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Others 12

Others 12

Others 12 related products

Structure Cat No. Product Name CAS No. Product Description
Udonitrectag (REC 0559) V61836 Udonitrectag (REC 0559) 1458063-04-1 Udonitrectag (REC 0559) is a low molecular weight analog of NGF that can improve the stability of NGF.
UDP-glucose dehydrogenase V61320 UDP-glucose dehydrogenase 9028-26-6 UDP-glucose dehydrogenase is a biochemical compound that could be utilized as a biomaterial or organic/chemical reagent for biomedical research.
UDP-β-D-glucose disodium V57535 UDP-β-D-glucose disodium 7333-33-7 UDP-β-D-glucose disodium is the stereoisomer of UDP-α-D-glucose.
UGT8-IN-1 V64325 UGT8-IN-1 2414349-93-0 UGT8-IN-1 is a BBB (blood-brain barrier) permeable (penetrable), orally bioactive inhibitor of ceramide galactosyltransferase (UGT8) and may be utilized in the study of lysosomal storage disorders.
UHMCP1 V60948 UHMCP1 2103079-87-2 UHMCP1 is a chemical probe of the U2AF homology motif (UHM) with a Kd of 79 μM.
UHMCP1 dihydrochloride V61137 UHMCP1 dihydrochloride 2925647-93-2 UHMCP1 di-HCl is a potent UHM domain splicing inhibitor (antagonist) with a Kd of 79 µM.
Ultrashort α,β-Peptide V57101 Ultrashort α,β-Peptide 2738334-37-5 Ultrashort α,β-Peptide was found to stabilize colloidal gold nanoparticles in physiological media for over 3 months.
UNC3474 V62354 UNC3474 1648707-79-2 UNC3474 is a small molecule ligand that binds to 53BP1.
UNC7467 V61949 UNC7467 2922283-43-8 UNC7467 is a potent IP6K inhibitor (antagonist) with IC50s of 4.9, 8.9 and 1320 nM for IP6K2, IP6K1 and IP6K6 respectively.
Uric acid sodium (monosodium urate) V72881 Uric acid sodium (monosodium urate) 1198-77-2 Uric acid sodium (Monosodium urate) is an oxygen radical scavenger and a very important antioxidant that helps maintain the stability of blood pressure and resist oxidative stress.
Uridine, 5'-P,P',P'',P''-tetrahydrogen imidotriphosphate V59306 Uridine, 5'-P,P',P'',P''-tetrahydrogen imidotriphosphate 497064-75-2 Uridine, 5'-(P,P',P'',P''-tetrahydrogen imidotriphosphate) is a non-hydrolyzable nucleotide that may be utilized to prepare RNA oligonucleotides.
Uridine-5'-diphosphoglucose pyrophosphorylase V57669 Uridine-5'-diphosphoglucose pyrophosphorylase 9026-22-6 Uridine-5'-diphosphoglucose pyrophosphorylase is a biochemical compound that could be utilized as a biomaterial or organic/chemical reagent for biomedical research.
Ursonic acid methyl ester (3-carbonyl-ursolic acid-28-methyl ester) V61634 Ursonic acid methyl ester (3-carbonyl-ursolic acid-28-methyl ester) 989-72-0 Ursonic acid methyl ester is an esterified analogue of ursonic acid.
UT-B-IN-1 V74252 UT-B-IN-1 892742-76-6 UT-B-IN-1 (UTBINH-14) is a reversible, competitive and selective urea transporter B (UT-B) inhibitor (antagonist) with IC50 of UT-B in humans and mice respectively.
UZH1b V75487 UZH1b 2814392-17-9 UZH1b is the enantiomer of UZH1a, a METTL3 inhibitor.
Vacquinol-1 dihydrochloride (NSC13316 dihydrochloride) V64403 Vacquinol-1 dihydrochloride (NSC13316 dihydrochloride) 2309312-85-2 Vacquinol-1 (NSC13316) di-HCl is a specific activator of MKK4 that activates the MAPK pathway.
Valethamate bromide (valethamate bromide) V62002 Valethamate bromide (valethamate bromide) 90-22-2 Valethamate bromide, an ester, is a potent, fast-acting anticholinergic antispasmodic and myotrophic agent that accelerates labor by improving cervical dilation.
Valiolamine V59087 Valiolamine 83465-22-9 Valiolamine is an aminocyclic alcohol.
Valnivudine hydrochloride (FV-100) V62205 Valnivudine hydrochloride (FV-100) 956483-03-7 FV-100 is a specific and orally bioactive antivaricella-zoster virus agent.
Vamagloxistat V58979 Vamagloxistat 2408241-62-1 Vamagloxistat is a glycolate oxidase inhibitor used to inhibit hyperoxaluria and kidney stones.
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