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Corticosterone

pharmaceutical raw materials
Corticosterone structure

Corticosterone 

structure
  • CAS No:

    50-22-6

  • Formula:

    C21H30O4

  • Chemical Name:

    Corticosterone

  • Synonyms:

    Pregn-4-ene-3,20-dione,11,21-dihydroxy-,(11β)-;Corticosterone;(11β)-11,21-Dihydroxypregn-4-ene-3,20-dione;11,21-Dihydroxyprogesterone;Kendall's compound B;4-Pregnene-11β,21-diol-3,20-dione;Reichstein's substance H;17-Deoxycortisol;11β,21-Dihydroxypregn-4-ene-3,20-dione;11-Hydroxycorticoaldosterone;11β,21-Dihydroxyprogesterone;Corticosteron;NSC 9705;67085-09-0;74339-96-1;1050677-95-6

  • Categories:

    Active Pharmaceutical Ingredients  >  Antibiotics

Description

Corticosterone is an adrenocortical steroid that has modest but significant activities as a mineralocorticoid and a glucocorticoid.


Solid


Corticosterone is a 21-hydroxy steroid that consists of pregn-4-ene substituted by hydroxy groups at positions 11 and 21 and oxo groups at positions 3 and 20. Corticosterone is a 21-carbon steroid hormone of the corticosteroid type produced in the cortex of the adrenal glands. It has a role as a human metabolite and a mouse metabolite. It is an 11beta-hydroxy steroid, a 21-hydroxy steroid, a 20-oxo steroid, a C21-steroid, a 3-oxo-Delta(4) steroid, a primary alpha-hydroxy ketone and a glucocorticoid. It derives from a hydride of a pregnane.|An adrenocortical steroid that has modest but significant activities as a mineralocorticoid and a glucocorticoid. (From Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed, p1437)|Corticosterone is a corticosteroid intermediate in the steroidogenic pathway that converts pregnenolone to aldosterone. In humans, corticosterone has limited glucocorticoid or mineralocorticoid activity.

Corticosterone Basic Attributes

346.46100

346.46

200-019-6

W980KJ009P

9705

DTXSID6022474

C393

29372900

Characteristics

74.60000

2.66670

Solid

1.21g/cm3

181 °C

529.2ºC at 760mmHg

288ºC

1.575

240.5mg/L(37 ºC)

Store at RT

186.8 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|186.46 Ų [M-H]- [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|186.9 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|208.4 Ų [M+K]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|211.8 Ų [M+Na]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|186.8 Ų [M-H]- [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|186.8 Ų [M-H]-

Safety Information

NONH for all modes of transport

3

R43

36-22

GM7650000

Xi; N; Xn; T

Stable, but light sensitive. Incompatible with strong oxidizing agents.

P280

H317

|Warning|H317 (97.5%): May cause an allergic skin reaction [Warning Sensitization, Skin]|P261, P272, P280, P302+P352, P321, P333+P313, P363, and P501|Aggregated GHS information provided by 40 companies from 2 notifications to the ECHA C&L Inventory.

Drug Information

Substances that reduce or suppress INFLAMMATION. (See all compounds classified as Anti-Inflammatory Agents.)

Corticosterone

Corticosterone Use and Manufacturing

Uses

1. Glucocorticoid; an intermediate in the biosynthesis of aldosterone, isolated from the adrenal cortex.
2. Corticosteroid is an activator of MCR.

Lipids -> Sterol Lipids [ST] -> Steroids [ST02] -> C21 steroids (gluco/mineralocorticoids, progestogins) and derivatives [ST0203]|Pharmaceuticals

Computed Properties

Molecular Weight:346.5
XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:346.21440943
Monoisotopic Mass:346.21440943
Topological Polar Surface Area:74.6
Heavy Atom Count:25
Complexity:638
Defined Atom Stereocenter Count:7
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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