Anthracenes
![Sigma Aldrich Fine Chemicals Biosciences Dibenz[a,j]anthracene BCR(R), certified reference material | 224-41-9 | MFCD00215859 | 100MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/501762352.PNG-250.jpg)
Sigma Aldrich Fine Chemicals Biosciences Dibenz[a,j]anthracene BCR(R), certified reference material | 224-41-9 | MFCD00215859 | 100MG
Dibenz[a,j]anthracene BCR(R), certified reference material | Mol Wt: 278.35 | 224-41-9 | MFCD00215859 | 100MG
![Medchemexpress LLC 1-Piperazinecarboxylic acid, 4-[[4-(4-chlorophenoxy)-3,5-difluorophenyl]sulfonyl]-3-[(hydroxyamino)carbonyl]-, 2-methoxyethyl ester, magnesium salt (2:1) | 1224964-36-6 | 98.3% | 548.92 | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000402606-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 1-Piperazinecarboxylic acid, 4-[[4-(4-chlorophenoxy)-3,5-difluorophenyl]sulfonyl]-3-[(hydroxyamino)carbonyl]-, 2-methoxyethyl ester, magnesium salt (2:1) | 1224964-36-6 | 98.3% | 548.92 | 1 ML
XL-784 is a selective matrix metalloproteinases (MMP) inhibitor. It potently inhibits MMP-2, MMP-13, and ADAM10 [TNF-α-converting enzyme (TACE)] activity in vitro, with IC50 values in the range of 1-2 nM. It also inhibits MMP-9 and ADAM17 activity, but exhibits low potency for inhibition of MMP-1.
- Selective matrix metalloproteinases (MMP) inhibitor.
- Potently inhibits MMP-2, MMP-13, and ADAM10 in vitro.
- Inhibits MMP-9 and ADAM17 activity.
- Demonstrated effectiveness in inhibiting aortic dilatation in mice.
eMolecules Ambeed TAK-779 100mg 837385137 A734428 0 000 229005-80-5 MFCD05662319 531 140 C33H39ClN2O2
Ambeed TAK-779 100mg 837385137 A734428 0 000 229005-80-5 MFCD05662319 531 140 C33H39ClN2O2
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.
TARGETMOL CHEMICALS INC TAK-779 10MG
Also available in 1 mL, 1 mg, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. TAK-779 (Takeda 779) is an antagonist of chemokine receptor 5 (CCR5), CCR2b, and CXC chemokine receptor 3 (CXCR3). Purity 99.58%
Sigma Aldrich Fine Chemicals Biosciences 9-Anthracenemethanol 97% | 1468-95-7 | MFCD00001264 | 10G
9-Anthracenemethanol 97% | Purity: 97% | Mol Wt: 208.26 | 1468-95-7 | MFCD00001264 | 10G
Medchemexpress LLC 9-Bromoanthracene-d9 | 183486-02-4 | 266.18 | 5 G
9-Bromoanthracene-d9 is a deuterium-labeled version of 9-Bromoanthracene. It is intended for research use only and is not sold to patients. This compound can be utilized as a tracer and an internal standard for quantitative analysis. Its appearance is a solid, light yellow to yellow in color.
- Used as a tracer
- Used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS