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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T7121 | Sulfaclozine | Sulfachloropyrazine,Sulfachloropyrazine sodium | Antibacterial , Antibiotic , Parasite |
Sulfachloropyrazine sodium(Sulfachloropyrazine) is an antiprotozoal,with antibacterial and anticoccidial effects | |||
T16501 | PF-3644022 | p38 MAPK , Serine Protease , MAPK | |
PF-3644022 is an effective, selective, and ATP-competitive MAPKAPK2 (MK2) inhibitor (IC50: 5.2 nM and a Ki of 3 nM). PF-3644022 potently inhibits TNFα production and has an anti-inflammatory effect. PF-3644022 also inhib... | |||
T15549 | Icosabutate | Others | |
Icosabutate is a structurally engineered and orally active ω-3 polyunsaturated fatty acid. Icosabutate is well tolerated, and efficacious in lowering non-high-density lipoprotein cholesterol (non-HDL-C) levels in persist... | |||
T3544 | SHP099 hydrochloride | Phosphatase , Others | |
SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor. | |||
T14217 | AMG 579 | AMG-579 | PDE |
AMG 579 is an efficacious and selective inhibitor of PDE10A (IC50 = 0.1 nM). | |||
T12462 | PI3Kδ-IN-1 | PI3K | |
PI3Kδ-IN-1 is an efficacious PI3Kδ inhibitor (IC50 of 1.7 nM). | |||
T3692 | GNE-477 | GNE 477 | PI3K , mTOR |
GNE-477 is a potent and efficacious dual PI3K/mTOR inhibitor. | |||
T2338 | JZL195 | FAAH , Lipase , Autophagy | |
JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor. | |||
T36526 | IL-17 modulator 4 | Interleukin | |
IL-17 modulator 4 is a prodrug of IL-17 modulator 1 which is an efficacious modulator of IL-17. | |||
T6148 | CX-6258 hydrochloride | CX-6258 HCl,Pim-Kinase Inhibitor X | Pim |
CX-6258 hydrochloride (Pim-Kinase Inhibitor X) is an effective, orally efficacious Pim1/2/3 kinase inhibitor (IC50: 5/25/16 nM). | |||
T3741 | (-)-borneol | L-Borneol | GABA Receptor |
(-)-borneol (L-Borneol) has a highly efficacious positive modulating action at GABA receptor with an EC50 of 237 μM. | |||
T4690 | Betrixaban hydrochloride(330942-05-7(free base)) | PRT054021 hydrochloride | Factor Xa |
Betrixaban hydrochloride(330942-05-7(free base)) (PRT054021 hydrochloride) is a potent, selective, and orally efficacious factor Xa (fXa) inhibitor (IC50: 1.5 nM). | |||
T16996 | TAS6417 | Apoptosis , EGFR | |
TAS6417 is an EGFR inhibitor and is an efficacious drug candidate for patients with NSCLC (IC50: ranging from 1.1-8.0 nM). | |||
T14302 | Olorinab | APD 371 | Cannabinoid Receptor |
Olorinab (APD 371) (APD 371) is a highly potent, selective and fully efficacious cannabinoid receptor type 2 (CB2) agonist. With an EC50 of 6.2 nM for hCB2. | |||
T12181 | NaV1.7 inhibitor-1 | Sodium Channel | |
NaV1.7 inhibitor-1, an efficacious inhibitor of voltage-gated sodium channel (NaV) 1.7 (IC50 of 0.6 nM for hNaV1.7). | |||
T2030 | Tiplaxtinin | PAI-039,Tiplasinin | PAI-1 , Apoptosis |
Tiplaxtinin (Tiplasinin)(PAI-039) is a selective and orally efficacious inhibitor of plasminogen activator inhibitor-1 (PAI-1) with IC50 of 2.7 uM. | |||
T28073 | MLS1547 | MLS000051547,MLS 1547,MLS-1547 | Dopamine Receptor |
MLS1547 (MLS000051547) is a highly efficacious agonist of G protein-biased dopamine D2 receptor with a Ki of 1.2 μM. MLS1547 stimulates D2R G protein-mediated signaling with EC50 of 0.37 μM in a calcium mobilization assa... | |||
T11980 | MD-224 | Mdm2 , E1/E2/E3 Enzyme , PROTACs | |
MD-224 is a highly potent and efficacious MDM2 degrader based on the proteolysistargeting chimera (PROTAC) concept,and as a new class of anticancer agent. | |||
T14087 | ABT-239 | TRP/TRPV Channel | |
ABT-239 is a novel, highly efficacious antagonist belonging to the non-imidazole class of histamine H3 receptor (H3R) antagonists. It also acts as a transient receptor potential vanilloid type 1 (TRPV1) antagonist. | |||
T12165 | NAChR agonist 1 | DUN71755 | AChR |
nAChR agonist 1 (DUN71755) is a brain-permeable and orally efficacious positive allosteric α7 nicotinic acetylcholine receptor (α7 nAChR)modulator. |