NP-MRD: Showing NP-Card for (6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate (NP0304434)

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Record Information

Version

2.0

Created at

2022-09-10 19:31:44 UTC

Updated at

2022-09-10 19:31:45 UTC

NP-MRD ID

NP0304434

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate

Description

(6R,7S,10S,15R,16S,18S,19R,22S)-6,18-dimethyl-5-oxa-16λ⁵-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]Docos-13-ene-4,16-dione belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring. (6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate is found in Daphniphyllum oldhamii. Based on a literature review very few articles have been published on (6R,7S,10S,15R,16S,18S,19R,22S)-6,18-dimethyl-5-oxa-16λ⁵-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]Docos-13-ene-4,16-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102221312D          

 26 31  0  0  1  0            999 V2000
    1.8384   -1.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6932   -0.7885    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2648   -0.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8758    0.5338    0.0000 N   0  3  1  0  0  0  0  0  0  0  0  0
    2.6986    0.5933    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    1.0636    0.3886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9508   -0.4287    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1728   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2422    0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318    1.0193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2803    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121    1.5048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318    2.2807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0636    2.9114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2803    2.4259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8121    1.7952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0924    2.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242    1.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9045    2.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7167    2.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2485    2.2309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0730    2.2041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024    1.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6195    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    1.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.3097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  4  1  1  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 21 25  1  0  0  0  0
 26 25  1  6  0  0  0
 18 26  1  0  0  0  0
  4 26  1  0  0  0  0
M  CHG  2   4   1   5  -1
M  END

     RDKit          3D

 57 62  0  0  0  0  0  0  0  0999 V2000
   -2.4474    3.4810   -0.8699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5623    2.7815    0.1153 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3523    2.1919   -0.6282 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1395    1.1794    0.2845 N   0  0  1  0  0  4  0  0  0  0  0  0
    0.8635    1.8376    1.2332 O   0  0  0  0  0  1  0  0  0  0  0  0
   -1.0039    0.6496    0.9555 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1641    1.5813    0.7520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1576    0.8899   -0.1541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5060   -0.3629   -0.6370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5399   -0.6569    0.5190 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4344   -1.1604    1.6506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9328   -2.5502    1.4540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7490   -3.4442    1.2609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8417   -4.7064    1.3818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5562   -2.8312    0.9460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5080   -1.6577    0.1154 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6379   -2.1537   -1.2941 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8603   -1.0670    0.3827 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8529   -2.1233   -0.0036 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2695   -1.6898    0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5527   -0.3267   -0.4704 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7391    0.3059    0.2203 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5005    1.7732   -0.1729 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9881    1.8668   -0.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4674    0.6631   -0.2907 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0166    0.2287   -0.3279 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0877    4.5455   -0.9264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3292    3.0890   -1.9055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5061    3.5516   -0.5538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2263    3.4699    0.9126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6548    1.7940   -1.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3308    3.0593   -0.7165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8452    0.5984    2.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7016    1.8200    1.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3645    1.5710   -1.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1441    0.7315    0.3313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3015   -1.1435   -0.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9994   -0.1770   -1.5794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7999   -1.1334    2.5630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2849   -0.4557    1.7499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4658   -2.8186    2.4047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5746   -2.6794    0.5831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2738   -3.2147   -1.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6972   -2.1911   -1.6386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0882   -1.5742   -2.0449 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9419   -0.8886    1.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6548   -2.5382   -1.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7043   -2.9758    0.6964 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8887   -2.4173   -0.5082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6813   -1.7715    1.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8397   -0.3740   -1.5575 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5914    0.1637    1.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7016   -0.0564   -0.1419 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9811    2.4705    0.5094 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8088    1.8572   -1.2326 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5462    2.8471    0.0399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8175    0.1415   -1.4366 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  1
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
 10  9  1  6
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
  7  2  1  0
 16 10  1  0
 26 18  1  0
 26  4  1  0
 10  6  1  0
 25 21  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  1
  3 31  1  0
  3 32  1  0
  6 33  1  1
  7 34  1  1
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  1
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  6
 22 52  1  0
 22 53  1  0
 23 54  1  0
 23 55  1  0
 24 56  1  0
 26 57  1  6
M  CHG  2   4   1   5  -1
M  END


