of organic compounds known as indolizidines. These are polycyclic compounds containing an indolizidine, which is a bicyclic heterocycle containing a saturated six-member ring fused to a saturated five-member ring, one of the bridging atoms being nitrogen. Embellicine C was first documented in 2021 (PMID: 34975502). Based on a literature review a small amount of articles have been published on Corynoxine (PMID: 35217810) (PMID: 35472200) (PMID: 35468648) (PMID: 34738856).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214162D          

 28 31  0  0  1  0            999 V2000
    4.4813   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8169    0.4987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3320    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5115    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1759    0.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6608   -0.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3554    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1839    1.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4302    1.5550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8984    1.6320    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5350    0.4987    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1994   -0.2549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8125   -0.8070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5270   -0.3945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3789   -0.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1060    0.3263    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2295    1.0799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0500    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2554    1.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0759    1.6611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4114    0.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2319    0.8212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0802    2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4047    3.1685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9007    2.5873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2362    3.3410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9265    0.2400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2620   -0.5136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  7  5  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 17 19  1  1  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 16 27  1  1  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
   -3.1531   -3.0546    0.0629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7869   -1.5809    0.1322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5921   -1.3857   -0.7779 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4931   -2.2561   -0.2601 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7979   -1.9995   -0.8117 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7659   -2.7237   -0.0214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6399   -1.6898    0.6439 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5984   -0.5989   -0.3985 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4828   -0.9529   -1.5346 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4104   -1.9975   -2.2717 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4352    0.0554   -1.6847 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1799    1.0347   -0.6900 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8986    2.2040   -0.4951 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5160    3.0532    0.5198 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4354    2.7143    1.3057 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7220    1.5293    1.0940 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1030    0.6784    0.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2046   -0.6357   -0.8720 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2210    0.2240   -0.0747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1046    0.0419   -0.7797 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1203    1.0476   -0.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1069    1.8632    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0677    1.8066    1.4221 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3962    1.4477    2.7606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2524    1.1539   -1.4538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3391    0.4123   -2.4560 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2595    2.0872   -1.2644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3206    2.1610   -2.1916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4435   -3.6238    0.7299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9268   -3.4354   -0.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1811   -3.2586    0.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6508   -0.9845   -0.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4638   -1.4113    1.1982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8904   -1.7583   -1.7789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7622   -3.3133   -0.5587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4595   -2.2922    0.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4335   -3.3369   -0.6719 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2662   -3.3779    0.7304 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1274   -1.2992    1.5464 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6606   -2.0515    0.8492 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1994    0.0534   -2.4247 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7489    2.4792   -1.1071 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0772    3.9722    0.6765 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1267    3.3786    2.1088 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8965    1.3468    1.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1228   -0.2445   -1.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4941    1.2973   -0.1926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2263   -0.1503    0.9445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8263    0.2211   -1.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8795    2.6021    0.6958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8618    0.4301    2.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4794    1.3741    3.3937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1031    2.1500    3.2203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2866    2.4016   -1.6734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1416    2.9665   -2.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4416    1.2256   -2.7822 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  8  7  1  1
  8 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 21 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 20  3  1  0
 17 12  1  0
 18  5  1  0
 17  8  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  6
  4 35  1  0
  4 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
 18 46  1  6
 19 47  1  0
 19 48  1  0
 20 49  1  6
 22 50  1  0
 24 51  1  0
 24 52  1  0
 24 53  1  0
 28 54  1  0
 28 55  1  0
 28 56  1  0
 11 41  1  0
 13 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  0
M  END


  Mrv1652304282214162D          

 28 31  0  0  1  0            999 V2000
    4.4813   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8169    0.4987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3320    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5115    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1759    0.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6608   -0.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3554    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1839    1.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4302    1.5550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8984    1.6320    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5350    0.4987    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1994   -0.2549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8125   -0.8070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5270   -0.3945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3789   -0.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1060    0.3263    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2295    1.0799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0500    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2554    1.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0759    1.6611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4114    0.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2319    0.8212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0802    2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4047    3.1685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9007    2.5873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2362    3.3410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9265    0.2400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2620   -0.5136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  7  5  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 17 19  1  1  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 16 27  1  1  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0331528

