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T4354KPT9274KPT 9274；PAK4-IN-1；KPT-9274
KPT-9274 is a non-competitive dual inhibitor of PAK4 and NAMPT(IC50= ~120 nM). It is an orally bioavailable small molecule.
价 格：￥电议型 号：T4354产 地：中国大陆
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T4353SR-18292SR 18292；SR18292
SR-18292 is a PPAR gamma coactivator-1α (PGC-1α) inhibitor, which increases PGC-1α acetylation, suppresses gluconeogenic gene expression and reduces glucose production in hepatocytes.
价 格：￥电议型 号：T4353产 地：中国大陆
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T4342PF-04929113 MesylatePF-04929113 (Mesylate)；SNX-5422 Mesylate
PF-04929113 Mesylate, a prodrug of SNX-2112, is an orally available Hsp90 inhibitor (Kd: 41 nM) and also induces Her-2 degradation (IC50: 37 nM).
价 格：￥电议型 号：T4342产 地：中国大陆
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T4317PF 429242
PF-429242 is a competitive inhibitor of sterol regulatory element-binding protein (SREBP) site 1 protease (IC50 = 0.175 μM). It is selective for site 1 protease against a panel of serine proteases. PF-429242 inhibits rate of cholesterol synthesis in CHO c
价 格：￥电议型 号：T4317产 地：中国大陆
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T4292ThiaprolineL-硫代脯氨酸；L-Thioproline；L-Thiaproline
Thiaproline has been used in peptide coupling reactions.
价 格：￥电议型 号：T4292产 地：中国大陆
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T4248T.cruzi Inhibitor (1350920-22-7(free base))
T.cruzi Inhibitor is a Trypanosoma cruzi inhibitor.
价 格：￥电议型 号：T4248产 地：中国大陆
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T4192hnps-PLA Inhibitor
Hnps-PLA Inhibitor is an inhibitor of human nonpancreatic secretory Phospholipase A (hnps-PLA).
价 格：￥电议型 号：T4192产 地：中国大陆
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T4113NBQX二羟基喹酮；FG9202
Potent, selective and competitive AMPA receptor antagonist. Neuroprotective and anticonvulsant; active in vivo.
价 格：￥电议型 号：T4113产 地：中国大陆
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T4092AG126AG 126；Tyrphostin AG126
The tyrphostin AG-126 selectively inhibits the phosphorylation of ERK1 (p44) and ERK2 (p42) at 25-50 μM. It blocks the production of TNF-α in vitro2 and in vivo, attenuating signaling through NF-κB, the induced expression of COX-2 and iNOS, and the inflam
价 格：￥电议型 号：T4092产 地：中国大陆
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T4063Delafloxacin德拉沙星；RX-3341；WQ-3034；ABT492
Delafloxacin (RX-3341, ABT-492) is a fluoroquinolone antibiotic agent. It has potent inhibitory against levofloxacin-resistant Streptococcus pneumoniae strains (MIC: 0.0078-0.125 μg/ml).
价 格：￥电议型 号：T4063产 地：中国大陆
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T4043ETC-159ETC159；ETC-1922159；ETC 159
ETC-159 is a potent, orally available PORCN inhibitor. It inhibits β-catenin reporter activity with an IC50 of 2.9 nM.
价 格：￥电议型 号：T4043产 地：中国大陆
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T4012UNC926UNC-926；UNC 926 hydrochloride
UNC-926 inhibits L3MBTL1 (IC50: 3.9 μM). UNC-926 also exhibits a low micromolar affinity for L3MBTL3. UNC-926 inhibits binding of the 3xMBT domain to H4K20me1. It selectively and dose-dependently inhibits the L3MBTL13xMBT-H4K20me1 interaction. UNC-926 has
价 格：￥电议型 号：T4012产 地：中国大陆
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T3S1892Crassicauline A粗茎乌头碱甲；Crassicauline I
1. Crassicauline A and Yunaconitine possesses feeding deterrent activity against T. castaneum adults, with EC(5) values of 1134.5 and 653.4 ppm, respectively.
价 格：￥电议型 号：T3S1892产 地：中国大陆
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T3S1692Octahydrocurcumin
Octahydrocurcumin has antioxidant and and anti-inflammatory activities, it can inhibit the lipopolysaccharide (LPS)-induced inflammatory response via the mechanism of inhibiting NF-kB translocation to the nucleus. Octahydrocurcumin exhibits potent cytotox
价 格：￥电议型 号：T3S1692产 地：中国大陆
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T39924NF-κΒ activator 2
NF-κΒ activator 2 is a potent and orally active NF-κB activator, with an EC 50 of 1.58 μM. NF-κΒ activator 2 induces SOD 2 through increasing NF-κB expression and activation. NF-κΒ activator 2 can be used for the research of amyotrophic lateral sclerosis
价 格：￥电议型 号：T39924产 地：中国大陆
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T3992MSX-122MSX 122；MSX122
MSX-122 is a novel small molecule and partial CXCR4 antagonist, with potent inhibition of CXCR4/CXCL12 actions(IC50 = 10 nM).
价 格：￥电议型 号：T3992产 地：中国大陆
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T39392LC-Type Natriuretic Peptide (CNP) (1-22), human acetateC-Type Natriuretic Peptide (CNP) (1-22), human
C-Type Natriuretic Peptide (CNP) (1-22), human acetate is an agonist of natriuretic peptide receptor B (NPR-B), an endothelial-derived relaxant and growth inhibitory factor. C-Type Natriuretic Peptide (CNP) (1-22), human acetate inhibits cAMP synthesis s
价 格：￥电议型 号：T39392L产 地：中国大陆
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T3929Kaurenoic acid异贝壳杉烯酸；kaur-16-en-18-oic acid；Kauren-19-Oic Acid；kaurenoate
Kaurenoic acid has anti-inflammatory potential in acetic acid-induced colitis, decreases in MDA level. Kaurenoic acid exerts a uterine relaxant effect acting principally through calcium blockade and in part, by the opening of ATP-sensitive potassium chann
价 格：￥电议型 号：T3929产 地：中国大陆
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T39284EST73502
EST73502 is an agonist of μ-opioid receptor(Ki = 64 nM) agonist and an antagonist of σ1 receptor (Ki = 118 nM). EST73502 displays antinociceptive activity.
价 格：￥电议型 号：T39284产 地：中国大陆
