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Filtered Search Results
Medchemexpress LLC HY-100895 5mg Medchemexpress, SAR-20347 CAS:1450881-55-6 Purity:>98%
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Medchemexpress, HY-100895 5mg SAR-20347 CAS:1450881-55-6 SAR-20347 is an inhibitor of TYK2 , JAK1 , JAK2 and JAK3 with IC 50 s of 0.6, 23, 26 and 41 nM, respectively. 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.
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eMolecules 214262-96-1 | 1-(2-Fluorophenyl)cyclopentane-1-carboxylic acid | Combi-Blocks | MFCD00800622 | 208.232 | C12H13FO2 | 98.000 | OC(=O)C1(CCCC1)c1ccccc1F | 1g | 205383708
1-(2-Fluorophenyl)cyclopentane-1-carboxylic acid | Combi-Blocks | 214262-96-1 | MFCD00800622 | 208.232 | C12H13FO2 | 98.000 | OC(=O)C1(CCCC1)c1ccccc1F | 1g | 205383708
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eMolecules 1702399-91-4 | 3,5-Dichloro-4-fluorobenzene-1,2-diamine | Apollo Scientific | MFCD29977177 | 195.020 | C6H5Cl2FN2 | 95.000 | Nc1cc(Cl)c(F)c(Cl)c1N | 1g | 591806807
3,5-Dichloro-4-fluorobenzene-1,2-diamine | Apollo Scientific | 1702399-91-4 | MFCD29977177 | 195.020 | C6H5Cl2FN2 | 95.000 | Nc1cc(Cl)c(F)c(Cl)c1N | 1g | 591806807
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![eMolecules 868734-73-0 | 2-carboxy-6-(4-fluorophenyl)pyridin-1-ium-1-olate | Synthonix233.198 | C12H8FNO3 | 95.000 | OC(=O)c1cccc(-c2ccc(F)cc2)[n+]1[O-] | 50mg | 786491292](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502473125.jpg-250.jpg)
eMolecules 868734-73-0 | 2-carboxy-6-(4-fluorophenyl)pyridin-1-ium-1-olate | Synthonix233.198 | C12H8FNO3 | 95.000 | OC(=O)c1cccc(-c2ccc(F)cc2)[n+]1[O-] | 50mg | 786491292
2-carboxy-6-(4-fluorophenyl)pyridin-1-ium-1-olate | Synthonix | 868734-73-0233.198 | C12H8FNO3 | 95.000 | OC(=O)c1cccc(-c2ccc(F)cc2)[n+]1[O-] | 50mg | 786491292
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Selleck Chemical LLC Teduglutide-5mg
Teduglutide (ALX-0600, Gattex, Revestive, TAK 633) is an analogue of human glucagon-like peptide-2 (GLP-2) and binds to the GLP-2 receptors. Teduglutide prolongs the intestinotrophic properties of GLP-2 in animal models.
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eMolecules 4-(4-Bromo-2-fluorophenyl)-2-methylpyridine | 1187168-25-7 | MFCD13152466 | 1g
Matrix Scientific | 4-(4-Bromo-2-fluorophenyl)-2-methylpyridine | 1g | 389723980 | 86308 | 97.000 | 1187168-25-7 | MFCD13152466 | 266.113 | C12H9BrFN
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eMolecules 554438-52-7 | Medchem Express | LASV inhibitor 3.3 | 5mg | 783660426 | HY-124871 | 471.645 | C30H37N3O2
Medchem Express | LASV inhibitor 3.3 | 5mg | 783660426 | HY-124871 | 554438-52-7 | 471.645 | C30H37N3O2
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eMolecules 1031496-06-6 | Medchem Express | CIM0216 | 5mg | 594229281 | HY-110220 | MFCD10627035 | 347.418 | C21H21N3O2
Medchem Express | SBE13 (Hydrochloride) | 10mg | 446265041 | HY-15158 | 1052532-15-6 | MFCD20036266 | 479.400 | C24H28Cl2N2O4
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Medchemexpress LLC PRX-08066 | 866206-54-4 | C19H17ClFN5S | 1 MG
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PRX-08066 is a selective and orally active 5-hydroxytryptamine receptor 2B (5-HT2BR) antagonist. It inhibits the MAPK pathway, 5-HT release, and the expression of fibrotic factors. This product can be used for research related to pulmonary Arterial Hypertension (PAH) and neuroendocrine tumors (NET).
- Selective and orally active 5-HT2BR antagonist (Ki of 3.4 nM)
- Inhibits MAPK pathway and 5-HT release
- Inhibits expression of fibrotic factors (TGFβ1, CTGF, and FGF2)
- Inhibits proliferation of KRJ-I cells
- Induces apoptosis via caspase-3 activation
- Inhibits pulmonary vascular remodeling
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Medchemexpress LLC 4-Chloro-2-fluoroben | 10G
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4-Chloro-2-fluoroben | 10G
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eMolecules 1262417-51-5 | Medchem Express | NMS-P118 | 2mg | 446269542 | HY-18954 | MFCD30533610 | 395.426 | C20H24F3N3O2
Medchem Express | S55746 (hydrochloride) | 5mg | 482204184 | HY-117288A | 1448525-91-4 | 747.290 | C43H43ClN4O6
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eMolecules 7589-27-7 | 4-FLUOROPHENETHYL ALCOHOL | AstaTech | MFCD00002898 | 140.157 | C8H9FO | 98.000 | OCCc1ccc(F)cc1 | 5g | 296375959
4-FLUOROPHENETHYL ALCOHOL | AstaTech | 7589-27-7 | MFCD00002898 | 140.157 | C8H9FO | 98.000 | OCCc1ccc(F)cc1 | 5g | 296375959
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Aobchem 1-Ethoxy-2 4-difluorobenzene | ≥97% | CAS 348-20-9 | C8H8F2O | 5g
1-Ethoxy-2 4-difluorobenzene | ≥97% | CAS 348-20-9 | C8H8F2O | 5g
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Selleck Chemical LLC SAR-020106
SAR-020106 is an ATP-competitive potent and selective CHK1 inhibitor with an IC50 of 13 3 nM
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Selleck Chemical LLC ASP5878
ASP5878 is a novel FGFR-selective inhibitor with IC50 values of 0 47 0 60 0 74 and 3 5 nmol/L for recombinant FGFR1 2 3 and 4 respectively
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