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Filtered Search Results
Medchemexpress LLC HY-14855 50mg , Tedizolid DA-7157;Torezolid;TR 700 CAS:856866-72-3 Purity:98%
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Medchemexpress, HY-14855 50mg Tedizolid DA-7157;Torezolid;TR 700 CAS:856866-72-3 Formula:C17H15FN6O3 Purity:98% Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens. 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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Medchemexpress LLC HY-15676 100mg , RG7388 Idasanutlin CAS:1229705-06-9 Purity:98%
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Medchemexpress, HY-15676 100mg RG7388 Idasanutlin CAS:1229705-06-9 Formula:C31H29Cl2F2N3O4 IC50: 6 nM (p53-MDM2) Purity:98% RG7388 is a potent and selective MDM2 antagonist, inhibiting p53-MDM2 binding, with IC 50 of 6 nM. 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 2102410-90-0 | (R)-2-AMINO-3-(4-FLUOROPHENYL)PROPAN-1-OL HCL | 1g
Ambeed | 2-Bromo-3-nitrotoluene | 5g | 525199731 | A375959 | 41085-43-2 | MFCD00134555 | 216.034 | C7H6BrNO2
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eMolecules 447-43-8 | 1-(4-Fluorophenyl)-2,2-dihydroxyethan-1-one | Combi-Blocks, Inc. | MFCD19982290 | 170.139 | C8H7FO3 | 98.000 | OC(O)C(=O)c1ccc(F)cc1 | 1g | 603140352
1-(4-Fluorophenyl)-2,2-dihydroxyethan-1-one | Combi-Blocks, Inc. | 447-43-8 | MFCD19982290 | 170.139 | C8H7FO3 | 98.000 | OC(O)C(=O)c1ccc(F)cc1 | 1g | 603140352
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Medchemexpress LLC HY-114395A 10mg Medchemexpress, (R)-NVS-ZP7-4 CAS: Purity:>98%
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Medchemexpress, HY-114395A 10mg (R)-NVS-ZP7-4 CAS: (R)-NVS-ZP7-4 is the R-isomer of NVS-ZP7-4. NVS-ZP7-4 is a Zinc transporter SLC39A7 (ZIP7) inhibitor that is also the first reported chemical tool to probe the impact of modulating ER zinc levels and investigate ZIP7 as a novel druggable node in the Notch pathway. 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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Medchemexpress LLC HY-106004 10mg Medchemexpress, Zamicastat CAS:1080028-80-3 Purity:>98%
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Medchemexpress, HY-106004 10mg Zamicastat CAS:1080028-80-3 Zamicastat (BIA 5-1058) is a dopamine β-hydroxylase (DBH) inhibitor that could cross the blood-brain barrier (BBB) and cause central as well as peripheral effects. Zamicastat is also a concentration-dependent dual P-gp and BCRP inhibitor with IC50 values of 73.8 μM and 17.0 μM, respectively. Reduces high blood pressure. 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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Medchemexpress LLC Ono-8430506 | 1354805-08-5 | 99.9% | C27H28FN3O3 | 50 MG
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This orally bioavailable and potent autotaxin (ATX)/ENPP2 inhibitor efficiently inhibits lysophosphatidic acid (LPA) formation with IC50s of approximately 10 nM. In vivo, it slows initial tumor growth, limits lung metastasis in mice, and enhances the antitumor effect of Paclitaxel in a breast cancer model. This product is for research use only.
- Potent autotaxin (ATX)/ENPP2 inhibitor
- Orally bioavailable
- Efficiently inhibits lysophosphatidic acid (LPA) formation
- Slows initial tumor growth and limits lung metastasis
- Enhances antitumor effect of Paclitaxel in breast cancer models
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Medchemexpress LLC Retagliptin | 1174122-54-3 | 98.5% | 464.36 | 50 MG
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Retagliptin (SP2086) is a selective, competitive, and orally active dipeptidyl peptidase-4 (DPP-4) inhibitor. It can be used for type 2 diabetes mellitus (T2DM) research. Retagliptin inhibits the degradation of GLP-1, thereby amplifying the incretin effect.
- Selective, competitive, and orally active DPP-4 inhibitor.
- Can be used for type 2 diabetes mellitus (T2DM) research.
- Inhibits the degradation of GLP-1.
- Amplifies the incretin effect.
