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Supplier: ALADDIN SCIENTIFIC
Description: 7-Azabicyclo[2.2.1]heptane hydrochloride ≥97%

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Supplier: ALADDIN SCIENTIFIC
Description: 2,5-Dioxopyrrolidin-1-yl hex-5-ynoate ≥95%

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Supplier: ALADDIN SCIENTIFIC
Description: Azetidin-3-amine dihydrochloride ≥97%

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Supplier: ALADDIN SCIENTIFIC
Description: 1H-Indol-6-ylmethylamine ≥97%

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Supplier: ALADDIN SCIENTIFIC
Description: RVX-208 ≥97%, Moligand™

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Supplier: ALADDIN SCIENTIFIC
Description: 3-(2-Amino-2-oxoethyl)-5-methylhexanoic acid ≥98%

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Supplier: ALADDIN SCIENTIFIC
Description: 6'-(Diethylamino)-3'-methyl-2'-(phenylamino)-3H-spiro[isobenzofuran-1,9'-xanthen]-3-one ≥98%

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Supplier: ALADDIN SCIENTIFIC
Description: 3-Amino-6-bromopyrazine-2-carbonitrile ≥97%

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Supplier: ALADDIN SCIENTIFIC
Description: N²-Methyl-5-(trifluoromethyl)pyridine-2,3-diamine ≥98%

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Supplier: ALADDIN SCIENTIFIC
Description: 2-Aminopyrimidine-5-carboxylic acid ≥98%

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Supplier: ALADDIN SCIENTIFIC
Description: A 83-01 is a potent inhibitor of TGF-β type I receptor ALK5 kinase, type I nodal receptor ALK4 and type I nodal receptor ALK7, with IC50s of 12 nM, 45 nM and 7.5 nM against the transcription induced by ALK5, ALK4 and ALK7, respectively。

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Supplier: ALADDIN SCIENTIFIC
Description: Product Introduction:Aminopurvalanol A is a potent, selective, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of physiological capacitation-dependent actin polymerization.

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Supplier: ALADDIN SCIENTIFIC
Description: Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.Product Introduction:A cell-permeable pyrimidinyl compound that displays anti-inflammatory properties. Acts as a potent, reversible, and ATP-competitive inhibitor of c-Jun N-terminal kinase (JNK, IC50 = 150, 220, and 70 nM for hJNK1, hJNK2, and hJNK3, respectively) with a 10- to 100-fold greater selectivity over a panel of 25 other commonly studied kinases (IC50 typically in the range of 1-10 µM or no effect at 10 µM). Its in vivo efficacy has been demonstrated in gerbils, mice, and rats via oral, i.v., or i.p. administration. Biochemical mechanism:Cell permeable: yesProduct competes with ATP.Primary TargethJNK 1, hJNK 2, hJNK 3Reversible: yesTarget IC50: 150, 220, and 70 nM for hJNK1, hJNK2, and hJNK3, respectively

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Supplier: ALADDIN SCIENTIFIC
Description: 5-Acetyl-2-fluorobenzeneboronic acid pinacol ester ≥96%

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Supplier: ALADDIN SCIENTIFIC
Description: 3-Amino-3-(4-bromophenyl)propionic acid ≥95%

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Supplier: ALADDIN SCIENTIFIC
Description: (2-Amino-6-chlorophenyl)methanol ≥97%

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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
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