Cat. No. | Product name | CAS No. |
DC11032 |
AZD9977
Featured
AZD9977 is a first-in-class, potent, selective, mineralocorticoid receptor (MR) modulator with IC50 of 0.37. 0.08 and 0.08 uM for human, mouse and rat MR, respectively. |
1850385-64-6 |
DC8338 |
Azeliragon(PF-04494700,TTP488)
Featured
Azeliragon is an oral, small-molecule inhibitor of RAGE. |
603148-36-3 |
DC20156 |
Azetidine-2-carboxylic acid
Featured
Azetidine-2-carboxylic acid is a non proteinogenic amino acid homologue of proline. Found in common beets. Azetidine-2-carboxylic acid can be misincorporated into proteins in place of proline in many species, including humans. Toxic and teratogenic agent. |
36476-78-5 |
DC4210 |
Azilsartan kamedoxomil
Featured
Azilsartan medoxomil is an angiotensin II receptor antagonist indicated for the treatment of mild to moderate essential hypertension. |
863031-24-7 |
DCAPI1469 |
azilsartan
Featured
Azilsartan(TAK-536) is a specific and potent angiotensin II type 1 receptor antagonist with IC50 of 2.6 nM. |
147403-03-0 |
DC9818 |
Azoramide
Featured
Azoramide is a small-molecule modulator of the unfolded protein response with antidiabetic activity. |
932986-18-0 |
DC12497 |
(Z)-Azoxystrobin
Featured
Azoxystrobin is a systemic, broad-spectrum fungicide belonging to the class of methoxyacrylates,which are derived from the naturally-occurring strobilurins. |
143130-94-3 |
DC21570 |
Azvudine
Featured
Azvudine (RO 0622) is a potent HCV NS5B RNA polymerase inhibitor, inhibits HCV replication in the replicon system with IC50 of 24 nM; inhibits RNA synthesis by HCV polymerases from either HCV genotypes 1a and 1b or containing S96T or S282T point mutations (IC50=10-100 nM). |
1011529-10-4 |
DC10026 |
B02
Featured
B02 is a cell-permeable pyridinylvinyl-quinazolinone compound that is shown to specifically inhibit human RAD51 (IC50 = 27.4 µM). |
1290541-46-6 |
DC12033 |
(S)-B-973B
Featured
B-973 (B973) is a potent, selective α7 nAChR ago-PAM, denonstrates analgesic effect with attenuating pain behavior and decreasing paw edema in vivo. |
2244989-34-0 |
DC10859 |
Baccatin III
Featured
Baccatin III is the precursor to paclitaxel/ taxol. Antileukaemic and antitumor agent isolated from the bark of the Pacific yew tree (Taxus breviofolia). |
27548-93-2 |
DC2013 |
Bafetinib (INNO-406)
Featured
Bafetinib (INNO-406) is a potent and selective dual Bcr-Abl/Lyn inhibitor with IC50 of 5.8 nM and 19 nM, respectively. |
859212-16-1 |
DC8858 |
Bafilomycin A1(Baf-A1)
Featured
Bafilomycin A1 is a vacuolar H+-ATPase inhibitor with IC50 of 0.44 nM. |
88899-55-2 |
DC7371 |
Balicatib
Featured
Balicatib(AAE-581) is a potent and selective inhibitor of cathepsin K; 10-100-fold more potent in cell-based enzyme occupancy assays than against cathepsin B, L, and S. |
354813-19-7 |
DC11516 |
Balovaptan
Featured
Balovaptan (RG7314, RG-7314) is a potent, selective vasopressin-1 receptor antagonist.. |
1228088-30-9 |
DC11057 |
Baloxavir acid
Featured
Baloxavir acid (S-033447) is an anti-influenza compound that potently and selectively inhibits the cap-dependent endonuclease within the polymerase PA subunit of influenza A and B viruses. |
1985605-59-1 |
DC11056 |
Baloxavir marboxil
Featured
Baloxavir marboxil is a prodrug of S-033447. S-033447 is a small molecule inhibitor of the cap-dependent endonuclease of influenza A and B viruses. |
1985606-14-1 |
DC8298 |
BAN ORL 24
Featured
BAN ORL 24 is a potent, selective, competitive ORL1 non-peptide agonist. Displays 1000-fold selectivity over classical opioid receptors. |
1401463-54-4 |
DC10502 |
BAPTA/AM(BAPTA-AM)
Featured
BAPTA/AM is a membrane permeable form of BAPTA, a selective chelator of Ca2+. |
126150-97-8 |
DC10385 |
BAR501
Featured
BAR501 is a potent and selective agonist of GPBAR1 with an EC50 of 1 μM. |
1632118-69-4 |
DC10564 |
BAR 502
Featured
BAR502 is a dual FXR and GPBAR1 agonist with IC50 values of 2 μM and 0.4 μM, respectively. |
1612191-86-2 |
DC4135 |
Bardoxolone methyl
Featured
Bardoxolone methyl (also known as “RTA 402” and “CDDO-methyl ester”) is an orally-available first-in-class synthetic triterpenoid belonging to the antioxidant inflammation modulator (AIM) class. |
218600-53-4 |