Pyrroles
AdipoGen L-Homoserine lactone HCl
Chemical. CAS 2185-03-7. Formula C4H7NO2 . HCl. MW 137.56. L-Homoserine lactone is a synthetic building block or intermediate used in the synthesis of organoselenium chemistry intermediates and analogs of bacterial quorum-sensing signaling molecules.
EMOLECULES INC 198765-34-3 | 4-AMINO-1-METHYL-1H-PYRROLE-2-CARBOXYLIC ACID HCL | AstaTech | MFCD18782086 | 176.600 | C6H9ClN2O2 | 95.000 | Cl.Cn1cc(N)cc1C(O)=O | 1g | 222806267
4-AMINO-1-METHYL-1H-PYRROLE-2-CARBOXYLIC ACID HCL | AstaTech | 198765-34-3 | MFCD18782086 | 176.600 | C6H9ClN2O2 | 95.000 | Cl.Cn1cc(N)cc1C(O)=O | 1g | 222806267
EMOLECULES INC 138907-68-3 | Ethyl 5-Amino-1-(4-fluorophenyl)pyrazole-4-carboxylate | Chem-Impex | MFCD00173917 | 249.245 | C12H12FN3O2 | 98.000 | CCOC(=O)c1cnn(c1N)-c1ccc(F)cc1 | 1g | 112749789
Ethyl 5-Amino-1-(4-fluorophenyl)pyrazole-4-carboxylate | Chem-Impex | 138907-68-3 | MFCD00173917 | 249.245 | C12H12FN3O2 | 98.000 | CCOC(=O)c1cnn(c1N)-c1ccc(F)cc1 | 1g | 112749789
Selleck Chemical LLC Atorvastatin
Atorvastatin is a lipid lowering agent It is a competitive inhibitor of hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase the rate-determining enzyme in cholesterol biosynthesis via the mevalonate pathway Atorvastatin activates autophagy
![EMOLECULES INC 7697-46-3 | PHENYL(1H-PYRROL-2-YL)METHANONE | AstaTech | MFCD00094048 | 171.199 | C11H9NO | 95.000 | O=C(c1ccc[nH]1)c1ccccc1 | 1g | 432789539](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502170462.JPG-250.jpg)
EMOLECULES INC 7697-46-3 | PHENYL(1H-PYRROL-2-YL)METHANONE | AstaTech | MFCD00094048 | 171.199 | C11H9NO | 95.000 | O=C(c1ccc[nH]1)c1ccccc1 | 1g | 432789539
PHENYL(1H-PYRROL-2-YL)METHANONE | AstaTech | 7697-46-3 | MFCD00094048 | 171.199 | C11H9NO | 95.000 | O=C(c1ccc[nH]1)c1ccccc1 | 1g | 432789539
Medchemexpress LLC HY-100025A 10mg Medchemexpress, HLCL-61 (hydrochloride) CAS:1158279-20-9 Purity:>98%
Medchemexpress, HY-100025A 10mg HLCL-61 (hydrochloride) CAS:1158279-20-9 HLCL-61 hydrochloride is a first-in-class inhibitor of protein arginine methyltransferase 5 (PRMT5) . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-111754 5mg Medchemexpress, DMX-5804 CAS:2306178-56-1 Purity:>98%
Medchemexpress, HY-111754 5mg DMX-5804 CAS:2306178-56-1 DMX-5804 is a potent, orally active and selective MAP4K4 inhibitor, with an IC 50 of 3 nM, a pIC 50 of 8.55 for human MAP4K4, less potent on MINK1/MAP4K6 ( pIC 50 , 8.18), and TNIK/MAP4K7 ( pIC 50 , 7.96). DMX-5804 enhances cardiomyocyte survival, and reduces ischemia-reperfusion injury in mice [1] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-15440A 5mg Medchemexpress, Fostemsavir CAS:864953-29-7 Purity:>98%
Medchemexpress, HY-15440A 5mg Fostemsavir CAS:864953-29-7 Fostemsavir (BMS-663068) is the phosphonooxymethyl prodrug of BMS-626529. Fostemsavir (BMS-663068) is a novel attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4 + T cells. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-15816A 5mg Medchemexpress, Ulixertinib (hydrochloride) CAS:1956366-10-1 Purity:>98%
Medchemexpress, HY-15816A 5mg Ulixertinib (hydrochloride) CAS:1956366-10-1 Ulixertinib hydrochloride is a potent, orally active, highly selective, ATP-competitive and reversible covalent inhibitor of ERK1/2 kinases, with an IC 50 of <0.3 nM against ERK2. Ulixertinib hydrochloride inhibits the phosphorylated ERK2 (pERK) and downstream kinase RSK (pRSK) in an A375 melanoma cell line [1] [2] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-108637 5mg Medchemexpress, PhiKan 083 CAS:880813-36-5 Purity:>98%
