Biochemicals

In this category you will find an extensive portfolio of biochemicals: inhibitors, ligands and substrates of various enzymes and receptors, regulatory compounds, assay components and dyes. Besides that it includes carbohydrates, amino acids, antioxidants and a wide array of other products and reagents for biochemical research.

In this category you will find an extensive portfolio of biochemicals: inhibitors, ligands and substrates of various enzymes and receptors, regulatory compounds, assay components and dyes. Besides... read more »
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Biochemicals

In this category you will find an extensive portfolio of biochemicals: inhibitors, ligands and substrates of various enzymes and receptors, regulatory compounds, assay components and dyes. Besides that it includes carbohydrates, amino acids, antioxidants and a wide array of other products and reagents for biochemical research.

10499 from 10504 pages
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GS-9901
GS-9901

Item number: Cay42105-1

A PI3Kdelta inhibitor (IC50 = 1 nM), selective for PI3Kdelta over PI3Kalpha, PI3Kbeta, and PI3Kgamma (IC50s = 750, 100, and 190 nM, respectively) and a panel of 456 additional kinases, including 11 lipid and 56 mutant kinases, at 10 µM, activates basophils in isolated human whole blood (EC50 = 1 nM), decreases ankle...
Keywords: 2,4-diamino-6-[[(S)-[5-chloro-8-fluoro-3,4-dihydro-4-oxo-3-(3-pyridinyl)-2-quinazolinyl]cyclopropylmethyl]amino]-5-pyrimid...
Application: PI3Kdelta inhibitor
CAS 1640247-87-5
MW: 477.9 D
From 122.00€ *
Review
Pyrotinib (maleate)
Pyrotinib (maleate)

Item number: Cay42108-1

An EGFR and HER2 inhibitor (IC50s = 13 and 38 nM, respectively), selectively inhibits the proliferation of HER2+ BT474 and SKOV3 cells (IC50s = 5.1 and 43 nM, respectively) over HER2- MDA-MB-231 cells (IC50 = 3,500 nM), decreases tumor growth without affecting body weight in BT474 and SKOV3 mouse xenograft models at...
Keywords: SHR-1258,...
Application: EGFR / HER2 inhibitor
CAS 1397922-61-0
MW: 815.2 D
From 214.00€ *
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2-Amino-9H-pyrido[2,3-b]indole
2-Amino-9H-pyrido[2,3-b]indole

Item number: Cay42114-10

A mutagenic heterocyclic amine, has been found in cooked foods, mutagenic to S. typhimurium in the Ames test and induces SCEs in NL3 cells, induces hepatic and blood vessel tumor formation in mice at 0.08% in the diet, has been found in the urine of cigarette smokers. Formulation: A solid. InChI:...
Keywords: 2-Amino-alpha-Carboline, AalphaC, 9H-pyrido[2,3-b]indol-2-amine
Application: Mutagenic heterocyclic amine
CAS 26148-68-5
MW: 183.2 D
From 122.00€ *
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Dendrophenol
Dendrophenol

Item number: Cay42115-1

A polyphenol with diverse biological activities, decreases viability of, and induces cell cycle arrest at the S phase in, HCT116 cells at 10 µM, inhibits the migration of MDA-MB-231 cells at 3 or 10 µM, inhibits LPS-induced increases in iNOS, COX-2, HIF-1alpha, and NF-kappaB levels and NF-kappaB nuclear...
Keywords: Aloifol II, Moscatilin, 4-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-2,6-dimethoxy-phenol
Application: Bioactive polyphenol
CAS 108853-14-1
MW: 304.3 D
From 101.00€ *
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Phepropeptin C
Phepropeptin C

Item number: Cay10008110-1

A cyclic peptide with proteasome inhibition activity, inhibits isolated mouse liver proteasomes (IC50 = 12.5 µg/ml). Formulation: A powder. InChI:...
Keywords: Cyclic(Leu-D-Leu-xi-Ile-Leu-D-Phe-D-Pro), cyclo(L-isoleucyl-L-leucyl-D-phenylalanyl-L-prolyl-L-leucyl-D-leucyl)
Application: Cyclic peptide, proteasome inhibition agent
CAS 396729-25-2
MW: 696.92 D
1,068.00€ *
Review
BM 567
BM 567

Item number: Cay10155-1

A dual acting antithrombogenic agent, inhibitor of TXA2 synthase (IC50 = 12 nM), acts as an TP receptor antagonist (IC50 = 1.1 nM). Formulation: A crystalline solid. InChI:...
Keywords: 2-(cyclohexylamino)-5-nitro-N-[(pentylamino)carbonyl]-benzenesulfonamide
Application: Dual thromboxane synthase inhibitor, TP receptor antagonist
CAS 284464-77-3
MW: 412.5 D
From 95.00€ *
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PDGFR TKI III
PDGFR TKI III

