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T15018CUDC-427
CUDC-427 is an orally bioactive and pan antagonist of inhibitor of apoptosis proteins(IAPs). CUDC-427 can be used in research on cancers.
价 格：￥电议型 号：T15018产 地：中国大陆
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TP1559LZiconotide Acetate (107452-89-1 free base)analgesic,non-opioid,Ziconotide Acetate (107452891 free
Ziconotide is an analgesic agent and has been used to treat neuropathic and non-neuropathic pain. Ziconotide acts by binding to N-type calcium channels situated on the terminal part of primary afferent neurons of the nociceptive pathway therefore reducing synaptic transmission with potent antinociceptive effects.
价 格：￥电议型 号：TP1559L产 地：中国大陆
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T15641K777
K777 is a potent, orally active and irreversible inhibitor of cysteine protease. K777 is a potent CYP3A4 inhibitor (IC50= 60 nM). K777 is also a selective CCR4 antagonist featuring the potent chemotaxis inhibition. K777 irreversibly inhibits Cruzain, which is the major cysteine protease of Trypansoma cruzi, and cathepsins B and L. K777 targets cathepsin-mediated cell entry and wxibits a broad-spectrum antiviral activity. K777 inhibits EBOV and SARS-CoV pseudovirus entry with IC50 values of 0.87
价 格：￥电议型 号：T15641产 地：中国大陆
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TP1881L1Pep 2-8 ammonium salt(1541011-97-5 free base)Pep 2 8 ammonium salt(1541011 97 5 free base),Pep 28 am
Pep 2-8 ammonium salt is Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor. Potent inhibitor of PCSK9 binding to LDL receptor (IC50 = 0.8 μM). Restores LDL uptake in HepG2 cells treated with PCSK9.
价 格：￥电议型 号：TP1881L1产 地：中国大陆
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TQ0150LevcromakalimPotassium Channel,KcsA,Inhibitor,inhibit,BRL38227,BRL-38227,Levcromakalim
Levcromakalim is an activator of the ATP-sensitive K+ channel.
价 格：￥电议型 号：TQ0150产 地：中国大陆
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T9645CU-115
CU-115 is a selective and potent TLR8 antagonist with IC50 of 1.04 ?M and =>50 ?M for TLR8 and TLR7, respectively. CU-115 decreases production of TNF-α and IL-1β activated by R-848 in THP-1 cells.
价 格：￥电议型 号：T9645产 地：中国大陆
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TQ0015PRN1371inhibit,CSF1R,PRN 1371,Inhibitor,colony stimulating factor 1 receptor,c-Fms,CSF-1R,FGFR,CSF-1
PRN1371 is a specific and potent FGFR1-4 and CSF1R inhibitor (IC50s: 0.6/1.3/4.1/19.3/8.1 nM for FGFR1/2/3/4 and CSF1R).
价 格：￥电议型 号：TQ0015产 地：中国大陆
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T61518TAK-653
TAK-653, an AMPA receptor potentiator with minimal agonistic activity, produces an antidepressant-like effect with a favorable safety profile in rats.
价 格：￥电议型 号：T61518产 地：中国大陆
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T6908NSC 228155Epidermal growth factor receptor,Histone Acetyltransferase,EGFR,HER1,HATs,inhibit,Inhibito
NSC228155 is an activator of EGFR, binding to the sEGFR dimerization domain II and modulate EGFR tyrosine phosphorylation.
价 格：￥电议型 号：T6908产 地：中国大陆
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T7815LAOD9604 acetate(221231-10-3 free base)AOD9604 acetate(221231103 free base),AOD-9604 acetate(221231-1
AOD9604 acetate is a potential anti-obesity peptide based on the human growth hormone.
价 格：￥电议型 号：T7815L产 地：中国大陆
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TP1545L1FFAGLDD amine saltFFAGLDD amine salt
FFAGLDD amine salt is MMP9 selective cleavage peptides, which used for cytosolic delivery of Doxorubi-cin (DOX) and achieve temporally and spatially controlled slow drug delivery and release.
价 格：￥电议型 号：TP1545L1产 地：中国大陆
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T38163ML-148ML-148,ML 148,selective,Inhibitor,prostaglandin-signaling,15-PGDH,15-Hydroxyprostaglandin dehy
ML-148 is a selective inhibitor of 15-hydroxy prostaglandin dehydrogenase (15-PGDH, IC50 = 56 nM). ML-148 can be used to profile across a panel of related dehydrogenase or reductase enzymes and in studies about prostaglandin-signaling pathways.
价 格：￥电议型 号：T38163产 地：中国大陆
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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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TN1519L(-)-Coclaurine hydrochloride
(-)-Coclaurine hydrochloride is an antagonist of nAChRs isolated from Sarcopetalum harveyanum.
价 格：￥电议型 号：TN1519L产 地：中国大陆
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T90597Compound 1549Compound 1549
SSR504734 is an orally active, selective and reversible inhibitor of human, rat, and mouse GlyT1 ( IC 50 =18, 15, and 38 nM, respectively). SSR504734 exhibits activity in schizophrenia, anxiety and depression models [1].
价 格：￥电议型 号：T90597产 地：中国大陆
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TN7215IsochiisanosideIsochiisanoside
Isochiisanoside is a natural product found in the leaves of Acanthopanax chiisanensis NAKAI.
价 格：￥电议型 号：TN7215产 地：中国大陆
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TN2315XanthopurpurinXanthopurpurin,Inhibitor,inhibit,Purpuroxanthin
Xanthopurpurin shows antiviral activity. Xanthopurpurin can effectively inhibit rotavirus multiplication by promoting virus-induced apoptosis in MA-104 cells. Xanthopurpurin shows mainly strong inhibition of collagen-induced platelet aggregation.
价 格：￥电议型 号：TN2315产 地：中国大陆
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T60152AZ5576AZ5576
AZ5576 is a potent and highly selective CDK9 inhibitor. AZ5576 can be used for the research of Hematological Malignancy [1].
价 格：￥电议型 号：T60152产 地：中国大陆
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TN1569DeoxylapacholDeoxylapachol,Fungal,inhibit,Inhibitor
Deoxylapachol has anti-wood rot activity, it can inhibit the brown rot fungi Gloeophyllum sepiarium CBS 353.74 and Gloeophyllum trabeum CBS 318.50 and the white rot fungi Merulius tremellosus CBS 280.73 and Phlebia brevispora CBS 509.92. It also can induce fungal cell wall stress.
价 格：￥电议型 号：TN1569产 地：中国大陆
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TN1527(-)-Corynoxidine
(-)-Corynoxidine is an AChE inhibitor derived from tubers of Stephania succifera. Corynoxidine exhibits antibacterial activities against Staphylococcus aureus and methicillin-resistant Staphylococcus aureus strains in different degrees.
价 格：￥电议型 号：TN1527产 地：中国大陆
