Compound Summary

CORTICOSTERONE
  Compound Information
 CORTICOSTERONE

Compound Name:

CORTICOSTERONE

Compound CID:

5753

Synonyms:

CORTICOSTERONE

50-22-6

17-Deoxycortisol

Kendalls compound B"

Reichsteins substance H

More...

Iupac Name:

(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

InChI:

InChI=1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3/t14-,15-,16+,17-,19+,20-,21-/m0/s1

InChIKey:

OMFXVFTZEKFJBZ-HJTSIMOOSA-N

Canonical Smiles:

CC12CCC(=O)C=C1CCC3C2C(CC4(C3CCC4C(=O)CO)C)O

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

Molecular Weight:

346.5

Molecular Formula:

C21H30O4

  Compound Structure
 2D Structure:
 3D Structure:
  Computed Properties
 CORTICOSTERONE

Molecular Weight:

346.5

Molecular Formula:

C21H30O4

Hydrogen Bond Donor Count:

2

Hydrogen Bond Acceptor Count:

4

Rotatable Bond Count:

2

Heavy Atom Count:

25

Complexity:

638

  Synonyms
 CORTICOSTERONE

CORTICOSTERONE CORTICOSTERONE

CORTICOSTERONE

50-22-6

17-Deoxycortisol

Kendalls compound B"

Reichsteins substance H

Corticosteron

11beta,21-Dihydroxyprogesterone

Compound B

Reichsteins B

(11beta)-11,21-Dihydroxypregn-4-ene-3,20-dione

11-Hydroxycorticoaldosterone

11beta,21-Dihydroxy-4-pregnene-3,20-dione

4-Pregnene-11beta,21-diol-3,20-dione

11,21-Dihydroxyprogesterone

11Beta,21-dihydroxypregn-4-ene-3,20-dione

UNII-W980KJ009P

11-beta,21-Dihydroxypregn-3,20-dione

CHEBI:16827

NSC9705

4-Pregnene-11-beta,21-diol-3,20-dione

NSC-9705

Pregn-4-ene-3,20-dione, 11,21-dihydroxy-, (11beta)-

Pregn-4-ene-3,20-dione, 11beta,21-dihydroxy-

Pregn-4-ene-3,20-dione, 11-beta,21-dihydroxy-

(11-beta)-11,21-Dihydroxypregn-4-ene-3,20-dione

MLS000028536

CHEMBL110739

(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-dodecahydrocyclopentaaphenanthren-3-one

W980KJ009P

11.beta.,21-Dihydroxyprogesterone

Pregn-4-ene-3,20-dione, 11,21-dihydroxy-, (11b)-

NCGC00022472-05

SMR000058318

DSSTox_CID_2474

DSSTox_RID_76598

DSSTox_GSID_22474

(8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3H-cyclopentaaphenanthren-3-one

11,12-Dihydroxyprogesterone

CCRIS 6753

11-beta,21-Dihydroxyprogesterone

Compound B nach Kendall

SR-01000075748

NSC 9705

EINECS 200-019-6

Substanz H nach Reichstein

BRN 2339601

Cortico

Pregn-4-ene-3,20-dione, 11,21-dihydroxy-, (11.beta.)-

Compd B

CAS-50-22-6

Prestwick_672

Kendalls Compound B

11Beta,21-dihydroxy-4-prenene-3,20-dione

Corticosterone solution

Reichsteins Substance H

21-dihydroxyprogesterone

(11-BETA)-11,21-DIHYDROXY-PREGN-4-ENE-3,20-DIONE

Opera_ID_1519

Prestwick0_000432

Prestwick1_000432

Prestwick2_000432

Prestwick3_000432

Corticosterone, >=92%

11-.beta.,20-dione

bmse000669

Epitope ID:152207

BIDD:PXR0063

Lopac0_000220

SCHEMBL22612

BSPBio_000444

4-Pregnene-11 Corticosteron

MLS001074095

MLS001424305

11b,21-Dihydroxyprogesterone

BIDD:ER0495

SPBio_002383

BPBio1_000490

GTPL2869

DTXSID6022474

Corticosterone, BRN 2339601

4-Pregnene-11.beta.,20-dione

HMS1569G06

HMS2052G21

HMS2090A08

HMS2096G06

HMS2231F16

HMS3260L21

HMS3713G06

HMS3885H22

AMY22288

HY-B1618

Tox21_110879

Tox21_201366

Tox21_303642

Tox21_500220

6866AB

BDBM50170653

CMC_13412

HSCI1_000383

LMST02030186

MFCD00037715

s4752

STL564760

ZINC13513592

Corticosterone, >=98.5% (HPLC)

