NP-MRD: Showing NP-Card for 3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid (NP0237495)

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Record Information

Version

2.0

Created at

2022-09-06 20:39:09 UTC

Updated at

2022-09-06 20:39:09 UTC

NP-MRD ID

NP0237495

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid

Description

Daphnezomine L belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid is found in Daphniphyllum calycinum and Daphniphyllum macropodum. 3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid was first documented in 2009 (PMID: 19739650). Based on a literature review very few articles have been published on Daphnezomine L (PMID: 28927287).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062222392D          

 25 28  0  0  1  0            999 V2000
   -0.4329    2.5058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5336    1.6473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3894    1.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0941    0.9954    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9289    1.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3539    0.3211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6954   -0.4971    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1177   -0.3681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3089   -1.3004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5054   -1.0972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7026   -0.2896    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0015    0.1967    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9925   -0.1135    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3964    0.8901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0200    1.5761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8262    1.4008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3811    2.0113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0774    0.6150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8583   -0.3345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5000    0.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1914   -0.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9770   -1.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1531   -1.1050    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6935   -1.8406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8633   -1.9098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  2  0  0  0  0
 12 11  1  1  0  0  0
  4 12  1  0  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  9 25  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
    4.1651    1.3146    1.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6680    1.0889    1.8178 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5683    0.0831    2.9192 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9900    0.6981    0.5430 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5426   -0.5679   -0.0569 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7974   -0.7548   -1.3267 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2853   -0.8955   -1.1494 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2125   -1.0562   -2.5685 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1359   -2.1663   -0.3406 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1768   -1.8358    1.1055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3870   -0.6892    1.5926 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5328    0.5226    0.7957 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3229    0.2902   -0.4297 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3700    1.4315   -1.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9399    2.7238   -0.8741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8748    3.7452   -1.9581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2837    4.9169   -1.8232 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3329    3.3686   -3.1712 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6857   -0.0856    0.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2007    0.6526    1.0788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5262    0.1734    1.5333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8875   -0.8387    0.5227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147   -1.1675   -0.2122 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1783   -2.5278    0.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0693   -2.9734   -0.6612 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6336    1.9120    2.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1968    1.8223    0.5518 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6195    0.3230    1.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3055    2.0724    2.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8520   -0.9055    2.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6053    0.1184    3.4678 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3419    0.3705    3.6860 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2185    1.4971   -0.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6001   -0.3535   -0.3287 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5550   -1.4262    0.6133 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1283   -1.7062   -1.7906 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0518    0.0481   -2.0341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0339   -2.0815   -2.9329 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4032   -0.3927   -3.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2313   -0.7569   -2.7594 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0167   -2.8631   -0.4926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0138   -2.6486    1.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1587    1.3387    1.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9638    1.1414   -2.2605 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6369    1.6926   -1.7953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3747    3.1888   -0.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9880    2.6190   -0.4989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8338    3.4175   -4.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7743    1.5550    1.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3727   -0.2680    2.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2919    0.9733    1.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6807   -0.4421   -0.1607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3396   -1.7226    1.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9022   -1.2850   -1.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587   -3.2088    0.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9526   -2.5898    1.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098   -4.0676   -0.5589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4473   -2.8226   -1.6981 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 25  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 19  2  0
 19 13  1  0
 13 14  1  6
 14 15  1  0
 15 16  1  0
 16 18  1  0
 16 17  2  0
 13 12  1  0
 12 11  1  0
 11 10  2  0
 12  4  1  0
 13  7  1  0
 10  9  1  0
 19 23  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  6
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  8 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  6
 25 57  1  0
 25 58  1  0
 24 55  1  0
 24 56  1  0
 23 54  1  6
 22 52  1  0
 22 53  1  0
 21 50  1  0
 21 51  1  0
 20 49  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 18 48  1  0
 12 43  1  1
 10 42  1  0
M  END


  Mrv1652309062222392D          

 25 28  0  0  1  0            999 V2000
   -0.4329    2.5058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5336    1.6473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3894    1.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0941    0.9954    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9289    1.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3539    0.3211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6954   -0.4971    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1177   -0.3681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3089   -1.3004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5054   -1.0972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7026   -0.2896    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0015    0.1967    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9925   -0.1135    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3964    0.8901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0200    1.5761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8262    1.4008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3811    2.0113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0774    0.6150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8583   -0.3345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5000    0.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1914   -0.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9770   -1.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1531   -1.1050    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6935   -1.8406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8633   -1.9098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  2  0  0  0  0
 12 11  1  1  0  0  0
  4 12  1  0  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  9 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237495

