Summary
SMILES: CO[C@H]1C[C@H](O[C@H]2CC[C@]3([C@H](C2)CC[C@@]2([C@@H]3C[C@@H](O)[C@]3([C@]2(O)CC[C@@]3(O)[C@@H](OC(=O)C)C)C)O)C)O[C@@H]([C@H]1O[C@H]1C[C@H](OC)[C@@H]([C@H](O1)C)O[C@@H]1O[C@H](C)[C@H]([C@@H]([C@H]1O)OC)O)CInChI: InChI=1S/C44H74O17/c1-21-34(47)38(54-10)35(48)39(57-21)61-37-23(3)56-33(19-29(37)53-9)60-36-22(2)55-32(18-28(36)52-8)59-27-12-13-40(6)26(17-27)11-14-43(50)30(40)20-31(46)41(7)42(49,15-16-44(41,43)51)24(4)58-25(5)45/h21-24,26-39,46-51H,11-20H2,1-10H3/t21-,22-,23-,24+,26+,27+,28+,29+,30-,31-,32+,33+,34-,35-,36-,37-,38+,39+,40+,41-,42-,43+,44-/m1/s1InChIKey: BBPXSUILPKNQKJ-XVMVROSKSA-N
DeepSMILES: CO[C@H]C[C@H]O[C@H]CC[C@][C@H]C6)CC[C@@][C@@H]6C[C@@H]O)[C@][C@]6O)CC[C@@]5O)[C@@H]OC=O)C)))C))))))C)))))O)))))C))))))O[C@@H][C@H]6O[C@H]C[C@H]OC))[C@@H][C@H]O6)C))O[C@@H]O[C@H]C)[C@H][C@@H][C@H]6O))OC)))O))))))))))))C
Scaffold Graph/Node/Bond level: C1CCC(OC2CCC(OC3CCC(OC4CCC5C(CCC6C7CCCC7CCC56)C4)OC3)OC2)OC1
Scaffold Graph/Node level: C1CCC(OC2CCC(OC3CCC(OC4CCC5C(CCC6C7CCCC7CCC56)C4)OC3)OC2)OC1
Scaffold Graph level: C1CCC(CC2CCC(CC3CCC(CC4CCC5C(CCC6C7CCCC7CCC56)C4)CC3)CC2)CC1
Functional groups: CC(=O)OC; CO; COC; CO[C@@H](C)OC; C[C@H](OC)OC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Steroids and steroid derivatives
ClassyFire Subclass: Steroidal glycosides
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Steroids
NP Classifier Class: Pregnane steroids
Synonymous chemical names:tenacissoside m
External chemical identifiers:CID:11622059; ZINC:ZINC000255197666
Chemical structure download
