Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C27H32O8 |
Molecular Weight | 484.5382 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12C[C@H]3O[C@]4([H])C=C(C)CC[C@]4(COC(=O)\C=C(C)\CCOC(=O)\C=C\C=CC(=O)O1)[C@]2(C)[C@]35CO5
InChI
InChIKey=GXCGYHWSYNQVHU-GYDJLPFWSA-N
InChI=1S/C27H32O8/c1-17-8-10-26-15-32-24(30)13-18(2)9-11-31-22(28)6-4-5-7-23(29)35-19-14-21(34-20(26)12-17)27(16-33-27)25(19,26)3/h4-7,12-13,19-21H,8-11,14-16H2,1-3H3/b6-4+,7-5-,18-13+/t19-,20-,21-,25-,26-,27+/m1/s1
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL366 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26320597 |
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Target ID: CHEMBL383 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11277768 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
A new macrocyclic trichothecene, 12,13-deoxyroridin E, produced by the marine-derived fungus Myrothecium roridum collected in Palau. | 2001 Mar |
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Macrocyclic trichothecenes are undetectable in kudzu (Pueraria montana) plants treated with a high-producing isolate of Myrothecium verrucaria. | 2001 Sep |
Patents
Sample Use Guides
Two sublethal doses of verrucarin J (0.9 and 0.5 mg/kg body weight) extracted from rice seeds were injected intraperitoneally to male mice for two, four, six and eight weeks (for each dose) and were compared with control groups.
Route of Administration:
Intraperitoneal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11277768
Verrucarin J inhibited HL-60 cells with IC50 2.5 ng/mL
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SUBSTANCE RECORD