Item number: Cay14925-1

A PDGFRalpha and PDGFRbeta inhibitor (IC50s = 0.05 and 0.13 µM, respectively), selective for PDGFRalpha and PDGFRbeta over FGFR, EGFR, PKA, and PKC (IC50s = 29.7, >30, >30, and >30 µM, respectively) but does inhibit c-Kit and FLT3 (IC50s = 0.05 and 0.23 µM, respectively), inhibits PDGF homodimer-induced...
Keywords: PDGFR Tyrosine Kinase Inhibitor III, Platelet-derived Growth Factor Receptor TKI III, Platelet-derived Growth Factor...
Application: PDGFRalpha / PDGFRbeta inhibitor
CAS 205254-94-0
MW: 485.5 D
From 55.00€ *
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GSK180
GSK180

Item number: Cay19217-1

An inhibitor of kynurenine 3-monooxygenase (IC50 = 6.3 nM), selective for human over P. fluorescens kynurenine 3-monooxygenase (IC50 = 500 nM), increases circulating levels of kynurenine and kynurenic acid in mice at 27 mg/kg, protects against secondary acute lung injury and renal injury in a rat model of...
Keywords: 5,6-dichloro-2-oxo-3(2H)-benzoxazolepropanoic acid
Application: Kynurenine 3-monooxygenase inhibitor
CAS 1799725-26-0
MW: 276.1 D
From 55.00€ *
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WAY-181187
WAY-181187

Item number: Cay23461-10

A 5-HT6 receptor agonist, increases intracellular cAMP levels in HeLa cells expressing 5-HT6 (EC50 = 6.5 nM), selectively binds to 5-HT6 over 5-HT2B, 5-HT2C, and 5-HT7 (Kis = 2,458, 124, and 679 nM, respectively), selective for 5-HT6 over a panel of 31 receptors and ion channels at 100 nM, increases extracellular...
Keywords: SAX 187, 1-[(6-chloroimidazo[2,1-b]thiazol-5-yl)sulfonyl]-1H-indole-3-ethanamine
Application: 5-HT6 receptor agonist
CAS 554403-49-5
MW: 380.87 D
From 105.00€ *
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Navoximod
Navoximod

Item number: Cay28440-1

An IDO1 inhibitor (IC50 = 28 nM for the recombinant human enzyme), decreases tumor volume in a Panc02 murine PDAC model at 500 mg/kg. Formulation: A solid. InChI: InChI=1S/C18H21FN2O2/c19-14-3-1-2-13-16-9-20-10-21(16)15(18(13)14)8-17(23)11-4-6-12(22)7-5-11/h1-3,9-12,15,17,22-23H,4-8H2/t11-,12-,15-,17+/m0/s1....
Keywords: GDC-0919, NLG-919, RG6078, (aR,5S)-6-fluoro-a-(trans-4-hydroxycyclohexyl)-5H-imidazo[5,1-a]isoindole-5-ethanol
Application: IDO1 inhibitor
CAS 1402837-78-8
MW: 316.4 D
From 239.00€ *
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TC 13172
TC 13172

Item number: Cay31034-1

An inhibitor of MLKL and necroptosis, selective for MLKL over RIPK1 and RIPK3 at 10 µM, inhibits TSZ-induced necroptosis in HT-29 cells (EC50 = 2 nM), inhibits TSZ-induced oligomerization of MLKL and translocation of MLKL to the plasma membrane in HT-29 cells at 100 nM. Formulation: A solid. InChI:...
Keywords: 3,7-dihydro-3-[3-(3-hydroxyphenyl)-2-propyn-1-yl]-1,7-dimethyl-8-(methylsulfonyl)-1H-purine-2,6-dione
Application: MLKL / necroptosis inhibitor
CAS 2093393-05-4
MW: 388.4 D
From 76.00€ *
Review
GLPG1205
GLPG1205

Item number: Cay33185-1

A GPR84 antagonist, inhibits DIM-induced GTPgammaS binding in cells overexpressing human GPR84 (IC50 = 54 nM), inhibits embelin-induced chemotaxis of isolated human neutrophils (IC50 = 11 nM), reduces body weight loss and rectal bleeding and improves stool consistency in a rat model of DSS-induced colitis....
Keywords: 9-(2-cyclopropylethynyl)-2-[(2S)-1,4-dioxan-2-ylmethoxy]-6,7-dihydro-4H-pyrimido[6,1-a]isoquinolin-4-one
Application: GPR84 antagonist
CAS 1445847-37-9
MW: 378.4 D
From 101.00€ *
Review
10499 from 10504 pages