RAC 8-HYDROXY EFAVIRENZ
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RAC 8-HYDROXY EFAVIRENZ 속성
- 녹는점
- 144-154°C
- 끓는 점
- 373.6±42.0 °C(Predicted)
- 밀도
- 1?+-.0.1 g/cm3(Predicted)
- 저장 조건
- Store at -20°C
- 용해도
- Acetonitrile: soluble; DMSO: soluble; Methanol: soluble
- 물리적 상태
- 고체
- 산도 계수 (pKa)
- 7.18±0.40(Predicted)
- 색상
- White to off-white
안전
RAC 8-HYDROXY EFAVIRENZ C화학적 특성, 용도, 생산
개요
8-hydroxy Efavirenz is a major oxidative metabolite of the non-nucleoside reverse transcriptase inhibitor efavirenz . 8-hydroxy Efavirenz is formed when efavirenz is metabolized by the cytochrome P450 (CYP) isoform CYP2B6. It induces apoptosis in rat primary hippocampal neurons and loss of dendritic spines in rat primary hippocampal neuronal cultures when used at a concentration of 0.01 μM.화학적 성질
Off-White Solid용도
A labellebed metabolite of Efavirenz, a nonnucleoside HIV-1 reverse transcriptase inhibitorRAC 8-HYDROXY EFAVIRENZ 준비 용품 및 원자재
원자재
준비 용품
RAC 8-HYDROXY EFAVIRENZ 공급 업체
글로벌( 33)공급 업체
공급자 | 전화 | 이메일 | 국가 | 제품 수 | 이점 |
---|---|---|---|---|---|
Standardpharm Co. Ltd. | 86-714-3992388 |
overseasales1@yongstandards.com | United States | 14335 | 58 |
Guangzhou PI PI Biotech Inc | 020-81716320 +86-13602409664 |
Sales@pipitech.com | China | 3635 | 55 |
Shanghai Devinchem Ltd | 027-65318838 13646286950 |
sales@devinchem.com | China | 2975 | 58 |
J & K SCIENTIFIC LTD. | 010-82848833 400-666-7788 |
jkinfo@jkchemical.com | China | 94658 | 76 |
Chemsky (shanghai) International Co.,Ltd | 021-50135380 |
shchemsky@sina.com | China | 15421 | 60 |
BOC Sciences | 16314854226 |
info@bocsci.com | United States | 9926 | 65 |
Shanghai EFE Biological Technology Co., Ltd. | 021-65675885 18964387627 |
info@efebio.com | China | 9806 | 58 |
Shanghai SuperLan Chemcial Technique Centre | 021-2022843681 15618226720 |
chaolaichem@foxmail.com | China | 7879 | 58 |
Shanghai Hongye Biotechnology Co. Ltd | 400-9205774 |
sales@glpbio.cn | China | 6870 | 58 |
Shenzhen Polymeri Biochemical Technology Co., Ltd. | +86-400-002-6226 |
sales@rrkchem.com | China | 56265 | 58 |
RAC 8-HYDROXY EFAVIRENZ 관련 검색:
SE 563
Efavirenz AMino Alcohol Ethyl CarbaMate
rac Methyl Efavirenz
Efavirenz Related Compound B (15 mg) ((S,E)-6-Chloro-4-(2-Cyclopropylvinyl)-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one)
rac 8-Hydroxy Efavirenz
Efavirenz Related Compound C (20 mg) (6-chloro-2-cyclopropyl-4-(trifluoromethyl)quinoline)
6-chloro-4-pent-1-ynyl-4-(trifluoromethyl)-1H-3,1-benzoxazin-2-one
L 741211
Efavirenz
rac 8,14-Dihydroxy Efavirenz
(S)-1-(2-Amino-5-chlorophenyl)-1-(trifluoromethyl)-3-cyclopropyl-2-propyn-1-ol
(4S)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-2-(4-methoxyphenyl)-4-(trifluoromethyl)-2H-3,1-benzoxazine(Mixture of 2 Diastereomers)
Efavirenz IP Impurity A
rac 7-Hydroxy Efavirenz
[4-Chloro-2-[(1S)-3-cyclopropyl-1-hydroxy-1-(trifluoromethyl)-2-propynyl)phenyl]carbamic Acid Methyl Ester
(S)-5-chloro-a-(Cyclopropylacetenyl)-2-[((4-methoxyphenyl)methyl)amino]-a- (trifluoromethyl) benzenemethanol (E-4)
Enantiomer Efavirenz
Efavirenz Impurity 13(7-Hydroxy Efavirenz)