  Mrv1652309102221312D          

 26 31  0  0  1  0            999 V2000
    1.8384   -1.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6932   -0.7885    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2648   -0.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8758    0.5338    0.0000 N   0  3  1  0  0  0  0  0  0  0  0  0
    2.6986    0.5933    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    1.0636    0.3886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9508   -0.4287    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1728   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2422    0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318    1.0193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2803    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121    1.5048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318    2.2807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0636    2.9114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2803    2.4259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8121    1.7952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0924    2.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242    1.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9045    2.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7167    2.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2485    2.2309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0730    2.2041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024    1.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6195    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    1.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.3097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  4  1  1  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 21 25  1  0  0  0  0
 26 25  1  6  0  0  0
 18 26  1  0  0  0  0
  4 26  1  0  0  0  0
M  CHG  2   4   1   5  -1
M  END
> <DATABASE_ID>
NP0304434

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[N@@+]2([O-])[C@H]3[C@@H]1CCC31CCC(=O)O[C@]1(C)[C@H]1CC[C@@H]3CCC=C3[C@H]21

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO3/c1-13-12-23(25)19-16-5-3-4-14(16)6-7-17(19)21(2)22(11-9-18(24)26-21)10-8-15(13)20(22)23/h5,13-15,17,19-20H,3-4,6-12H2,1-2H3/t13-,14+,15-,17+,19+,20+,21-,22?,23+/m1/s1

> <INCHI_KEY>
PTOMOLGIAURSGE-LPSODYPNSA-N

> <FORMULA>
C22H31NO3

> <MOLECULAR_WEIGHT>
357.494

> <EXACT_MASS>
357.230393862

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
39.9150474676492

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6R,7S,10S,15R,16S,18S,19R,22S)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-16-ium-16-olate

> <JCHEM_LOGP>
2.3057293370000016

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.1198933965208595

> <JCHEM_POLAR_SURFACE_AREA>
49.36

> <JCHEM_REFRACTIVITY>
99.63219999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(6R,7S,10S,15R,16S,18S,19R,22S)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-16-ium-16-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       3.432  -2.988   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.161  -1.472   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.228  -0.362   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       3.501   0.996   0.000  0.00  0.00           N+1
HETATM    5  O   UNK     0       5.037   1.108   0.000  0.00  0.00           O-1
HETATM    6  C   UNK     0       1.985   0.725   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.775  -0.800   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.323  -0.214   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.452   1.105   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.993   1.903   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.523   1.632   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.516   2.809   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.993   4.257   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.985   5.435   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       0.523   4.528   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.516   3.351   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.039   4.799   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.032   3.622   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.555   5.071   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.071   5.342   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.064   4.164   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.603   4.114   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.031   2.635   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.756   1.771   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.541   2.716   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.025   2.445   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6   26                                             
CONECT    5    4                                                            
CONECT    6    4    7   10                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6   11   16                                             
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   10   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   21   26                                                  
CONECT   26   25   18    4                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₁NO₃

Average Mass

357.4940 Da

Monoisotopic Mass

357.23039 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[N@@+]2([O-])[C@H]3[C@@H]1CCC31CCC(=O)O[C@]1(C)[C@H]1CC[C@@H]3CCC=C3[C@H]21

InChI Identifier

InChI=1S/C22H31NO3/c1-13-12-23(25)19-16-5-3-4-14(16)6-7-17(19)21(2)22(11-9-18(24)26-21)10-8-15(13)20(22)23/h5,13-15,17,19-20H,3-4,6-12H2,1-2H3/t13-,14+,15-,17+,19+,20+,21-,22?,23+/m1/s1

InChI Key

PTOMOLGIAURSGE-LPSODYPNSA-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 oldhamii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolidines

Sub Class

Not Available

Direct Parent

Quinolidines

Alternative Parents

Substituents

Quinolidine
Indolizidine
Delta_valerolactone
Delta valerolactone
N-alkylpyrrolidine
Piperidine
Oxane
Trialkyl amine oxide
Pyrrolidine
Lactone
Carboxylic acid ester
Oxacycle
Azacycle
Trisubstituted n-oxide
Monocarboxylic acid or derivatives
Carboxylic acid derivative
N-oxide
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic zwitterion
Organooxygen compound
Organonitrogen compound
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

163189853

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate (NP0304434)

MOL for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)

3D MOL for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)

3D SDF for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)

3D-SDF for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)

PDB for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)

3D PDB for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)

SMILES for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)

INCHI for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)

Structure for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)

3D Structure for NP0304434 ((6r,7s,10s,15r,16s,18s,19r,22s)-6,18-dimethyl-4-oxo-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-16-ium-16-olate)