Summary
SMILES: OC(=O)CCC(=O)OCC(=O)[C@@]1(O)CCC2C1(C)C[C@H](O)C1C2CCC2=CC(=O)CCC12C.[Na]InChI: InChI=1S/C25H34O8.Na/c1-23-9-7-15(26)11-14(23)3-4-16-17-8-10-25(32,24(17,2)12-18(27)22(16)23)19(28)13-33-21(31)6-5-20(29)30;/h11,16-18,22,27,32H,3-10,12-13H2,1-2H3,(H,29,30);/t16?,17?,18-,22?,23?,24?,25-;/m0./s1InChIKey: LGKJVUKNTHOZJH-QNHJWQTFSA-N
DeepSMILES: OC=O)CCC=O)OCC=O)[C@@]O)CCCC5C)C[C@H]O)CC6CCC=CC=O)CCC%106C.[Na]
Scaffold Graph/Node/Bond level: O=C1C=C2CCC3C4CCCC4CCC3C2CC1
Scaffold Graph/Node level: OC1CCC2C(CCC3C4CCCC4CCC23)C1
Scaffold Graph level: CC1CCC2C(CCC3C4CCCC4CCC23)C1
Functional groups: CC(=O)C=C(C)C; CC(=O)O; CC(C)=O; CO; COC(C)=O; [Na]
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Steroids and steroid derivatives
ClassyFire Subclass: Pregnane steroids
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Steroids
NP Classifier Class: Pregnane steroids
Synonymous chemical names:hydrocortisone sodium succinate
External chemical identifiers:CID:122130677
Chemical structure download