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T16401Org-12962Org 12962,Org12962
Org-12962 is an effective and selective 5-HT2C?receptor agonist pEC50: 7.01). Org-12962 shows antiaversive effects in a rat model of panic-like anxiety. Org-12962 also shows high effacy for the 5-HT2A?and 5-HT2B receptors (pEC50s: 6.38 and 6.28, respectively).
价 格：￥电议型 号：T16401产 地：中国大陆
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T34374RO5203648 HClRO5203648 HCl,RO-5203648 HCl
RO5203648 HCl is a partial agonist of trace amine-related receptor 1 (TAAR1) with antipsychotic and antidepressant-like activities. RO5203648 HCl can be used in studies about neuropsychiatric therapeutics.
价 格：￥电议型 号：T34374产 地：中国大陆
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T6407β-LapachoneARQ 501,ARQ501,Topoisomerase,Inhibitor,NSC26326,β-Lapachone,Apoptosis,NSC 26326,Autophagy
Beta-Lapachone is a specific DNA topoisomerase I inhibitor, and no inhibitory activities against DNA topoisomerase II or ligase.
价 格：￥电议型 号：T6407产 地：中国大陆
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T7064Valproic AcidHistone deacetylases,Mitochondrial Autophagy,bipolar disorder,epilepsy,Autophagy,Apopto
Valproic Acid is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid have not been completely elucidated. Valproic Acid has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally,
价 格：￥电议型 号：T7064产 地：中国大陆
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T9991WAY-620645WAY 620645,WAY620645
WAY-620645 is a CCK antagonist with antitumor and analgesic activities.
价 格：￥电议型 号：T9991产 地：中国大陆
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T64328Fmoc-L-aspartic acid
Fmoc-L-aspartic acid is an aspartic acid derivative.
价 格：￥电议型 号：T64328产 地：中国大陆
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T7648HA-100protein,PKC,Rho-associated kinase,ROCK,kinase,PKG,HA100,inhibit,Inhibitor,Myosin,HA 100,MLCK,H
HA-100 is an inhibitor of protein kinase
价 格：￥电议型 号：T7648产 地：中国大陆
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T6426Buclizine dihydrochlorideteratogen,Inhibitor,MCF-7,anti-tumor activity,antiallergic,antihistamine,in
Buclizine HCl is the hydrochloride salt form of buclizine, a piperazine histamine H1 receptor antagonist with primarily antiemetic and antivertigo activities. Buclizine binds to and blocks the histamine H1 receptor, thereby preventing the symptoms that are caused by histamine activity. Buclizine exerts its anti-emetic effect by binding to and blocking the muscarinic and histamine receptors in the vomiting center of the central nervous system (CNS). This may prevent activation of the chemorecepto
价 格：￥电议型 号：T6426产 地：中国大陆
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T6441CGS 21680 HydrochlorideCGS-21680,Inhibitor,CGS 21680,inhibit,CGS21680,CGS 21680 Hydrochloride,Adenos
CGS 21680 HCl（ IC50=22 nM）, an adenosine receptor agonist, exhibits 140-fold potency in A2 receptor over A1 receptor.
价 格：￥电议型 号：T6441产 地：中国大陆
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T101645,6-Dihydroxyindole
5,6-Dihydroxyindole is a melanin precursor and has a broad-spectrum antibacterial, antiviral, antifungal, antiparasitic activity. It has cytotoxic effects and is strongly toxic against various pathogens.
价 格：￥电议型 号：T10164产 地：中国大陆
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T7505Azimilide DihydrochlorideInhibitor,Azimilide,Azimilide Dihydrochloride,Potassium Channel,NE 10064,NE
Azimilide Dihydrochloride, a novel class III antiarrhythmic agent, blocks both the slowly activating (IKs) and rapidly activating (IKr) components of the delayed rectifier potassium current
价 格：￥电议型 号：T7505产 地：中国大陆
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T9640Diethylnorspermine HCl
Diethylnorspermine HCl potently induces SSAT (spermidine/spermine N1-acetyltransferase) mRNA and effectively stabilizes SSAT enzyme activity.
价 格：￥电议型 号：T9640产 地：中国大陆
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T6447Clindamycinbroad-spectrum,Antibiotic,Parasite,Inhibitor,Clindamycin,inhibit,bacteriostatic,Bacterial
Clindamycin dissociates peptidyl-tRNA from the bacterial ribosome, thereby disrupting bacterial protein synthesis. Clindamycin is a semisynthetic broad-spectrum antibiotic produced by chemical modification of the parent compound lincomycin.
价 格：￥电议型 号：T6447产 地：中国大陆
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T8646URB937FAAH,URB 937,Inhibitor,URB937,low,toxicity,inhibit,Fatty acid amide hydrolase,OEA,URB-937
URB937 is an inhibitor of FAAH and increases anandamide levels(IC50 : 26.8 nM).
价 格：￥电议型 号：T8646产 地：中国大陆
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T9641Aβ42-IN-2Aβ42 IN 2,Aβ42IN2
Aβ42-IN-2 is a γ-secretase modulator (patent WO2016070107, compound example 36). Aβ42-IN-2 exhibits an IC50 of 6.5 nM for Αβ42. Aβ42-IN-2 has research value in Alzheimer´s disease.
价 格：￥电议型 号：T9641产 地：中国大陆
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T8864Thymidylate Kinase Inhibitor, YMU1YMU 1,inhibit,YMU-1,YMU1,Thymidylate Kinase Inhibitor, YMU1,Inhibi
YMU1 is a human thymidylate kinase (hTMPK) inhibitor. YMU1 stabilizes the conformation of ligand-induced degradation (LID) region of hTMPK and blocks the catalytic site or ATP-binding site.
价 格：￥电议型 号：T8864产 地：中国大陆
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T6440CGP 57380CGP-57380,CGP 57380,Mitogen activated protein kinase interacting kinase,Inhibitor,MAPK inte
CGP 57380 is a potent MNK1 inhibitor with IC50 of 2.2 μM, exhibiting no inhibitory activity on p38, JNK1, ERK1 and -2, PKC, or c-Src-like kinases.
价 格：￥电议型 号：T6440产 地：中国大陆
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T18640(S,R,S)-AHPC-C4-NH2 hydrochlorideinhibit,E3 Ligase Ligand-Linker Conjugates,(S,R,S)AHPCC4NH2 hydroch
(S,R,S)-AHPC-C4-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate incorporating the (S,R,S)-AHPC based VHL ligand and a linker.
价 格：￥电议型 号：T18640产 地：中国大陆
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T9064LY3143921 hydrateLY-3143921 hydrate,LY3143921 hydrate
LY3143921 ((S)-Example 2) hydrate is an orally active CDC7 kinase inhibitor with broad in vitro anticancer activity [1].
价 格：￥电议型 号：T9064产 地：中国大陆
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T7644DPNinhibit,neuroprotection,estrogen,beta,anti-inflammation,receptor,Autophagy,peptide,amyloid,DPN,In
DPN is an selective agonist of estrogen receptor β (ERβ) .
价 格：￥电议型 号：T7644产 地：中国大陆
