Home Sulfos 4-amino-N-(1-phenyl-1H-pyrazol-5-yl)benzene-1-sulfonamide

4-amino-N-(1-phenyl-1H-pyrazol-5-yl)benzene-1-sulfonamide

CAS No.:
526-08-9
Catalog Number:
AG003UGQ
Molecular Formula:
C15H14N4O2S
Molecular Weight:
314.3623
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
100mg
1 week
United States
$94
- +
250mg
1 week
United States
$149
- +
500mg
≥98%
1 week
United States
$241
- +
1g
≥98%
1 week
United States
$321
- +
5g
≥98%
1 week
United States
$1112
- +
Product Description
Catalog Number:
AG003UGQ
Chemical Name:
4-amino-N-(1-phenyl-1H-pyrazol-5-yl)benzene-1-sulfonamide
CAS Number:
526-08-9
Molecular Formula:
C15H14N4O2S
Molecular Weight:
314.3623
MDL Number:
MFCD00057226
IUPAC Name:
4-amino-N-(2-phenylpyrazol-3-yl)benzenesulfonamide
InChI:
InChI=1S/C15H14N4O2S/c16-12-6-8-14(9-7-12)22(20,21)18-15-10-11-17-19(15)13-4-2-1-3-5-13/h1-11,18H,16H2
InChI Key:
QWCJHSGMANYXCW-UHFFFAOYSA-N
SMILES:
Nc1ccc(cc1)S(=O)(=O)Nc1ccnn1c1ccccc1
EC Number:
208-384-3
UNII:
0J8L4V3F81
NSC Number:
757859
Properties
Complexity:
451  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
314.084g/mol
Formal Charge:
0
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
314.363g/mol
Monoisotopic Mass:
314.084g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
98.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5  
Literature
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In vitro sulfoxidation of thioether compounds by human cytochrome P450 and flavin-containing monooxygenase isoforms with particular reference to the CYP2C subfamily. Drug metabolism and disposition: the biological fate of chemicals 20040301
Mediators of bradykinin-induced vasorelaxation in human coronary microarteries. Hypertension (Dallas, Tex. : 1979) 20040201
Utility of microtiter plate assays for human cytochrome P450 inhibition studies in drug discovery: application of simple method for detecting quasi-irreversible and irreversible inhibitors. Drug metabolism and pharmacokinetics 20040201
Inhibition of cytochrome P450 2C9 improves endothelium-dependent, nitric oxide-mediated vasodilatation in patients with coronary artery disease. Circulation 20040120
Effects of the dietary flavonoid chrysin in isolated rat mesenteric vascular bed. Journal of vascular research 20040101
Identification of the cytochrome P450 enzymes involved in the metabolism of domperidone. Xenobiotica; the fate of foreign compounds in biological systems 20040101
Involvement of CYP 2C9 in mediating the proinflammatory effects of linoleic acid in vascular endothelial cells. Journal of the American College of Nutrition 20031201
Identification of the human cytochrome P450s responsible for the in vitro metabolism of a leukotriene B4 receptor antagonist, CP-195,543. Xenobiotica; the fate of foreign compounds in biological systems 20031201
Baseline blood flow and bradykinin-induced vasodilator responses in the human forearm are insensitive to the cytochrome P450 2C9 (CYP2C9) inhibitor sulphaphenazole. Clinical science (London, England : 1979) 20031001
Aged spontaneously hypertensive rats exhibit a selective loss of EDHF-mediated relaxation in the renal artery. Hypertension (Dallas, Tex. : 1979) 20031001
Demethylation of radiolabelled dextromethorphan in rat microsomes and intact hepatocytes. European journal of biochemistry 20030901
Role of human hepatic cytochrome P-450s in territrem A metabolism. Journal of toxicology and environmental health. Part A 20030711
Cytochrome p-450 epoxygenase products contribute to attenuated vasoconstriction after chronic hypoxia. American journal of physiology. Heart and circulatory physiology 20030701
Electron spin resonance detection of hydrogen peroxide as an endothelium-derived hyperpolarizing factor in porcine coronary microvessels. Arteriosclerosis, thrombosis, and vascular biology 20030701
Selectivities of human cytochrome P450 inhibitors toward rat P450 isoforms: study with cDNA-expressed systems of the rat. Drug metabolism and disposition: the biological fate of chemicals 20030701
Cytochrome P450 inhibition using recombinant proteins and mass spectrometry/multiple reaction monitoring technology in a cassette incubation. Drug metabolism and disposition: the biological fate of chemicals 20030701
Sulfaphenazole derivatives as tools for comparing cytochrome P450 2C5 and human cytochromes P450 2Cs: identification of a new high affinity substrate common to those enzymes. Biochemistry 20030603
Induction of hepatic heme oxygenase-1 by diclofenac in rodents: role of oxidative stress and cytochrome P-450 activity. Journal of hepatology 20030601
EDHF-mediated vasodilation involves different mechanisms in normotensive and hypertensive rat lungs. American journal of physiology. Heart and circulatory physiology 20030501
