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omtriptolide

Description

omtriptolide: a water-soluble, semisynthetic derivative of PG490 (triptolide) purified from the Chinese herb Tripterygium Wilfordii; structure in first source [MeSH]

Cross-References

ID SourceID
PubMed CID6918522
CHEMBL ID2110669
SCHEMBL ID16312527
MeSH IDM0578170

Synonyms (19)

Synonym
unii-d36elm729p
d36elm729p ,
omtriptolide [inn]
pg490-88
195883-06-8
omtriptolide
ym 262
butanedioic acid, mono((3bs,4as,5ar,6r,6as,7as,7bs,8as,8bs)-1,3,3b,4,4a,6,6a,7a,7b,8b,9,10-dodecahydro-8b-methyl-6a-(1-methylethyl)-1-oxotrisoxireno(6,7:8a,9:4b,5)phenanthro(1,2-c)furan-6-yl) ester
4-(((3bs,4as,5ar,6r,6as,7as,7bs,8as,8bs)-6a-isopropyl-8b-methyl-1-oxo-1,3,3b,4,4a,6,6a,7a,7b,8b,9,10-dodecahydrotrisoxireno(6,7:8a,9:4b,5)phenanthro(1,2-c)furan-6-yl)oxy)-4-oxobutanoic acid
omtriptolide [who-dd]
SCHEMBL16312527
CHEMBL2110669
CS-6982
HY-16363
Q27276034
MS-28442
4-[[(1s,2s,4s,5s,7s,8r,9r,11s,13s)-1-methyl-17-oxo-7-propan-2-yl-3,6,10,16-tetraoxaheptacyclo[11.7.0.02,4.02,9.05,7.09,11.014,18]icos-14(18)-en-8-yl]oxy]-4-oxobutanoic acid
VHA88306
AKOS040742336

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's7 (58.33)29.6817
2010's4 (33.33)24.3611
2020's1 (8.33)2.80

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (7.69%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other12 (92.31%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
camptothecindelta-lactone;
pyranoindolizinoquinoline;
quinoline alkaloid;
tertiary alcohol
antineoplastic agent;
EC 5.99.1.2 (DNA topoisomerase) inhibitor;
genotoxin;
plant metabolite
2003200321.0low000100
irinotecancarbamate ester;
delta-lactone;
N-acylpiperidine;
pyranoindolizinoquinoline;
ring assembly;
tertiary alcohol;
tertiary amino compound
antineoplastic agent;
apoptosis inducer;
EC 5.99.1.2 (DNA topoisomerase) inhibitor;
prodrug
2003200321.0low000100
triptolidediterpenoid;
epoxide;
gamma-lactam;
organic heteroheptacyclic compound
antispermatogenic agent;
plant metabolite
2003202012.0high000130
tacrolimusmacrolide lactambacterial metabolite;
immunosuppressive agent
2005200618.7high000300
trelstar2005200519.0low000100
phenanthrenes2003202012.0high000130
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
Acute Kidney Failure02014201410.0low000010
Acute Kidney Injury02014201410.0low000010
Acute Lung Injury0201920195.0low000010
Age-Related Osteoporosis0202020204.0low000010
Arthritis, Rheumatoid0202020204.0low000010
Benign Neoplasms0202020204.0low000010
Bronchiolitis Obliterans02002200222.0low000100
Bronchiolitis, Exudative02002200222.0low000100
Cancer of Colon02003200321.0low000100
Cancer of Lung02003200321.0low000100
Cardiovascular Diseases0202020204.0low000010
Colonic Neoplasms02003200321.0low000100
Disease Models, Animal02002200222.0low000100
Graft vs Host Disease02000200223.0low001100
Graft-Versus-Host Disease02000200223.0low001100
Injury, Ischemia-Reperfusion0201920195.0low000010
Lung Injury, Acute0201920195.0low000010
Lung Injury, Ventilator-Induced02012201212.0low000010
Lung Neoplasms02003200321.0low000100
Neoplasms0202020204.0low000010
Osteoporosis0202020204.0low000010
Reperfusion Injury0201920195.0low000010
Rheumatoid Arthritis0202020204.0low000010
Sensitivity and Specificity02002200222.0low000100

Safety/Toxicity (1)

ArticleYear
The Study of Cellular Mechanism of Triptolide in the Treatment of Cancer, Bone Loss and Cardiovascular Disease and Triptolide's Toxicity.
Current stem cell research & therapy, , Volume: 15, Issue:1
2020

Dosage (2)

ArticleYear
Protective effects of PG490-88 on chronic allograft rejection by changing intragraft gene expression profiles.
Transplantation proceedings, , Volume: 37, Issue:4
2005
PG490-88, a derivative of triptolide, causes tumor regression and sensitizes tumors to chemotherapy.
Molecular cancer therapeutics, , Volume: 2, Issue:9
2003