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产品数：86101
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T6826EmricasanInhibitor,Caspase,IDN6556,Emricasan,Influenza Virus,IDN 6556,PF-03491390,PF03491390,inhibit
Emricasan is an effective and irreversible pan-caspase inhibitor.
价 格：￥电议型 号：T6826产 地：中国大陆
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T12655(Rac)-AMG8379
(Rac)-AMG8379 is a racemate of AMG8379 which is an orally active and selective sulfonamide NaV1.7 antagonist.
价 格：￥电议型 号：T12655产 地：中国大陆
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TQ0055AMG-3969Hexokinase IV,AMG 3969,Hexokinase D,Glucokinase,Inhibitor,AMG3969,AMG-3969,inhibit
AMG-3969 is an effective glucokinase-glucokinase regulatory protein interaction (GK-GKRP) disruptor (IC50: 4 nM).
价 格：￥电议型 号：TQ0055产 地：中国大陆
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T9275ART558ART558
ART558 is a potent, selective, low molecular weight, allosteric DNA polymerase activity of Polθ inhibitor (IC50=7.9 nM). ART558 can be used for the research of cancer.
价 格：￥电议型 号：T9275产 地：中国大陆
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TN1557Decursinol angelateProtein kinase C,inhibit,Inhibitor,Decursinol angelate,PKC
Decursinol angelate has anti-tumor, anti-inflammatory, anti-oxidant, and hepatoprotective activities, it inhibits VEGF-induced angiogenesis via suppression of the VEGFR-2-signaling pathway; it also suppresses invasion and inflammatory activation of cancer cells through modulation of PI3K/AKT, ERK and NF-kappaB, its anti-inflammatory activity may contribute to its anti-cancer activity.
价 格：￥电议型 号：TN1557产 地：中国大陆
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T8850sbp-7455SBP-7455,ULK,TNBC,ULK2,ULK1,Unc-51 like kinase,sbp7455,Ser318,sbp 7455,Inhibitor,inhibit,Aut
SBP-7455 potently inhibited ULK1/2 enzymatic activity in vitro and in cells, reduced the viability of TNBC cells and had oral bioavailability in mice.
价 格：￥电议型 号：T8850产 地：中国大陆
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T23554(Z)-FeCP-oxindole(Z)FeCPoxindole,(Z) FeCP oxindole
(Z)-FeCP-oxindole is a selective inhibitor of VEGFR2 with an IC50 of 200 nM for human. (Z)-FeCP-oxindole shows anticancer activity.
价 格：￥电议型 号：T23554产 地：中国大陆
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TP1385Neurokinin A(4-10) TFA(97559-35-8 free base)Neurokinin A(410) TFA(97559358 free base),Neurokinin A(4
Neurokinin A (4-10) TFA is a tachykinin NK2 receptor agonist[1].
价 格：￥电议型 号：TP1385产 地：中国大陆
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TP2334PMX 53 acetate(219639-75-5 free base)PMX 53 acetate(219639755 free base),PMX 53 acetate(219639 75 5
PMX-53 is a potent and orally active CD88 (C5aR) antagonist (IC50: 20 nM) and inhibits C5a-induced neutrophil myeloperoxidase release and chemotaxis with IC50 values of 22 nM and 75 nM, respectively. PMX-53 is also an agonist of Mas-related gene 2 (MrgX2).
价 格：￥电议型 号：TP2334产 地：中国大陆
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T6S1559Aurantio-obtusinAurantio obtusin,inhibit,Aurantio-obtusin,Inhibitor,Aurantioobtusin
1. Biotransformation of glucoAurantio-obtusin towards Aurantio-obtusin increased the toxicity of irinotecan through increased inhibition of SN-38 glucuronidation. 2. Aurantio-obtusin, stimulated chemotactic migration of MC3T3-E1 osteoblast cells in a concentration-dependent manner. Besides migration, the compound stimulated osteoblast differentiation and mineralization. 3. Aurantio-obtusin is a promising osteoanabolic compound of natural origin with potential therapeutic applications in the prev
价 格：￥电议型 号：T6S1559产 地：中国大陆
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TP2165Urotensin II, mouse acetate (9047-55-6 free base)Urotensin II, mouse acetate (9047556 free base),Uro
Urotensin II, mouse acetate is an endogenous ligand for the orphan GPR14 or SENR. It is a potent vasoconstrictor.
价 格：￥电议型 号：TP2165产 地：中国大陆
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T6955Propafenone hydrochlorideSodium Channel,Na+ channels,Na channels,Propafenone hydrochloride,Inhibitor
Propafenone HCl is a classic anti-arrhythmic medication, which treats illnesses associated with rapid heartbeats such as atrial and ventricular arrhythmias.
价 格：￥电议型 号：T6955产 地：中国大陆
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TP1155LHuman growth hormone-releasing factor acetateHuman growth hormone releasing factor acetate,Human gro
Human growth hormone-releasing factor acetate is a hypothalamic polypeptide and stimulates GH production and release by binding to the GHRH Receptor (GHRHR) on cells in the anterior pituitary[1].
价 格：￥电议型 号：TP1155L产 地：中国大陆
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T7216MirogabalinDS 5565,DS-5565,Calcium Channel,Mirogabalin,inhibit,Inhibitor,Ca channels,Ca2+ channels
Mirogabalin is a calcium channel blocker with analgesic effects.
价 格：￥电议型 号：T7216产 地：中国大陆
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T3511PF-1355
PF-1355 is a selective 2-thiouracil mechanism-based MPO inhibitor. PF-1355 is used for treatment of vasculitic diseases.
价 格：￥电议型 号：T3511产 地：中国大陆
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T7551Belotecan hydrochlorideBelotecan,Topoisomerase,CKD 602,Inhibitor,Belotecan hydrochloride,CKD602,inhi
Belotecan hydrochloride is a synthetic water-soluble camptothecin derivative and topoisomerase I inhibitor with potential antitumor activity
价 格：￥电议型 号：T7551产 地：中国大陆
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T7554Substance P (7-11)Inhibitor,Substance P (7-11),inhibit,NK receptor,Neurokinin Receptor,Substance P (
Substance P 7-11(TFA) is a C-terminal fragment of Substance P .
价 格：￥电议型 号：T7554产 地：中国大陆
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T8262Fosfomycin sodiumXDR,multidrug-resistant,Bacterial,inhibit,Fosfomycin sodium,Antibiotic,MK-0955,drug
Fosfomycin is a bactericidal, low-molecular weight, broad-spectrum antibiotic, with putative activity against several bacteria, including multidrug-resistant Gram-negative bacteria, by irreversibly inhibiting an early stage in cell wall synthesis.
价 格：￥电议型 号：T8262产 地：中国大陆
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T9554SN-008STING,Stimulator of Interferon Genes,SN-011,TMEM173,MITA,inhibit,ERIS,SN008,Inhibitor,SN 008,M
SN-008 is a less active analog SN-011 which is a STING antagonist. SN-008 can be used as a negative control.
价 格：￥电议型 号：T9554产 地：中国大陆
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T14551BevenopranInhibitor,CB 5945,Bevenopran,CB5945,inhibit,Opioid Receptor,ADL 5945,ADL5945
Bevenopran is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.
价 格：￥电议型 号：T14551产 地：中国大陆
