corticosterone (Q422543)

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chemical compound
  • 11beta,21-dihydroxyprogesterone
  • 17-deoxycortisol
  • (11beta)-11,21-dihydroxypregn-4-ene-3,20-dione
  • (1S,2R,10S,11S,14S,15S,17S)-17-hydroxy-14-(2-hydroxyacetyl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one
  • 11,21-Dihydroxyprogesterone
  • 11,21-Dihydroxypregn-4-ene-3,20-dione
  • 4-Pregnene-11 Corticosteron
  • 11-Hydroxycorticoaldosterone
  • (8S,9S,10R,11S,13S,14S,17S)-17-glycoloyl-11-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • (8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-17-(2-hydroxyethanoyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • (8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • (8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-17-(2-hydroxy-1-oxoethyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • (11β)-11,21-dihydroxypregn-4-ene-3,20-dione
  • 11beta,21-Dihydroxy-4-pregnene-3,20-dione
  • Reichstein's substance H
  • 11β,21-dihydroxyprogesterone
  • Corticosterone
  • Kendall's compound B
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Language Label Description Also known as
English
corticosterone
chemical compound
  • 11beta,21-dihydroxyprogesterone
  • 17-deoxycortisol
  • (11beta)-11,21-dihydroxypregn-4-ene-3,20-dione
  • (1S,2R,10S,11S,14S,15S,17S)-17-hydroxy-14-(2-hydroxyacetyl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one
  • 11,21-Dihydroxyprogesterone
  • 11,21-Dihydroxypregn-4-ene-3,20-dione
  • 4-Pregnene-11 Corticosteron
  • 11-Hydroxycorticoaldosterone
  • (8S,9S,10R,11S,13S,14S,17S)-17-glycoloyl-11-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • (8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-17-(2-hydroxyethanoyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • (8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • (8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-17-(2-hydroxy-1-oxoethyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • (11β)-11,21-dihydroxypregn-4-ene-3,20-dione
  • 11beta,21-Dihydroxy-4-pregnene-3,20-dione
  • Reichstein's substance H
  • 11β,21-dihydroxyprogesterone
  • Corticosterone
  • Kendall's compound B

Statements

subclass of
pregnane steroid
0 references
steroid
0 references
chemical structure
Corticosterone-2D-skeletal.svg
512 × 358; 5 KB
0 references
mass
346.214 dalton
1 reference
stated in
PubChem
PubChem CID
5753
language of work or name
English
title
50-22-6 (English)
retrieved
19 October 2016
chemical formula
C₂₁H₃₀O₄
1 reference
stated in
PubChem
PubChem CID
5753
language of work or name
English
title
50-22-6 (English)
retrieved
19 October 2016
canonical SMILES
CC12CCC(=O)C=C1CCC3C2C(CC4(C3CCC4C(=O)CO)C)O
1 reference
stated in
PubChem
PubChem CID
5753
language of work or name
English
title
50-22-6 (English)
retrieved
19 October 2016
isomeric SMILES
C[C@]12CCC(=O)C=C1CC[C@@H]3[C@@H]2[C@H](C[C@]4([C@H]3CC[C@@H]4C(=O)CO)C)O
1 reference
stated in
PubChem
PubChem CID
5753
language of work or name
English
title
50-22-6 (English)
retrieved
19 October 2016
has part(s)
carbon
0 references
Commons category
Corticosterone
0 references

Identifiers

Reaxys registry number
2339601
1 reference
stated in
ChEBI
ChEBI ID
16827
language of work or name
English
title
corticosterone (English)
retrieved
19 October 2016
NSC number
9705
0 references
AGROVOC ID
c_10123
0 references
MeSH descriptor ID
D003345
subject named as
Corticosterone
0 references
KEGG ID
C02140
0 references
PDB ligand ID
C0R
0 references
CAB ID
113522
1 reference
stated in
CAB Thesaurus
retrieved
6 April 2020
Elhuyar ZTH ID
132055
0 references
WordNet 3.1 Synset ID
14770070-n
0 references
YSO ID
23119
subject named as
kortikosteroni
kortikosteron
corticosterone
1 reference
stated in
YSO-Wikidata mapping project
retrieved
2 February 2022
 
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