JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

Setting

Ordered before 17:30, shipped today - Support: (012) 800 456 789

Track Your Order

Home
Search results for: 'research area gpcr g protein leukotriene receptor'

Search results for: 'research area gpcr g protein leukotriene receptor'

A8180 KN-62

Target: Ca2 /calmodulin-dependent protein kinases (CaMKs)|P2X Receptors

Summary: CaM kinase II inhibitor

≥36.1 mg/mL
A3530 KN-92 hydrochloride

Target: Ca2 /calmodulin-dependent protein kinases (CaMKs)

Summary: Inactive derivative of KN-93,control compound

≥24.65 mg/mL
A3532 KN-93

Target: Ca2 /calmodulin-dependent protein kinases (CaMKs)

Summary: CaMKII inhibitor,selective and cometitive

insoluble in H2O; ≥19.15 mg/mL
A8895 p-Cresyl sulfate

2 Citation

Summary: Protein-bound uremic retention solute

insoluble in EtOH; ≥30.1 mg/mL
A8537 Thioridazine HCl

Target: Cytochrome P450 (CYP450)|D1 and D5 Receptors|D2 Receptors|D3 Receptors|D4 Receptors

Summary: Calcium channel protein inhibitor
B1274 AP20187

4 Citation

Target: FKBP

Summary: Dimerizer,synthetic and cell-permeable

≥74.14 mg/mL
A8380 Bexarotene

Target: Retinoid X receptors (RXR)

Summary: Retinoid Receptor agonist

insoluble in H2O; ≥10.35 mg/mL
A8534 Terfenadine

Target: Voltage-gated Potassium (KV) Channels|Histamine H1 Receptors|Inward Rectifier Potassium (Kir) Channels

Summary: Histamine H1-receptor antagonist

insoluble in H2O; ≥18 mg/mL
B1527 GW4064

Target: FXR

Summary: Non-steroidal FXR agonist,potent and selective

insoluble in H2O; insoluble in EtOH; ≥24.7 mg/mL
A8809 Vorapaxar

Target: Protease-Activated Receptors

Summary: PAR-1 antagonist,potent and orally active

≥24.65 mg/mL