NP-MRD: Showing NP-Card for (1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile (NP0201883)

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Record Information

Version

2.0

Created at

2022-09-04 21:00:08 UTC

Updated at

2022-09-04 21:00:08 UTC

NP-MRD ID

NP0201883

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile

Description

(1S,4S,4aS,5S,6R,8aS)-4-[(2R,5S)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-decahydronaphthalene-1,6-dicarbonitrile belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated. (1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile is found in Acanthella cavernosa. Based on a literature review very few articles have been published on (1S,4S,4aS,5S,6R,8aS)-4-[(2R,5S)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-decahydronaphthalene-1,6-dicarbonitrile.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042223002D          

 28 30  0  0  1  0            999 V2000
    3.5635   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3920   -3.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2204   -4.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1989   -3.4855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0059   -3.6570    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5850   -3.1424    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9719   -3.6945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2574   -3.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6085   -2.3888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8986    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4895    1.2640    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3848   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8545   -2.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1367   -2.7880    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2494   -2.3888    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  3  0  0  0  0
  6  2  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  6  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  3  0  0  0  0
 14 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  1  0  0  0
 21 23  1  6  0  0  0
 23 24  3  0  0  0  0
 21 25  1  0  0  0  0
 25 26  1  1  0  0  0
 27 25  1  6  0  0  0
 18 27  1  0  0  0  0
 11 27  1  0  0  0  0
  9 28  1  0  0  0  0
  6 28  1  0  0  0  0
M  END

     RDKit          3D

 61 63  0  0  0  0  0  0  0  0999 V2000
    3.6605   -2.2851   -0.9010 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9623   -1.0935   -0.0227 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4111   -0.6945   -0.3305 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9036   -1.4384    1.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8719   -1.7269    2.4936 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1113    0.1081   -0.3771 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4780    1.2245    0.5358 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1205    1.5950    1.1433 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1340    1.0039    0.1649 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0175    1.9656   -0.9905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1727    0.7476    0.8621 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6684    2.0799    1.3792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7329    2.6846    0.5017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9123    1.7410    0.5802 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9638    2.3051   -0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4951    1.9397    1.9312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9359    2.0871    2.9892 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5982    0.3288    0.3251 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4291   -0.1303   -0.8818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8708   -1.4140   -1.3973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2302   -2.2415   -0.3135 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7442   -3.5250   -1.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2812   -2.6630    0.6142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1157   -3.0070    1.3492 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1030   -1.5361    0.3847 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0818   -2.1057    0.0625 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1680   -0.0268    0.1008 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7711   -0.1230   -0.2806 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4767   -3.0317   -0.6973 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7750   -1.9655   -1.9579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6780   -2.7203   -0.6816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7508    0.1266    0.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4220   -0.3073   -1.3748 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0934   -1.5449   -0.2001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3494    0.3453   -1.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1706    0.9463    1.3477 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9014    2.0493   -0.0536 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1102    2.7105    1.1450 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0401    1.1628    2.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2671    1.5884   -1.6915 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0026    1.8971   -1.5410 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9188    3.0114   -0.6968 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0905    0.1522    1.7865 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1125    2.8241    1.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1502    1.9445    2.3927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0114    3.6552    0.9600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4634    2.7887   -0.5460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8448    1.6705   -0.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5186    2.6154   -1.3394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3106    3.2621    0.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0079   -0.2814    1.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4009    0.6109   -1.6985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4692   -0.3330   -0.5320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7025   -2.0210   -1.8150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1661   -1.2630   -2.2666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3187   -3.3130   -1.9984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1203   -4.1351   -0.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6854   -4.1100   -1.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2684   -1.6291    1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1436   -2.5872   -0.7751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9662    0.0809   -1.0006 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  3  0
  2  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  6
  9 28  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  1
 16 17  3  0
 14 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  1
 23 24  3  0
 21 25  1  0
 25 26  1  0
 25 27  1  0
 28  6  1  0
 27 11  1  0
 27 18  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  6 35  1  6
  7 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
 10 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  1
 12 44  1  0
 12 45  1  0
 13 46  1  0
 13 47  1  0
 15 48  1  0
 15 49  1  0
 15 50  1  0
 18 51  1  1
 19 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 22 56  1  0
 22 57  1  0
 22 58  1  0
 25 59  1  1
 26 60  1  0
 27 61  1  6
M  END


