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CN

P8629

5β-Pregnane-3α,17α,20α-triol

≥98.00% (TLC), Inactive progestrone metabolite, powder

Synonym(s):

3α,17α,20α-Trihydroxy-5β-pregnane, Pregnanetriol

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About This Item

Empirical Formula (Hill Notation):
C21H36O3
CAS Number:
1098-45-9
Molecular Weight:
336.51
NACRES:
NA.77
PubChem Substance ID:
24898959
UNSPSC Code:
12352202
EC Number:
214-148-0
MDL number:
MFCD00003678
Beilstein/REAXYS Number:
2619975
Assay:
≥98.00% (TLC)
Form:
powder
Quality level:
200

Key Documents

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Product Name

5β-Pregnane-3α,17α,20α-triol,

assay

≥98.00% (TLC)

Quality Level

200

form

powder

solubility

chloroform: methanol (1:1): 19.60-20.40 mg/mL, clear, colorless

shipped in

ambient

storage temp.

room temp

SMILES string

[H][C@]12CC[C@]3([H])[C@]([H])(CC[C@@]4(C)[C@@]3([H])CC[C@]4(O)[C@H](C)O)[C@@]1(C)CC[C@@H](O)C2

InChI

1S/C21H36O3/c1-13(22)21(24)11-8-18-16-5-4-14-12-15(23)6-9-19(14,2)17(16)7-10-20(18,21)3/h13-18,22-24H,4-12H2,1-3H3/t13-,14+,15+,16+,17-,18-,19-,20-,21-/m0/s1

InChI key

SCPADBBISMMJAW-UHHUKTEYSA-N

Related Categories

General description

5β-Pregnane-3α,17α,20α-triol (pregnanetriol) is a urinary steroid metabolite of 17α-hydroxyprogesterone.

Biochem/physiol Actions

5β-Pregnane-3α,17α,20α-triol (pregnanetriol) plays a role in the synthesis of adrenal corticoids. Levels of pregnanetriol are elevated in the urine of 21-hydroxylase deficiency and congenital adrenal hyperplasia (CAH) patients.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

涉药品监管产品

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Certificates of Analysis (COA)

Lot/Batch Number
0000192511
0000188064
0000192511
0000188064
0000128630

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A V Canario et al.
General and comparative endocrinology, 83(2), 258-264 (1991-08-01)
In a previous study, plasma sex steroid levels were measured in female dab (Limanda limanda) induced to ovulate by injections of human chorionic gonadotrophin (HCG). In the present study, a similar experiment was carried out on male dabs. In common
A V Canario et al.
General and comparative endocrinology, 76(1), 147-158 (1989-10-01)
Dab (Limanda limanda) ovarian fragments were incubated in vitro with either [4,7-3H]pregnenolone or 17 alpha-hydroxy[1,2,6,7-3H]progesterone to investigate the pattern of steroidogenesis. A major enzyme found in the dab ovary was 20 alpha-hydroxysteroid dehydrogenase. Among the steroids that were tentatively identified
Toshihiko Takada et al.
Gut microbes, 11(6), 1662-1676 (2020-06-20)
Probiotic products have been shown to have beneficial effects on human hosts, but what happens in the gastrointestinal tract after its ingestion remains unclear. Our aim was to investigate the changes within the small intestines after a single intake of

Global Trade Item Number

SKUGTIN
P8629-100MG04061832851310

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