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New10

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Structure Cat No. Product Name CAS No. Product Description
V5198 (R)-Oxiracetam (ISF-2522) 68252-28-8 R)-Oxiracetam is the R-isomer of oxiracetam (also known as ISF 2522), which is a widely used nootropic drug and improves memory and learning in patients with cognitive impairments.
V2169 (Rac)-LM11A-31 dihydrochloride 1214672-15-7 Rac)-LM11A-31 dihydrochloride is an isomer of LM11A-31 dihydrochloride.
V5092 Alclofenac 22131-79-9 Alclofenac, adrug of the non-steroidal anti-inflammatory drug (NSAIDs) class, has been used to treat patients with chronic rheumatic diseases but was withdrawn from the UK market in 1979 due to concerns with its association with vasculitis and rash.
V4560 Alendronate sodium hydrate 121268-17-5 Alendronate sodium hydrate, the sodium salt of alendronate, is a novel and potent farnesyl diphosphate synthase inhibitor withIC50of 460 nM.
V5116 Apomorphine HCl (APL130277; TAK251) 314-19-2 Apomorphine HCl (APL-130277; TAK-251) is a novel and potent dopamine D2 agonist used for the treatment of Parkinsons disease.
V4740 BD-AcAc 2 1208313-97-6 BD-AcAc 2, usually added in diet and given orally, can elevate mean blood ketone bodies of 3.5 mm and lowered plasma glucose, insulin, and leptin in animals.
V2192 CCRP2 2113650-04-5 CCRP2(also known as TLX agonist 1 and SUN-23314) ,is a novel orphan nuclear receptor tailless (TLX, NR2E1) modulator (EC50=1μM; Kd= 650 nM).
V5001 Debrisoquin sulfate 581-88-4 Debrisoquine sulfate (Ro5-3307;Debrisochinum; Tendor), the sulfate salt ofDebrisoquin which isa guanidine derivative, is a potent antihypertensive and adrenergic neuron-blocking drugsimilar to guanethidine.
V4897 Dexrazoxane (NSC-169780) 24584-09-6 Dexrazoxane (formerly also known as ICRF-187; ADR-529; NSC-169780) is an intracellular iron chelator, which decreases the formation of superoxide radicals, and is mainly used as a cardioprotective agent.
V5073 Dicyclohexylamine 101-83-7 Dicyclohexylamine, an inhibitor of Spd synthesis, is a secondary amine with the chemical formula HN(C6H11)2.
V4956 Eniluracil (5-Ethynyluracil; GW-776C85) 59989-18-3 Eniluracil (also known as 5-Ethynyluracil; GW776C85) is a novel and potent uracil analog and also a mechanism-based irreversible inhibitor of dihydropyrimidine dehydrogenase (DPD), which increases the oral bioavailability of 5-fluorouracil (5-FU) to 100%, facilitating uniform absorption and predictable toxicity.
V4835 EphB1-IN-10 2097512-73-5 EphB1-IN-10 is a novel, potent, selective and irreversible/covalent inhibitor of receptor tyrosine kinase EphB1.
V4802 EXP-3174 151801-76-2 EXP-3174 (also known as losartan aarboxylic acid), a physiologically active metabolite of losartan produced by cytochrome P450 isoforms in the liver, is a non-peptide, potent angiotensin II (AII) receptor, type 1 (AT1) antagonist, which inhibits the AII induced cellular responses.
V5161 Fenazaquin (EL436; XDE 436) 120928-09-8 Fenazaquin(EL-436; XDE-436) is a quinazoline-based insecticide/acaricide which exhibits contact and ovicidal activity against a broad spectrum of mites in grapes, pome fruit, citrus, peaches, cucurbits, tomatoes, cotton and ornamentals.
V4947 Fluticasone furoate 397864-44-7 Fluticasone furoate is a topical, intranasal, enhanced affinity synthetic trifluorocorticosteroid with Kd of 0.3 nM.
V4921 GLL-398 2077980-83-5 GLL398 (GLL-398) is a novel, potent, orally bioavailable, and selective estrogen receptor downregulator.
V4545 GNE-140 racemate 1809794-70-4 GNE-140 racemate is a novel and potent lactate dehydrogenase (LDHA) inhibitor which is a racemic mixture of (R)-GNE-140 and (S)-GNE-140.
V4863 GSK-3008348 1629249-33-7 GSK-3008348 (GSK3008348), an investigational drug, is a novel and potent integrin alpha(v)beta6 antagonist thatis being developed by GlaxoSmithKline Research and Development Limited (the Sponsor, a pharmaceutical company based in the UK) for the treatment of Idiopathic Pulmonary Fibrosis (IPF).
V2171 Isocanadine 6656-19-5 Isocanadine is an isomer of canadine.
V4871 LY334370 HCl 199673-74-0 LY-334370 HCl, the hydrochloride of LY-334370, is a novel, potent and selective 5-HT1F receptor agonist with Ki values of 1.6 nM.
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