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MEDCHEMEXPRESS LLC HELIOXANTHIN DERIVATIVE 5-4-2
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501873476 HELIOXANTHIN DERIVATIVE 5-4-2
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Medchemexpress LLC Mps1-IN-3 hydrochloride | 2989453-29-2 | 98.0% | 574.09 | C26H32ClN7O4S | 25MG
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Mps1-IN-3 hydrochloride is the hydrochloride salt of a potent and selective MPS1 (TTK) kinase inhibitor (reported IC50 ≈ 50 nM) provided for research use. The compound is supplied as a solid with high purity, chemical formula C26H32ClN7O4S, and molecular weight 574.09 g/mol; it is commonly packaged in small quantities for in vitro biochemical and cell-based studies.
- Potent MPS1 kinase inhibitor with reported IC50 ≈ 50 nM.
- High purity solid suitable for research applications.
- Chemical formula C26H32ClN7O4S and molecular weight 574.09 g/mol.
- Hydrochloride salt form to aid solubility for assays.
- Packaged in small quantities for laboratory testing and method development.
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MEDCHEMEXPRESS LLC TIRABRUTINIB 5MG
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501873353 TIRABRUTINIB 5MG
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eMolecules 146662-42-2 | Medchem Express | SR2640 (hydrochloride) | 5mg | 716993407 | HY-107610 | MFCD04971976 | 406.87 | C23H19ClN2O3
Medchem Express | LLY-283 | 5mg | 485251275 | HY-107777 | 2040291-27-6 | 342.355 | C17H18N4O4
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eMolecules 646995-35-9 | Medchem Express | Cinaciguat (hydrochloride) | 2mg | 446263916 | HY-14181A | MFCD28127267 | 602.17 | C36H40ClNO5
Medchem Express | Cinaciguat (hydrochloride) | 2mg | 446263916 | HY-14181A | 646995-35-9 | MFCD28127267 | 602.170 | C36H40ClNO5
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Apexbio Technology LLC LY2606368 5MG
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502240112 LY2606368 5MG
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MEDCHEMEXPRESS LLC NRC-2694 5MG
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501873788 NRC-2694 5MG
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eMolecules Medchem Express | O-Demethyl Lenvatinib (hydrochloride) | 5mg | 783660462 | HY-133980A | 449.29 | C20H18Cl2N4O4
Medchem Express | O-Demethyl Lenvatinib (hydrochloride) | 5mg | 783660462 | HY-133980A | | 449.290 | C20H18Cl2N4O4
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MEDCHEMEXPRESS LLC UNC 0631 5MG
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501872968 UNC 0631 5MG
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MEDCHEMEXPRESS LLC A 839977 10MG
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501872993 A 839977 10MG
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Medchemexpress LLC HY-N0693 10mg Medchemexpress, Schisandrin A CAS:61281-38-7 Purity:>98%
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Medchemexpress, HY-N0693 10mg Schisandrin A CAS:61281-38-7 Schisandrin A inhibits CYP3A activity with an IC 50 of 6.60 μM and K i of 5.83 μM, 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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Medchemexpress LLC HY-N0700 1g Medchemexpress, alpha-Asarone CAS:2883-98-9 Purity:>98%
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Medchemexpress, HY-N0700 1g alpha-Asarone CAS:2883-98-9 alpha-Asarone (α-Asarone) is one of the main psychoactive compounds, and possesses an antidepressant-like activity in mice. 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 1-[3,5-bis(trifluoromethyl)benzoyl]-N-(4-chlorophenyl)-3-piperidinecarboxamide | 1207113-88-9 | 99.3% | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000230844.png-250.jpg)
Medchemexpress LLC 1-[3,5-bis(trifluoromethyl)benzoyl]-N-(4-chlorophenyl)-3-piperidinecarboxamide | 1207113-88-9 | 99.3% | 10 MG
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Small-molecule inhibitor of myocardin-related transcription factor A/serum response factor (MRTF-A/SRF) signaling used in research to block MRTF-A nuclear localization and probe Rho/MKL1-SRF transcriptional pathways.
- Specific inhibitor of MRTF-A/SRF signaling for cell and molecular studies.
- High purity suitable for research applications.
- Molecular weight 478.82 g/mol; formula C21H17ClF6N2O2.
- Supplied in small mg quantities for experimental use.
- Used to study fibrosis, cytoskeletal regulation, and transcriptional pathways.
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![eMolecules 583837-94-9 | [4-(ETHANESULFONYL)PHENYL]METHANAMINE | MFCD10032480 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502180232.JPG-250.jpg)
eMolecules 583837-94-9 | [4-(ETHANESULFONYL)PHENYL]METHANAMINE | MFCD10032480 | 1g
AstaTech | [4-(ETHANESULFONYL)PHENYL]METHANAMINE | 1g | 596576189 | P10910 | 95.000 | 583837-94-9 | MFCD10032480 | 199.270 | C9H13NO2S
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Medchemexpress LLC Bi 639667 (compound 19n) | 1295298-26-8 | 98.9% | 10 MG
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BI 639667 is a small-molecule CCR1 antagonist chemical probe with low-nanomolar potency in biochemical and cellular assays. It is intended for in vitro pharmacology and target-validation studies exploring CCR1-mediated chemotaxis and signaling.
- Chemical probe for CCR1 with potent receptor antagonism.
- Ca2+ flux IC50 ≈ 1.8 nM; SPA binding ~5.4 nM; chemotaxis IC50 ~2.4 nM.
- CAS 1295298-26-8; molecular formula C22H18FN5O3S; molecular weight 451.47 Da.
- High chemical purity (reported 98.87%).
- Supplied as a 10 mg sample suitable for in vitro assays.
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