  Mrv1652309042223002D          

 28 30  0  0  1  0            999 V2000
    3.5635   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3920   -3.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2204   -4.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1989   -3.4855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0059   -3.6570    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5850   -3.1424    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9719   -3.6945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2574   -3.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6085   -2.3888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8986    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4895    1.2640    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3848   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8545   -2.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1367   -2.7880    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2494   -2.3888    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  3  0  0  0  0
  6  2  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  6  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  3  0  0  0  0
 14 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  1  0  0  0
 21 23  1  6  0  0  0
 23 24  3  0  0  0  0
 21 25  1  0  0  0  0
 25 26  1  1  0  0  0
 27 25  1  6  0  0  0
 18 27  1  0  0  0  0
 11 27  1  0  0  0  0
  9 28  1  0  0  0  0
  6 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0201883

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(C#N)[C@@H]1CC[C@@](C)(O1)[C@H]1CC[C@](C)(C#N)[C@H]2CC[C@](C)(C#N)[C@@H](O)[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C23H33N3O2/c1-20(2,12-24)17-8-11-23(5,28-17)16-7-9-21(3,13-25)15-6-10-22(4,14-26)19(27)18(15)16/h15-19,27H,6-11H2,1-5H3/t15-,16-,17-,18-,19-,21+,22+,23+/m0/s1

> <INCHI_KEY>
BAFWSRLHCKLKHU-NGTVHILMSA-N

> <FORMULA>
C23H33N3O2

> <MOLECULAR_WEIGHT>
383.536

> <EXACT_MASS>
383.257277315

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
42.98960204913057

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4S,4aS,5S,6R,8aS)-4-[(2R,5S)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-decahydronaphthalene-1,6-dicarbonitrile

> <JCHEM_LOGP>
3.436694117000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.890671581626105

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2840202501967406

> <JCHEM_POLAR_SURFACE_AREA>
100.83000000000001

> <JCHEM_REFRACTIVITY>
106.4918

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,4aS,5S,6R,8aS)-4-[(2R,5S)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       6.652  -4.680   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.332  -6.186   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.011  -7.692   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.838  -6.506   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       9.344  -6.826   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       4.825  -5.866   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.681  -6.896   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.347  -6.126   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.136  -4.459   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.677   1.180   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.657   1.180   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       4.647   2.359   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.185  -2.043   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.195  -3.757   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       7.722  -5.204   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.199  -4.459   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    6                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4                                                            
CONECT    6    2    7   28                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   28                                             
CONECT   10    9                                                            
CONECT   11    9   12   27                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   18                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   14   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   25                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23                                                            
CONECT   25   21   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   18   11                                                  
CONECT   28    9    6                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₃N₃O₂

Average Mass

383.5360 Da

Monoisotopic Mass

383.25728 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)(C#N)[C@@H]1CC[C@@](C)(O1)[C@H]1CC[C@](C)(C#N)[C@H]2CC[C@](C)(C#N)[C@@H](O)[C@H]12

InChI Identifier

InChI=1S/C23H33N3O2/c1-20(2,12-24)17-8-11-23(5,28-17)16-7-9-21(3,13-25)15-6-10-22(4,14-26)19(27)18(15)16/h15-19,27H,6-11H2,1-5H3/t15-,16-,17-,18-,19-,21+,22+,23+/m0/s1

InChI Key

BAFWSRLHCKLKHU-NGTVHILMSA-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
Acanthella cavernosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Diterpene glycosides

Alternative Parents

Substituents

Diterpene glycoside
Diterpenoid
Biflorane diterpenoid
Cyclic alcohol
Tetrahydrofuran
Secondary alcohol
Dialkyl ether
Ether
Carbonitrile
Nitrile
Oxacycle
Organoheterocyclic compound
Organic nitrogen compound
Alcohol
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Organopnictogen compound
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

163187837

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile (NP0201883)

MOL for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)

3D MOL for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)

3D SDF for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)

3D-SDF for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)

PDB for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)

3D PDB for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)

SMILES for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)

INCHI for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)

Structure for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)

3D Structure for NP0201883 ((1s,4s,4as,5s,6r,8as)-4-[(2r,5s)-5-(1-cyano-1-methylethyl)-2-methyloxolan-2-yl]-5-hydroxy-1,6-dimethyl-octahydronaphthalene-1,6-dicarbonitrile)