Ulipristal Acetate

Ulipristal Acetate 구조식 이미지
카스 번호:
126784-99-4
상품명:
Ulipristal Acetate
동의어(영문):
Ulipristal;17α-Acetoxy-11β-(4-dimethylaminophenyl)-19-norpregna-4,9-dien-3,20-dione;Uliprisnil Acetate;Esmya;EllaOne;CDB2914;VA 2914;RU 44675;CBD 2914;HRP 2000
CBNumber:
CB31400406
분자식:
C30H37NO4
포뮬러 무게:
475.62
MOL 파일:
126784-99-4.mol
MSDS 파일:
SDS

Ulipristal Acetate 속성

녹는점
183-185 ºC
끓는 점
640.1±55.0 °C(Predicted)
밀도
1.19
저장 조건
-20°C
용해도
클로로포름, 에틸아세테이트, 메탄올에 용해됨
산도 계수 (pKa)
5.49±0.24(Predicted)
물리적 상태
가루
색상
흰색에서 베이지색
optical activity
[α]/D +165 to +185°, c = 1 in dichloromethane
안전
  • 위험 및 안전 성명
HS 번호 2937.29.9095
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
예방조치문구:
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
NFPA 704
0
2 0

Ulipristal Acetate C화학적 특성, 용도, 생산

개요

Ulipristal acetate is a synthetic steroid derived from 19-nor-progesterone that exerts potent progesterone receptor (PR) antagonist activity at the transcriptional level. It is an orally administered drug indicated for emergency contraception (i.e., postcoital contraception) up to 120 h following unprotected intercourse. Ulipristal acetate is the second oral progestogen marketed for this indication behind levonorgestrel. As PR antagonists, both drugs are believed to act via delay of ovulation and inhibition of follicular development. Levonorgestrel 1.5 mg is approved for contraception up to 72 h following unprotected intercourse and is widely accessible via prescription, and directly from clinics and community pharmacies. Prior to ulipristal acetate, the only approved postcoital contraceptive option between 72 and 120 h was the insertion of an intrauterine device (IUD). The recommended dose of ulipristal acetate is one 30-mg tablet taken as soon as possible and no more than 120 h following intercourse. The vast majority of PR antagonists belonging to the mifepristone (RU486) family also bind to the glucocorticoid receptor (GR) with high affinity and thereby exert antiglucocorticoid activity.
The most common adverse effects with ulipristal acetate were headache, dysmenorrhea, nausea, abdominal pain, dizziness, fatigue, and upper abdominal pain.

화학적 성질

Pale Yellow Solid

용도

Ulipristal acetate is a selective progesterone receptor modulator

정의

ChEBI: A 20-oxo steroid obtained by acetylation of the 17-hydroxy group of (11beta,17alpha)-17-acetyl-11-[4-(dimethylamino)phenyl]-3-oxoestra-4,9-dien-17-ol (ulipristal). A selective progesterone receptor modulator, which is empl yed as an emergency contraceptive.

Clinical Use

Ulipristal acetate, a selective progesterone receptor modulator (SPRM), was developed at the Research Triangle Institute. In 2009, HRA Pharma received FDA approval for emergency contraception within 120 h (5 days) of unprotected sexual intercourse or contraceptive failure. Ulipristal acetate is a well-known steroid that possesses antiprogestational and antiglucocorticoid activity. It is the first SPRM that was specifically designed as an oral emergency contraceptive. Unlike earlier levonorgestrel-based emergency contraceptives, this SPRM drug maintains efficacy for 5 days after unprotected intercourse while having safety profile comparable to levonorgestrel.

Ulipristal Acetate 준비 용품 및 원자재

원자재

준비 용품


Ulipristal Acetate 공급 업체

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+86-21-33585366 - 03@
sales03@shyrchem.com CHINA 738 60

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