Hydrocortisone Hemisuccinate Anhydrous
drug drugOn this page
Also known as NSC-7576Oristar hcshsHydrocortisone hemisuccinateSID855704SID56422426C0164806hydrocortisone succinate
Summary
Hydrocortisone Hemisuccinate Anhydrous (CHEMBL977) is an approved small molecule.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- Clinical trials: 1
- Chemistry: 462.5 Da · C25H34O8
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL977 |
| Name | Hydrocortisone Hemisuccinate Anhydrous |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 16623 |
| ChEBI | CHEBI:31677 |
| Molecular formula | C25H34O8 |
| Molecular weight | 462.5 |
| InChIKey | VWQWXZAWFPZJDA-CGVGKPPMSA-N |
SMILES: C[C@]12CCC(=O)C=C1CC[C@@H]3[C@@H]2[C@H](C[C@]4([C@H]3CC[C@@]4(C(=O)COC(=O)CCC(=O)O)O)C)O
IUPAC name: 4-[2-[(8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-oxoethoxy]-4-oxobutanoic acid
ChEBI definition: A derivative of succinic acid in which one of the carboxy groups is esterified by the C-21 hydroxy group of cortisol (hydrocortisone).
Also known as: Hydrocortisone hemisuccinate anhydrous, NSC-7576, Oristar hcshs, Hydrocortisone hemisuccinate, SID855704, SID56422426, HYDROCORTISONE HEMISUCCINATE, HYDROCORTISONE HEMISUCCINATE ANHYDROUS, C0164806, hydrocortisone succinate
Parent form; salt/anhydrous children: CHEMBL1200495, CHEMBL3989663
Patent coverage: 784 distinct patent families (2,639 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 4 (assay-derived). Sample: Survival motor neuron protein, Beta-lactamase, Glucocorticoid receptor, Hypoxia-inducible factor 1-alpha.
Bioactivity
ChEMBL activities: 5 potent at pChembl ≥ 5 of 5 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P06537 | 6.72 | Kd | 190 | nM | CHEMBL_ACT_14698041 |
| P00811 | 6.2 | Potency | 631 | nM | CHEMBL_ACT_4630788 |
| HIF1A | 6.1 | Potency | 794.3 | nM | CHEMBL_ACT_4127901 |
| HIF1A | 6.1 | Potency | 794.3 | nM | CHEMBL_ACT_4520510 |
| SMN1 | 5.9 | Potency | 1259 | nM | CHEMBL_ACT_3882835 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
0 indication records carry no mapped disease name (EFO/MeSH-only); none shown.
Clinical trials
Total trials: 1.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02768740 | PHASE4 | COMPLETED | Hydrocortisone 50 mg Every 6 Hours Compared to Hydrocortisone 300 mg Per Day in Treatment of Septic Shock. |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.