AKOS016008541

Tox21_110879_1

11-b,21-Dihydroxypregn-3,20-dione

ACN-036935

CCG-101146

CS-5105

DB04652

LP00220

MCULE-1874567277

NC00396

SDCCGSBI-0050208.P002

SMP1_000079

NCGC00022472-06

NCGC00022472-07

NCGC00022472-08

NCGC00022472-10

NCGC00022472-17

NCGC00091029-01

NCGC00256539-01

NCGC00258918-01

NCGC00260905-01

11|A

AS-75743

11,21-Dihydroxypregn-4-ene-3,20-dione

11-.beta.,21-Dihydroxypregn-3,20-dione

11b,21-Dihydroxy-4-pregnene-3,20-dione

Pregn-4-ene-3, 11.beta.,21-dihydroxy-

4-Pregnen-11.beta.,21-diol-3,20-dione

4-Pregnene-11.beta.,21-diol-3,20-dione

B7469

EU-0100220

Corticosterone 100 microg/mL in Acetonitrile

7061-EP2269977A2

7061-EP2270008A1

7061-EP2272835A1

7061-EP2272844A1

7061-EP2292228A1

7061-EP2292617A1

7061-EP2295411A1

7061-EP2301931A1

7061-EP2308851A1

C 2505

C02140

D94656

Preg-4-ene-3,20-dione,11-b,21-dihydroxy-

11.beta.,21-dihydroxypregn-4-ene-3,20-dione

Corticosterone, VETRANAL(TM), analytical standard

Q422543

SR-01000000082

(11?)-11,21-Dihydroxypregn-4-ene-3,20-dione

Pregn-4-ene-3,20-dione, 11.beta.,21-dihydroxy-

SR-01000000082-3

SR-01000075748-1

SR-01000075748-4

W-105977

WLN: L E5 B666 OV MUTJ A1 CQ E1 FV1Q

(11beta)-11,21-Dihydroxypregn-4-ene-3,2 0-dione

BRD-K73589401-001-04-6

Pregn-4-ene-3, 11,21-dihydroxy-, (11.beta.)-

(11.beta.)-11,21-Dihydroxypregn-4-ene-3,20-dione

(9beta,11alpha)-11,21-dihydroxypregn-4-ene-3,20-dione

11,21-Dihydroxypregn-4-ene-3,20-dione, (11.beta.)- #

4793EB71-D789-498E-B641-C5C1C377B9FF

17-Deoxycortisol;11|A,21-Dihydroxyprogesterone;Kendalls compound B

Pregn-4-ene-3,20-dione, 11,21-dihydroxy-, (11-beta)- (9CI)

Kendalls Compound B; 4-Pregnene-11beta,21-diol-3,20-dione; Reichsteins Substance H

Corticosterone solution, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material
  Experimental Data
 CORTICOSTERONE

Species Dose Unit Control(Avg days) Treatment(Avg days) Avg/Med Lifespan Change(%) Control(Max days) Treatment(Max days) Max Lifespan Change(%) Significant Strain Gender PubMed Avg/Med Lifespan Change tab
Caenorhabditis elegans 33.000000000000000 umol/L -2.000000000000000 NS N2 24134630 Inactive
  Experimental Data Visualization
 CORTICOSTERONE

  Statistics Data
 CORTICOSTERONE

Species Avg/Med Lifespan Change(%) Max Lifespan Change(%) Count Reference Count Data point
Caenorhabditis elegans -2.000000000000000 1 1
  Statistics Data Visualization
 CORTICOSTERONE

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