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产品数：86101
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TP1885L1[(pF)Phe4]Nociceptin(1-13)NH2 acetate[(pF)Phe4]Nociceptin(113)NH2 acetate,[(pF)Phe4]Nociceptin(1 13)
[(pF)Phe4]Nociceptin(1-13)NH2 acetate is a selective agonist of NOP receptor with a pKi of 10.68 and a pEC50 of 9.31. [(pF)Phe4]Nociceptin(1-13)NH2 acetate displays high selectivity over δ, κ, and μ opioid receptors (>3000 fold).
价 格：￥电议型 号：TP1885L1产 地：中国大陆
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T7777M4284Bacterial,M-4284,M4284,inhibit,Inhibitor,UPEC,UTI,mannoside,E.Coil
M 4284 is a selective and orally active biphenyl mannoside FimH antagonist.
价 格：￥电议型 号：T7777产 地：中国大陆
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T8034Dimethyl TrisulfideEndogenous Metabolite,Inhibitor,inhibit,Dimethyl Trisulfide
Dimethyl trisulfide is the simplest organic trisulfide found in garlic, onion, broccoli, and similar plants. Dimethyl trisulfide is a cyanide antidote.
价 格：￥电议型 号：T8034产 地：中国大陆
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TN1849Kuwanon HInhibitor,Kuwanon H,Bombesin Receptor,inhibit
Kuwanon H is a specific antagonist for the gastrin-releasing peptide (GRP) -preferring receptor with Ki values of 290 nM and can be useful for studying the physiological and pathological role of GRP. Kuwanon H is a potent non-peptide bombesin receptor antagonist.
价 格：￥电议型 号：TN1849产 地：中国大陆
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TQ01722’’-O-Rhamnosylicariside IIInhibitor,2’’ O Rhamnosylicariside II,inhibit,2’’ORhamnosylicariside II
2´´-O-Rhamnosylicariside II is beneficial for improving postmenopausal osteoporosis. It shows potent antioxidant activity, with IC50 values of 90.5 uM.
价 格：￥电议型 号：TQ0172产 地：中国大陆
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T8392L(+)-Asparagine monohydrateL-Asparagine,amino,non-essential,Inhibitor,L(+) Asparagine monohydrate,ti
L(+)-Asparagine monohydrate is a non-essential amino acid, participate in neurological and metabolic regulation of tissue cell function.
价 格：￥电议型 号：T8392产 地：中国大陆
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T9330MIPS521A1AR,inhibit,MIPS-521,pain,Adenosine Receptor,MIPS 521,MIPS521,Inhibitor,P1 receptor
MIPS-521 is a positive allosteric modulator of the A1R.
价 格：￥电议型 号：T9330产 地：中国大陆
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T8394D-Serineinhibit,D-Serine,Ionotropic glutamate receptors,Endogenous Metabolite,Inhibitor,DSerine,iGlu
(R)-Serine is an endogenous amino acid,is a potent co-agonist at the NMDA glutamate receptor.
价 格：￥电议型 号：T8394产 地：中国大陆
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T8517BelinostatHistone deacetylases,PX-105684,PX 105684,Inhibitor,HDAC,Belinostat,PXD 101,inhibit,Autopha
Belinostat is an inhibitor of hydroxamic acid-type histone deacetylase (HDAC, IC50 of 27 nM in HeLa cell extracts),and with antineoplastic activity.
价 格：￥电议型 号：T8517产 地：中国大陆
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TN2296Vinaginsenoside R4Vinaginsenoside R 4,Vinaginsenoside R4,inhibit,Vinaginsenoside R-4,Inhibitor
Vinaginsenoside R4 has melanogenic inhibitory activity, it may have potential as a new skin whitening compound.
