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Fr12799Compound Fr12799Compound Fr12799
AChE-IN-23 (compound 3h) is an inhibitor of acetylcholinesterase (AChE) with an IC 50 value of 48.3 μM [1].
价 格：￥电议型 号：Fr12799产 地：中国大陆
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T86274-Acetamidobenzenesulfonamide4 Acetamidobenzenesulfonamide,4Acetamidobenzenesulfonamide
4-Acetamidobenzenesulfonamide used in proteomics research and is an anti-infective agent
价 格：￥电议型 号：T8627产 地：中国大陆
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T12733Rislenemdaz
Rislenemdaz (CERC-301) is an antagonist of the N-methyl-D-aspartate (NMDA) receptor subunit 2B (GluN2B).
价 格：￥电议型 号：T12733产 地：中国大陆
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T82743-Methyl-L-histidineInhibitor,3 Methyl L histidine,Endogenous Metabolite,3MethylLhistidine,inhibit
3-Methylhistidine belongs to the class of organic compounds known as histidine and derivatives. Histidine and derivatives are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. It is also a biomarker for the consumption of soy products. 3-Methylhistidine is a very strong basic compound (based on its pKa). 3-Methylhistidine exists in all eukaryotes, r
价 格：￥电议型 号：T8274产 地：中国大陆
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T27554HS38HS38
HS38 is a specific and ATP-competitive DAPK inhibitor with Kds of 300 nM, 200 nM, and 280 nM for DAPK1, PIM3, and ZIPK. HS38 can be used in studies about smooth muscle-related disorders.
价 格：￥电议型 号：T27554产 地：中国大陆
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T9220Naftopidil hydrochlorideBM-15275,BM15275,canine,prostatic,Naftopidil,prostate,hyperplasia,inhibit,In
Naftopidil hydrochloride is a selective alpha1-adrenoceptor antagonist with Ki of 3.7 nM, 20 nM and 1.2 nM for the cloned human α1a-adrenoceptor, α1b-adrenoceptor and α1d-adrenoceptor, respectively. Naftopidil hydrochloride has antiproliferative effects.
价 格：￥电议型 号：T9220产 地：中国大陆
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T7668VTP-27999 TFAinhibit,VTP27999 TFA,Renin,VTP-27999,VTP 27999 TFA,VTP 27999,Inhibitor,VTP27999
VTP-27999 TFA is an inhibitor of Renin (IC50 : 0.47 nM).
价 格：￥电议型 号：T7668产 地：中国大陆
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T7005UlixertinibERK,VRT 752271,Ulixertinib,inhibit,VRT-752271,BVD 523,BVD523,Inhibitor,Extracellular sign
Ulixertinib (BVD-523, VRT752271) is an effective and reversible ERK1/ERK2 inhibitor. The IC50 of Ulixertinib is less than 0.3 nM for ERK2.
价 格：￥电议型 号：T7005产 地：中国大陆
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T9497Niraparib tosylate monohyrateNiraparib tosylate,Apoptosis,cancer,MK-4827 tosylate,inhibit,breast,PAR
Niraparib, also know as MK-4827, is an inhibitor of poly (ADP-ribose) polymerase (PARP) with potential antineoplastic activity. MK4827 inhibits PARP activity, enhancing the accumulation of DNA strand breaks and promoting genomic instability and apoptosis. The PARP family of proteins detect and repair single strand DNA breaks by the base-excision repair (BER) pathway.
价 格：￥电议型 号：T9497产 地：中国大陆
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T14271Aminooxy-PEG4-alcoholAminooxy PEG4 alcohol,AminooxyPEG4alcohol,Aminooxy-PEG-4-alcohol
Aminooxy-PEG4-alcohol is both a non-cleavable 4-unit PEG ADC linker and a PEG-based PROTAC linker.
价 格：￥电议型 号：T14271产 地：中国大陆
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T12527LMavodelpar free acid hydrochloride
Mavodelpar free acid hydrochloride is a potent PPARδ agonist (patent US20180071304, compound example 10).
价 格：￥电议型 号：T12527L产 地：中国大陆
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T27467GSK270822AGSK270822A
GSK270822A is a selective ROCK1 inhibitor. GSK270822A exhibits IC50 of 9nM, 1100nM, 1550nM for ROCK1, RSK1, p70S6K, respectively.
价 格：￥电议型 号：T27467产 地：中国大陆
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T22789FPR A14FPR A-14,FPR A14
FPR A14 is an agonist of formyl peptide receptor (FPR) and induces cell differentiation.
价 格：￥电议型 号：T22789产 地：中国大陆
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T10727Cdc7-IN-5Cdc7IN5,Cdc7 IN 5,Cdc-7-IN-5
Cdc7-IN-5 is a potent inhibitor of Cdc7 kinase. Cdc7, a serine-threonine protein kinase enzyme, is essential for the initiation of DNA replication in the cell cycle.
价 格：￥电议型 号：T10727产 地：中国大陆
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T12777RTC-5
RTC-5 (TRC-382) is an optimized phenothiazine with anti-cancer potency. RTC-5 demonstrates efficacy against a xenograft model of an EGFR driven cancer, its effects is attributed to concomitant negative regulation of PI3K-AKT and RAS-ERK signaling.
价 格：￥电议型 号：T12777产 地：中国大陆
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TMA2270Alisol F 24-acetateAlisol F 24 acetate,Alisol F 24acetate
Alisol F 24-acetate is a natural product isolated from Alisma plantago-aquatica Linn[1]. Alisol F 24 Acetate enhances chemosensitivity and apoptosis of MCF-7/DOX Cells by inhibiting P-Glycoprotein-Mediated drug efflux[2].
价 格：￥电议型 号：TMA2270产 地：中国大陆
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T8270DeserpidineDeserpidine,Reserpine,Angiotensin-converting Enzyme (ACE),cortex,antihypertensive,Alkaloi
Deserpidine is only found in individuals that have used or taken this drug. It is an ester alkaloid drug isolated from Rauwolfia canescens (family Apocynaceae) with antipsychotic and antihypertensive properties that has been used for the control of high blood pressure and for the relief of psychotic behavior.Deserpidine´s mechanism of action is through inhibition of the ATP/Mg2+ pump responsible for the sequestering of neurotransmitters into storage vesicles located in the presynaptic neur
价 格：￥电议型 号：T8270产 地：中国大陆
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T10381AS2717638AS2717638,AS-2717638
AS2717638 is an orally active and selective lysophosphatidic acid receptor 5 (LPA5) antagonist (IC50: 38 nM for hLPA5). It also significantly improves PGF2α-, PGE2-, and AMPA-induced allodynia.
价 格：￥电议型 号：T10381产 地：中国大陆
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T27319FIIN-4FIIN 4
FIIN-4 is a covalent inhibitor of FGFR and can be used in studies about metastatic breast cancer.
价 格：￥电议型 号：T27319产 地：中国大陆
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TQ0273Neopterininhibit,Endogenous Metabolite,Inhibitor,Neopterin
D-(+)-Neopterin is produced by human monocytes/macrophages upon stimulation with the cytokine interferon-γ. In humans, neopterin is involved in purine biosynthesis.
价 格：￥电议型 号：TQ0273产 地：中国大陆
