| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V31999 | ZEN-3411 | 1952264-36-6 | ZEN-3411 is a BET inhibitor, inhibiting BRD4(BD1), BRD4(BD2) and BRD4(BD1BD2) with IC50 of 0.05, 0.05 and 0.06 μM respectively. |
|
V32001 | ZEN-3862 | 1952264-33-3 | ZEN-3862 is a BET inhibitor (antagonist) with IC50s of 0.16 and 0.13 μM for BRD4(BD1) and BRD4(BD2), respectively. |
|
V32029 | Zeylenone | 193410-84-3 | Zeylenone is a naturally occurring cyclohexene oxide that can inhibit cervical cancer/tumor cell growth/proliferation and causes apoptosis through the PI3K/AKT/mTOR and MAPK/ERK signaling pathways. |
|
V32336 | Zidebactam sodium salt | 1706777-46-9 | Zidebactam sodium (WCK5107 sodium; WCK-5107 Na) is a novel and potent dual β-lactamase and penicillin-binding protein2 (PBP2) inhibitor with an IC50 of 0.26 μg/mL. |
|
V33664 | Zileuton sodium | 118569-21-4 | Zileuton sodium(also known as A-64077 sodium;Abbott-64077; ZYFLO; ZYFLO CR)is a novel, potent and orally bioactive inhibitor of 5-lipoxygenase, and thus inhibits leukotrienes (LTB4, LTC4, LTD4, and LTE4) formation, it was introduced in 1996 to decrease the symptoms of asthma. |
|
V32872 | Zinc phthalocyanine | 14320-04-8 | Zinc phthalocyanine is extensively used in industry (catalysts, photoconductors) and biomedicine (photodynamic therapy, PDT). |
|
V32636 | Zinc Protoporphyrin | 15442-64-5 | Zinc Protoporphyrin is a novel and potent heme oxygenase-1 (HO-1) inhibitor. |
|
V32267 | ZINC03129319 | 1777807-64-3 | ZINC03129319 (ZINC-03129319) is a novel and potent dengue virus (DENV) NS2B-NS3 protease inhibitor(extracted from patent US20150141521A1) with inhibition constants (Ki1) of 92±15 μM and Ki3 of 20±4 μM. |
|
V33685 | ZINC13466751 | 117953-17-0 | ZINC13466751 is a potent inhibitor of HIF-1α/von Hippel-Lindau interaction with IC50 of 2.0 µM. |
|
V32673 | Zinquin | 151606-29-0 | Zinquin is a fluorescent sensor that may be utilized to observe active zinc ions. |
|
V40582 | Zinterol | 37000-20-7 | Zinterol (MJ 9184) is a potent and specific β2-adrenoceptor (β2-adrenoceptor) agonist. |
|
V33817 | Ziprasidone D8 | 1126745-58-1 | Ziprasidone D8 is the deuterium labeled form of Ziprasidone, which is a dual 5-HT (serotonin) and dopamine receptor antagonist with antipsychotic activity. |
|
V30785 | Ziyuglycoside I | 35286-58-9 | Ziyuglycoside I, extracted from S. officinalis roots, has anti-wrinkle activity and increases the expression of type I collagen. |
|
V30784 | Ziyuglycoside II | 35286-59-0 | Ziyuglycoside II is a triterpene saponin compound found in Sanguisorba officinalis L. |
|
V41940 | ZK-994 | 686773-12-6 | ZK-994, β-oxidation-resistant lipoxin A4 receptor agonist |
|
V40003 | ZK168281 | 186371-96-0 | ZK168281, a 25-carboxylic ester derivative of 1α,25(OH)2D3, is a novel, potent and pure VDR antagonist with a Kd value of 0.1 nM. |
|
V39637 | ZK824190 | 2254001-81-3 | ZK824190 is an orally bioavailable, selective urokinase plasminogen activator (uPA) inhibitor for use in multiple sclerosis research. |
|
V37769 | ZL0580 | 2377151-10-3 | ZL0580 is a structural analog of ZL0590 that induces apparent suppression of HIV by selectively binding to the BRD4 domain of BD1. |
|
V39935 | ZLDI-8 | 667880-38-8 | ZLDI-8 is an inhibitor (blocker/antagonist) of Notch activating/cleaving enzyme ADAM-17, which inhibits the cleavage of Notch protein and reduces the expression of pro-survival/anti-apoptotic and epithelial-to-mesenchymal transition-related proteins. |
|
V32030 | ZM323881 | 193001-14-8 | ZM323881 is a potent and specific inhibitor of VEGFR2 with IC50 of less than 2 nM. |
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