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D4000

trans-Dehydroandrosterone

≥99%

Synonym(s):

3β-Hydroxy-5-androsten-17-one, 5-Androsten-3β-ol-17-one, DHEA, Dehydroepiandrosterone, Dehydroisoandrosterone, Prasterone

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Size/SKUAvailabilityPrice
10 g
Please contact Customer Service for Availability
4 600,00 CZK
3 772,00 CZK
25 g
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10 200,00 CZK
8 364,00 CZK
250 g
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69 400,00 CZK
56 908,00 CZK

About This Item

Empirical Formula (Hill Notation):
C19H28O2
CAS Number:
Molecular Weight:
288.42
UNSPSC Code:
51111800
NACRES:
NA.77
PubChem Substance ID:
EC Number:
200-175-5
Beilstein/REAXYS Number:
2058110
MDL number:
Biological source:
synthetic (organic)
Form:
crystalline powder
Assay:
≥99%

3 772,00 CZK

List Price4 600,00 CZKSave 18%

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biological source

synthetic (organic)

Quality Segment

assay

≥99%

form

crystalline powder

drug control

Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada

mp

149-151 °C (lit.)

solubility

chloroform: 50 mg/mL, clear, colorless

shipped in

ambient

storage temp.

room temp

SMILES string

C[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O)CC[C@]34C)[C@@H]1CCC2=O

InChI

1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3,13-16,20H,4-11H2,1-2H3/t13-,14-,15-,16-,18-,19-/m0/s1

InChI key

FMGSKLZLMKYGDP-USOAJAOKSA-N

Biochem/physiol Actions

Dehydroandrosterone (DHEA) is a negative modulator of GABAA receptors. It is a steroid secreted by the adrenal gland with both estrogenic and androgenic properties. DHEAs conversion to 5-androstenediol, a potent estrogen, enhances the growth and survival of estrogen-sensitive breast tumors.
Negative modulator of GABAA receptors. Steroid secreted by the adrenal gland with both estrogenic and androgenic properties. Its conversion to 5-androstenediol, a potent estrogen, enhances the growth and survival of estrogen-sensitive breast tumors.
Negative modulator of GABAA receptors. Steroid secreted by the adrenal gland with both estrogenic and androgenic properties. Its conversion to 5-androstenediol, a potent estrogen, enhances the growth and survival of estrogen-sensitive breast tumors. At high but physiologically valid concentrations, DHEA inhibits proliferation of chromaffin progenitor cells and induces dopaminergic differentiation.

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This Item
252805700087PE3375
description

≥99%

description

Major secretory steroidal product of the adrenal gland.

description

Avanti Research™ - A Croda Brand

description

-

biological source

synthetic (organic)

biological source

-

biological source

-

biological source

synthetic (organic)

assay

≥99%

assay

≥97% (HPLC)

assay

>99% (TLC)

assay

≥98% (HPLC)

Quality Level

200

Quality Level

100

Quality Level

-

Quality Level

200

form

crystalline powder

form

powder

form

powder

form

powder

Gene Information

human ... GABRA1(2554), GABRA2(2555), GABRA3(2556), GABRA4(2557), GABRA5(2558), GABRA6(2559), GABRB1(2560), GABRB2(2561), GABRB3(2562), SERPINA6(866)
rat ... Ar(24208)

Gene Information

-

Gene Information

-

Gene Information

human ... HSD17B3(3293)

shipped in

ambient

shipped in

ambient

shipped in

dry ice

shipped in

ambient


Pictograms

Health hazard

Signal Word

Warning

Hazard Codes

Hazard Classifications

Repr. 2

Storage Class

11 - Combustible Solids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

PPE (personal protective equipment)

dust mask type N95 (US), Eyeshields, Gloves



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