UCSF

ZINC03833823

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
September 30th, 2005 24 No

Popular Name: Desoxycorticosterone Desoxycorticosterone

Find On: PubMed — Wikipedia — Google

CAS Numbers: , 64-85-7 , [64-85-7]

Other Names:

(8S,9S,10R,13S,14S,17S)-17-(2-Hydroxy-acetyl)-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-3-one

1,2(3H)-Deoxycorticosterone; 11-Dehydroxycorticosterone; 11-Deoxycorticosterone; 11-Desoxycorticosterone; 21-Hydroxy-4-pregnene-3,20-dione; 21-hydroxypregn-4-ene-3,20-dione; 21-hydroxyprogesterone; 4-Pregnen-21-ol-3,20-dione; Cortexone; Corticosterone, 11

1,2(3H)-Deoxycorticosterone; 11-Dehydroxycorticosterone; 11-Deoxycorticosterone; 11-Desoxycorticosterone; 21-Hydroxypregn-4-ene-3,20-dione; 21-Hydroxyprogesterone; 4-Pregnen-21-ol-3,20-dione; C21H30O3; Cortexone; Corticosterone, 11-deoxy-; DOC; Deoxycorto

11-Dehydroxycorticosterone; 11-Deoxy-Corticosterone; 11-Deoxycorticosterone; 11-Desoxycorticosterone; 21-Hydroxy-3,20-dioxopregn-4-ene; 21-Hydroxy-D4-pregnane-3,20-dione; 21-Hydroxy-D4-pregnene-3,20-dione; 21-Hydroxy-Pregn-4-ene-3,20-dione; 21-Hydroxy-Pro

11-Dehydroxycorticosterone;11-Deoxy-Corticosterone;11-Deoxycorticosterone;11-Desoxycorticosterone;21-Hydroxy-3,20-dioxopregn-4-ene;21-Hydroxy-D4-pregnane-3,20-dione;21-Hydroxy-D4-pregnene-3,20-dione;21-Hydroxy-Pregn-4-ene-3,20-dione;21-Hydroxy-Progesteron

11-deoxycorticosterone

11-Deoxycorticosterone; 21-Hydroxy-4-pregnene-3,20-dione; 64-85-7; C03205; Cortexone; DOC; Deoxycorticosterone; Desoxycortone

11-deoxycorticosterone; 21-hydroxy-4-pregnene-3,20-dione; cortexone; deoxycorticosterone

11-deoxycorticosterone; 21-hydroxyprogesterone; 4-pregnen-21-ol-3,20-dione; Kendall's desoxy compound B; Reichstein's substance Q; desoxycortone

21-Hydroxypregn-4-ene-3,20-dione

21-HYDROXYPROGESTERONE

64-85-7; D07792; Desoxycorticosterone; Desoxycortone (INN)

BRD-A77816529-001-01-4

BRD-K98521173-001-03-8

CHEBI:713; CHEBI:11314; CHEBI:39642; CHEBI:19123

Cortexon

Cortexone

Corthormon

Corticormon

Decortene

Deoxycorticosterone

Deoxycortone

Desoxycortone

Kendall's desoxy compound B

MFCD00003661

MFCD03225549

Ocriten

Ormosurrenol

pregn-4-ene-3,20-dione, 21-hydroxy-

Reichstein's substance Q

Download: MOL2 SDF SMILES Flexibase

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) 2.80 8.44 -13.86 1 3 0 54 330.468 2 ↓

Vendor Notes

Note Type Comments Provided By
UniProt Database Links 5BPOR_DIGLA; APC10_ARATH; APC10_BOVIN; APC10_DICDI; APC10_DROME; APC10_HUMAN; APC10_MOUSE; APC10_SCHPO; APC10_YEAST; CDKA1_HUMAN; CDKA1_MESAU; CDKA1_MOUSE; CDKA2_BOVIN; CDKA2_HUMAN; CDKA2_MOUSE; CP2C4_RABIT; CP2C5_RABIT; CPXM_BACME; CUL7_HUMAN; CUL7_MOUSE ChEBI
mechanism ACTH secretion inhibitor IBScreen Bioactives IBScreen Bioactives
mechanism ACTH secretion inhibitor; Gluconeogenesis promoter ZereneX Building Blocks
mechanism Gluconeogenesis promoter IBScreen Bioactives
mechanism Glycogen deposition inhibitor IBScreen Bioactives
biological_use Mineralocorticoid IBScreen Bioactives
biological_source Obt. by incubation of 9b,10a-pregn-4-ene-3,20-dione with Curvularia spp. ZereneX Building Blocks
Reactome Database Links REACT_10032; REACT_10117; REACT_13700; REACT_9966 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Endogenous sterols
Mineralocorticoid biosynthesis

Analogs ( Draw Identity 99% 90% 80% 70% )