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T11665Ionomycin calciumCa2+ channels,PKC,ionophore,Calcium Channel,Ionomycin,SQ 23377,Ionomycin calcium,An
lonomycin calcium is a potent, selective calcium ionophore and an antibiotic produced by Streptomyces conglobatus. also induces the activation of protein kinase C (PKC). Ionomycin calcium is highly specific for divalent cations (Ca>Mg>Sr=Ba). Ionomycin promotes apoptosis.
价 格：￥电议型 号：T11665产 地：中国大陆
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T7811Pilsicainide HClatrial tachyarrhythmias,SUN-1165,Pilsicainide HCl,antiarrhythmic,inhibit,orally acti
Pilsicainide HCl is a pure sodium channel blocker
价 格：￥电议型 号：T7811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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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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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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T9116SMCCSMCC,ADC Linkers,inhibit,Antibody-drug conjugates linkers,Inhibitor
N-Succinimidyl 4-(N-maleimidomethyl)cycl(SMCC), also known as succinimidyl-4-[N-maleimidomethyl]cyclohexane-1-carboxylate, is a heterobifunctional protein crosslinker.
价 格：￥电议型 号：T9116产 地：中国大陆
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TP1167Fmoc-Arg-OHFmoc Arg OH,FmocArgOH,inhibit,Inhibitor
Fmoc-Arg-OH (Fmoc-L-Arginine) is a used in peptide synthesis.
价 格：￥电议型 号：TP1167产 地：中国大陆
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T10343AOH1160
AOH1160 is an inhibitor of proliferating cell nuclear antigen (PCNA). AOH1160 induces apoptosis and causes cell-cycle arrest by interfering with DNA replication.
价 格：￥电议型 号：T10343产 地：中国大陆
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T6S2116Ginkgolic acid C17:1Phosphatase and tensin homolog,PTEN,Phosphatase,Inhibitor,MMAC1,inhibit,Ginkgoli
1. Ginkgolic acid C17:1 can significantly inhibit enterohemorrhagic Escherichia coli O157:H7(EHEC) biofilm formation on the surfaces of polystyrene and glass, and on nylon membranes.
价 格：￥电议型 号：T6S2116产 地：中国大陆
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T9696β-catenin-IN-2HCT116,inhibit,cancer,β-catenin,cell,Beta catenin,HT-29,Tcf/4,Colorectal,Inhibitor,β c
β-catenin-IN-2 is a potent inhibitor of β-catenin that can be used in colorectal cancer research.
价 格：￥电议型 号：T9696产 地：中国大陆
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T11693LIT1t dihydrochlorideIT1t dihydrochloride,IT-1t dihydrochloride
IT1t dihydrochloride inhibits CXCL12/CXCR4 interaction with IC50 of 2.1 nM. IT1t dihydrochloride is an antagonist of CXCR4.
价 格：￥电议型 号：T11693L产 地：中国大陆
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T6458CYC-116CYC116,inhibit,Inhibitor,CYC-116,CYC 116,Aurora Kinase
CYC116 is a potent inhibitor of Aurora A/B with Ki of 8.0 nM/9.2 nM, is less potent to VEGFR2 (Ki of 44 nM), with 50-fold greater potency than CDKs, not active against PKA, Akt/PKB, PKC, no effect on GSK-3α/β, CK2, Plk1 and SAPK2A. Phase 1.
价 格：￥电议型 号：T6458产 地：中国大陆
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T8116Azulenenaphthalene,chamomile,scaffold,Azulene,oil,Cyclopentacycloheptene,distillation,inhibit,Human
Bicyclo[5.3.0]Decapentaene is a natural product.
价 格：￥电议型 号：T8116产 地：中国大陆
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T7369LGemigliptin Tartrate(911637-19-9 free base)type,Gemigliptin,products,mellitus,peptidase-4,Gemiglipti
Gemigliptin tartrate is a highly selective, reversible and competitive inhibitor of dipeptidyl peptidase-4 (DPP-4). It has an IC50 of 10.3 nM for human recombinant DPP-4. Gemigliptin tartrate exhibits potent anti-glycation properties.
价 格：￥电议型 号：T7369L产 地：中国大陆
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T8668HM03shock,HM 03,inhibit,heat,tumor,cancer,cell,HM03,protein,Heat shock proteins,HSP,Inhibitor,HCT116
HM03 is a potent and selective inhibitor of HSPA5, and has anticancer activity.
价 格：￥电议型 号：T8668产 地：中国大陆
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TP1305LEP(116-130)(mouse)LEP(116-130)(mouse),Inhibitor,LEP(116130)(mouse),inhibit,LEP(116 130)(mouse)
Leptin (116-130),mouse(C64H109N19O24S),a peptide with the sequence Ser-Cys-Ser-Leu-Pro-Gln-Thr-Ser-Gly-Leu-Gln-Lys-Pro-Glu-Ser-NH2. Leptin is an adipocyte-derived hormone that acts as a major regulator for food intake and energy homeostasis.
价 格：￥电议型 号：TP1305产 地：中国大陆
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T9638CCT241161CCT241161
CCT241161 is an orally active pan- RAF inhibitor with IC 50 s of 3, 6, 10, 15 and 30 nM for LCK, CRAF, SRC, V600E-BRAF and BRAF, respectively. CCT241161 shows good activity to in BRAF and NRAS mutant melanomas. CCT241161 also shows anticancer cell proliferative activity [1].
价 格：￥电议型 号：T9638产 地：中国大陆
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T6116Bleomycin Sulfate硫酸博来霉素；硫酸博莱霉素；Blenoxane；NSC125066
Bleomycin Sulfate, a glycopeptide antibiotic, is an anticancer agent for squamous cell carcinomas (SCC). In UT-SCC-19A cells, the IC50 of Bleomycin Sulfate is 4 nM.
价 格：￥电议型 号：T6116产 地：中国大陆
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T5697BMS-1166BMS1166
BMS-1166 is a potent PD-1/PD-L1 interaction inhibitor.
价 格：￥电议型 号：T5697产 地：中国大陆
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T5677SAR125884 hydrochlorid (1116743-46-4(free base))
SAR125844 is a potent and selective MET kinase inhibitor with a favorable preclinical toxicity profile,(IC50=4.2 nM).
价 格：￥电议型 号：T5677产 地：中国大陆
