| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V1741 | Medroxyprogesterone acetate | 71-58-9 | Medroxyprogesterone acetate (formerly NSC26386;NSC 26386;Medroxyprogesterone 17-acetate;MPA), the17-ester form ofMedroxyprogesterone,is a steroidal progestin and a synthetic variant of the human hormone progesterone. |
|
V1739 | Mestranol | 72-33-3 | Mestranol (Ethinyl Estradiol 3 Methyl Ether; Devocin; Norquen; Ovastol), the 3-methyl ether of ethinyl estradiol, is a potent estrogen receptor agonist that has been used as an oral contraceptive. |
|
V1725 | Mifepristone (RU486) | 84371-65-3 | Mifepristone (formerly RU-486; C-1073; RU-38486; Mifegyne; Pictovir; Mifepristonum; Mifepristona; Mifeprex; Corlux)is a synthetic steroid compound that has been approved asa medication used in combination with misoprostol to bring about an abortion during pregnancy. |
|
V15544 | Norethindrone acetate | 51-98-9 | Norethindrone acetate (NSC-22844;NSC22844;NSC 22844;ENTA) is the 17-O-acetylated ester of Norethindrone (Norethisterone; sold under many trade names), which is a synthetic progestin and an orally active contraceptive for preventing pregnancy. |
|
V1730 | Ospemifene (FC-1271a) | 128607-22-7 | Ospemifene (FC-1271a; FC1271a;Osphena) is an orally bioactive medication anda non-hormonal selective estrogen receptor modulator (SERM), used for the treatment of dyspareunia. |
|
V1744 | Pregnenolone | 145-13-1 | Pregnenolone (NSC-1616; NSC-18158; Prenolon; Regnosone; Skinostelon; Enelone; Natolone; Pregnetan; Pregneton; Pregnolon) is an endogenous/naturally occurring steroidal hormone that has been used in the treatment of fatigue, Alzheimers disease, trauma and injuries. |
|
V1747 | Pritelivir (BAY 57-1293) | 348086-71-5 | Pritelivir (formerly known as AIC-316; BAY-57-1293;AIC316;BAY571293) is a novel and potent helicase primase inhibitor thatdisplays antiviral effects against herpes simplex virus (HSV) with an IC50 of 20 nM for both HSV-1 and HSV-2. |
|
V1737 | Progesterone | 57-83-0 | Progesterone (Pregn-4-ene-3,20-dione;Hormoflaveine; Lutociclina; Agolutin; Crinone; Luteohormone; Utrogestan; Cyclogest) is an endogenous steroidal hormone and a universal precursor for the biosynthesis of other steroidal hormones. |
|
V13519 | Quinestrol (W-3566) | 152-43-2 | Quinestrol(W3566) is a novel steroid compound used in estrogen/hormone replacement therapy, and may also be used to treat breast cancer and prostate cancer. |
|
V1723 | Raloxifene HCl (LY-139481) | 82640-04-8 | Raloxifene HCl (also known as LY-156758; LY-139481; trade names: Evista; Keoxifene; RALOX), the hydrochloride salt ofRaloxifene,is a selective estrogen antagonist or estrogen strogen receptor modulator (SERM) that has been approved as a medication to prevent and treat osteoporosis in postmenopausal women. |
|
V81275 | Raloxifene-d10 | Raloxifene-d10 is the deuterated form of Raloxifene. | |
|
V40395 | SAR439859 | 2114339-57-8 | Amcenestrant (SAR-439859; SAR439859) is a potent, orally available, and nonsteroidalestrogen receptor degrader (SERD)with potential anticancer activity. |
|
V1755 | Sinomenine (Cucoline) | 568-72-9 | Sinomenine(Coculine; Cucoline; Kukoline) is a naturally occuring alkaloid found in the root of the climbing plant Sinomenium acutum which is native to Japan and China. |
|
V1756 | Tariquidar dimesylate | 625375-84-0 | Tariquidar dimesylate (formerly known as XR9576; D06008; XR-9576; D-06008), the dimesylate salt ofTariquidar, is a novel potent and selective noncompetitive inhibitor of P-glycoprotein (P-gp) with potential antitumor activity. |
|
V16600 | Toremifene | 89778-26-7 | Toremifene (NSC 613680; NK 622; FC 1157a)is an orally bioavailable and second-generation SERM (selective estrogen receptor modulator) used in the treatment of advanced breast cancer. |
|
V1726 | Toremifene Citrate (FC 1157a) | 89778-27-8 | Toremifene Citrate (NSC-613680; NK-622; FC-1157a; NSC613680;NSC613680;FC1157a;Fareston), the citrate salt of toremifene, is an orally bioavailable SERM (selective estrogen receptor modulator) approved for use in the treatment of advanced breast cancer. |
|
V1752 | Ulipristal (CDB-2914) | 159811-51-5 | Ulipristal(CDB-2914;HRP2000, VA2914,RTI 3021-012, RU 44675, EllaOne, Ella, Esmya) is a potent and selective SPRM (selective progesterone receptor modulator) used for emergency contraception after an unprotected intercourse or contraceptive failure. |
|
V25388 | Ulipristal acetate (CDB-2914) | 126784-99-4 | Ulipristalacetate (also known as CDB-2914) is a potent and selective SPRM (selective progesterone receptor modulator) for emergency contraception after an unprotected intercourse or contraceptive failure. |
|
V73484 | Yp537 TFA (Anti-estrogen TFA) | Yp537 TFA is an estrogen receptor (ER) inhibitor that prevents dimerization of the human estrogen receptor. | |
|
V5135 | Zearalenone (Mycotoxin F2; Toxin F2) | 17924-92-4 | Zearalenone is a novel mycotoxin found mainly by fungi/Fusarium, belonging to the genusFusariumin foods and feeds. |
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