Summary

SMILES: O=C1O[C@@H]2[C@@]([C@@H]1C)(O)[C@@]13[C@]4([C@H]2O)[C@H](OC3=O)[C@@H]([C@H]([C@@]24C(O1)OC(=O)[C@@H]2O)C(C)(C)C)O
InChI: InChI=1S/C20H24O11/c1-5-12(24)28-11-8(22)18-10-6(21)7(16(2,3)4)17(18)9(23)13(25)30-15(17)31-20(18,14(26)29-10)19(5,11)27/h5-11,15,21-23,27H,1-4H3/t5-,6-,7+,8+,9+,10-,11+,15?,17+,18-,19-,20-/m1/s1
InChIKey: AMOGMTLMADGEOQ-BSJQODTGSA-N
DeepSMILES: O=CO[C@@H][C@@][C@@H]5C))O)[C@][C@][C@H]5O))[C@H]OC5=O)))[C@@H][C@H][C@]5CO8)OC=O)[C@@H]5O))))))CC)C)C)))O
Scaffold Graph/Node/Bond level: O=C1CC2C(CC34C5CCC36CC(=O)OC6OC24C(=O)O5)O1
Scaffold Graph/Node level: OC1CC2C(CC34C5CCC36CC(O)OC6OC24C(O)O5)O1
Scaffold Graph level: CC1CC2CC34C5CCC36CC(C)CC6CC4(C(C)C5)C2C1
Functional groups: COC(=O)C; CO; COC1CCC(=O)O1

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Chemical classification

ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like molecules
ClassyFire Class: Prenol lipids
ClassyFire Subclass: Terpene lactones
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Sesquiterpenoids
NP Classifier Class: Picrotoxane sesquiterpenoids

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Synonymous chemical names:
ginkgolide c

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External chemical identifiers:
CID:CID_102004391; MolPort-039-052-356

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Chemical structure download