4-(4-Methylperhydro-1,4-diazepin-1-yl)benzoic acid hydrochloride hydrate, 95%, Thermo Scientific™

CAS: 303134-03-4 Molecular Formula: C13H19ClN2O2 Molecular Weight (g/mol): 270.757 MDL Number: MFCD09064999 InChI Key: KJZVHMAKWMCIBB-UHFFFAOYSA-N Synonym: 4-4-methyl-1,4-diazepan-1-yl benzoic acid hydrochloride,4-4-methyl-1,4-diazepan-1-yl benzoic acid-hydrogen chloride 1/1 PubChem CID: 24229616 IUPAC Name: 4-(4-methyl-1,4-diazepan-1-yl)benzoic acid;hydrochloride SMILES: CN1CCCN(CC1)C2=CC=C(C=C2)C(=O)O.Cl

2-(4-Methylperhydro-1,4-diazepin-1-yl)benzoic acid hydrochloride hemihydrate, 95%, Thermo Scientific™

CAS: 921938-77-4 Molecular Formula: C13H19ClN2O2 Molecular Weight (g/mol): 270.757 MDL Number: MFCD09065004 InChI Key: UCYNEWGETFFMQY-UHFFFAOYSA-N Synonym: 2-4-methyl-1,4-diazepan-1-yl benzoic acid hydrochloride,2-4-methyl-1,4-diazepan-1-yl benzoic acid hcl,2-4-methylhomopiperazin-1-yl benzoic acid hydrochloride hemihydrate,2-4-methyl-1,4-diazepan-1-yl benzoic acid-hydrogen chloride 1/1,2-4-methylperhydro-1,4-diazepin-1-yl benzoic acid hydrochloride 0.5 hydrate,benzoicacid, 2-hexahydro-4-methyl-1h-1,4-diazepin-1-yl-, hydrochloride 1:1,benzoicacid,2-hexahydro-4-methyl-1h-1,4-diazepin-1-yl-,hydrochloride 1:1 PubChem CID: 24229621 IUPAC Name: 2-(4-methyl-1,4-diazepan-1-yl)benzoic acid;hydrochloride SMILES: CN1CCCN(CC1)C2=CC=CC=C2C(=O)O.Cl

TARGETMOL CHEMICALS INC BIIB 722 Mesylate 1MG

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Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. BIIB 722 Mesylate is a selective sodium-hydrogen exchange inhibitor with cardioprotective properties and can be used to study myocardial ischemia and myocardial infarction. Purity 99.49%

AdipoGen Manumycin A

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Chemical. CAS 52665-74-4. Formula C31H38N2O7. MW 550.6. Isolated from Streptomyces parvulus. Antibiotic. Apoptosis and endoplasmic reticulum stress-mediated cell death inducer. Potent, selective and competitive cell permeable rasfarnesyltransferase inhibitor IC50 = 30 nM. Does not affect geranylgeranyltransferase IC50 = 180 µM. Inhibition is competitive with respect to farnesyl pyrophosphate and non-competitive with respect to Ras. Neutral sphingomyelinase inhibitor. Blocks insulin-induced MAP kinase activation in rat cardiac myocytes 19 µM. Targets protein phosphatase 1alpha PP1alpha and reduces hydrogen peroxide. Corrects aberrant splicing of the muscle chloride channel Clcn1 in myotonic dystrophy type 1 DM1. Shows potential anti-inflammatory activity.