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Filtered Search Results
MEDCHEMEXPRESS LLC TASQUINIMOD 5MG
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501872126 TASQUINIMOD 5MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000379010 MAO-B-IN-2 100MG
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Apexbio Technology LLC PIRIBEDIL 10MG
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PIRIBEDIL 10MG APEXBIO TECHNOLOGIES
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![Medchemexpress LLC 1-cyclobutyl-3-(2,6-dimethylphenyl)-3,4-dihydro-pyrimido[4,5-d]pyrimidin-2(1H)-one (methoxy-piperazinyl substituted) | 2172617-15-9 | 99.8% | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00132390-MCE-LOGO.JPG-250.jpg){kind=logo}
Medchemexpress LLC 1-cyclobutyl-3-(2,6-dimethylphenyl)-3,4-dihydro-pyrimido[4,5-d]pyrimidin-2(1H)-one (methoxy-piperazinyl substituted) | 2172617-15-9 | 99.8% | 5 MG
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YKL-06-061 is a potent, selective, second-generation salt-inducible kinase (SIK) inhibitor for research use. It inhibits SIK1, SIK2, and SIK3 with IC50 values of 6.56 nM, 1.77 nM, and 20.5 nM, respectively. The compound is supplied as a high-purity solid with good DMSO solubility for biochemical and cellular studies.
- Potent inhibition of SIK1, SIK2, and SIK3 at low-nanomolar concentrations.
- High purity suitable for research applications.
- Soluble in DMSO at 16.67 mg/mL (31.59 mM).
- Solid storage recommended at -20°C; in solution store at -80°C for long-term stability.
- Available in small research sizes for assay development.
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Medchemexpress LLC HY-119243 5mg Medchemexpress, LY2794193 CAS:2173037-97-1 Purity:>98%
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Medchemexpress, HY-119243 5mg LY2794193 CAS:2173037-97-1 LY2794193 is a highly potent and selective mGlu3 receptor agonist ( hmGlu3 K i =0.927 nM， EC 50 =0.47 nM; hmGlu2 K i =412 nM， EC 50 =47.5 nM) [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.
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Medchemexpress LLC HY-114379 5mg Medchemexpress, AS2717638 CAS:2148339-28-8 Purity:>98%
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Medchemexpress, HY-114379 5mg AS2717638 CAS:2148339-28-8 AS2717638 is an oral active and selective lysophosphatidic acid receptor 5 (LPA5) antagonist, with an IC 50 of 38 nM for hLPA5. AS2717638 also significantly improves PGE 2 -, PGF 2α -, and AMPA-induced allodynia [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.
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Medchemexpress LLC HY-15200 10mg Medchemexpress, Agerafenib CAS:1188910-76-0 Purity:>98%
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Medchemexpress, HY-15200 10mg Agerafenib CAS:1188910-76-0 Agerafenib (CEP-32496; RXDX-105) is a highly potent and orally efficacious inhibitor of BRAFV600E with a Kd of 14 nM. 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 2070015-13-1 | Medchem Express | ML241 (hydrochloride) | 5mg | 446270363 | HY-19797A | MFCD30187511 | 408.93 | C23H25ClN4O
Medchem Express | 8-Hydroxyguanosine | 5mg | 482204092 | HY-113262 | 3868-31-3 | 299.243 | C10H13N5O6
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Medchemexpress LLC HY-N0270 10mg Medchemexpress, Ononin CAS:486-62-4 Purity:>98%
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Medchemexpress, HY-N0270 10mg Ononin CAS:486-62-4 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 173952-44-8 | Medchem Express | SYM2206 | 5mg | 446269307 | HY-18689 | MFCD00946571 | 366.421 | C20H22N4O3
Medchem Express | EST73502 (monohydrochloride) | 5mg | 569407474 | HY-134189A | 2535970-65-9 | 388.880 | C19H27ClF2N2O2
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000383660 DSM705 HYDROCHLORID 50MG
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MEDCHEMEXPRESS LLC SULTOPRIDE HYDROCHLORIDE 5MG
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501873844 SULTOPRIDE HYDROCHLORIDE 5MG
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eMolecules 131179-95-8 | Medchem Express | Efaproxiral | 50mg | 446263211 | HY-13619 | MFCD00899086 | 341.407 | C20H23NO4
Ambeed | Benzyl 5-aminopentanoate hydrochloride | 5g | 572859746 | A1037243 | 154407-91-7 | MFCD25371665 | 243.730 | C12H18ClNO2
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Medchemexpress LLC Olmutinib | 1353550-13-6 | 99.5% | 486.59 | 5 MG
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Olmutinib is an orally active and irreversible third EGFR tyrosine kinase inhibitor that binds to a cysteine residue near the kinase domain. It is used for non-small cell lung cancer.
- Orally active.
- Irreversible third EGFR tyrosine kinase inhibitor.
- Binds to a cysteine residue near the kinase domain.
- Used for non-small cell lung cancer.
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Medchemexpress LLC Acebilustat | 943764-99-6 | 99.7% | 481.54 | 100 MG
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Acebilustat is a leukotriene A4 hydrolase inhibitor, used as an oral antiinflammatory agent. It is safe and well tolerated in phase 1 trials. This antiinflammatory drug is in development for the treatment of CF and other diseases, acting as a potent inhibitor of the enzyme leukotriene A4 hydrolase (LTA4H), which catalyzes the rate-limiting step in the formation of leukotriene B4 (LTB4), a powerful chemoattractant and activator of inflammatory immune cells like neutrophils.
- Leukotriene A4 hydrolase inhibitor
- Oral antiinflammatory agent
- Safe and well tolerated in phase 1 trials
- Potent inhibitor of LTA4H
- Inhibits the formation of leukotriene B4 (LTB4)
- Being developed for the treatment of cystic fibrosis (CF) and other diseases
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