trabectedin
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trabectedin
Summary
trabectedin is a type of chemical entity[1]. trabectedin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (53 views/month).[2]
Key Facts
- trabectedin's instance of is recorded as type of chemical entity[3].
- trabectedin's physically interacts with is recorded as Nuclear receptor subfamily 1, group I, member 2[4].
- trabectedin's canonical SMILES is recorded as CC1=C(C(=C2C3C4C5C6=C(C(N4C(C(N3C)CC2=C1)O)COC(=O)C7(CS5)C8=CC(=C(C=C8CCN7)O)OC)C9=C(C(=C6OC(=O)C)C)OCO9)O)OC[5].
- trabectedin's canonical SMILES is recorded as O=C(OC=1C(=C2OCOC2=C3C1C4SCC5(NCCC6=CC(O)=C(OC)C=C65)C(=O)OCC3N7C(O)C8N(C)C(C9=C(O)C(OC)=C(C=C9C8)C)C74)C)C[6].
- trabectedin's chemical formula is recorded as C₃₉H₄₃N₃O₁₁S[7].
- trabectedin is a type of 5,6',12-trihydroxy-6,7'-dimethoxy-7,21,30-trimethyl-27-oxo-3',4'-dihydro-2'H-17,19,28-trioxa-24-thia-13,30-diazaspiro[heptacyclo[12.9.6.1³,¹¹.0²,¹³.0⁴,⁹.0¹⁵,²³.0¹⁶,²⁰]triacontane-26,1'-isoquinoline]-4,6,8,15,20,22-hexaen-22-yl acetate[8].
- trabectedin is a type of CID 372978[9].
- trabectedin is used for medication[10].
- trabectedin's Commons category is recorded as Trabectedin[11].
- trabectedin's found in taxon is recorded as Ecteinascidia turbinata[12].
- trabectedin's isomeric SMILES is recorded as CC1=C(C(=C2[C@@H]3[C@@H]4[C@H]5C6=C(C@@HCOC(=O)[C@@]7(CS5)C8=CC(=C(C=C8CCN7)O)OC)C9=C(C(=C6OC(=O)C)C)OCO9)O)OCC@@HCOC(=O)[C@@]7(CS5)C8=CC(=C(C=C8CCN7)O)OC)C9=C(C(=C6OC(=O)C)C)OCO9)O)OC">[13].
- trabectedin's isomeric SMILES is recorded as COc1cc2c(cc1O)CCN[C@@]21CS[C@@H]2c3c(OC(C)=O)c(C)c4c(c3C@HN1C@@H[C@@H]3Cc5cc(C)c(OC)c(O)c5C@HN3C)OCO4C@HN1C@@H[C@@H]3Cc5cc(C)c(OC)c(O)c5C@HN3C)OCO4">[14].
- trabectedin's mass is recorded as {'unit': 'Q483261', 'amount': '+761.262'}[15].
- trabectedin's mass is recorded as {'unit': 'Q483261', 'amount': '+761.261830196'}[16].
- trabectedin's World Health Organisation international non-proprietary name is recorded as {'lang': 'en', 'text': 'trabectedin'}[17].
- trabectedin's subject has role is recorded as alkylating agent[18].
- trabectedin's subject has role is recorded as alkylating antineoplastic agent[19].
- trabectedin's stereoisomer of is recorded as Q105210696[20].
- trabectedin's active ingredient in is recorded as Yondelis[21].
- trabectedin's has active ingredient is recorded as Trabectedin[22].
Why It Matters
trabectedin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (53 views/month).[2] trabectedin has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[23] trabectedin is known by 14 alternative names across languages and contexts.[24]