20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T79772 | RARα antagonist 1 | ||
Compound 21, an orally active and selective RARα antagonist, exhibits a potent inhibition of the retinoic acid receptor α with an IC50 of 4.6 nM [1]. | |||
T1093 | Adapalene | CD271 | Apoptosis , Retinoid Receptor , Autophagy |
Adapalene (CD271) is a dual RAR and RXR agonist, utilized in the treatment of skin conditions. | |||
T21714 | BMS453 | BMS 453,BMS-189453 | Retinoid Receptor |
BMS453 (BMS-189453), a synthetic retinoid, is a potent and selective agonist of RARβ and a potent testicular toxin. BMS453 inhibits breast cell growth predominantly through the induction of active TGFβ. | |||
T22049 | BMS 753 | Retinoid Receptor | |
BMS 753 is an agonist of isotype-selective retinoic acid receptor α (RARα, Ki= 2 nM). | |||
T22920 | LE135 | LE 135 | Retinoid Receptor |
LE135 is a potent RAR antagonist that binds selectively to RARα (Ki of 1.4 μM) and RARβ (Ki of 220 nM), and has a higher affinity to RARβ. LE135 is highly selective over RARγ, RXRα, RXRβ and RXRγ. LE135 is also a potent ... | |||
TQ0097 | AGN 193109 | Retinoid Receptor , Autophagy | |
AGN 193109, a retinoid analog, is a potent and specific antagonist of RARs (Kds: 2 nM, 2 nM, and 3 nM for RARα, RARβ, and RARγ). | |||
T1288 | TTNPB | AGN191183,Arotinoid acid,Ro 13-7410,AGN-191183,Ro 13-7410 | Apoptosis , Retinoid Receptor , Autophagy |
TTNPB (Ro 13-7410,AGN-191183), a potent RAR agonist, inhibits binding of [3H]tRA of human RARα (IC50: 5.1 nM), β (IC50: 4.5 nM), and γ (IC50: 9.3 nM), respectively. | |||
T10261 | AGN 196996 | Others , Retinoid Receptor , Autophagy | |
AGN 196996 is a potent and selective inhibitor of RARα (Ki: 2 nM).AGN 196996 has very low affinity for RARβ and RARγ, with a Ki of 1087 nM and 8523 nM, respectively. | |||
T22192 | BMS 195614 | BMS614 | Retinoid Receptor |
BMS 195614 (BMS614) is a selective RARα antagonist. BMS 195614 can bind to the RARα subunit. | |||
T7586 | Trifarotene | CD5789 | Retinoid Receptor , Autophagy |
Trifarotene (CD5789) is a potent and selective RARγ agonist with 65-fold and 16-fold selectivitiy for the RARγ (EC50=7.7 nM) over RARα (EC50=500 nM) and RARβ (EC50=125 nM). | |||
T1051 | Retinoic acid | Vitamin A acid,ATRA,all-trans-Retinoic acid,Tretinoin | Retinoid Receptor , Endogenous Metabolite , PPAR , Autophagy |
Retinoic acid (Tretinoin), a metabolite of vitamin A, is a natural agonist of the retinoic acid receptor RAR and inhibits RARα/β/γ (IC50=14 nM). Retinoic acid induces cellular differentiation, reduces cellular proliferat... | |||
T3955 | AR7 | Retinoid Receptor | |
AR7 is a retinoic acid receptor α (RARα) antagonist. | |||
T5854 | AM580 | NSC608001,CD336,Ro 40-6055 | Retinoid Receptor , Autophagy |
AM580 (CD336) is a retinoic acid receptor agonist that is selective for RARα( IC50 : 8 nM ) | |||
T22767 | ER 50891 | Retinoid Receptor | |
ER-50891 is a potent retinoic acid receptor alpha (RARα) antagonist. er-50891 reduces the inhibitory effect of allosteric retinoic acid and restores osteoblast differentiation induced by bone morphogenetic protein 2. | |||
T61588 | AGN 192870 | Apoptosis , Retinoid Receptor | |
AGN 192870 is a potent retinoic acid receptor (RAR) antagonist.AGN 192870 can be used to study cell growth arrest, differentiation and apoptosis. | |||
T10265 | AGN 194078 | Others | |
AGN 194078 is a selective RARα agonist (Kd: 3 nM; EC50: 112 nM). | |||
T21314 | Amsilarotene | TAC-101,TAC 101,TAC101 | CDK |
Amsilarotene (TAC101) inhibits the phosphorylation of retinoblastoma gene product (RB) and increases the presence of 2 cyclin-dependent kinases (CDK) inhibitors resulting in cell cycle arrest. This agent also causes a cy... | |||
T14144 | AGN-195183 | Others | |
AGN 195183 is a potent and selective agonist of RARα(Kd=3 nM) with improved binding selectivity relative to AGN 193836; no activity on RARβ/γ. IC50 value: 3 nM (Kd); 200 nM (EC80, RAR Trans.) Target: RARα agonist Compoun... | |||
T14143 | AGN 194310 | VTP-194310 | Retinoid Receptor |
AGN 194310 (VTP-194310) is retinioic acid receptors (RARs) pan-antagonist. The Kd values of 3 nM, 2 nM, 5 nM for RARα, RARβ, RARγ, respectively[1][2]. | |||
T28589 | Ro 41-5253 | Ro-41-5253,Ro 415253 | Apoptosis , Retinoid Receptor |
Ro 41-5253 is an orally active RARα antagonist, ligand and partial agonist of peroxisome proliferator-activated receptor (PPAR)-γ. It exhibits antitumor activity, inhibits proliferation and induces apoptosis in MCF-7 and... |