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SB-T-1212 ID: ALA339531
PubChem CID: 9940743
Max Phase: Preclinical
Molecular Formula: C43H57NO15
Molecular Weight: 827.92
Molecule Type: Small molecule
This compound is available for customization.
Associated Items:
Names and Identifiers Synonyms: SB-T-1212 | SB-T-1212|CHEMBL339531|SCHEMBL12168467
Canonical SMILES: CC(=O)O[C@H]1C(=O)[C@@]2(C)[C@H]([C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@H](C=C(C)C)NC(=O)OC(C)(C)C)C(C)=C1C3(C)C)[C@]1(OC(C)=O)CO[C@@H]1C[C@@H]2O
Standard InChI: InChI=1S/C43H57NO15/c1-21(2)17-26(44-38(52)59-39(6,7)8)31(48)37(51)56-27-19-43(53)35(57-36(50)25-15-13-12-14-16-25)33-41(11,28(47)18-29-42(33,20-54-29)58-24(5)46)34(49)32(55-23(4)45)30(22(27)3)40(43,9)10/h12-17,26-29,31-33,35,47-48,53H,18-20H2,1-11H3,(H,44,52)/t26-,27-,28-,29+,31+,32+,33-,35-,41+,42-,43+/m0/s1
Standard InChI Key: NRISGROGJFACOP-LYEXFJIESA-N
Molfile:
RDKit 2D
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M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 827.92Molecular Weight (Monoisotopic): 827.3728AlogP: 3.42#Rotatable Bonds: 9Polar Surface Area: 230.52Molecular Species: NEUTRALHBA: 15HBD: 4#RO5 Violations: 2HBA (Lipinski): 16HBD (Lipinski): 4#RO5 Violations (Lipinski): 2CX Acidic pKa: 11.95CX Basic pKa: ┄CX LogP: 2.99CX LogD: 2.99Aromatic Rings: 1Heavy Atoms: 59QED Weighted: 0.16Np Likeness Score: 2.13
References 1. Ojima I, Duclos O, Kuduk SD, Sun C, Slater JC, Lavelle F, Veith JM, Bernacki RJ. (1994) Synthesis and biological activity of 3-alkyl- and 3-alkenyl-3-dephenyldocetaxels, 4 (21): [10.1016/S0960-894X(01)80298-5 ] 2. Ojima I, Kuduk SD, Pera P, Veith JM, Bernacki RJ.. (1997) Synthesis and structure-activity relationships of nonaromatic taxoids: effects of alkyl and alkenyl ester groups on cytotoxicity., 40 (3): [PMID:9022794 ] [10.1021/jm9606711 ] 3. Ojima I, Slater JC, Michaud E, Kuduk SD, Bounaud PY, Vrignaud P, Bissery MC, Veith JM, Pera P, Bernacki RJ.. (1996) Syntheses and structure-activity relationships of the second-generation antitumor taxoids: exceptional activity against drug-resistant cancer cells., 39 (20): [PMID:8831755 ] [10.1021/jm9604080 ]