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@H]4CCC=C4[C@@]2(CCC(O)=O)[C@H]1N=C3

> <INCHI_IDENTIFIER>
InChI=1S/C22H33NO2/c1-14(2)17-9-11-21(3)16-8-7-15-5-4-6-18(15)22(21,12-10-19(24)25)20(17)23-13-16/h6,13-17,20H,4-5,7-12H2,1-3H3,(H,24,25)/t15-,16-,17-,20+,21+,22+/m1/s1

> <INCHI_KEY>
UJDROKCPMXMUHR-SQXXJVNJSA-N

> <FORMULA>
C22H33NO2

> <MOLECULAR_WEIGHT>
343.511

> <EXACT_MASS>
343.251129307

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
39.80091391326148

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(1S,2S,7R,10S,13S,14R)-1-methyl-14-(propan-2-yl)-12-azatetracyclo[8.6.0.0^{2,13}.0^{3,7}]hexadeca-3,11-dien-2-yl]propanoic acid

> <JCHEM_LOGP>
1.4908541808162852

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.795720922311865

> <JCHEM_PKA_STRONGEST_BASIC>
8.623295932735253

> <JCHEM_POLAR_SURFACE_AREA>
49.66

> <JCHEM_REFRACTIVITY>
100.41129999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-[(1S,2S,7R,10S,13S,14R)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0^{2,13}.0^{3,7}]hexadeca-3,11-dien-2-yl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.808   4.677   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.996   3.075   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.593   2.827   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.176   1.858   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.734   2.049   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.527   0.599   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.298  -0.928   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.220  -0.687   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.577  -2.427   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.943  -2.048   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -1.312  -0.541   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -0.003   0.367   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.853  -0.212   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.607   1.661   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.771   2.942   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.275   2.615   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.311   3.754   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       5.744   1.148   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.469  -0.624   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.667   0.343   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.957  -0.497   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.557  -1.984   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.019  -2.063   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.161  -3.436   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.612  -3.565   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   13                                             
CONECT    8    7                                                            
CONECT    9    7   10   25                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    4   13                                                  
CONECT   13   12    7   14   19                                             
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   13   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   19   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24    9                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₃NO₂

Average Mass

343.5110 Da

Monoisotopic Mass

343.25113 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@H]4CCC=C4[C@@]2(CCC(O)=O)[C@H]1N=C3

InChI Identifier

InChI=1S/C22H33NO2/c1-14(2)17-9-11-21(3)16-8-7-15-5-4-6-18(15)22(21,12-10-19(24)25)20(17)23-13-16/h6,13-17,20H,4-5,7-12H2,1-3H3,(H,24,25)/t15-,16-,17-,20+,21+,22+/m1/s1

InChI Key

UJDROKCPMXMUHR-SQXXJVNJSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Daphniphyllum calycinum	LOTUS Database	35616633
Daphniphyllum macropodum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Carbocyclic fatty acid
Tetrahydropyridine
Fatty acyl
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organoheterocyclic compound
Azacycle
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic oxide
Organic nitrogen compound
Imine
Hydrocarbon derivative
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102245575

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang CR, Liu HB, Feng T, Zhu JY, Geng MY, Yue JM: Alkaloids from the leaves of Daphniphyllum subverticillatum. J Nat Prod. 2009 Sep;72(9):1669-72. doi: 10.1021/np9003799. [PubMed:19739650 ]
Liu S, Zhang J, Di Y, Dong J, Hao X: Daphniphyllum alkaloids with cytotoxic activity from Daphniphyllum angustifolium. Nat Prod Res. 2018 Sep;32(18):2165-2170. doi: 10.1080/14786419.2017.1371155. Epub 2017 Sep 19. [PubMed:28927287 ]
LOTUS database [Link]

Showing NP-Card for 3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid (NP0237495)

MOL for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)

3D MOL for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)

3D SDF for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)

3D-SDF for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)

PDB for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)

3D PDB for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)

SMILES for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)

INCHI for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)

Structure for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)

3D Structure for NP0237495 (3-[(1s,2s,7r,10s,13s,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoic acid)