价 格：￥电议型 号：TN2296产 地：中国大陆
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T8976PD-089828EGFR,ATP,nonselective,PD 089828,PDGFR,autophosphorylation,PD089828,HER1,Epidermal growth fa
PD 089828 is a competitive inhibitor of the receptor tyrosine kinases FGFR1, PDGFRβ, and EGFR (IC50s = 0.15, 1.76, and 5.47 μM, respectively) and a noncompetitive inhibitor of the nonreceptor tyrosine kinase c-Src (IC50 = 0.18 μM)
价 格：￥电议型 号：T8976产 地：中国大陆
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TN71812-Pentadecanone
2-Pentadecanone is a marine derived natural products found in Caulocystis cephalornithos.
价 格：￥电议型 号：TN7181产 地：中国大陆
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T6S1369Vitexinneurodegeneration,Vitexin,anti-cancer,anti-nociceptive,inhibit,Medicinal,anti-hypertensive,an
1. Vitexin has antinociceptive and antispasmodic activities. 2. Vitexin exhibits a prominent first-pass effect. 3. Vitexin has antioxidant, antimyeloperoxidase, and α-glucosidase inhibitory activities. 4. Vitexin can either inhibit or induce activities of CYP2C11 and CYP3A1. 5. Vitexin induces the novel p53-dependent metastatic and apoptotic pathway. 6. Vitexin protects brain against cerebral I/R injury, and this effect may be regulated by mitogen-activated protein kinase (MAPK) and apoptosis si
价 格：￥电议型 号：T6S1369产 地：中国大陆
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T8461SKI VPI3K,SKI V,Inhibitor,Apoptosis,GST-hSK,sphingosine,second,mitogenic,Phosphoinositide 3-kinase,S
SKI V is a potent and noncompetitive non-lipid sphingosine kinase (SPHK; SK) inhibitor (GST-hSK,IC50 : 2 μM), and is a PI3K inhibitor(hPI3k,IC50 : 6 μM), induces apoptosis and has antitumor activity
价 格：￥电议型 号：T8461产 地：中国大陆
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T76963-Cyano-7-ethoxycoumarininhibit,Inhibitor,3Cyano7ethoxycoumarin,3 Cyano 7 ethoxycoumarin
3-Cyano-7-ethoxycoumarin is cytochrome P450 (CYP) isoforms CYP1A1 and CYP1A2 .
价 格：￥电议型 号：T7696产 地：中国大陆
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T8849PF-9601Nexcitotoxicity,neurodegenerative diseases,MAO,PF9601N,Monoamine Oxidase,MAO-B inhibitor,neur
PF-9601N showed high potency and selectivity as a MAO-BI (monoamine oxidase type B inhibitor) and also demonstrated remarkable neuroprotective properties in several in vivo and cellular models of PD.
价 格：￥电议型 号：T8849产 地：中国大陆
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T7476AS057278Prepulse inhibition,Inhibitor,Non-peptidic,D-amino acid oxidase,AS 057278,inhibit,Schizophre
AS057278 is an D-amino acid oxidase (DAAO) inhibitor.
价 格：￥电议型 号：T7476产 地：中国大陆
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T19343sn-Glycerol 3-phosphateinhibit,Endogenous Metabolite,sn Glycerol 3 phosphate,snGlycerol 3phosphate,I
Glycerol 3-phosphate is produced by the reduction of dihydroxyacetone phosphate by NADH formed during glycolysis of the cytoplasmic glycerol 3-phosphate dehydrogenase pathway.
价 格：￥电议型 号：T19343产 地：中国大陆
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T99683-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride3Piperidinyl(1pyrrolidinyl)methanone hydrochlori
3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride can be used in the synthesis of piperidin-4-yl-urea derivatives which are MCH-R1 antagonists.
价 格：￥电议型 号：T9968产 地：中国大陆
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T6425BTZ043 RacemateBenzothiazinone10526038,inhibit,Benzothiazinone-10526038,BTZ043 Racemate,BTZ 10526038
BTZ043 racemate is a decaprenylphosphoryl-β-D-ribose 2´-epimerase (DprE1) inhibitor, used as a new antimycobacterial agent.
价 格：￥电议型 号：T6425产 地：中国大陆
