Drug Standards
Medchemexpress LLC 2,6-di-tert-butyl-4-methylphenol | 128-37-0 | MFCD00011644 | 99.9% | 220.35 g/mol | C15H24O | 1mL
Butylated hydroxytoluene is an antioxidant widely used in foods and in food-related products[1] Butylated hydroxytoluene is a Ferroptosis inhibitor[2]
eMolecules 496775-62-3 | ELTROMBOPAG OLAMINE | AstaTech | MFCD22380664 | 564.643 | C29H36N6O6 | 95.000 | NCCO.NCCO.CC1=NN(C(=O)\C1=N/Nc1cccc(-c2cccc(c2)C(O)=O)c1O)c1ccc(C)c(C)c1 | 5g | 381456806
ELTROMBOPAG OLAMINE | AstaTech | 496775-62-3 | MFCD22380664 | 564.643 | C29H36N6O6 | 95.000 | NCCO.NCCO.CC1=NN(C(=O)\C1=N/Nc1cccc(-c2cccc(c2)C(O)=O)c1O)c1ccc(C)c(C)c1 | 5g | 381456806
Selleck Chemical LLC Hydroxychloroquine (HCQ) Sulfate S4430-200mg
Hydroxychloroquine (HCQ) Sulfate is an antimalarial agent used for the treatment of systemic lupus erythematosus rheumatoid arthritis and other autoimmune inflammatory and dermatologic conditions Also acts as an inhibitor of autophagy and toll-like receptor (TLR) 7/9
Selleck Chemical LLC Isradipine 50mg 75695-93-1 PN 200-110
Isradipine (PN 200-110) is a potent and selective L-type voltage-gated calcium channel blocker, used to treat high blood pressure. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Cayman Chemical Pantoprazole 1g
A proton pump inhibitor; inhibits H+/K+-ATPase activity in porcine gastric membrane vesicles (IC50 = 6.8 µM); reduces basal gastric acid secretion in pylorus-ligated rats (ED50 = 1.3 mg/kg); inhibits mepirizole-induced increases in gastric acid secretion in an anesthetized rat model of gastric fistula (ED50 = 0.8 mg/kg); inhibits formation of mepirizole-induced duodenal lesions in rats (ED50 = 0.5 mg/kg)
Selleck Chemical LLC Dapoxetine HCl 25mg 129938-20-1 LY-210448
Dapoxetine HCl (LY-210448) is a short-acting novel selective serotonin reuptake inhibitor, used for the treatment of premature ejaculation. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Sigma Aldrich Fine Chemicals Biosciences Calcifediol United States Pharmacopeia (USP) Reference Standard | 63283-36-3 | MFCD00867077 | 75MG
Calcifediol United States Pharmacopeia (USP) Reference Standard | Mol Wt: 418.65 | 63283-36-3 | MFCD00867077 | 75MG
Selleck Chemical LLC Estradiol dipropionate
Estradiol dipropionate (17-Beta-Estradiol-3 17-Dipropionate) is a semisynthetic steroidal estrogen which has been used in hormone therapy for menopausal symptoms and low estrogen levels in women and in the treatment of gynecological disorders
TARGETMOL CHEMICALS INC R-Naproxen 200MG
Also available in 1 mL, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. (R)-Naproxen, an anti-inflammatory agent, has antipyretic and analgesic properties. Both the acid and its sodium salt are used in the therapy of acute gout or dysmenorrhea, musculoskeletal disorders, rheumatoid arthritis and other rheumatic. Purity 99.2%
Selleck Chemical LLC Capecitabine S1156-1g
Capecitabine is a tumor-selective fluoropyrimidine carbamate which achieves higher intratumoral 5-FU level with lower toxicity than 5-FU Capecitabine treatment of HCT-15 cells causes condensation of DNA and induces apoptosis
Medchemexpress LLC Δ14-Triamcinolone acetonide | 1260149-96-9 | 432.48 | 1 MG
Δ14-Triamcinolone acetonide is identified as a potential impurity. It is known to inhibit basic fibroblast growth factor (bFGF) induced proliferation of retinal endothelial cells. This compound also contributes to the reduction of chondrocyte viability, which can lead to cartilage destruction. Furthermore, Δ14-Triamcinolone acetonide has applications in the study of various diseases, including atopic dermatitis.
- Potential impurity.
- Inhibits basic fibroblast growth factor (bFGF) induced proliferation of retinal endothelial cells.
- Reduces chondrocyte viability and leads to cartilage destruction.
- Can be used in the study of diseases such as atopic dermatitis.
Selleck Chemical LLC Volasertib (BI 6727) 10mM/1mL 755038-65-4
Volasertib (BI 6727) is a highly potent Plk1 inhibitor with IC50 of 0.87 nM in a cell-free assay. It shows 6- and 65-fold greater selectivity against Plk2 and Plk3. Volasertib induces cell cycle arrest and apoptosis in various cancer cells. Phase 3. *For Research & Development use only. Product is not intended for drug, household, or human consumption.