Summary
SMILES: CC[C@]12C=CCN3[C@@H]2[C@@]2([C@H]([C@@]([C@@H]1OC(=O)C)(O)C(=O)OC)N(c1c2cc(c(c1)OC)[C@@]1(C(=O)OC)C2OC4(C[C@H]2CN(C4)CCc2c1[nH]c1c2cccc1)CC)C)CC3InChI: InChI=1S/C46H56N4O9/c1-8-42-23-27-24-49(25-42)19-15-29-28-13-10-11-14-32(28)47-35(29)45(36(27)59-42,40(52)56-6)31-21-30-33(22-34(31)55-5)48(4)38-44(30)17-20-50-18-12-16-43(9-2,37(44)50)39(58-26(3)51)46(38,54)41(53)57-7/h10-14,16,21-22,27,36-39,47,54H,8-9,15,17-20,23-25H2,1-7H3/t27-,36?,37-,38+,39+,42?,43+,44+,45-,46-/m0/s1InChIKey: KMWVJRBQGMUMID-CIASJWMASA-N
DeepSMILES: CC[C@@]C=CCN[C@@H]6[C@@][C@H][C@@][C@@H]%10OC=O)C))))O)C=O)OC))))Ncc5cccc6)OC)))[C@@]C=O)OC)))COCC[C@H]5CNC6)CCcc%12[nH]cc5cccc6)))))))))))))))CC))))))))))C)))CC5
Scaffold Graph/Node/Bond level: C1=CC2CCC3Nc4ccc(C5c6[nH]c7ccccc7c6CCN6CC7CC(C6)C5O7)cc4C34CCN(C1)C24
Scaffold Graph/Node level: C1CCC2C(C1)NC1C2CCN2CC3CC(C2)C(O3)C1C1CCC2NC3CCC4CCCN5CCC3(C2C1)C45
Scaffold Graph level: C1CCC2C(C1)CC1C2CCC2CC3CC(C2)C(C3)C1C1CCC2CC3CCC4CCCC5CCC3(C2C1)C45
Functional groups: CC(=O)OC; CC=CC; CN(C)C; CO; COC; COC(C)=O; cN(C)C; cOC; c[nH]c
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Alkaloids and derivativesClassyFire Class: Vinca alkaloids
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Tryptophan alkaloids
NP Classifier Class: Aspidosperma type|Aspidosperma-Iboga hybrid type (Vinca alkaloids)
Synonymous chemical names:catharanthamine
External chemical identifiers:CID:327791
Chemical structure download