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Medchemexpress LLC Vorapaxar sulfate | 705260-08-8 | MFCD16038877 | 99.8% | 590.66 g/mol | C29H35FN2O8S | 5 MG
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Vorapaxar sulfate is the sulfate salt of vorapaxar, a selective, orally active protease-activated receptor-1 (PAR-1) antagonist used in antiplatelet research. Supplied as a high-purity research chemical for biochemical, pharmacology, and assay development.
- Selective PAR-1 antagonism for antiplatelet studies.
- High purity, ≈99.8%.
- Molecular formula C29H35FN2O8S; molecular weight 590.66 g/mol.
- CAS number 705260-08-8 for unambiguous identification.
- Available in small quantities, including 5 MG, for research use.
- Intended for research and analytical applications only, not for human consumption.
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eMolecules 530145-53-0 | 6-Bromo-2,3,4-trifluorobenzoic acid | Apollo Scientific | MFCD09910412 | 254.990 | C7H2BrF3O2 | 98.000 | OC(=O)c1c(Br)cc(F)c(F)c1F | 1g | 562428423
6-Bromo-2,3,4-trifluorobenzoic acid | Apollo Scientific | 530145-53-0 | MFCD09910412 | 254.990 | C7H2BrF3O2 | 98.000 | OC(=O)c1c(Br)cc(F)c(F)c1F | 1g | 562428423
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![eMolecules 1189729-43-8 | [2-(4-Fluorophenyl)phenyl]methylaminehydrochloride | Chem-Impex | MFCD02089421 | 237.700 | C13H13ClFN | 90.000 | Cl.NCc1ccccc1-c1ccc(F)cc1 | 1g | 386898282](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502178123.JPG-250.jpg)
eMolecules 1189729-43-8 | [2-(4-Fluorophenyl)phenyl]methylaminehydrochloride | Chem-Impex | MFCD02089421 | 237.700 | C13H13ClFN | 90.000 | Cl.NCc1ccccc1-c1ccc(F)cc1 | 1g | 386898282
[2-(4-Fluorophenyl)phenyl]methylaminehydrochloride | Chem-Impex | 1189729-43-8 | MFCD02089421 | 237.700 | C13H13ClFN | 90.000 | Cl.NCc1ccccc1-c1ccc(F)cc1 | 1g | 386898282
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eMolecules 1263094-82-1 | (S)-3-AMINO-2,2-DIFLUORO-3-(4-METHOXYPHENYL)PROPIONIC ACID HCL | MFCD12068661 | 0.25g
AstaTech | 2-BIPHENYL-2-CHLORO-CARBOXYLIC ACID | 0.25g | 256640579 | 82122 | 98.000 | 14498-95-4 | MFCD00093800 | 232.660 | C13H9ClO2
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Medchemexpress LLC HY-14557 25mg Medchemexpress, Pimavanserin CAS:706779-91-1 Purity:>98%
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Medchemexpress, HY-14557 25mg Pimavanserin CAS:706779-91-1 Pimavanserin is a selective inverse agonist of the 5-HT2A receptor with pIC50 and pKd of 8.73 and 9.3, 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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Apexbio Technology LLC ID-8 147591-46-6 10mg
ID-8 (CAS 147591-46-6) is a small-molecule inhibitor targeting dual-specificity tyrosine phosphorylation-regulated kinases (DYRKs) enzymes involved in the phosphorylation of tyrosine and serine/threonine residues In human embryonic stem cells (hESCs) ID-8 enhances cell survival and proliferation notably increasing hESC viability and when combined with Wnt3a suppressing Wnt-induced morphological differentiation and downregulating differentiation markers such as GATA6 GSC SOX17 and CDX2 In mouse embryonic stem cells ID-8 sustains self-renewal and pluripotency in serum-free culture supporting expansion and differentiation into derivatives of all three germ layers These properties make ID-8 a valuable tool for research on stem cell maintenance and cell fate regulation
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eMolecules 10540-41-7 | 3-(4-Fluorophenyl)phenol | Combi-Blocks | MFCD06802305 | 188.201 | C12H9FO | 98.000 | Oc1cccc(c1)-c1ccc(F)cc1 | 1g | 117577928
3-(4-Fluorophenyl)phenol | Combi-Blocks | 10540-41-7 | MFCD06802305 | 188.201 | C12H9FO | 98.000 | Oc1cccc(c1)-c1ccc(F)cc1 | 1g | 117577928
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