20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T3S0081 | Oxypeucedanin | (+-)-Oxypeucedanin,Oxypeucadanin | Potassium Channel |
1. Oxypeucedanin ((+-)-Oxypeucedanin) has novel anticancer effect, mediated via induction of G2-M cell cycle arrest and apoptosis in human prostate carcinoma DU145 cells. 2. Oxypeucedanin is a kind of open-channel blocke... | |||
T8118 | Bekanamycin | Kanamycin B | Antibacterial , Antibiotic |
Bekanamycin (Kanamycin B) is an aminoglycoside antibiotic. | |||
T20766 | Sulfisoxazole acetyl | Gantrisin,Acetylsulfisoxazole,Gantrisin Pediatric,Lipo Gantrisin | Antibacterial |
Sulfisoxazole acetyl (Gantrisin) is an agent with antibacterial activity. Sulfisoxazole acetyl is a Sulfisoxazole derivative with antibacterial activity. Sulfisoxazole acetyl is an inhibitor of dihydropteroate synthase. | |||
T3158 | Harmane | Loturine,Harman,Aribine | Adrenergic Receptor , Monoamine Oxidase , Imidazoline Receptor |
Harmane (Loturine) is a bio-active β-Carboline and monoamine oxidase inhibitor found in coffee and tobacco smoke. | |||
T1320 | Disopyramide | Triombrin,Hypaque sodium,amidotrizoate sodium | Potassium Channel , Sodium Channel , AChR |
Disopyramide (Triombrin) is a class I anti-arrhythmic agent (one that interferes directly with the depolarization of the cardiac membrane and thus serves as a membrane-stabilizing agent) with a depressant action on the h... | |||
T1676 | Rosuvastatin | ZD 4522 | Potassium Channel , HMG-CoA Reductase , Autophagy |
Rosuvastatin (ZD 4522) is an antilipemic agent that competitively inhibits hydroxymethyl-glutaryl-coenzyme A (HMG-CoA) reductase. HMG-CoA reductase catalyzes the conversion of HMG-CoA to mevalonic acid, the rate-limiting... | |||
T7894 | Tazarotenic acid | AGN-190299 | Others |
Tazarotenic acid (AGN-190299) is a retinoid prodrug which is converted to its active form | |||
T1510 | Rosuvastatin calcium | ZD 4522 Calcium,ZD4522,Rosuvastatin hemicalcium | Potassium Channel , HMG-CoA Reductase , Autophagy |
Rosuvastatin calcium (ZD4522) , a selective and competitive inhibitor of hepatic hydroxymethyl-glutaryl coenzyme A (HMG-CoA) reductase, has antilipidemic activity. | |||
T3189 | B7/CD28 interaction inhibitor 1 | CTLA-4 inhibitor | Others |
B7/CD28 interaction inhibitor 1 (CTLA-4 inhibitor) is a potent CTLA-4 inhibitor. | |||
T9044 | SORT-PGRN interaction inhibitor 1 | Neurotensin Receptor | |
SORT-PGRN interaction inhibitor 1 is a potent sortilin-progranulin interaction inhibitor(IC50 of 2 μM). | |||
T12350 | P53 and MDM2 proteins-interaction-inhibitor dihydrochloride | Others | |
p53 and MDM2 proteins-interaction-inhibitor dihydrochloride is a interaction inhibitor between p53 and MDM2 proteins. | |||
T80381 | SAAP Fraction 3 | ||
SAAP Fraction 3, an antimicrobial peptide, exhibits activity against P. haemolytica in Zn-saline buffer [1]. | |||
T28219 | NusB-NusE interaction inhibitor-1 | ||
NusB-NusE interaction inhibitor-1 is a modulator of the NusB-NusE interaction. | |||
T82245 | HA-CD44 interaction inhibitor 1 | ||
Antitumor agent-109 (compound 6) is a dual-function inhibitor that targets hyaluronic acid and CD44, which are involved in tumor progression and invasion. It demonstrates potent antitumor activity, specifically inhibitin... | |||
T82902 | Beclin1-Bcl-2 interaction inhibitor 1 | ||
Beclin1-Bcl-2 Interaction Inhibitor 1 effectively disrupts the binding of Beclin 1 to Bcl-2, and is utilized in cancer and neurodegeneration research [1]. | |||
T79756 | Beclin1-ATG14L interaction inhibitor 1 | Autophagy | |
Beclin1-ATG14L Interaction Inhibitor 1 (COM 19) is a selective inhibitor targeting the specific interaction between Beclin1 and ATG14L. It impedes the formation of complex I in the lipid kinase VPS34, thus inhibiting aut... | |||
T12351 | P53 and MDM2 proteins-interaction-inhibitor (racemic) | p53-and-mdm2-proteins-interaction-inhibitor-racemic | Others |
p53 and MDM2 proteins-interaction-inhibitor (racemic) is an inhibitor of the interaction between p53 and MDM2 proteins. | |||
T82244 | HA-CD44 interaction inhibitor 2 | ||
Antitumor Agent-108 (Compound 5), an inhibitor of the Hyaluronic Acid (HA)-CD44 interaction, effectively disrupts cancer spheroid integrity and exhibits antiproliferative activity against cancer cells [1]. | |||
T81126 | SORT-PGRN interaction inhibitor 2 | ||
SORT-PGRN Interaction Inhibitor 2 is a compound that downregulates SORT1 protein expression and enhances extracellular progranulin (PGRN) secretion in various mammalian cell lines, and is utilized in the study of neurolo... | |||
T79106 | SORT-PGRN interaction inhibitor 3 | Neurotensin Receptor | |
SORT-PGRN Interaction Inhibitor 3 (Compound 13), with an IC50 value of 0.17 μM, acts as an inhibitor of the SORT-PGRN interaction, and is utilized in the study of neurodegenerative diseases [1]. |