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TN119216-Epivoacarpine16-Epivoacarpine,Inhibitor,16 Epivoacarpine,16Epivoacarpine,inhibit
16-Epivoacarpine is a natural product from Gelsemium elegans.
价 格：￥电议型 号：TN1192产 地：中国大陆
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TP1888L1[Ala113]-MBP (104-118) acetate[Ala113] MBP (104 118) acetate,[Ala113]MBP (104118) acetate
[Ala113]MBP(104-118) acetate is an noncompetitive peptide inhibitors of protein kinase C (PKC), with IC50s ranging from 28-62 μM.
价 格：￥电议型 号：TP1888L1产 地：中国大陆
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T7828[Sar9,Met(O2)11]-Substance PInhibitor,Tachykinin receptor,[Sar9,Met(O2)11]-Substance P,NK receptor,N
Bhsar-sp is an agonist of NK1 receptor.
价 格：￥电议型 号：T7828产 地：中国大陆
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T17115TolycaineTolycaine,anesthetic,inhibit,analog,convulsion,Inhibitor
Tolycaine is a compound of local anesthetic.
价 格：￥电议型 号：T17115产 地：中国大陆
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T23349SF 11SF 11
SF 11 is a potent and brain penetrant neuropeptide Y Y2 receptor antagonist with IC50 of 199 nM. Antidepressant-like activity
价 格：￥电议型 号：T23349产 地：中国大陆
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TP1174Endothelin-2 (49-69), humanpeptide,21-amino,inhibit,Human endothelin 2,vasoactive,acid,ET-RB,Endothe
Endothelin-2, human is a 21-amino acid vasoactive peptide that binds to G-protein-linked transmembrane receptors, ET-RA and ET-RB.
价 格：￥电议型 号：TP1174产 地：中国大陆
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T24437MCP110astrocytomas,Inhibitor,Raf kinases,colorectal,cancer,MCP110,inhibit,Raf-1,Raf,Ras
MCP110 is an inhibitor of the interaction of Ras with Raf-1 and can be used in studies about the treatment of human tumors.
价 格：￥电议型 号：T24437产 地：中国大陆
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T7018WZB117GLUT,Inhibitor,WZB-117,WZB 117,WZB117,inhibit,Glucose transporter
WZB117 is a Glucose Transporter 1 (GLUT1) inhibitor. when IC50 of WZB117 approximate 10 μM, it inhibits lung cancer A549 cells and breast cancer MCF7 cells proliferation.
价 格：￥电议型 号：T7018产 地：中国大陆
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T60016VV116VV116
VV116 is a selective and orally active nucleoside antiviral agent against respiratory syncytial virus (RSV) and SARS-CoV-2 infection.
价 格：￥电议型 号：T60016产 地：中国大陆
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T9711OGT-IN-2OGT,mono- acylglycerol acyltransferase,articular diseases,Inhibitor,articular cartilage,Acyl
OGT-IN-2 is a potent O-GlcNAc transferase (OGT) inhibitor. OGT-IN-2 inhibits sOGT and ncOGT with IC50 values of 30 μM and 53 μM, respectively[1]. OGT-IN-2 can be used for the research of articular diseases[1].
价 格：￥电议型 号：T9711产 地：中国大陆
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T7373CDN1163Inhibitor,CDN 1163,Calcium Channel,Ca channels,Ca2+ channels,CDN-1163,CDN1163,inhibit
CDN1163 is a small molecule activator of sarco/endoplasmic reticulum Ca2+-ATPase (SERCA).
价 格：￥电议型 号：T7373产 地：中国大陆
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TN1150Procyanidin B3Histone Acetyltransferase,Procyanidin B-3,Procyanidin B 3,HAT,HATs,inhibit,Inhibitor,P
Procyanidin B3(B3) is a procyanidin dimer that is widely studied due to its high abundance in the human diet and antioxidant activity.
价 格：￥电议型 号：TN1150产 地：中国大陆
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T7112Ibutamoren MesylateMK 0677,MK 677,Inhibitor,Ibutamoren,MK677,inhibit,Ibutamoren Mesylate,Growth horm
Ibutamoren Mesylate is a potent, non-peptide Growth hormone secretagogue receptor (GHSR) agonist.
价 格：￥电议型 号：T7112产 地：中国大陆
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T8474Dabrafenib MesylateDabrafenib Mesylate,Dabrafenib,Raf kinases,Inhibitor,GSK2118436,Raf,inhibit,GSK 2
Dabrafenib Mesylate is a B-Raf inhibitor(IC50s of 0.6 and 5.0 nM for RafV600E and c-Raf, respectively).
价 格：￥电议型 号：T8474产 地：中国大陆
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T7143Alagebrium chlorideAlagebrium chloride,Endogenous Metabolite,ALT-711,Inhibitor,inhibit,Alagebrium,AL
Alagebrium Chloride is an advanced glycation end product (AGE) inhibitor, and has proven effective in reducing systolic blood pressure and providing therapeutic benefit for patients with diastolic
价 格：￥电议型 号：T7143产 地：中国大陆
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T11019DHODH-IN-1DHODHIN1,DHODH IN 1
DHODH-IN-1 is a potent dihydroorotate dehydrogenase (DHODH) inhibitor with IC50 of 25 nM. DHODH-IN-1 is an inhibitor of the pyrimidine biosynthetic pathway.
价 格：￥电议型 号：T11019产 地：中国大陆
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TP1164N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFANFormylNleLeuPheNleTyrLys TFA,N Formyl Nle Leu Phe Nle Tyr Lys T
N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFA (For-Nle-Leu-Phe-Nle-Tyr-Lys-OH TFA) is a formyl peptide receptor (FPR) agonist[1].Potent chemoattractant for human neutrophils.Radioiodinated molecule has full biological activity.
价 格：￥电议型 号：TP1164产 地：中国大陆
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T11079NMI 8739
NMI 8739 is an agonist of D2 autoreceptor. NMI 8739 reduces NO production and elicits concentration-dependent suppression of CCL-20, MCP-1 and IL-6 release.
价 格：￥电议型 号：T11079产 地：中国大陆
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T11319FR183998 free baseFR-183998 free base,FR183998 free base
FR183998 free base is an inhibitor of Na+/Ca2+ Exchanger.
价 格：￥电议型 号：T11319产 地：中国大陆
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T8825Capmatinib 2HCl.H2OS114,SNU-5,ATP competitive,Balb/c nu/nu mice,U-87MG,INCB-28060 dihydrochloride,or
Capmatinib 2HCl.H2O is an orally bioavailable inhibitor of the proto-oncogene c-Met (HGFR)with potential antineoplastic activity.
价 格：￥电议型 号：T8825产 地：中国大陆
