Anthracenes

Polycyclic aromatic hydrocarbon compounds that consist of fourteen carbon atoms and ten hydrogen atoms linearly fused into three benzene rings; also called paranaphthalene, or green oil.

Search Within Results

226 – 240 of 373 results

226

Ambeed AMBEED

5000846979 3 3 - ETHANE-1 1-DIYL B 1G

Pricing & Availability

227

Ambeed AMBEED

5000891501 ANTHRACENE-910-DIYL DIAC 250MG

Pricing & Availability

228

MOLTOX Molecular Toxicology Inc 2-Aminoanthracene, 100 ug/vial, 5 vials/pack, Store in Refrigerator

For use in Ames test with the following corresponding tester strains and dosage: - TA1538. Dose 2 - 10 µg/plate. - TA97a, TA98, TA100. Dose 1 - 5 µg/plate. - TA102. Dose 5 - 10 µg/plate. - E. coli WP2, E. coli WP2 uvra, E. coli WP2 pKM101, E. coli WP2 uvra pKM101. Dose 20 µg/plate. Reconstitute with organic solvents such as DMSO or sterile dH2O as applicable. Indirect acting mutagens require the use of S9 metabolic activation to cause mutagenicity. CONTROLCHEM™ chemicals are obtained from major suppliers of research chemicals and are employed without further characterization or purification. Packaged quantities are precise within 1%. Please Note: CONTROLCHEM™ chemicals are known mutagens/carcinogens/toxins and are sold only to those experienced in the safe handling and disposal of hazardous materials. Consult your Institutional Safety Officer before ordering.

Pricing & Availability

229

Apexbio Technology LLC A 779 159432-28-7 1mg

A 779 (CAS 159432-28-7) is a selective antagonist of the angiotensin-(1-7)/Mas receptor By competitively inhibiting angiotensin-(1-7) a bioactive peptide of the renin-angiotensin system (RAS) involved in cardiovascular and renal homeostasis A 779 enables detailed study of Mas receptor-mediated signaling In vivo A 779 blocks the antidiuretic and pressor effects of angiotensin-(1-7) in rats and modulates the response to bradykinin potentiation by ACE inhibition It has been used to explore interactions among angiotensin receptors and the role of Mas signaling in cardiovascular and renal physiology

Pricing & Availability

230

Medchemexpress LLC A 779 | 159432-28-7 | 99.3% | 872.97 | 100 MG

A 779 is a specific antagonist of the G-protein coupled receptor (Mas receptor), which is an Ang1-7 receptor distinct from the classical AngII. It is for research use only.

Inhibits the effect of Ang-(1-7)
Suppresses PCNA protein expression up-regulated by Ang II
Blocks Ang II-induced inflammatory responses of VSMCs
Blocks Ang II-induced Akt and ERK1/2 phosphorylation
Elevates serum BALP, CTX, TRAcP 5b, OC, and urinary DPD
Abolishes Ang-(1-7)'s favorable effects on bone health by blocking the Mas receptor
Erradicates captopril protective effects on bone metabolism, mineralization, and micro-structure
Restores OVX effects on RANKL expression and ACE-1/AngII/AT1R cascade
Down-regulates OPG expression and ACE-2/Ang1-7/Mas pathway

Pricing & Availability

231

eMolecules 229005-80-5 | TAK-779 | Ambeed | MFCD05662319 | 531.140 | C33H39ClN2O2 | 98.000 | [Cl-].Cc1ccc(cc1)-c1ccc2CCCC(=Cc2c1)C(=O)Nc1ccc(C[N+](C)(C)C2CCOCC2)cc1 | 25mg | 832562838

TAK-779 | Ambeed | 229005-80-5 | MFCD05662319 | 531.140 | C33H39ClN2O2 | 98.000 | [Cl-].Cc1ccc(cc1)-c1ccc2CCCC(=Cc2c1)C(=O)Nc1ccc(C[N+](C)(C)C2CCOCC2)cc1 | 25mg | 832562838

Pricing & Availability

232

eMolecules 117820-97-0 | 2,3-Dibromoanthracene | Toronto Research Chemicals | MFCD30497387 | 336.026 | C14H8Br2Brc1cc2cc3ccccc3cc2cc1Br | 50mg | 483399302

2,3-Dibromoanthracene | Toronto Research Chemicals | 117820-97-0 | MFCD30497387 | 336.026 | C14H8Br2Brc1cc2cc3ccccc3cc2cc1Br | 50mg | 483399302

Pricing & Availability

233

Medchemexpress LLC (2S)-N-[7-chloro-6-[4-[(3R,4R)-4-hydroxy-3-methyloxolan-3-yl]piperazin-1-yl]isoquinolin-3-yl]-6-o... | 2769107-89-1 | 99.7% | 501.02 g·mol⁻1 | C26H33ClN4O4 | 10 MG

MK-1468 is an orally active, selective, blood-brain barrier-permeable inhibitor of leucine-rich repeat kinase 2 (LRRK2) used in preclinical research of Parkinson's disease and LRRK2-related pathways.

Orally active and brain-penetrant LRRK2 inhibitor suitable for in vivo and in vitro studies.
High purity (≈99.7%) for research-grade experiments.
Molecular weight 501.02 g·mol⁻1 and formula C26H33ClN4O4.
Available in small-scale quantities for dosing and assay optimization.
Store powder at -20°C; solutions stable at -80°C for 6 months.