All ProductsDisplaying Products by Catalog Number (5300 - 5399)
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Cat. No. | Product Name / Activity |
---|---|
5301 | BPTES |
Selective allosteric glutaminase (GLS1) inhibitor | |
5303 | GSK 2194069 |
Potent human fatty acid synthase (hFASN) inhibitor | |
5304 | FICZ |
High affinity aryl hydrocarbon receptor (AhR) agonist | |
5305 | Verteporfin |
YAP inhibitor | |
5306 | KJ Pyr 9 |
High affinity Myc inhibitor | |
5307 | MM 102 |
Potent WDR5/MLL interaction inhibitor | |
5308 | ASP 2535 |
Potent and selective GlyT1 inhibitor | |
5309 | SP 100030 |
NF-κB and AP-1 dual inhibitor | |
5310 | ASP 3026 |
Potent anaplastic lymphoma kinase (ALK) inhibitor; also potent ACK inhibitor | |
5311 | RHPS 4 methosulfate |
Telomerase inhibitor | |
5312 | BRACO 19 trihydrochloride |
Telomerase inhibitor | |
5314 | SMBA 1 |
High affinity and selective activator of Bax | |
5315 | Rostafuroxin |
Na+/K+ ATPase modulator; antihypertensive agent | |
5316 | Elinogrel |
P2Y12 antagonist | |
5317 | WWL 123 |
α/β-hydrolase domain 6 (ABHD6) inhibitor; antiepileptic | |
5318 | AEE 788 |
Potent EGFR and VEGFR inhibitor | |
5319 | ACT 462206 |
Potent, dual orexin receptor antagonist | |
5320 | CORM 3 |
Water-soluble carbon monoxide-releasing molecule | |
5321 | PSNCBAM-1 |
Negative allosteric modulator of CB1 receptors | |
5323 | WDR5 0103 |
WDR5 antagonist | |
5324 | M8 B hydrochloride |
Potent and selective TRPM8 channel blocker | |
5325 | Rosiglitazone |
Potent and selective PPARγ agonist; antidiabetic agent | |
5326 | CHR 6494 trifluoroacetate |
Potent and selective haspin inhibitor | |
5327 | BGC 20-1531 hydrochloride |
High affinity and selective EP4 antagonist | |
5328 | TY 52156 |
S1P3 receptor antagonist | |
5329 | CKI 7 dihydrochloride |
CK1 inhibitor | |
5331 | CPI 203 |
BET bromodomain inhibitor; arrests cell cycle at G1 phase | |
5332 | SP 141 |
High affinity MDM2 inhibitor | |
5337 | ML 365 |
Potent and selective K2P3.1 (TASK-1) channel blocker | |
5338 | PK-THPP |
Potent K2P9.1 (TASK-3) channel blocker | |
5339 | PFK 15 |
Selective PFKFB3 inhibitor | |
5340 | NSC 617145 |
Werner syndrome helicase (WRN) inhibitor | |
5342 | SCR7 pyrazine |
Enhances HDR efficiency | |
5343 | TPPB |
High affinity PKC activator; also APP modulator | |
5348 | 6,8-Bis(benzylthio)octanoic acid |
PDH and KGDH inhibitor | |
5349 | Treprostinil |
Potent prostacyclin (PGI2) analog | |
5353 | Gap19 |
Cx43 hemichannel blocker | |
5355 | TC-G 1008 |
Potent and selective GPR39 agonist | |
5356 | SGX 523 |
Selective and potent c-MET kinase inhibitor | |
5357 | DC 260126 |
FFA1 (GPR40) antagonist | |
5358 | Cariporide |
Selective NHE1 inhibitor; cardioprotective and antitumor | |
5361 | GSK LSD 1 dihydrochloride |
Potent and selective LSD1 inhibitor | |
5362 | TASP 0433864 |
Selective positive allosteric modulator of mGlu2 receptors | |
5363 | NHI 2 |
LDHA inhibitor | |
5364 | Hydroxy Dynasore |
Dynamin inhibitor; analog of dynasore (Cat. No. 2897) | |
5367 | SGC 707 |
Potent and selective allosteric inhibitor of PRMT3 | |
5373 | C34 |
TLR4 inhibitor | |
5374 | GLP-1 (7-37) |
Endogenous bioactive GLP-1 receptor ligand | |
5376 | Pregnenolone sulfate sodium salt |
NMDA potentiator; also GABAA inhibitor and TRPM3 activator | |
5378 | VU 0422288 |
Selective positive allosteric modulator of group III mGlu receptors | |
5379 | VU 0469650 hydrochloride |
Potent and selective negative allosteric modulator of mGlu1 receptors | |
5380 | ML 297 |
Selective Kir3.1/3.2 (GIRK1/2) channel activator | |
5382 | C16 |
PKR inhibitor | |
5388 | RQ 00203078 |
Potent and selective TRPM8 antagonist; orally active | |
5389 | Ro 48-8071 fumarate |
2,3-Oxidosqualene cyclase (OSC) inhibitor; blocks cholesterol synthesis | |
5390 | Tobramycin |
Aminoglycoside antibiotic | |
5391 | SPP 86 |
Potent RET inhibitor | |
5393 | ERK5-IN-1 |
Potent and selective ERK5 inhibitor | |
5397 | A01 |
High affinity Smurf1 inhibitor; enhances BMP signaling | |
5399 | BTB1 |
Selective and ATP-competitive Kif18A inhibitor |