Summary

IMPPAT Phytochemical identifier: IMPHY002059

Phytochemical name: Hydrocortisone sodium succinate

Synonymous chemical names:
hydrocortisone sodium succinate

External chemical identifiers:
CID:122130677

---

Chemical structure information

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./s1

InChIKey:
LGKJVUKNTHOZJH-QNHJWQTFSA-N

DeepSMILES:
OC=O)CCC=O)OCC=O)[C@@]O)CCCC5C)C[C@H]O)CC6CCC=CC=O)CCC%106C.[Na]

Functional groups:
CC(=O)C=C(C)C, CC(=O)O, CC(C)=O, CO, COC(C)=O, [Na]

---

Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1C=C2CCC3C4CCCC4CCC3C2CC1

Scaffold Graph/Node level:
OC1CCC2C(CCC3C4CCCC4CCC23)C1

Scaffold Graph level:
CC1CCC2C(CCC3C4CCCC4CCC23)C1

---

Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Lipids and lipid-like molecules

ClassyFire Class: Steroids and steroid derivatives

ClassyFire Subclass: Pregnane steroids

NP Classifier Biosynthetic pathway: Terpenoids

NP Classifier Superclass: Steroids

NP Classifier Class: Pregnane steroids

NP-Likeness score: 1.739

---

Chemical structure download