Catalog |
name |
Description |
price |
R-R-1557 |
CUR61414 CAS No.334998-36-6 |
CUR61414/CAS No.334998-36-6 is a novel, potent and cell permeable Hedgehog signaling pathway inhibitor (IC50 =100-200 nM). CUR61414 is a small-molecule aminoproline class compound and selectively binds to smoothened (Smo) with a Ki value of 44 nM. CUR-61414 can induce apoptosis in cancer cells without affecting neighboring non-tumor cells. |
price> |
R-R-1558 |
Forodesine hydrochloride CAS No.284490-13-7 |
Forodesine hydrochloride (BCX-1777 hydrochloride)/CAS No.284490-13-7 is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP. Forodesine hydrochloride is a potent human lymphocyte proliferation inhibitor. Forodesine hydrochloride could induce apoptosis in leukemic cells by increasing the dGTP levels. |
price> |
R-R-1560 |
IACS-010759 hydrochloride CAS No.1807523-99-4 |
IACS-010759 hydrochlorideis/CAS No.1807523-99-4 an orally active, potent mitochondrial complex I of oxidative phosphorylation (OXPHOS) inhibitor. IACS-010759 hydrochlorideinhibits proliferation and induces apoptosis in models of brain cancer and acute myeloid leukemia (AML) reliant on OXPHOS. IACS-010759 hydrochloride has the potential for relapsed/refractory AML and solid tumors research. |
price> |
R-R-1561 |
Forodesine CAS No.209799-67-7 |
Forodesine (BCX-1777)/CAS No.209799-67-7 is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP. Forodesine is a potent human lymphocyte proliferation inhibitor. Forodesine could induce apoptosis in leukemic cells by increasing the dGTP levels. |
price> |
R-R-1562 |
Indinavir sulfate CAS No.157810-81-6 |
Indinavir sulfate (MK-639)/CAS No.157810-81-6 is an orally active and selective HIV-1 protease inhibitor with a Ki of 0.54 nM for PR. Indinavir sulfate exhibits anticancer activity by inhibiting the activation of MMPs-2 hydrolysis, anti-angiogenesis and inducing apoptosis. Indinavir sulfate is also a SARS-CoV 3CLpro inhibitor. |
price> |
R-R-1563 |
Bullatine A CAS No.1354-84-3 |
Bullatine A/CAS No.1354-84-3, a diterpenoid alkaloid of the genus Aconitum, possesses anti-rheumatic, anti-inflammatory and anti-nociceptive effects. Bullatine A is a potent P2X7 antagonist, inhibits ATP-induced cell death/apoptosis and P2X receptor-mediated inflammatory responses. Bullatine A attenuates pain hypersensitivity, regardless of the pain models employed. |
price> |
R-R-1564 |
(Rac)-CCT 250863 CAS No.1364269-06-6 |
(Rac)-CCT 250863 (compound rac-21)/CAS No.1364269-06-6 is a selective and reversible NEK 2 inhibitor with an IC50 of 0.073 µM. (Rac)-CCT 250863 shows good effects of inducing cell cycle arrest and also can antiproliferative in cells (Pomalidomide sensitive/resistant). (Rac)-CCT 250863 induces apoptosis when combines with Pomalidomide. |
price> |
R-R-1565 |
NSC 48160 CAS No.6640-90-0 |
NSC 48160/CAS No.6640-90-0 inhibits the growth of the pancreatic cancer cells with IC50s of 84.3 μM for CPFAC-1 and 94.5 μM for BxPC-3. NSC 48160 also induces pancreatic cancer cell apoptosis. NSC 48160 can improve metabolic syndromes, such as NASH, obesity and lipid metabolism disorders. |
price> |
R-R-1566 |
Cantrixil CAS No.2135511-22-5 |
Cantrixil (TRX-E-002-1)/CAS No.2135511-22-5, an active enantiomer of TRX-E-002, is a second-generation super-benzopyran (SBP) compound. Cantrixil increases phosphorylated c-Jun levels resulting in caspase-mediated apoptosis in ovarian cancer cells. Cantrixil has potent pan anti-cancer activity against a broad range of cancer phenotypes. |
price> |
R-R-1567 |
GSK-843 CAS No.1601496-05-2 |
GSK-843/CAS No.1601496-05-2 is a receptor-interacting protein kinase 3 (RIP3 or RIPK3) inhibitor, which binds RIP3 kinase domain with an IC50 of 8.6 nM, and inhibits kinase activity with an IC50 of 6.5 nM. GSK-843 can be used for the research of inflammation. |
price> |