Unsaturated hydrocarbons

Organic compounds made up entirely of hydrogen and carbon elements that contain both double and triple carbon - carbon bonds in their structures.

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991 – 1,005 of 1,117 results

991

Medchemexpress LLC DJ-V-159 | 2253744-53-3 | 99.9% | 502.37 | 50 MG

DJ-V-159 is an agonist for G protein-coupled receptor family C group 6 member A (GPRC6A). It activates ERK in HEK-293 cells transfected with GPRC6A and dose-dependently stimulates cAMP production. DJ-V-159 also stimulates insulin secretion in mouse beta-cell MIN-6 cells, similar to the effects of Ocn, a known ligand of GPRC6A, and has been shown to reduce blood glucose levels in wildtype mice.

Activates ERK in HEK-293 cells transfected with GPRC6A.
Stimulates cAMP production in GPRC6A expressing HEK-293 cells.
Stimulates insulin secretion in mouse beta-cell MIN-6 cells.
Reduces blood glucose levels in wildtype mice.
For research use only.

Pricing & Availability

992

Medchemexpress LLC Dichlorobis(tricyclohexylphosphine)palladium(II) | 29934-17-6 | MFCD00191830 | 98.0% | 738.2 g/mol | C36H66Cl2P2Pd | 5 G

Dichlorobis(tricyclohexylphosphine)palladium(II) is a palladium(II) phosphine complex used as a homogeneous catalyst in organic synthesis. It is commonly employed for C-C and C-N cross-coupling reactions and for the carbonylation of chloroarenes under mild conditions, and is supplied as a solid for research use.

Used as a homogeneous catalyst for C-C and C-N cross-coupling reactions.
Effective in the carbonylation of chloroarenes under mild conditions.
High purity suitable for research applications.
Solid form for straightforward handling and storage.

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993

Medchemexpress LLC Acetamide, 2-[[7-(3,4-dimethoxyphenyl)-2-quinoxalinyl)amino]-N-methyl- | 1513879-21-4 | 99.9% | 352.39 | 25 MG

BQR-695 is a PI4KIIIβ inhibitor with IC50s of 80 nM for human PI4KIIIβ and 3.5 nM for the *Plasmodium* variant of PI4KIIIβ. For research use only.

Treatment with 0.5 μM of either KAI407 or BQR695 causes GFP-PHOsh2 to redistribute to the parasite plasma membrane, consistent with depletion of intracellular PI4P upon inhibition of PfPI4K function.
BQR695 shows no evidence of toxicity against mature red blood cells (RBCs).
It induces a schizont-stage arrest indistinguishable from that observed in imidazopyrazine-treated parasites and exhibits cross-resistance with the imidazopyrazine-resistant lines.
DMSO: 50 mg/mL (141.89 mM; requires ultrasonic; hygroscopic DMSO has a significant impact on solubility, use newly opened DMSO).
Powder: -20°C for 3 years, 4°C for 2 years.
In solvent: -80°C for 2 years, -20°C for 1 year.

Pricing & Availability

994

Medchemexpress LLC ETC-159 | 1638250-96-0 | 99.1% | 391.38 | 1 ML

ETC-159 is a potent, orally available PORCN inhibitor that inhibits β-catenin reporter activity with an IC50 of 2.9 nM. It is intended for research use only.