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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8188 | Podophyllotoxone | Others , Microtubule Associated | |
Podophyllotoxinone, a natural compound found in Dysosma versipellis, shows inhibitory activity against L1210 leukemia and KB cells in vitro. | |||
TN2054 | Periplocymarin | Calcium Channel | |
Periplocymarin is a cardiac glycoside with anticancer potential isolated from Periploca sepium and Periploca graeca. | |||
T12928 | SK33 | Androgen Receptor | |
SK33 is a potent and tissue selective anti-androgen agent. SK33 reduces androgen receptor (AR) transcriptional activity. | |||
T1267 | Abacavir | Epzicom,Ziagen,Abacavir sulfate | Apoptosis , HIV Protease , Reverse Transcriptase |
Abacavir (Ziagen) is a nucleoside reverse transcriptase inhibitor analog of guanosine. This agent decreases HIV viral loads, retards or prevents the damage to the immune system, and reduces the risk of developing AIDS. | |||
T1448 | Dasatinib | BMS-354825 | Apoptosis , Bcr-Abl , Src , c-Kit , Autophagy |
Dasatinib (BMS-354825) is a tyrosine kinase inhibitor that inhibits Src and Bcr-Abl (Ki=16/30 pM) and is orally active and ATP-competitive. Dasatinib has antitumor activity and is used in the treatment of leukemia and ly... | |||
T6967 | RHPS4 | RHPS 4 methosulfate,NSC714187 | Apoptosis , Telomerase |
RHPS4 (RHPS 4 methosulfate) is a potent inhibitor of Telomerase at submicromolar. | |||
T6367 | Abacavir sulfate | Abacavir Hemisulfate,1592U89,ABC sulfate,Ziagen | Apoptosis , HIV Protease , Reverse Transcriptase |
Abacavir sulfate (Ziagen) , a nucleoside analogue, effectively utilize its antiviral activity | |||
T1448L | Dasatinib monohydrate | BMS-354825 Monohydrate | Apoptosis , Bcr-Abl , Src , c-Kit , Ephrin Receptor , Autophagy |
Dasatinib monohydrate (BMS-354825 Monohydrate) is an orally bioavailable synthetic small molecule-inhibitor of SRC-family protein-tyrosine kinases. Dasatinib monohydrate binds to and inhibits the growth-promoting activit... | |||
T79054 | TRPC3/6-IN-2 | ||
TRPC3/6-IN-2 is a potent inhibitor of TRPC3 and TRPC6, exhibiting IC50 values of 16 nM for TRPC3 and 29.8 nM for TRPC6, respectively [1]. | |||
T29113 | VPC32183 | VPC-32183,VPC 32183 | |
VPC32183 is a competitive antagonist of LPA1 and LPA3 receptors. | |||
T61407 | TRPC3/6-IN-1 | ||
TRPC3/6-IN-1 is a highly potent and selective inhibitor that specifically blocks the activity of the canonical transient receptor channels TRPC3 and TRPC6. It exhibits a significant blocking potency against the human iso... | |||
T35071 | VPC32179 | VPC 32179,VPC-32179 | |
VPC32179 is a bioactive chemical. | |||
T10657 | C75 | C-75 | Fatty Acid Synthase |
C75 is an inhibitor synthetic fatty-acid synthase (FASN) and inhibits prostate cancer cells PC3 (IC50: 35 μM). | |||
TN1198 | 19-Hydroxybufalin | Others | |
19-Hydroxybufalin is a natural product, inhibits epithelial-mesenchymal transition and attenuates the migration and invasion of PC3 cells. | |||
T35666 | PRGL493 | Others | |
PRGL493 is an inhibitor of long-chain acyl-CoA synthetase 4 (ACSL4).1It inhibits formation of arachidonoyl-CoA (AA-CoA) from arachidonic acid in, as well as the proliferation and migration of, PC3 and MDA-MB-231 cancer c... | |||
T29110 | VPC-13163 | 2,3-dihydro-2,3'-Bi-1H-indole,VPC13163,NSC52361,NSC 52361,VPC 13163 | Others |
VPC-13163 (NSC-52361) has strong anti-proliferative activity against LNCaP and Enzalutamide-resistant prostate cancer cell lines (MR49F) whereas it did not affect the growth of AR independent PC3 cell line. It also inhib... | |||
TP1895L1 | KYL acetate(676657-00-4 free base) | Ephrin Receptor | |
KYL acetate is a EphA4 receptor tyrosine kinase inhibitor (Kd = 0.8 μM). KYL inhibits EphA4-EphrinA5 interactions (IC50 = 6.34 μM). | |||
T3989 | SMI-16a | PIM1/2 Kinase Inhibitor VI | Pim |
SMI-16a (PIM1/2 Kinase Inhibitor VI) , a cell-permeable thiazolidinedione compound, acts as an effective, ATP-competitive inhibitor against Pim-1/2 kinases (IC50: 150/20 nM) while exhibiting little or no activity against... | |||
T10656 | Trans-C75 | (±)-C75 | Others , Fatty Acid Synthase |
trans-C75 ((±)-C75) is an enantiomer of C75. C75 is an inhibitor of fatty-acid synthase (FASN). | |||
T64222 | Antitumor agent-55 | ||
Antitumor agent-55 (compound 5q) is a potent antitumour agent that effectively inhibits PC3 (IC50: 0.91 μM). antitumor agent-55 blocks the G1/S phase of the PC3 cell cycle, induces apoptosis, inhibits cell migration and ... |