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Details

Stereochemistry ABSOLUTE
Molecular Formula C30H44O8
Molecular Weight 532.6656
Optical Activity UNSPECIFIED
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of WIKSTROTOXIN D

SMILES

CCCCCCCCC[C@]12O[C@@H]3[C@@H]4[C@@H]5O[C@]5(CO)[C@@H](O)[C@@]6(O)[C@@H](C=C(C)C6=O)[C@@]4(O1)[C@H](C)C[C@@]3(O2)C(C)=C

InChI

InChIKey=JAQJQYMDHBSCKO-JDVVNZBPSA-N
InChI=1S/C30H44O8/c1-6-7-8-9-10-11-12-13-28-36-23-21-24-27(16-31,35-24)25(33)29(34)20(14-18(4)22(29)32)30(21,38-28)19(5)15-26(23,37-28)17(2)3/h14,19-21,23-25,31,33-34H,2,6-13,15-16H2,1,3-5H3/t19-,20-,21-,23-,24+,25-,26-,27+,28-,29-,30+/m1/s1

HIDE SMILES / InChI

Approval Year

Name Type Language
WIKSTROTOXIN D
Common Name English
J37.161K
Preferred Name English
(2S,3AR,3BS,3CS,4AR,5S,5AS,8AR,8BR,9R,10AR)-5,5A-DIHYDROXY-4A-(HYDROXYMETHYL)-7,9-DIMETHYL-2-NONYL-10A-(PROP-1-EN-2-YL)-3A,3B,3C,4A,5,5A,8A,9,10,10A-DECAHYDRO-6H-2,8B-EPOXYOXIRENO(6,7)AZULENO(5,4-E)(1,3)BENZODIOXOL-6-ONE
Systematic Name English
(1R,2R,6S,7S,8R,10S,11S,12R,14S,16R,18R)-6,7-DIHYDROXY-8-(HYDROXYMETHYL)-16-ISOPROPENYL-4,18-DIMETHYL-14-NONYL-9,13,15,19-TETRAOXAHEXACYCLO(12.4.1.01,11.0(SUP 2,6).0(SUP 8,10).0(SUP 12,16))NONADEC-3-EN-5-ONE
Systematic Name English
DAPHNOPSIS FACTOR R3
Common Name English
PIMELEA FACTOR P1
Common Name English
SIMPLEXIN
Common Name English
6H-2,8B-EPOXYOXIRENO(6,7)AZULENO(5,4-E)-1,3-BENZODIOXOL-6-ONE, 3A,3B,3C,4A,5,5A,8A,9,10,10A-DECAHYDRO-5,5A-DIHYDROXY-4A-(HYDROXYMETHYL)-7,9-DIMETHYL-10A-(1-METHYLETHENYL)-2-NONYL-, (2S,3AR,3BS,3CS,4AR,5S,5AS,8AR,8BR,9R,10AR)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID90930781
Created by admin on Mon Mar 31 22:51:12 GMT 2025 , Edited by admin on Mon Mar 31 22:51:12 GMT 2025
PRIMARY
FDA UNII
9QZ71FI0LO
Created by admin on Mon Mar 31 22:51:12 GMT 2025 , Edited by admin on Mon Mar 31 22:51:12 GMT 2025
PRIMARY
CAS
1404-62-2
Created by admin on Mon Mar 31 22:51:12 GMT 2025 , Edited by admin on Mon Mar 31 22:51:12 GMT 2025
PRIMARY
PUBCHEM
119045
Created by admin on Mon Mar 31 22:51:12 GMT 2025 , Edited by admin on Mon Mar 31 22:51:12 GMT 2025
PRIMARY