Medchemexpress, HY-108637 5mg PhiKan 083 CAS:880813-36-5 PhiKan 083 is a carbazole derivative, which binds to the surface cavity and stabilizes Y220C (a p53 mutant), with a K d of 167 μM [1] , and a relative binding affinity ( K d ) of 150 μM in Ln229 cells [3] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-109020 5mg Medchemexpress, Acrizanib CAS:1229453-99-9 Purity:>98%
Medchemexpress, HY-109020 5mg Acrizanib CAS:1229453-99-9 Acrizanib is a VEGFR-2 inhibitor, with an IC 50 of 17.4 nM for BaF3-KDR. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Apexbio Technology LLC Sunitinib malate(Synonyms: Sutent, SU11248, Sunitinib L-malate, Sunitinib malate salt, SU-11248 malate, Sutent malate), 100mg, CAS: 341031-54-7.
Sunitinib malate (CAS 341031-54-7) is a small molecule orally bioavailable multitargeted receptor tyrosine kinase inhibitor It inhibits various receptor tyrosine kinases including platelet-derived growth factor receptor (PDGFR) vascular endothelial growth factor receptors (VEGFR-1 2 and 3) c-KIT FLT3 kinase colony-stimulating factor-1 receptor (CSF-1R) and RET kinase In neuroblastoma cell lines (e g SK-N-BE(2) SH-SY5Y LAN-5) treatment with sunitinib malate significantly suppresses proliferation in a dose-dependent manner (IC50 10-20 ng/ml) Preclinical studies show tumor growth inhibition and reduced metastasis in neuroblastoma mouse models highlighting its potential for research in oncology therapeutics
Apexbio Technology LLC Sunitinib malate(Synonyms: Sutent, SU11248, Sunitinib L-malate, Sunitinib malate salt, SU-11248 malate, Sutent malate), 2g, CAS: 341031-54-7.
Sunitinib malate (CAS 341031-54-7) is a small molecule orally bioavailable multitargeted receptor tyrosine kinase inhibitor It inhibits various receptor tyrosine kinases including platelet-derived growth factor receptor (PDGFR) vascular endothelial growth factor receptors (VEGFR-1 2 and 3) c-KIT FLT3 kinase colony-stimulating factor-1 receptor (CSF-1R) and RET kinase In neuroblastoma cell lines (e g SK-N-BE(2) SH-SY5Y LAN-5) treatment with sunitinib malate significantly suppresses proliferation in a dose-dependent manner (IC50 10-20 ng/ml) Preclinical studies show tumor growth inhibition and reduced metastasis in neuroblastoma mouse models highlighting its potential for research in oncology therapeutics
Apexbio Technology LLC Sunitinib malate(Synonyms: Sutent, SU11248, Sunitinib L-malate, Sunitinib malate salt, SU-11248 malate, Sutent malate), 500mg, CAS: 341031-54-7.
Sunitinib malate (CAS 341031-54-7) is a small molecule orally bioavailable multitargeted receptor tyrosine kinase inhibitor It inhibits various receptor tyrosine kinases including platelet-derived growth factor receptor (PDGFR) vascular endothelial growth factor receptors (VEGFR-1 2 and 3) c-KIT FLT3 kinase colony-stimulating factor-1 receptor (CSF-1R) and RET kinase In neuroblastoma cell lines (e g SK-N-BE(2) SH-SY5Y LAN-5) treatment with sunitinib malate significantly suppresses proliferation in a dose-dependent manner (IC50 10-20 ng/ml) Preclinical studies show tumor growth inhibition and reduced metastasis in neuroblastoma mouse models highlighting its potential for research in oncology therapeutics
CAYMAN CHEMICAL 4-hydroxy Atorvastatin lacton
A metabolite of atorvastatin; formed by metabolism of atorvastatin by CYP3A4