Summary
IMPPAT Phytochemical identifier: IMPHY010010
Phytochemical name: Jurubin
Synonymous chemical names:25s-3β-amino-5α-furostane-22α,26-diol-o(26)-β-d-glucopyranoside (jurubine)
External chemical identifiers:CID:12304762
Chemical structure information
SMILES:
OC[C@H]1O[C@@H](OC[C@H](CC[C@@]2(O)O[C@@H]3[C@H]([C@@H]2C)[C@@]2([C@@H](C3)[C@@H]3CC[C@@H]4[C@]([C@H]3CC2)(C)CC[C@@H](C4)N)C)C)[C@@H]([C@H]([C@@H]1O)O)OInChI:
InChI=1S/C33H57NO8/c1-17(16-40-30-29(38)28(37)27(36)25(15-35)41-30)7-12-33(39)18(2)26-24(42-33)14-23-21-6-5-19-13-20(34)8-10-31(19,3)22(21)9-11-32(23,26)4/h17-30,35-39H,5-16,34H2,1-4H3/t17-,18-,19-,20-,21+,22-,23-,24-,25+,26-,27+,28-,29+,30+,31-,32-,33+/m0/s1InChIKey:
YEWUMIMAJWFDQG-YHLUJPQISA-NDeepSMILES:
OC[C@H]O[C@@H]OC[C@H]CC[C@@]O)O[C@@H][C@H][C@@H]5C))[C@@][C@@H]C5)[C@@H]CC[C@@H][C@][C@H]6CC%10)))C)CC[C@@H]C6)N))))))))))C))))))))C))))[C@@H][C@H][C@@H]6O))O))OFunctional groups:
CN, CO, CO[C@@H](C)OC, C[C@@](C)(O)OC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
C(CCC1CC2C(CC3C2CCC2C4CCCCC4CCC23)O1)COC1CCCCO1Scaffold Graph/Node level:
C(CCC1CC2C(CC3C2CCC2C4CCCCC4CCC23)O1)COC1CCCCO1Scaffold Graph level:
C1CCC(CCCCCC2CC3CC4C(CCC5C6CCCCC6CCC54)C3C2)CC1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire 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: Furostane steroids
NP-Likeness score: 2.742
Chemical structure download