Chemicals

As the former name of Biomol GmbH (Biomol Fine Chemicals GmbH) already suggests: For more than 50 years, we provide a wide range of organic and inorganic chemicals for your laboratory. Search for your desired chemical substance using a compound name or, even better, a CAS number (Chemical Abstracts Service Registry Number), unique identifiers for chemicals. In contrast to the different spelling options of a substance, a CAS number will directly lead you to the product you are looking for. According to our slogan: "You have the vision, we have the substance."

As the former name of Biomol GmbH (Biomol Fine Chemicals GmbH) already suggests: For more than 50 years, we provide a wide range of organic and inorganic chemicals for your laboratory . Search... read more »
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Chemicals

As the former name of Biomol GmbH (Biomol Fine Chemicals GmbH) already suggests: For more than 50 years, we provide a wide range of organic and inorganic chemicals for your laboratory. Search for your desired chemical substance using a compound name or, even better, a CAS number (Chemical Abstracts Service Registry Number), unique identifiers for chemicals. In contrast to the different spelling options of a substance, a CAS number will directly lead you to the product you are looking for. According to our slogan: "You have the vision, we have the substance."

11340 from 11341 pages
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Paltusotine
Paltusotine

Item number: Cay42041-10

An SST2 agonist, selectively inhibits cAMP production in cells expressing SST2 over cells expressing SST1, SST3, SST4, or SST5 (EC50s = 25, >1,000, >1,000, >1,000, and >1,000 nM, respectively), reduces GHRH-stimulated growth hormone release in rats at 3, 10, and 30 mg/kg, reduces plasma levels of IGF-1 in beagle...
Keywords: CRN00808, 3-[4-(4-amino-1-piperidinyl)-3-(3,5-difluorophenyl)-6-quinolinyl]-2-hydroxy-benzonitrile
Application: SST2 agonist
CAS 2172870-89-0
MW: 456.5 D
From 421.00€ *
Review
BI-87G3
BI-87G3

Item number: Cay42045-1

A JNK1 inhibitor (IC50 = 1.804 µM), selective for JNK1 over p38alpha MAPK, Akt, furin, and lethal factor (IC50s = >100, >100, >100, and >50 µM, respectively), inhibits TNF-alpha-induced JNK1 phosphorylation in HeLa cells (IC50 = ~15 µM). Formulation: A solid. InChI:...
Keywords: c-Jun N-terminal Kinase Inhibitor XI, JNK Inhibitor XI, 2-[(5-nitro-2-thiazolyl)thio]-benzothiazole
Application: JNK1 inhibitor
CAS 2207-44-5
MW: 295.4 D
From 40.00€ *
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KEA1-97
KEA1-97

Item number: Cay42049-10

An inhibitor of the protein-protein interaction between Trx and caspase-3, binds to K72 of Trx and inhibits DCT-alkyne labeling of recombinant Trx (IC50 = 10 µM), inhibits the interaction between thioredoxin and caspase-3 in a cell-free assay at 100 µM, reduces survival and proliferation of and induces apoptosis in...
Keywords: 4,6-dichloro-N-(4'-fluoro[1,1'-biphenyl]-4-yl)-1,3,5-triazin-2-amine
Application: Trx-caspase-3 protein-protein interaction inhibitor
CAS 2138882-71-8
MW: 335.16 D
From 70.00€ *
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CFT-7455
CFT-7455

Item number: Cay42053-1

A cereblon ligand 1-containing degrader of IKZF1 and IKZF3, reduces levels of IKZF1 and IKZF3 in NCI H929 cells at 0.1 nM, decreases the growth of NCI H929 cells (GI50 = 0.0743 nM), reduces tumor volume in an RPMI-8226 plasmocytoma mouse xenograft model at 30 or 100 µg/kg per day. Formulation: A solid. InChI:...
Keywords: Cemsidomide, 3S-[6-[[4-(4-morpholinylmethyl)phenyl]methyl]-2-oxobenz[cd]indol-1(2H)-yl]-2,6-piperidinedione
Application: Cereblon ligand 1-containing IKZF1 / IKZF3 degrader
CAS 2504235-67-8
MW: 469.53 D
From 110.00€ *
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AZ 13705339
AZ 13705339

Item number: Cay42087-10

A PAK1 inhibitor (IC50 = 0.33 nM), selective for PAK1 over a panel of 117 kinases at 100 nM, binds to PAK1 and PAK2 (Kd = 0.28 and 0.32 nM, respectively), inhibits S. enterica infection in HAP1 cells at 10 µM, inhibits cell death induced by an antibody targeting Siglec-8 in IL-5-stimulated primary human eosinophils...
Keywords: 2-[[[2-[[3-(ethylsulfonyl)-4-(4-methyl-1-piperazinyl)phenyl]amino]-5-fluoro-4-pyrimidinyl][5-(hydroxymethyl)-2-methylpheny...
Application: PAK1 (p21-activated kinase 1) inhibitor
CAS 2016806-57-6
MW: 629.8 D
From 116.00€ *
Review
GAPDH Inhibitor Compound F8
GAPDH Inhibitor Compound F8