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H]1CN2CC[C@]3([C@@H]2C[C@@H]1\C(=C/OC)C(=O)OC)C(=O)NC1=CC=CC=C31

> <INCHI_IDENTIFIER>
InChI=1S/C22H28N2O4/c1-4-14-12-24-10-9-22(17-7-5-6-8-18(17)23-21(22)26)19(24)11-15(14)16(13-27-2)20(25)28-3/h5-8,13-15,19H,4,9-12H2,1-3H3,(H,23,26)/b16-13+/t14-,15+,19+,22+/m1/s1

> <INCHI_KEY>
DAXYUDFNWXHGBE-NRAMRBJXSA-N

> <FORMULA>
C22H28N2O4

> <MOLECULAR_WEIGHT>
384.476

> <EXACT_MASS>
384.20490739

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
41.486462314585445

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2E)-2-[(3S,6'S,7'S,8'aS)-6'-ethyl-2-oxo-1,2,3',5',6',7',8',8'a-octahydro-2'H-spiro[indole-3,1'-indolizine]-7'-yl]-3-methoxyprop-2-enoate

> <ALOGPS_LOGP>
2.85

> <JCHEM_LOGP>
2.6094639083333337

> <ALOGPS_LOGS>
-3.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.16702338486493

> <JCHEM_PKA_STRONGEST_BASIC>
10.712527798380334

> <JCHEM_POLAR_SURFACE_AREA>
67.87

> <JCHEM_REFRACTIVITY>
108.00599999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.40e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2E)-2-[(3S,6'S,7'S,8'aS)-6'-ethyl-2-oxo-3',5',6',7',8',8'a-hexahydro-1H,2'H-spiro[indole-3,1'-indolizine]-7'-yl]-3-methoxyprop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       8.365  -0.476   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.991   0.931   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.086   2.177   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.555   2.016   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.928   0.609   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.834  -0.637   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.397   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.077   2.276   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.670   2.903   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0       5.410   3.046   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       2.865   0.931   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       2.239  -0.476   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       3.383  -1.506   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.717  -0.736   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.707  -0.637   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.198   0.609   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.428   2.016   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.960   2.177   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.477   3.262   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.008   3.101   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.635   1.694   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -4.166   1.533   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.150   4.669   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.756   5.915   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       1.681   4.830   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.308   6.236   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.729   0.448   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.356  -0.959   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   11   14                                             
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    4                                                       
CONECT   11    7   12   18                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    7                                                       
CONECT   15   12   16                                                       
CONECT   16   15   17   27                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   11                                                       
CONECT   19   17   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   19   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27   16   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₁NO₅

Average Mass

543.7040 Da

Monoisotopic Mass

543.29847 Da

IUPAC Name

methyl (2E)-2-[(3S,6'S,7'S,8'aS)-6'-ethyl-2-oxo-1,2,3',5',6',7',8',8'a-octahydro-2'H-spiro[indole-3,1'-indolizine]-7'-yl]-3-methoxyprop-2-enoate

Traditional Name

methyl (2E)-2-[(3S,6'S,7'S,8'aS)-6'-ethyl-2-oxo-3',5',6',7',8',8'a-hexahydro-1H,2'H-spiro[indole-3,1'-indolizine]-7'-yl]-3-methoxyprop-2-enoate

CAS Registry Number

Not Available

SMILES

[H][C@@]12C[C@H](C)C[C@H](C)[C@@]1([H])[C@H]1OC3=CC=C(C[C@]4(O)NC(=O)[C@]5(O[C@@H]45)C(=O)[C@H]4[C@]1([H])[C@]2([H])C(C)=C1[C@H](C)C(C)=C[C@@]41C)C=C3

InChI Identifier

InChI=1S/C34H41NO5/c1-15-11-16(2)23-22(12-15)24-19(5)26-18(4)17(3)13-32(26,6)27-25(24)28(23)39-21-9-7-20(8-10-21)14-33(38)30-34(40-30,29(27)36)31(37)35-33/h7-10,13,15-16,18,22-25,27-28,30,38H,11-12,14H2,1-6H3,(H,35,37)/t15-,16+,18-,22-,23-,24-,25+,27-,28-,30+,32-,33-,34+/m1/s1

