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PREMARIN, also known as Estrone Sulfate, is a steroid sulfate that serves as a precursor to estrogen. It is a circulating steroid found in men, non-pregnant women, and post-menopausal women. PREMARIN plays a crucial role in the hormonal balance and overall health of individuals.

481-97-0

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481-97-0 Usage

Uses

Used in Pharmaceutical Industry:
PREMARIN is used as a hormone replacement therapy for post-menopausal women. It helps alleviate symptoms associated with menopause, such as hot flashes, night sweats, and vaginal dryness. Additionally, it can be used to prevent osteoporosis and reduce the risk of heart disease in post-menopausal women.
Used in Hormone Regulation:
PREMARIN is used as a hormone regulator in both men and non-pregnant women. It helps maintain hormonal balance and supports overall health by providing the necessary precursor to estrogen.
Used in Research and Development:
As a precursor to estrogen, PREMARIN is also used in research and development for the study of hormonal effects and the development of new medications related to hormone regulation and treatment of hormone-related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 481-97-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 481-97:
(5*4)+(4*8)+(3*1)+(2*9)+(1*7)=80
80 % 10 = 0
So 481-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H22O5S/c1-18-9-8-14-13-5-3-12(23-24(20,21)22)10-11(13)2-4-15(14)16(18)6-7-17(18)19/h3,5,10,14-16H,2,4,6-9H2,1H3,(H,20,21,22)/t14-,15-,16+,18+/m1/s1

481-97-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name estrone 3-sulfate

1.2 Other means of identification

Product number -
Other names estrone-3-sulfate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:481-97-0 SDS

481-97-0Relevant academic research and scientific papers

Piperazine estrone sulfate preparation method

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Paragraph 0027-0029; 0033-0035; 0039-0041, (2020/01/03)

The invention relates to a high-purity estra-1,3,5(10)-triene-17-one-3-piperazine sulfate (1:1) (i.e., piperazine estrone sulfate) preparation method, which has characteristics of mild reaction conditions, simple post-treatment operation and easy impurity control, so that the quality of the prepared piperazine estrone sulfate is controllable, and the stability is high. The preparation method comprises the following main steps: 1) dissolving estrone in an organic solvent, and carrying a reaction with a sulfonating reagent to obtain estra-1,3,5(10)-triene-17-one-3-sulfate; and 2) dissolving piperazine in an organic solvent, then adding into the organic solution of the estra-1,3,5(10)-triene-17-one-3-sulfate, separating out a solid, filtering, washing, and drying to obtain the high-purity piperazine estrone sulfate product.

Testosterone sulfotransferase: Evidence in the guinea pig that this reaction is carried out by 3α-hydroxysteroid sulfotransferase

Park, Byoung C.,Lee, Young C.,Strott, Charles A.

, p. 510 - 517 (2007/10/03)

During the course of isolating, characterizing, and cloning estrogen and 3-hydroxysteroid sulfotransferases from the guinea pig adrenal gland, it was noted that cytosolic preparations from this tissue would also sulfonate testosterone. Therefore, we set out to isolate and clone the enzyme that performs this reaction. Testosterone sulfotransferase (TST) was isolated from the guinea pig adrenal by using the standard procedures of ion exchange, affinity, and high-performance liquid chromatography. When purified, TST was examined by liquid-phase nondenaturing isoelectric focusing, it was found that the TST activity profile completely overlapped with the activity profile of the 3α-hydroxysteroid sulfotransferase (3αHST) isoform, but not the 3β-hydroxysteroid sulfotransferase (3βHST) isoform. This finding was further investigated by overexpressing the cDNAs for 3αHST and 3βHST in Escherichia coli and examining the expressed proteins for TST activity. This experiment confirmed that 3αHST does indeed function as a TST. In addition, 3αHST was also found to sulfonate estradiol but not estrone, a finding that further suggested that 3αHST may function as a general 17β-hydroxysteroid sulfotransferase. Copyright (C) 1999.

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