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T16704LQuilseconazole Formic acid(1340593-70-5 Free base)
Quilseconazole Formic acid is a selective inhibitor of fungal Cyp51 with potent activities against Cryptococcus neoformans and Cryptococcus gattii.
价 格：￥电议型 号：T16704L产 地：中国大陆
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TQ0011PF-06869206inhibit,PF-06869206,Na+ channels,Sodium Channel,Na channels,PF 06869206,Inhibitor,PF06869
PF-06869206 is an oral selective inhibitor of the sodium-phosphate cotransporter NaPi2a (SLC34A1, IC50: 380 nM).
价 格：￥电议型 号：TQ0011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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T86131-Ethyl-6-aminouracil1 Ethyl 6 aminouracil,1Ethyl6aminouracil
1-Ethyl-6-aminouracil is an intermediate in the synthesis of a series of new substituted Xanthines which have high affinity and selectivity for the human adenosine A2B receptors.
价 格：￥电议型 号：T8613产 地：中国大陆
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TP2309NEUROTENSIN TFA (39379-15-2 free base)NEUROTENSIN TFA (39379 15 2 free base),NEUROTENSIN TFA (393791
Neurotensin (NT) is an endogenous 13 amino acid neuropeptide with profound opioid-independent analgesic effects. It behaves as a neurotransmitter in the brain, as a hormone in the gut, and also as a neuromodulator. It is implicated in the pathophysiology of several CNS disorders (including schizophrenia, Parkinson´s disease, drug abuse, pain, cancer, inflammation, eating disorders and central control of blood pressure) due to its association with a wide variety of neurotransmitter systems
价 格：￥电议型 号：TP2309产 地：中国大陆
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TP1591LOVA G4 peptide acetate(148274-82-2 free base)OVA G-4 peptide acetate(148274-82-2 free base),OVA G4 p
G4 peptide acetate is a variant of the agonist ovalbumin (OVA) peptide (257-264), SIINFEKL. OVA Peptide is a class I (Kb)-restricted peptide epitope of ovalbumin presented by the class I MHC (major histocompatibility complex) molecule, H-2Kb (class I genes of the mouse MHC).
价 格：￥电议型 号：TP1591L产 地：中国大陆
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TN1474Caulilexin Cantifungal,inhibit,Caulilexin C,phytoalexin,Inhibitor,Fungal
Caulilexin C shows inhibitory activity on human Acyl CoA: cholesterol transferase I (hACATI) and on human Acyl CoA: cholesterol transferase 2 (hACAT2) at 100 mug/ml.
价 格：￥电议型 号：TN1474产 地：中国大陆
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TN1012LFebrifugine dihydrochlorideInhibitor,Parasite,Febrifugine dihydrochloride,antimalarial,alkaloid,Quin
Febrifugine dihydrochloride is a biochemical with therapeutic activity regarding malaria, cancer, fibrosis and inflammatory diseases.
价 格：￥电议型 号：TN1012L产 地：中国大陆
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TP1889MCL0020inhibit,Melanocortin Receptor,COS-1,Inhibitor,MCL0020,MC Receptor,anorexia,dose-dependently,s
Potent and selective melanocortin MC4 receptor antagonist (IC50 values are 11.63, 1115 and > 10 000 nM at MC4, MC3 and MC1 receptors respectively). Significantly reverses stress-induced anorexia but has no effect on food intake in free-feeding rats. Exhibits anxiolytic-like activity in vivo.
价 格：￥电议型 号：TP1889产 地：中国大陆
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TP1018LUrechistachykinin II acetateUrechistachykinin II acetate
Urechistachykinin II acetate is an invertebrate rapid kinin-related peptide (TRPs) isolated from carotenoid worms, shows antimicrobial activities without a hemolytic effect
价 格：￥电议型 号：TP1018L产 地：中国大陆
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T7123AMG-47aInhibitor,signal,kinases,AMG 47a,JAK,Janus kinase,AMG-47a,transduction,Src,VEGFR,cytoplamic,p
AMG-47a is a potent inhibitor of Lck and T cell proliferation. AMG-47a could promote the degradation of the KRAS oncoprotein. AMG-47a selectively reduced the levels of EGFP-KRASG12V protein but did not affect EGFP protein in cells.
价 格：￥电议型 号：T7123产 地：中国大陆
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T60889RP-6306
RP-6306 is a potent, selective and orally active PKMYT1 inhibitor (IC50= 14 nM). RP-6306 exhibits a high degree of selectivity for PKMYT1 over other kinases in cellular binding assays. RP-6306 exhibits anticancer effects.
价 格：￥电议型 号：T60889产 地：中国大陆
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T7449o-Phenanthroline monohydrateInhibitor,inhibit,Matrix metalloproteinases,o-Phenanthroline,MMP,1,10-Ph
1,10-Phenanthroline monohydrate is an inhibitor of metallopeptidases, inhibits zinc-dependent hydrolysis of Fa-Gly-Leu-NH2 by B. subtilis neutral protease and B. thermoproteolyticus thermolysin.
价 格：￥电议型 号：T7449产 地：中国大陆
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T14362LAY 9944 dihydrochloride1(2chlorophenyl)N[[4[(2chlorophenyl)methylaminomethyl]cyclohexyl]methyl]metha
AY 9944 dihydrochloride is a intermediate.
价 格：￥电议型 号：T14362L产 地：中国大陆
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T10269AHR antagonist 2AHR antagonist 2
AHR antagonist 2 is an antagonist of the aryl hydrocarbon receptor. The IC50s for human AHR and mouse AHR are 0.885 and 2.03 nM, respectively.
价 格：￥电议型 号：T10269产 地：中国大陆
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TN1539Cussosaponin CCussosaponin C,Inhibitor,inhibit
Cussosaponin C is a natural product isolated from Pulsatilla koreana Nakai.
价 格：￥电议型 号：TN1539产 地：中国大陆
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TN1089Hydroxy-β-sanshool
Hydroxy-β-sanshool is a pungent compound obtained from Zanthoxylum piperitum.
价 格：￥电议型 号：TN1089产 地：中国大陆
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TP1159LBoc-Gly-Gly-Phe-Gly-OH acetateBocGlyGlyPheGlyOH acetate,Boc Gly Gly Phe Gly OH acetate
Boc-Gly-Gly-Phe-Gly-OH acetate is a self-assembly of N- and C-protected tetrapeptide.
价 格：￥电议型 号：TP1159L产 地：中国大陆
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TN25491-Methoxycarbonyl-β-carboline1 Methoxycarbonyl β carboline,1Methoxycarbonylβcarboline
1-Methoxycarbonyl-β-carboline is an alkaloid from Ailanthus altissima.
价 格：￥电议型 号：TN2549产 地：中国大陆
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T7334NP118809NP118809,NP 118809,NP-118809,Inhibitor,inhibit,Ca2+ channels,Calcium Channel,Ca channels
NP118809 is a potent N-type calcium channel blocker(IC50 : 0.11 μM).
价 格：￥电议型 号：T7334产 地：中国大陆