Characterization of the endothelium-derived hyperpolarizing factor (EDHF) response in the human interlobar artery. Kidney international 20030501
Identification of the cytochrome P450 enzymes involved in the N-oxidation of voriconazole. Drug metabolism and disposition: the biological fate of chemicals 20030501
Cytochrome P450 2C9-derived epoxyeicosatrienoic acids induce angiogenesis via cross-talk with the epidermal growth factor receptor (EGFR). FASEB journal : official publication of the Federation of American Societies for Experimental Biology 20030401
Oxidative metabolism of amprenavir in the human liver. Effect of the CYP3A maturation. Drug metabolism and disposition: the biological fate of chemicals 20030301
Metabolism and metabolic inhibition of cilnidipine in human liver microsomes. Acta pharmacologica Sinica 20030301
Mediation of arachidonic acid metabolite(s) produced by endothelial cytochrome P-450 3A4 in monkey arterial relaxation. Hypertension research : official journal of the Japanese Society of Hypertension 20030301
Essential requirements for substrate binding affinity and selectivity toward human CYP2 family enzymes. Archives of biochemistry and biophysics 20030101
Substrate selectivity of human cytochrome P450 2C9: importance of residues 476, 365, and 114 in recognition of diclofenac and sulfaphenazole and in mechanism-based inactivation by tienilic acid. Archives of biochemistry and biophysics 20030101
High-throughput inhibition screening of major human cytochrome P450 enzymes using an in vitro cocktail and liquid chromatography-tandem mass spectrometry. Journal of pharmaceutical and biomedical analysis 20030101
Cytochrome P450 2C9 plays an important role in the regulation of exercise-induced skeletal muscle blood flow and oxygen uptake in humans. The Journal of physiology 20030101
Liquid chromatography/tandem mass spectrometric determination of inhibition of human cytochrome P450 isozymes by resveratrol and resveratrol-3-sulfate. Rapid communications in mass spectrometry : RCM 20030101
Identification of glutathione conjugates of troglitazone in human hepatocytes. Chemico-biological interactions 20021110
Mechanisms underlying endothelium-dependent, nitric oxide- and prostanoid-independent relaxation in monkey and dog coronary arteries. Naunyn-Schmiedeberg's archives of pharmacology 20021101
The contribution of cytochrome P-450 isoenzymes to the metabolism of phenothiazine neuroleptics. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 20021001
EDHF, but not NO or prostaglandins, is critical to evoke a conducted dilation upon ACh in hamster arterioles. American journal of physiology. Heart and circulatory physiology 20020901
Effects of herbal components on cDNA-expressed cytochrome P450 enzyme catalytic activity. Life sciences 20020816
The N-demethylation of the doxepin isomers is mainly catalyzed by the polymorphic CYP2C19. Pharmaceutical research 20020701
Cytochrome P450 2C9-induced endothelial cell proliferation involves induction of mitogen-activated protein (MAP) kinase phosphatase-1, inhibition of the c-Jun N-terminal kinase, and up-regulation of cyclin D1. The Journal of biological chemistry 20020503
Metabolism of (+)- and (-)-limonenes to respective carveols and perillyl alcohols by CYP2C9 and CYP2C19 in human liver microsomes. Drug metabolism and disposition: the biological fate of chemicals 20020501
In vitro metabolic characteristics of cytochrome P-450 2A6 in Chinese liver microsomes. Acta pharmacologica Sinica 20020501
Sustained ER Ca2+ depletion suppresses protein synthesis and induces activation-enhanced cell death in mast cells. The Journal of biological chemistry 20020419
Dynamic modulation of interendothelial gap junctional communication by 11,12-epoxyeicosatrienoic acid. Circulation research 20020419
Human cytochrome P450s involved in the metabolism of 9-cis- and 13-cis-retinoic acids. Biochemical pharmacology 20020301
Cytochrome P450 enzymes contributing to demethylation of maprotiline in man. Pharmacology & toxicology 20020301
Oxidation of the flavonoids galangin and kaempferide by human liver microsomes and CYP1A1, CYP1A2, and CYP2C9. Drug metabolism and disposition: the biological fate of chemicals 20020201
Contribution of cytochrome P450 metabolites to bradykinin-induced vasodilation in endothelial NO synthase deficient mouse hearts. British journal of pharmacology 20020201
Hydrogen peroxide is an endothelium-derived hyperpolarizing factor in human mesenteric arteries. Biochemical and biophysical research communications 20020125
Design and application of fluorometric assays for human cytochrome P450 inhibition. Methods in enzymology 20020101
