Company Name: |
Alta Scientific Co., Ltd.
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Tel: |
022-6537-8550 15522853686 |
Email: |
sales@altasci.com.cn |
Products Intro: |
Product Name:Norethindrone-13C2 CAS:201741-02-8 Purity:99% Package:10mg;100mg;1g
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Company Name: |
ShangHai Anpel Co, Ltd.
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Tel: |
18017382783 18017382783 |
Email: |
shanpel@anpel.com.cn |
Products Intro: |
Product Name:Norethindrone-[13C2 CAS:201741-02-8 Purity:100ppm Package:100mg/L于甲醇,1.2ml Remarks:CDAA-S-590159C2-AA-1.2ml
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Company Name: |
Reer Technology (Shanghai) Co., LTD
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Tel: |
021-64400900 15800436310 |
Email: |
bessey@reertech.com |
Products Intro: |
Product Name:NORETHINDRONE(ETHYNYL-13C2, 99%) CAS:201741-02-8 Purity:98% Package:0.01 G Remarks:CLM-2468-0.01
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Company Name: |
Shanghai Yifei Biotechnology Co. , Ltd.
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Tel: |
021-65675885 18964387627 |
Email: |
customer_service@efebio.com |
Products Intro: |
Product Name:Norethindrone (Ethynyl-13C2) CAS:201741-02-8 Purity:95% Package:1mg;5mg
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Norethindrone-13C2 Solution, 100ppm manufacturers
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| Norethindrone-13C2 Solution, 100ppm Basic information |
| Norethindrone-13C2 Solution, 100ppm Chemical Properties |
| Norethindrone-13C2 Solution, 100ppm Usage And Synthesis |
Uses | Norethindrone-13C2 (Norethisterone-13C2) is the 13C labeled Norethindrone (HY-B0554)[1]. Norethindrone is a female progestin approved by FDA for the treatment of endometriosis, uterine bleeding caused by abnormal hormone levels, and secondary amenorrhea[2][3][4][5]. | References | [1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110 [2] Muneyyirci-Delale O, et al. Effect of norethindrone acetate in the treatment of symptomatic endometriosis. Int J Fertil Womens Med. 1998 Jan-Feb;43(1):24-7. PMID:9532466 [3] Kaser DJ, et al. Use of norethindrone acetate alone for postoperative suppression of endometriosis symptoms. J Pediatr Adolesc Gynecol. 2012 Apr;25(2):105-8. DOI:10.1016/j.jpag.2011.09.013 [4] Maier WE, et al. Pharmacology and toxicology of ethinyl estradiol and norethindrone acetate in experimental animals. Regul Toxicol Pharmacol. 2001 Aug;34(1):53-61. DOI:10.1006/rtph.2001.1483 [5] Cheng DC, et al. Norethindrone acetate inhibition of triglyceride synthesis and release by rat hepatocytes. Atherosclerosis. 1983 Jan;46(1):41-8. DOI:10.1016/0021-9150(83)90162-4 |
| Norethindrone-13C2 Solution, 100ppm Preparation Products And Raw materials |
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