Item number: Cay42090-1

A covalent inhibitor of GAPDH (IC50 = 39.31 µM), decreases viability of, and glucose metabolism in, HEK293 cells in a concentration-dependent manner. Formulation: A solid. InChI: InChI=1S/C20H18N2O5/c1-3-13(7-15(5-1)23-9-17-11-25-17)19-21-22-20(27-19)14-4-2-6-16(8-14)24-10-18-12-26-18/h1-8,17-18H,9-12H2. InChIKey:...
Keywords: 2,5-bis[3-(2-oxiranylmethoxy)phenyl]-1,3,4-oxadiazole
Application: GAPDH covalent inhibitor
CAS 252212-58-1
MW: 366.37 D
From 55.00€ *
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Martinostat
Martinostat

Item number: Cay42100-10

An HDAC inhibitor (IC50s = 0.3, 2, 0.6, and 4.1 nM for HDAC1, -2, -3, and -6, respectively), selective for these HDACs over HDAC4, -5, -7, -8, and -9 (IC50s = 1,970, 352, >20,000, >15,000, and >15,000 nM, respectively), reduces H3K9ac and H4K12ac in primary mouse neuronal cells (EC50s = 100 nM for both)....
Keywords: N-hydroxy-3-[4-[[methyl(tricyclo[3.3.1.13,7]dec-1-ylmethyl)amino]methyl]phenyl]-2E-propenamide
Application: HDAC inhibitor
CAS 1629052-58-9
MW: 354.5 D
From 153.00€ *
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GSK467
GSK467

Item number: Cay42103-1

A JARID1B inhibitor (IC50 = 0.02-0.1 µM), selective for JARID1B over KMD2, -3, -4, and -5 (IC50s = 1-10 µM). Formulation: A solid. InChI: InChI=1S/C17H13N5O2/c23-16-14-6-7-18-9-15(14)20-17(21-16)24-13-8-19-22(11-13)10-12-4-2-1-3-5-12/h1-9,11H,10H2,(H,20,21,23). InChIKey: ZTYRLXUTLYBVHH-UHFFFAOYSA-N. SMILES:...
Keywords: 2-[[1-(phenylmethyl)-1H-pyrazol-4-yl]oxy]- pyrido[3,4-d]pyrimidin-4(3H)-one
Application: JARID1B (KDM5B) inhibitor
CAS 1628332-52-4
MW: 319.3 D
From 60.00€ *
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GSK3beta Inhibitor 1
GSK3beta Inhibitor 1

Item number: Cay42107-10

A GSK3beta inhibitor (IC50 = 4.19 nM), decreases blood glucose levels in an OGTT in a rat model of high-fat diet and STZ-induced diabetes at 50 mg/kg. Formulation: A solid. InChI: InChI=1S/C14H10N2O/c17-14-12(9-10-5-3-4-8-15-10)11-6-1-2-7-13(11)16-14/h1-9H,(H,16,17)/b12-9-. InChIKey: YKQONSWBHGBDSB-XFXZXTDPSA-N....
Keywords: Glycogen Synthase Kinase 3beta Inhibitor I, (3Z)-1,3-dihydro-3-(2-pyridinylmethylene)-2H-indol-2-one
Application: GSK3beta inhibitor
CAS 187325-53-7
MW: 222.2 D
From 223.00€ *
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A-425619
A-425619

Item number: Cay42117-10

A TRPV1 antagonist, selective for TRPV1 over a panel of 83 receptors, enzymes, transporters, and ion channels at 10 µM, inhibits capsaicin-, NADA-, anandamide-, or acid-induced increases in intracellular calcium in HEK293 cells expressing human TRPV1 (IC50s = 5, 4, 3, and 2 nM, respectively), increases core body...
Keywords: N-5-isoquinolinyl-N'-[[4-(trifluoromethyl)phenyl]methyl]-urea
Application: TRPV1 antagonist
CAS 581809-67-8
MW: 345.3 D
From 208.00€ *
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D-Amino Acid Oxidase Inhibitor
D-Amino Acid Oxidase Inhibitor

Item number: Cay23894-100

An inhibitor of DAAO (IC50s = 145 and 114 nM in CHO cells expressing human and rat DAAO, respectively), selective for DAAO over a panel of 150 enzymes, receptors and ion channels (30 µM), inhibits DAAO activity in rat kidney and cerebellum in a dose- and time-dependent manner (10-200 mg/kg, i.p.), increases levels...
Keywords: DAAO inhibitor, 4H-thieno[3,2-b]pyrrole-5-carboxylic acid
Application: DAAO inhibitor
CAS 39793-31-2
MW: 167.2 D
From 40.00€ *
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Voacanga africana Ethanol Extract
Voacanga africana Ethanol Extract

Item number: Cay43250-1

A natural extract, contains a crude mixture of bioactive natural products extracted from V. africana. Formulation: A solution in methanol. InChI: . InChIKey: . SMILES:
Keywords: V. africana Ethanol Extract
Application: Natural extract, crude mixture of bioactive natural products
76.00€ *
Review
11340 from 11341 pages