Major cytochrome P450 enzymes responsible for microsomal aldehyde oxygenation of 11-oxo-Delta8-tetrahydrocannabinol and 9-anthraldehyde in human liver. Drug metabolism and pharmacokinetics 20020101
Quantitative determination of sulfonamide in meat by liquid chromatography-electrospray-mass spectrometry. Talanta 20011224
Synthesis of sulfaphenazole derivatives and their use as inhibitors and tools for comparing the active sites of human liver cytochromes P450 of the 2C subfamily. Journal of medicinal chemistry 20011025
Interaction of new sulfaphenazole derivatives with human liver cytochrome p450 2Cs: structural determinants required for selective recognition by CYP 2C9 and for inhibition of human CYP 2Cs. Archives of biochemistry and biophysics 20011015
Metabolism of vanoxerine, 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine, by human cytochrome P450 enzymes. Drug metabolism and disposition: the biological fate of chemicals 20010901
Role of CYP2C9 polymorphism in losartan oxidation. Drug metabolism and disposition: the biological fate of chemicals 20010701
The coronary endothelium-derived hyperpolarizing factor (EDHF) stimulates multiple signalling pathways and proliferation in vascular cells. Pflugers Archiv : European journal of physiology 20010701
Involvement of CYP2B6 in n-demethylation of ketamine in human liver microsomes. Drug metabolism and disposition: the biological fate of chemicals 20010601
Establishment of the transformants expressing human cytochrome P450 subtypes in HepG2, and their applications on drug metabolism and toxicology. Toxicology in vitro : an international journal published in association with BIBRA 20010601
Metabolism of sulfinpyrazone sulfide and sulfinpyrazone by human liver microsomes and cDNA-expressed cytochrome P450s. Drug metabolism and disposition: the biological fate of chemicals 20010501
Inhibition of phenytoin hydroxylation in human liver microsomes by several selective serotonin re-uptake inhibitors. Epilepsy research 20010401
Relative contributions of CYP2C9 and 2C19 to phenytoin 4-hydroxylation in vitro: inhibition by sulfaphenazole, omeprazole, and ticlopidine. European journal of clinical pharmacology 20010401
Metabolic characterization of the major human small intestinal cytochrome p450s. Drug metabolism and disposition: the biological fate of chemicals 20010301
CYP3A4 is the major CYP isoform mediating the in vitro hydroxylation and demethylation of flunitrazepam. Drug metabolism and disposition: the biological fate of chemicals 20010201
Inhibition of cytochrome P450 2C9 activity in vitro by 5-hydroxytryptamine and adrenaline. Pharmacogenetics 20010201
Endothelium-derived hyperpolarizing factor synthase (Cytochrome P450 2C9) is a functionally significant source of reactive oxygen species in coronary arteries. Circulation research 20010119
A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry. Drug metabolism and disposition: the biological fate of chemicals 20010101
Effects of CYP2C19 genotype and CYP2C9 on fluoxetine N-demethylation in human liver microsomes. Acta pharmacologica Sinica 20010101
Cytochrome P-450 2C9 sensitizes human prostate tumor cells to cyclophosphamide via a bystander effect. Antimicrobial agents and chemotherapy 20001001
Metabolism of 3-methylindole by porcine liver microsomes: responsible cytochrome P450 enzymes. Toxicological sciences : an official journal of the Society of Toxicology 20000601
Oxidation of histamine H1 antagonist mequitazine is catalyzed by cytochrome P450 2D6 in human liver microsomes. The Journal of pharmacology and experimental therapeutics 19980201
Roles of two allelic variants (Arg144Cys and Ile359Leu) of cytochrome P4502C9 in the oxidation of tolbutamide and warfarin by human liver microsomes. Xenobiotica; the fate of foreign compounds in biological systems 19980201
Inhibition of tolbutamide 4-methylhydroxylation by a series of non-steroidal anti-inflammatory drugs in V79-NH cells expressing human cytochrome P4502C10. Xenobiotica; the fate of foreign compounds in biological systems 19961201
Efficacy of 101 antimicrobials and other agents on the development of Cryptosporidium parvum in vitro. Annals of tropical medicine and parasitology 19961201
Specificity of substrate and inhibitor probes for cytochrome P450s: evaluation of in vitro metabolism using cDNA-expressed human P450s and human liver microsomes. Xenobiotica; the fate of foreign compounds in biological systems 19960701
Tolbutamide and phenytoin hydroxylations by cDNA-expressed human liver cytochrome P4502C9. Biochemical and biophysical research communications 19910329
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