Tetrapyrroles and derivatives
Abcam Jasplakinolide, Actin polymerization and stabilization inducer, 50UG
MW 709.7 Da, Purity >95%. Cell-permeable actin polymerization and stabilization inducer. Potent antiproliferative activity (IC₅₀ = 15 nM). Antitumor and antifungal agent. Active in vitro.
The product is subject to the following: Abcam Restricted Use Statement
Strem, An Ascensus Company CAS# 574-93-6. 5g. Phthalocyanine. MFCD00005085
CAS# 574-93-6. 5g. Phthalocyanine. MFCD00005085. Molecular Weight: 514.55. Molecular Formula: C32H18N8. Color/form: blue black pwdr. Strem# 07-1700. http://www.strem.com/catalog/v/07-1700/
Abcam SCD1 Inhibitor, SCD1(stearoyl-CoA desaturase 1) inhibitor, 1MG
MW 387.9 Da, Purity >99%. Potent, selective SCD1 (stearoyl-CoA desaturase 1) inhibitor (IC₅₀ = 4.5 nM). Inhibits the conversion of saturated, long-chain fatty acyl-CoAs to monounsaturated, long-chain fatty acyl-CoAs in vitro, when heptadecanoic acid and palmitic acid are used as the substrate (IC₅₀ = 7.9 and 6.8 nM, respectively). Active in vivo. Orally bioavailable.
The product is subject to the following: Abcam Restricted Use Statement
![Abcam [Pyr1]-Apelin 13, endogenous apelin receptor (APJ) agonist, 1MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502583378.JPG-250.jpg)
Abcam [Pyr1]-Apelin 13, endogenous apelin receptor (APJ) agonist, 1MG
MW 1533.8 Da, Purity >95%. [Pyr1]-Apelin 13, endogenous apelin receptor (APJ) agonist. Achieve your results faster with highly validated, pure and trusted compounds.
The product is subject to the following: Abcam Restricted Use Statement
Abcam x anomeline o x alate, M1 muscarinic acetylcholine receptor agonist, 50MG
MW 371.5 Da, Purity >99%. Functionally preferring M₁ muscarinic acetylcholine receptor agonist (pKi values are 7.1 (M₁), 6.9 (M₂), 7.4 (M₃), 7.7 (M₄) and 7.4 (M₅)). Able to cross blood-brain barrier. Displays antipsychotic activity.
The product is subject to the following: Abcam Restricted Use Statement
Abcam Radicicol, Heat shock protein (HSP) 90 inhibitor, 1MG
MW 364.8 Da, Purity >99%. Heat shock protein 90 inhibitor and antifungal antibiotic. Binds to the N-terminal ATP/ADP-binding domain suppressing cell transformation induced by src, ras and mos. Induces cell cycle arrest at G₁-S phase. Shows antiangiogenic effects in vivo.
The product is subject to the following: Abcam Restricted Use Statement
Medchemexpress LLC 3-(4-bromo-2-chlorophenyl)piperidine-2,6-dione | 2923549-60-2 | MFCD35454792 | 98.9% | 302.55 g/mol | C11H9BrClNO2 | 100mg
3-(4-Bromo-2-chlorophenyl)piperidine-2 6-dione is a CRBN-type E3 ubiquitin ligase ligand that can be used to prepare PROTAC
Abcam QNZ, NF-kB inhibitor, 1MG
MW 358.4 Da, Purity >98%. Potent, selective NF-kB inhibitor (IC₅₀ = 11 nM). Inhibits LPS-induced TNFα production (IC₅₀ = 7 nM). Reduces edema in inflammation in vivo..
The product is subject to the following: Abcam Restricted Use Statement
Sigma Aldrich Fine Chemicals Biosciences Cytochrome c from equine heart | 9007-43-6 | MFCD00130890 | 10 mg
Cytochrome c from equine heart | Purity: ≥99% | Mol Wt: 12,384 | 9007-43-6 | MFCD00130890 | 10 mg
Sigma Aldrich Fine Chemicals Biosciences Cytochrome c from equine heart | 9007-43-6 | MFCD00130890 | 250mg
Cytochrome c from equine heart | Purity: ≥95% | Mol Wt: 12384 | 9007-43-6 | MFCD00130890 | 250mg
Selleck Chemical LLC Vitamin B12 S1902-1g
Vitamin B12 (Cobalamin Cyanocobalamin) is a water soluble vitamin with a key role in the normal functioning of the brain and nervous system and for the formation of blood
Abcam GsMT x -4, mechanosensitive and stretch-activated ion channel inhibitor, 100UG
MW 4096 Da. GsMTx-4, mechanosensitive and stretch-activated ion channel inhibitor. Achieve your results faster with highly validated, pure and trusted compounds.
The product is subject to the following: Abcam Restricted Use Statement
Cayman Chemical CobaltIc III ProtoporphyrIn
An inducer of HO-1 activity; induces HO-1 activity in vitro and in vivo; reduces δ-aminolevulinate synthase and CYP activities in rat liver microsomes ex vivo at 125 µmol/kg; prevents liver injury and increases in the percentage of hepatic apoptotic cells in a mouse model of liver ischemia-reperfusion injury at 5 mg/kg; increases survival and decreases the number of lung CFUs in mice infected with Y. pestis; has also been used as a catalyst for the electrochemical reduction of carbon dioxide in carbon electrodes