InChI Key

NQFJAFJMOUIAAX-LVGIWTBVSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2024-02-26	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2024-02-26	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-14	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-13	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-11	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-10	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-09	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCL3, experimental)	zyalsubeh@just.edu.jo	Not Available	Not Available	2023-03-08	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indolizidines. These are polycyclic compounds containing an indolizidine, which is a bicyclic heterocycle containing a saturated six-member ring fused to a saturated five-member ring, one of the bridging atoms being nitrogen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indolizidines

Sub Class

Not Available

Direct Parent

Indolizidines

Alternative Parents

Substituents

Indole or derivatives
Dihydroindole
Indolizidine
Aralkylamine
Piperidine
N-alkylpyrrolidine
Benzenoid
Pyrrolidine
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Vinylogous ester
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid ester
Lactam
Azacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Amine
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Organonitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

indolizines (CHEBI:70072 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.85	ALOGPS
logP	2.61	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	13.17	ChemAxon
pKa (Strongest Basic)	10.71	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	67.87 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	108.01 m³·mol⁻¹	ChemAxon
Polarizability	41.49 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00025163

Chemspider ID

8650526

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10475115

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhu Z, Liu LF, Su CF, Liu J, Tong BC, Iyaswamy A, Krishnamoorthi S, Sreenivasmurthy SG, Guan XJ, Kan YX, Xie WJ, Zhao CL, Cheung KH, Lu JH, Tan JQ, Zhang HJ, Song JX, Li M: Corynoxine B derivative CB6 prevents Parkinsonian toxicity in mice by inducing PIK3C3 complex-dependent autophagy. Acta Pharmacol Sin. 2022 Feb 25. pii: 10.1038/s41401-022-00871-0. doi: 10.1038/s41401-022-00871-0. [PubMed:35217810 ]
Zhang M, Sharma A, Leon F, Avery B, Kjelgren R, McCurdy CR, Pearson BJ: Plant growth and phytoactive alkaloid synthesis in kratom [Mitragyna speciosa (Korth.)] in response to varying radiance. PLoS One. 2022 Apr 26;17(4):e0259326. doi: 10.1371/journal.pone.0259326. eCollection 2022. [PubMed:35472200 ]
Manwill PK, Flores-Bocanegra L, Khin M, Raja HA, Cech NB, Oberlies NH, Todd DA: Kratom (Mitragyna speciosa) Validation: Quantitative Analysis of Indole and Oxindole Alkaloids Reveals Chemotypes of Plants and Products. Planta Med. 2022 Apr 25. doi: 10.1055/a-1795-5876. [PubMed:35468648 ]
Zeng P, Su HF, Ye CY, Qiu SW, Tian Q: Therapeutic Mechanism and Key Alkaloids of Uncaria rhynchophylla in Alzheimer's Disease From the Perspective of Pathophysiological Processes. Front Pharmacol. 2021 Dec 15;12:806984. doi: 10.3389/fphar.2021.806984. eCollection 2021. [PubMed:34975502 ]
Liang XX, Yang JX, Li JM, Huang JB, Yang LM, Sun TT, Luo RH, Xiao WL, Zheng YT, Li XL: A pair of new oxindole alkaloids isolated from Uncaria macrophylla. Nat Prod Res. 2021 Nov 5:1-7. doi: 10.1080/14786419.2021.2000982. [PubMed:34738856 ]

Showing NP-Card for Embellicine C (NP0331528)

MOL for NP0331528 (Embellicine C)

3D MOL for NP0331528 (Embellicine C)

3D SDF for NP0331528 (Embellicine C)

3D-SDF for NP0331528 (Embellicine C)

PDB for NP0331528 (Embellicine C)

3D PDB for NP0331528 (Embellicine C)

SMILES for NP0331528 (Embellicine C)

INCHI for NP0331528 (Embellicine C)

Structure for NP0331528 (Embellicine C)

3D Structure for NP0331528 (Embellicine C)