Anthracenes
![Sigma Aldrich Ethyl 8-chloro-4H-thieno[3,2-c]chromene-2-carboxylate](https://assets.fishersci.com/TFS-Assets/CCG/Sigma-Aldrich/product-images/6966afd6-9457-435f-be99-8713d36edfe5.jpg-250.jpg)
Sigma Aldrich Ethyl 8-chloro-4H-thieno[3,2-c]chromene-2-carboxylate
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 1-Aminoanthracene
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
eMolecules 9,10-Dimethylanthracene | 781-43-1 | MFCD00001262 | 10g
Combi-Blocks | 9,10-Dimethylanthracene | 10g | 482934476 | QF-5809 | 95.000 | 781-43-1 | MFCD00001262 | 206.288 | C16H14
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
![Medchemexpress LLC Spiro[3H-indole-3,4'-[4H]thiopyran]-5-carboxamide, N-[[3-chloro-5-(trifluoromethyl)-2-pyridinyl]methyl]... | 1631164-24-3 | 99.5% | 672.11 g/mol | C29H26ClF4N3O5S2 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000262274.png-250.jpg)
Medchemexpress LLC Spiro[3H-indole-3,4'-[4H]thiopyran]-5-carboxamide, N-[[3-chloro-5-(trifluoromethyl)-2-pyridinyl]methyl]... | 1631164-24-3 | 99.5% | 672.11 g/mol | C29H26ClF4N3O5S2 | 5 MG
BAY-784 is a small-molecule gonadotropin releasing hormone receptor (GnRH-R) antagonist used as a research probe to inhibit GnRH-mediated signaling in vitro and in vivo. It is characterized by nanomolar potency, defined physicochemical properties, and high chemical purity for reliable assay performance.
- Small-molecule GnRH receptor antagonist with nanomolar potency.
- Reported IC50: 21 nM (human), 24 nM (rat).
- Molecular formula C29H26ClF4N3O5S2; molecular weight 672.11 g/mol.
- High chemical purity (99.5%).
- Supplied as a 5 mg research pack for assay and pharmacology studies.
- Useful for pharmacology, receptor biology, and signaling research.
eMolecules Target Molecule TAK-779 25mg 517682757 T7499 0 000 229005-80-5 MFCD05662319 531 140 C33H39ClN2O2
Target Molecule TAK-779 25mg 517682757 T7499 0 000 229005-80-5 MFCD05662319 531 140 C33H39ClN2O2
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
eMolecules ChemScene / 1-(Anthracen-9-yl)-222-trifluoroethanol / 100mg / 712788670 / CS-0436386 / 0.000 / 65487-67-4 / MFCD00062967 / 276.258 / C16H11F3O
ChemScene / 1-(Anthracen-9-yl)-222-trifluoroethanol / 100mg / 712788670 / CS-0436386 / 0.000 / 65487-67-4 / MFCD00062967 / 276.258 / C16H11F3O
eMolecules Ambeed TAK-779 25mg 832562838 A734428 0 000 229005-80-5 MFCD05662319 531 140 C33H39ClN2O2
Ambeed TAK-779 25mg 832562838 A734428 0 000 229005-80-5 MFCD05662319 531 140 C33H39ClN2O2
Accela Chembio Inc MF: C15H12O | MW: 208.26 | ?98% | Flash Point: 196.3?.
MF: C15H12O | MW: 208.26 | ?98% | Flash Point: 196.3?.
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
Apexbio Technology LLC A 779 159432-28-7 5mg
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