WARNING: This product is for research use only, not for human or veterinary use.
MedKoo CAT#: 100880
CAS#: 89778-27-8 (citrate)
Description: Toremifene citrate is an oral selective estrogen receptor modulator (SERM) which helps oppose the actions of estrogen in the body. Licensed in the United States under the brand name Fareston, toremifene citrate is FDA-approved for use in advanced (metastatic) breast cancer. It is also being evaluated for prevention of prostate cancer under the brand name Acapodene.
MedKoo Cat#: 100880
Name: Toremifene Citrate
CAS#: 89778-27-8 (citrate)
Chemical Formula: C32H36ClNO8
Exact Mass:
Molecular Weight: 598.089
Elemental Analysis: C, 64.26; H, 6.07; Cl, 5.93; N, 2.34; O, 21.40
Toremifene Citrate, purity > 98%, is in stock. Current shipping out time is about 2 weeks after order is received. CoA, QC data and MSDS documents are available in one week after order is received. Delivery time: overnight (USA/Canada); 3-5 days (worldwide). Shipping fee: from $30.00 (USA); from $45.00 (Canada); from $70.00 (international).
Related CAS #: 89778-27-8 (citrate) 89778-26-7 (free base)
Synonym: Fareston; FC 1157a; FC-1157a; NK 622; NSC 613680; Toremifene citrate.
IUPAC/Chemical Name: (Z)-2-(4-(4-chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)-N,N-dimethylethan-1-amine 2-hydroxypropane-1,2,3-tricarboxylate
InChi Key: IWEQQRMGNVVKQW-OQKDUQJOSA-N
InChi Code: InChI=1S/C26H28ClNO.C6H8O7/c1-28(2)19-20-29-24-15-13-23(14-16-24)26(22-11-7-4-8-12-22)25(17-18-27)21-9-5-3-6-10-21;7-3(8)1-6(13,5(11)12)2-4(9)10/h3-16H,17-20H2,1-2H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/b26-25-;
SMILES Code: ClCC/C(C1=CC=CC=C1)=C(C2=CC=C(OCCN(C)C)C=C2)\C3=CC=CC=C3.O=C(CC(C(O)=O)(O)CC(O)=O)O
The following data is based on the product molecular weight 598.089 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 1.15 mL | 5.76 mL | 11.51 mL |
5 mM | 0.23 mL | 1.15 mL | 2.3 mL |
10 mM | 0.12 mL | 0.58 mL | 1.15 mL |
50 mM | 0.02 mL | 0.12 mL | 0.23 mL |
1: Saylor PJ, Smith MR. Bone health and prostate cancer. Prostate Cancer Prostatic Dis. 2010 Mar;13(1):20-7. Epub 2009 Nov 10. Review. PubMed PMID: 19901958.
2: Fitzpatrick JM, Schulman C, Zlotta AR, Schröder FH. Prostate cancer: a serious disease suitable for prevention. BJU Int. 2009 Apr;103(7):864-70. Review. PubMed PMID: 19302133.
3: Bonkhoff H, Berges R. The evolving role of oestrogens and their receptors in the development and progression of prostate cancer. Eur Urol. 2009 Mar;55(3):533-42. Epub 2008 Nov 6. Review. PubMed PMID: 19013008.
4: Shelly W, Draper MW, Krishnan V, Wong M, Jaffe RB. Selective estrogen receptor modulators: an update on recent clinical findings. Obstet Gynecol Surv. 2008 Mar;63(3):163-81. Review. PubMed PMID: 18279543.
5: Sieber PR. Treatment of bicalutamide-induced breast events. Expert Rev Anticancer Ther. 2007 Dec;7(12):1773-9. Review. PubMed PMID: 18062751.
6: Smith MR. Androgen deprivation therapy for prostate cancer: new concepts and concerns. Curr Opin Endocrinol Diabetes Obes. 2007 Jun;14(3):247-54. Review. PubMed PMID: 17940447.
7: Thompson IM. Chemoprevention of prostate cancer: agents and study designs. J Urol. 2007 Sep;178(3 Pt 2):S9-S13. Epub 2007 Jul 20. Review. PubMed PMID: 17644117.
8: Musa MA, Khan MO, Cooperwood JS. Medicinal chemistry and emerging strategies applied to the development of selective estrogen receptor modulators (SERMs). Curr Med Chem. 2007;14(11):1249-61. Review. PubMed PMID: 17504144.
9: Gennari L, Merlotti D, Valleggi F, Martini G, Nuti R. Selective estrogen receptor modulators for postmenopausal osteoporosis: current state of development. Drugs Aging. 2007;24(5):361-79. Review. PubMed PMID: 17503894.
10: Palacios S. The future of the new selective estrogen receptor modulators. Menopause Int. 2007 Mar;13(1):27-34. Review. PubMed PMID: 17448265.
Related CAS#
89778-27-8 (Toremifene Citrate)
89778-26-7 (Toremifene free base)