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T17239VU0155069
VU0155069 strongly inhibits the invasive migration of several cancer cell lines in transwell assays. VU0155069 is a selective phospholipase D1 inhibitor (IC50: 46 nM in vitro).
价 格：￥电议型 号：T17239产 地：中国大陆
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T9428HM43239HM43239,HM-43239
HM43239 is an orally active and selective FLT3 inhibitor with IC 50 s of 1.1 nM, 1.8 nM and 1.0 nM for FLT3 WT, FLT3 internal tandem duplication (ITD) and FLT3 D835Y kinases, respectively. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1. HM43239 inhibits the proliferation and induces the apoptosis of leukemic cells [1] [2] [3].
价 格：￥电议型 号：T9428产 地：中国大陆
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T27462GSK-239512
GSK-239512 is an antagonist of H3 receptor and can be used in studies about the treatment of cognitive dysfunction in neurodegenerative disorders.
价 格：￥电议型 号：T27462产 地：中国大陆
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T8457NPS2390Inhibitor,NPS2390,Calcium-sensing receptor,NPS-2390,mGluR,inhibit,Metabotropic glutamate rece
NPS2390 is a first generation quinoxaline derivative that acts as a noncompetitive antagonist of mGluR1 and mGluR5 (IC50 of 5.2 and 82 nM, respectively)
价 格：￥电议型 号：T8457产 地：中国大陆
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T6976SB 239063inhibit,SB 239063,SB-239063,Inhibitor,Autophagy,p38 MAPK
SB239063 is a potent and selective p38 MAPKα/β inhibitor with IC50 of 44 nM, showing no activity against the γ- and δ-kinase isoforms.
价 格：￥电议型 号：T6976产 地：中国大陆
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T80272-Ethylbutyric Acid2-Ethylbutyric acid,inhibit,2Ethylbutyric Acid,2 Ethylbutyric Acid,Inhibitor,3239
2-Ethylbutyric Acid is a natural compound.
价 格：￥电议型 号：T8027产 地：中国大陆
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T60063WAY-323975
WAY-323975 is a nonfluorescent inhibitors of Fluorogen–Fluorogen Activating Protein Binding Pairn.
价 格：￥电议型 号：T60063产 地：中国大陆
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TN2239Strictosamidepain,antifungal,Anti-inflammatory,Parasite,inhibit,Inhibitor,antiplasmodial,Fungal,Stri
Strictosamide possesses antibacterial and antiviral activities, it also may have important effects on inflammation and inflammatory pain.
价 格：￥电议型 号：TN2239产 地：中国大陆
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TMA2394DL-alpha-TocopherolFerroptosis,Inhibitor,inhibit,DL alpha Tocopherol,DLalphaTocopherol
Antioxidant.
价 格：￥电议型 号：TMA2394产 地：中国大陆
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T14087ABT-239ABT239,ABT 239
ABT-239 is a novel, highly efficacious, non-imidazole?class of H3R antagonist. Its a transient receptor potential vanilloid type 1 (TRPV1) antagonist.
价 格：￥电议型 号：T14087产 地：中国大陆
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T10239Acolbifene
Acolbifene is a selective antagonist of estrogen receptors with IC50s of 2 nM and 0.4 nM for estradiol-induced transcriptional activity of ERα and ERβ. Acolbifene shows an anticarcinogenic property.
价 格：￥电议型 号：T10239产 地：中国大陆
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TQ0239PF-06291874inhibit,Inhibitor,glucagon,bioavailability,Glucagon Receptor,PF 06291874,Glucagon recepto
PF-06291874 (Glucagon receptor antagonists-4) is a highly effective and orally active antagonist of the glucagon receptor.
价 格：￥电议型 号：TQ0239产 地：中国大陆
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TJA2398Taurodeoxycholic acid sodium hydrateTaurodeoxycholic acid sodium,Inhibitor,Taurodeoxycholic acid sod
Taurohyodeoxycholic acid sodium salt, a hydrophilic bile salt, on bile salt and biliary lipid secretion in the rat.
价 格：￥电议型 号：TJA2398产 地：中国大陆
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TP1246LACTH (22-39) acetateACTH (2239) acetate,ACTH (22 39) acetate
ACTH (22-39) acetate is a fragment of adrenocorticotropic hormone (ACTH) containing two proline residues at positions 3 and 15 from the N-terminus.
价 格：￥电议型 号：TP1246L产 地：中国大陆
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T8239Cromoglicic acidallergic rhinitis,Cromolyn,bronchial asthma,Cromoglicic acid,cell stabilizer,inhibit
Cromoglicic acid prevents the release of inflammatory chemicals such as histamine from mast cells.
价 格：￥电议型 号：T8239产 地：中国大陆
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T9239RS-25344RS25344,RS 25344
RS-25344 is a potent and selective phosphodiesterase (PDE) 4 inhibitor. It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.
价 格：￥电议型 号：T9239产 地：中国大陆
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T6S2391L-Chicoric Acidreplication,Inhibitor,L-Chicoric Acid,HIV Integrase,L Chicoric Acid,dicaffeoyltartari
L-Chicoric acid has been shown to inhibit hyaluronidase and HIV-1 integrase, and to possess phagoeytosis stimulatory activity in vitro and in vivo and antiviral acitivy. L-Chicoric acid may reduce acute alcohol-induced steatosis in mice through interfering with the induction of iNOS and iNOS-dependent signaling cascades in the liver. 3. L-Chicoric acid inhibited cell viability and induced apoptosis in 3T3-L1 preadipocytes which was characterized by chromatin condensation and poly ADP-ribose-poly
价 格：￥电议型 号：T6S2391产 地：中国大陆
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T24239K201
K201 is a Ca2+-dependent blocker and prevents abnormal Ca(2+) leak from the sarcoplasmic reticulum in the ischemic heart and skeletal muscle (SkM) by stabilizing the ryanodine receptors.
价 格：￥电议型 号：T24239产 地：中国大陆
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T12395PDE9-IN-1PDE-9-IN-1,PDE9IN1,PDE9 IN 1
PDE9-IN-1 is a selective and orally bioavailable Inhibitor of PDE9A(IC50 of 8.7 nM).
价 格：￥电议型 号：T12395产 地：中国大陆
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T60002Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylateHistone Methyltransferase,
Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate is a selective inhibitor of histone methyltransferase SETD7 (IC50 = 4.59 μM) with anticancer activity.
价 格：￥电议型 号：T60002产 地：中国大陆
