Signal Transduction Reagents and Kits
Medchemexpress LLC Malic enzyme inhibitor ME1 | 522649-59-8 | 99.7% | 351.40 g·mol⁻¹ | C20H21N3O3 | 50MG
Malic enzyme inhibitor ME1 is a small-molecule, selective inhibitor of cytosolic malic enzyme (ME1) used for biochemical and cellular research. It exhibits potent inhibition of ME1 (IC50 = 0.15 μM) and is supplied as a white to off-white solid with high purity and defined storage recommendations.
- Potent ME1 inhibition (IC50 = 0.15 μM).
- High purity suitable for biochemical assays (99.7%).
- Supplied as a solid, white to off-white.
- Highly soluble in DMSO; may require sonication and warming.
- Stable when stored under recommended conditions in powder or solution.
Enzo Life Sciences D609 (5 mg). CAS: 83373-60-8
Selective inhibitor of phosphatidylcholine-specific phospholipase C (PC-PLC). Has been used to study the coupling of phosphatidylcholine-specific phospholipase C with sphingomyelinase. Shows antitumor and antiviral activity. Inhibits basement membrane collagen synthesis, which is the last step in the development of a new blood vessel. Inhibits induction of nitric oxide synthases (NOS). Induces apoptosis. It indirectly inhibits phorbol ester stimulated PLD activity. Alternative name: Tricyclodecan-9-yl xanthogenate . K. Purity: ≥98% (TLC). Solubility: Soluble in water (25mg/ml). Long Term Storage: -20°C.
Revvity Health Sciences Inc HTRF Human IL-17A / IL17RA Binding Kit, 10,000 Assay Points
HTRF Human IL-17A / IL17RA Binding Kit, 10,000 Assay Points
![CPC Scientific 4-(4-Dimethylaminophenylazo)benzoyl-Tyr-Val-Ala-Asp-Ala-Pro-Val-5-[(2-aminoethyl)amino]-naphthalene-1-sulfonic acid 1MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00111436-SUBS-016.PNG-250.jpg)
CPC Scientific 4-(4-Dimethylaminophenylazo)benzoyl-Tyr-Val-Ala-Asp-Ala-Pro-Val-5-[(2-aminoethyl)amino]-naphthalene-1-sulfonic acid 1MG
SEQUENCE: 4-(4-Dimethylaminophenylazo)benzoyl-Tyr-Val-Ala-Asp-Ala-Pro-Val-5-[(2-aminoethyl)amino]-naphthalene-1-sulfonic acidONE-LETTER SEQUENCE: 4-(4-Dimethylaminophenylazo)benzoyl-YVADAPV-5-[(2-aminoethyl)amino]-naphthalene-1-sulfonic acidMOLECULAR FORMULA: C61H76N12O14S1MOLECULAR WEIGHT: 1233.39STORAGE CONDITIONS: -20 5 CCAS REGISTRY NUMBER: [161877-70-9]SYNONYMS: Caspase 1 (ICE) Substrate; dabcyl-yvadapv-edans; dabcyl-tyr-val-ala-asp-ala-pro-val-edans; ICE Substrate Ii; il-1-beta Converting Enzyme Substrate Ii; il-1b Converting Enzyme Substrate Ii; 4-(4-dimethylaminophenylazo)benzoyl-tyr-val-ala-asp-ala-pro-val-5-[(2-aminoethyl)amino]-naphthalene-1-sulfonic acid; 4-(4'-dimethylaminophenylazo)benzoyl-tyrosyl-valyl-alanyl-aspartyl-alanyl-prolyl-valyl-5((2-aminoethyl)amino)naphthalene-1-sulfonic acidRESEARCH AREA: ApoptosisREFERENCES:M.W. Pennington et al., Peptide Res., 7, 72 (1994)M. Los et al., Nature 375, 81 (1995)SKU(s): SUBS-016A, SUBS-016B
Medchemexpress LLC HY-112815 5mg Medchemexpress, ALK2-IN-2 CAS:2254409-25-9 Purity:>98%
Medchemexpress, HY-112815 5mg ALK2-IN-2 CAS:2254409-25-9 ALK2-IN-2 is a potent and selective inhibitor of activin receptor-like kinase 2 (ALK2) with an IC50 of 9 nM, and over 700-fold selectivity against ALK3. 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.
Enzo Life Sciences BML-210 (1mg). CAS: 537034-17-6
HDAC inhibitor developed at Enzo Life Sciences. Inhibits HDAC activity in HeLa nuclear extracts (IC50=5-10µM). Purity: ≥98% (TLC). Solubility: Soluble in DMSO (25mg/ml) or 100% ethanol (10mg/ml, warm). Long Term Storage: -20°C.
Sigma Aldrich Fine Chemicals Biosciences Oleoyl-L--lysophosphatidic acid sodium salt 98, solid, 22556-62-3, MFCD00133427
Oleoyl-L--lysophosphatidic acid sodium salt 98, solid
Medchemexpress LLC Reticuline | 485-19-8 | 329.39 | 1 MG
Reticuline exhibits anti-inflammatory effects by influencing JAK2/STAT3 and NF-κB signaling pathways. It inhibits the mRNA expression of TNF-α and IL-6, and reduces the phosphorylation levels of JAK2 and STAT3. Reticuline also demonstrates cardiovascular effects.
- Inhibits JAK2/STAT3 and NF-κB signaling pathways.
- Reduces TNF-α and IL-6 mRNA expression.
- Decreases JAK2 and STAT3 phosphorylation.
- Shows cardiovascular effects.
- Purity of 98.89%.
- Appearance: white to yellow solid.
- Soluble in DMSO.