Acrylic acids and derivatives
Medchemexpress LLC HY-106443A 5mg Medchemexpress, Arimoclomol maleate CAS:289893-26-1 Purity:>98%
Medchemexpress, HY-106443A 5mg Arimoclomol maleate CAS:289893-26-1 Arimoclomol maleate (BRX-220) is a co-inducer of heat shock proteins (HSP). 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.
Medchemexpress LLC HY-107322 10mg Medchemexpress, Barnidipine (hydrochloride) CAS:104757-53-1 Purity:>98%
Medchemexpress, HY-107322 10mg Barnidipine (HCl) CAS:104757-53-1 Barnidipine hydrochloride (Mepirodipine hydrochloride) is an L-type calcium antagonist (CaA) with high affinity for [3H] initrendipine binding sites (Ki=0.21 nmol/l), has selective action against CaA receptors.Barnidipine hydrochloride (Mepirodipine hydrochloride) is an antihypertensive drug and acts by the reduction of peripheral vascular resistance secondary to its vasodilatory action. 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.
eMolecules Scopoletin | 92-61-5 | MFCD00006872 | 1g
Apollo Scientific | Scopoletin | 1g | 562451991 | BIS1402 | | 92-61-5 | MFCD00006872 | 192.170 | C10H8O4
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Apexbio Technology LLC Vinpocetine 42971-09-5 100mg
Vinpocetine (CAS 42971-09-5) is a selective inhibitor of cyclic GMP phosphodiesterase (PDE) exhibiting a Ki of 14 2 M for Ca2 -dependent PDE in vitro It acts as a non-competitive inhibitor effectively modulating intracellular cGMP levels in smooth muscle In rat aortic cytosolic preparations vinpocetine inhibits Ca2 -PDE activity significantly while demonstrating minimal inhibition of Ca2 -independent cGMP PDE and cAMP PDE (Ki values 1000 M) Additionally vinpocetine attenuates 5-HT-induced contractions in intact rat aorta with an EC50 of 1 M This compound is used in research to explore mechanisms of smooth muscle relaxation and PDE regulation
eMolecules Ambeed 3-Bromo-4-chloropyridin-2-amine 250mg 552600702 A160126 0 000 221297-82-1 MFCD15143381 207 460 C5H4BrClN2
Ambeed 3-Bromo-4-chloropyridin-2-amine 250mg 552600702 A160126 0 000 221297-82-1 MFCD15143381 207 460 C5H4BrClN2
Apexbio Technology LLC KW-2478 819812-04-9 50mg
KW-2478 (CAS 819812-04-9) is a potent non-ansamycin inhibitor of heat shock protein 90 (Hsp90) Unlike traditional Hsp90 inhibitors such as 17-AAG KW-2478 exhibits improved aqueous solubility and reduced hepatotoxicity In multiple myeloma cell models KW-2478 induces degradation of Hsp90 client proteins and leads to downregulation of IgH translocation products including FGFR3 c-Maf and cyclin D1 thereby inhibiting cell proliferation and promoting apoptosis Additionally KW-2478 reduces levels of Cdk9 and phosphorylated 4E-BP1 further suppressing oncogenic transcriptional regulators This compound is a valuable tool for studying Hsp90-mediated pathways and evaluating therapeutic strategies in hematological malignancies
Selleck Chemical LLC Prochlorperazine dimaleate salt S4631-100mg
Prochlorperazine dimaleate salt is a dopamine (D2) receptor antagonist
Medchemexpress LLC Praeruptorin E | 78478-28-1 | 99.2% | 428.47 g·mol⁻¹ | C24H28O7 | 10 MG
Praeruptorin E is a pyranocoumarin natural product isolated from the roots of Peucedanum praeruptorum. It is used as a research reagent and is reported to have calcium channel antagonist activity; related compound Praeruptorin C has a reported pD2′ value of 5.2. The compound is supplied as a high-purity solid and is commonly offered in small milligram quantities for laboratory studies.
- Natural pyranocoumarin isolated from Peucedanum praeruptorum.
- Reported calcium channel antagonist activity; related compound shows pD2′ ≈ 5.2.
- High reported purity (~99.2%), suitable for research use.
- Available in small solid packs (for example, 10 mg) and as a 10 mM solution in DMSO.
- Soluble in DMSO; solvent preparations available for immediate use.
- Store at -20°C protected from light; in solvent store at -80°C for long-term stability.
Medchemexpress LLC HY-10349A 5mg Medchemexpress, WAY-100635 Maleate CAS:1092679-51-0 Purity:>98%
Medchemexpress, HY-10349A 5mg WAY-100635 Maleate CAS:1092679-51-0 WAY-100635 maleate is a potent and selective 5-hydroxytryptamine 1A (5-HT1A) receptor antagonist with an IC50 value of 0.91 nM and Ki value of 0.39 nM. WAY-100635 maleate has pIC50 values for 5-HT1A and α1-adrenergic receptors of 8.9 and 6.6, respectively. WAY-100635 maleate is also a potent dopamine D4 receptor agonist. 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.
Matrix Scientific 2-(PERFLUOROBUTYL)ETHYL ACR-5G
2-(Perfluorobutyl)ethyl acrylate, 97%; 5g,C9H7F9O2, MFCD00236104, mw 318.14, [117374-41-1]
Apexbio Technology LLC Monastrol 329689-23-8 10mg
Monastrol (CAS 329689-23-8) is a cell-permeable small molecule inhibitor that selectively targets the mitotic kinesin Eg5 a motor protein essential for bipolar spindle formation in cell division Monastrol impedes microtubule motility mediated by Eg5 resulting in mitotic arrest without affecting progression through S or G2 phases or centrosome duplication In vitro it demonstrates an IC50 of 14 M for Eg5 inhibition and induces reversible mitotic arrest with chromosomes attached to microtubules extending from centrosomes Monastrol is widely utilized in cell biology research to probe spindle assembly mechanisms and investigate mitotic kinesin function