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Filtered Search Results
Santa Cruz Biotechnology SELENOSULFURIC ACID DIPOT 50MG
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selenosulfuric acid dipotassium salt MW: 237.22 | 15571-89-8 | 50mg
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eMolecules 1782970-28-8 | Medchem Express | PTC-028 | 5mg | 459606791 | HY-103696 | 405.332 | C19H12F5N5
Medchem Express | OncoFAP | 5mg | 719836901 | HY-145938 | 2639365-69-6 | 459.410 | C21H19F2N5O5
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Medchemexpress LLC HY-103154 10mg Medchemexpress, SB228357 CAS:181629-93-6 Purity:>98%
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Medchemexpress, HY-103154 10mg SB228357 CAS:181629-93-6 SB228357 is a selective, potent oral active 5-HT2C/2B receptor antagonist with pKi values of 6.9, 8.0 and 9.0 for 5-HT2A, 5-HT2B and 5-HT2C, respectively. SB228357 has antidepressant/anxiolytic effects. 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 5960-69-0 | 2-Acetylphenanthrene | Combi-Blocks | MFCD00001171 | 220.271 | C16H12O | 95.000 | CC(=O)c1ccc2c(ccc3ccccc23)c1 | 25g | 528668988
2-Acetylphenanthrene | Combi-Blocks | 5960-69-0 | MFCD00001171 | 220.271 | C16H12O | 95.000 | CC(=O)c1ccc2c(ccc3ccccc23)c1 | 25g | 528668988
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eMolecules 2137047-43-7 | Medchem Express | VU6005649 | 5mg | 446259212 | HY-107982 | 357.284 | C16H12F5N3O
2-Fluoroacrylic acid | Ambeed | 430-99-9 | MFCD03424474 | 90.053 | C3H3FO2 | 98.000 | OC(=O)C(F)=C | 1g | 524985310
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eMolecules 1076225-26-7 | Medchem Express | (Rac)-PF-998425 | 5mg | 686921871 | HY-14250A | 269.267 | C14H14F3NO
Ambeed | (S)-4-Amino-N-(1-(4-chlorophenyl)-3-hydroxypropyl)-1-(7H-pyrrolo[23-d]pyrimidin-4-yl)piperidine-4-carboxamide | 1mg | 491170748 | A260907 | 1143532-39-1 | MFCD22628785 | 428.920 | C21H25ClN6O2
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Selleck Chemical LLC Pamiparib
Pamiparib is a potent and selective inhibitor of PARP1 and PARP2 with IC50 values of 0 83 and 0 11 nM respectively in biochemical assays It shows high selectivity over other PARP enzymes
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Medchemexpress LLC KRAS inhibitor-9 | 300809-71-6 | 99.9% | 292.81 | 50 MG
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KRAS inhibitor-9 is a potent inhibitor that blocks the formation of GTP-KRAS and downstream activation of KRAS. It causes G2/M cell cycle arrest and induces apoptosis. This inhibitor selectively inhibits the proliferation of NSCLC cells with KRAS mutation but not normal lung cells.
- Binds to KRAS G12D, KRAS G12C, and KRAS Q61H protein
- Induces G2/M cell cycle arrest
- Promotes apoptosis
- Selectively inhibits NSCLC cells with KRAS mutation
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Apexbio Technology LLC DEUCRAVACITINIB 5MG
DEUCRAVACITINIB 5MG APEXBIO TECHNOLOGIES
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Rieke Metals LLC 2,5-DIFLUOROBENZYL ZN BR
2,4-Difluorobenzylzinc bromide, 0.5M THF, 50mL
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Medchemexpress LLC HY-10562 50mg Medchemexpress, Ketanserin CAS:74050-98-9 Purity:>98%
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Medchemexpress, HY-10562 50mg Ketanserin CAS:74050-98-9 Ketanserin is a selective 5-HT receptor antagonist. Ketanserin also blocks hERG current (IhERG) in a concentration-dependent manner (IC50=0.11 μM). 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 Fht-1015 5Mg | HY-144896-5MG
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Fht-1015 5Mg
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![Medchemexpress LLC 2-[1-[(2S,3S)-2-(2,3-dihydro-1H-inden-2-ylmethyl)-3-(3,5-dimethoxy-4-methylphenyl)...]acetic acid | 856691-44-6 | 99.9% | 521.60 | C30H35NO7 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000227749.png-250.jpg)
Medchemexpress LLC 2-[1-[(2S,3S)-2-(2,3-dihydro-1H-inden-2-ylmethyl)-3-(3,5-dimethoxy-4-methylphenyl)...]acetic acid | 856691-44-6 | 99.9% | 521.60 | C30H35NO7 | 25 MG
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ONO-9780307 is a synthetic antagonist of the lysophosphatidic acid receptor 1 (LPA1) with high potency (IC50 = 2.7 nM). It has been used as a pharmacological tool and as a co-crystallized ligand for human LPA1 (PDB 4Z34). Supplied as a 25 mg solid, the compound has formula C30H35NO7 and a molecular weight of 521.60; store protected from light and follow recommended solvent storage conditions.
- High potency LPA1 antagonist (IC50 2.7 nM).
- Validated for receptor binding and structural biology applications.
- High purity confirmed by certificate of analysis (>99.9%).
- Supplied as a solid suitable for dissolution in common solvents (e.g., DMSO).
- Short- and long-term storage guidance provided for solid and solvent solutions.
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Medchemexpress LLC Phd-1-in-1 | 2009343-14-8 | 99.2% | 220.23 | C13H8N4 | 5 MG
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PHD-1-IN-1 is a potent, orally active small-molecule inhibitor of hypoxia-inducible factor prolyl-hydroxylase domain-1 (PHD-1) for preclinical research into HIF regulation and hypoxia signaling. It binds the active-site Fe2+ with a unique monodentate interaction and induces an Arg367-out pocket. Supplied as a white to off-white solid with high purity for in vitro and in vivo studies.
- Potent PHD-1 inhibition (IC50 0.034 μM).
- Unique monodentate binding to the active-site iron that alters pocket conformation.
- High purity suitable for research and assay development.
- Soluble in DMSO; manufacturer provides in vivo formulation protocols.
- Stable powder storage conditions for long-term preservation.
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Selleck Chemical LLC Ipragliflozin
Ipragliflozin (ASP1941) is a highly selective sodium-glucose cotransporter 2 (SGLT2) inhibitor with an IC50 value of 7 4 nM for hSGLT2 and a 254-fold selectivity versus SGLT1
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