Halophenols
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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
5000414553 TACCALONOLIDE E 1MG
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eMolecules METHYLTRIPHENYLPHOSPHONIUM 5G
5000189488 METHYLTRIPHENYLPHOSPHONIUM 5G
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eMolecules 1-METHYLCYCLOPROPANAMINE H 10G
5000189524 1-METHYLCYCLOPROPANAMINE H 10G
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eMolecules HOAT 25G
5000189216 HOAT 25G
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Medchemexpress LLC Pevonedistat Hydroch 10Mm 1Ml | HY-10484-10MM 1ML
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Pevonedistat Hydroch 10Mm 1Ml
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Ambeed 2 4 6Triisopropylbenzenethiol
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2,4,6-Triisopropylbenzenethiol, 22693-41-0, 97%
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Ambeed 2R 3S 4R 5R 5 6Amino9Hpurin
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(((2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-4-hydroxy-2-(((hydroxy((hydroxy((R)-3-hydroxy-2,2-dimethyl-3-((2-((2-sulfanylethyl)carbamoyl)ethyl)carbamoyl)propoxy)phosphoryl)oxy)phosphoryl)oxy)methyl)oxolan-3-yl)oxy)phosphonic acid, 85-61-0, 85%
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000437456 LV-320 10MM 1ML
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Medchemexpress LLC Samuraciclib hydroch 25mg | 1805789-54-1 | 25MG
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Samuraciclib hydrochloride (CT7001 hydrochloride) is a potent selective ATP-competitive and orally active CDK7 inhibitor with an IC50 of 41 nM Samuraciclib hydrochloride displays 45- 15- 230- and 30-fold selectivity over CDK1 CDK2 (IC50 of 578 nM) CDK5 and CDK9 respectively Samuraciclib hydrochloride inhibits the growth of breast cancer cell lines with GI50 values between 0 2-0 3 M Samuraciclib hydrochloride has anti-tumor effects[1 [2
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eMolecules 2 4-DIFLUOROPHENOL 25G
5000189162 2 4-DIFLUOROPHENOL 25G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000400732 N N -DIBENZYLETHYLEN 100G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000408422 OXACILLIN SODIUM MO 10MM 1ML
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000418781 26-DEOXYACTEIN 1MG
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Apexbio Technology LLC Rabeprazole sodium 117976-90-6 10mM (in 1mL DMSO)
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Rabeprazole sodium (CAS 117976-90-6) is a small-molecule inhibitor targeting gastric H /K -ATPase It is designed to irreversibly inhibit this proton pump enzyme thereby suppressing gastric acid secretion Rabeprazole sodium exerts its biological activity primarily through irreversible inhibition of H /K -ATPase It also induces apoptosis and inhibits uridine nucleoside hydrolase (UNH) with an IC50 value of 0 3 M Based on these pharmacological properties Rabeprazole sodium holds research potential in studies of gastric ulcer gastroesophageal reflux disease and the investigation of proton pump inhibition apoptosis induction and nucleoside metabolism regulation
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Ambeed 2R 3S 4R 5R 5 6Amino9Hpurin
(((2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-4-hydroxy-2-(((hydroxy((hydroxy((R)-3-hydroxy-2,2-dimethyl-3-((2-((2-sulfanylethyl)carbamoyl)ethyl)carbamoyl)propoxy)phosphoryl)oxy)phosphoryl)oxy)methyl)oxolan-3-yl)oxy)phosphonic acid, 85-61-0, 85%
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