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T2819Methyl p-coumarate；4-羟基肉桂酸甲酯Methyl 4-hydroxycinnamate|||inhibit|||A. alternata|||melanoma|||Methyl p
"Methyl 4-hydroxycinnamate is an esterified derivative of p-coumaric acid isolated from the flowers of Trixis michuacana var. longifolia, exhibiting antibacterial and anti-melanogenesis properties."
价 格：￥电议型 号：T2819产 地：中国大陆
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T28132NaV1.7 Blocker-801；化合物 T28132NaV1.7 Blocker-801
NaV1.7 Blocker-801 is a potent NaV1.7 blocker.
价 格：￥电议型 号：T28132产 地：中国大陆
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T27982MBRI-001；化合物 T27982MBRI 001|||MBRI001. BPI-2358-d|||plinabulin-d|||NPI-2358-d；MBRI 001|||MBRI001. BP
MBRI-001 is a deuterium-substituted plinabulin derivative and a potent anti-cancer agent with better pharmacokinetic characteristics tand lower toxicity.
价 格：￥电议型 号：T27982产 地：中国大陆
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T27832Lifibrol；利弗布罗U 83860|||K-12148|||K-12.148|||U-83860|||K12148；U 83860|||K-12148|||K-12.148|||U-83860|
Lifibrol (U-83860) is an inhibitor of cholesterol synthesis.Lifibrol has anticholesterol and hypolipidemic properties and promotes the conversion of LDL Apo B-100 in patients with hypercholesterolemia and mixed hyperlipidemia.
价 格：￥电议型 号：T27832产 地：中国大陆
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T27757Kv1.5-IN-IIII；化合物 T27757Kv1.5INIIII|||Kv1.5INIV|||Compound IIII|||Kv1.5IN4|||Compound 4；Kv1.5INIIII|
Kv1.5-IN-IIII is a potent inhibitor of Kv1.5.
价 格：￥电议型 号：T27757产 地：中国大陆
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T27354Fozivudine tidoxil；化合物 T27354FZT|||HDP-99.0002|||W-09726867|||HDP-990002|||BM-211290；FZT|||HDP-99.00
Fozivudine tidoxil, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.
价 格：￥电议型 号：T27354产 地：中国大陆
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T27348Fosalvudine tidoxil；化合物 T27348HDP-990003|||HDP990003|||HDP 99.0003|||HDP99.0003|||HDP-99.0003|||HDP
Fosalvudine tidoxil, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.
价 格：￥电议型 号：T27348产 地：中国大陆
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T27310Fengabine；酚加宾SL79229|||SL 79.229-00|||SL-79229|||SL 79229|||SL 79-229|||SL 79,229-00；SL79229|||SL 79
Fengabine (SL-79229) is a GABA receptor agonist with antidepressant activity and is used to treat depression.
价 格：￥电议型 号：T27310产 地：中国大陆
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T27306Fasidotril；化合物 T27306BP 1137|||BP1137|||BP-1.137|||BP1.137|||BP-1137|||BP 1.137；BP 1137|||BP1137|||B
Fasidotril is a NEP/ACE inhibitor. Fasidotril was an effective oral antihypertensive agent during chronic treatment in high-renin renovascular rats, normal-renin SHR, and low-renin DOCA-salt hypertensive rats and in patients with essential hypertension.
价 格：￥电议型 号：T27306产 地：中国大陆
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T27239Edaglitazone；依格列宗Edaglitazone sodium|||BM-13.1258|||RO-2052349-602|||R-483|||RO-2052349-000；Edaglita
Edaglitazone is a PPARγ agonist. Edarglitazone restores acute inflammatory responses to cerebral hypoxia-ischemia in the diabetic ob/ob mouse.
价 格：￥电议型 号：T27239产 地：中国大陆
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T27174Dihydrocelastrol；化合物 T27174DHCE. (-)-Triptohypol C|||Triptohypol C；DHCE. (-)-Triptohypol C|||Triptoh
Dihydrocelastrol is synthesized by hydrogenation of celastrol, a treterpene isolated from Chinese medicinal plant Tripterygium regelii. Dihydrocelastrol could inhibit cell proliferation and promote apoptosis through caspase-dependent way in vitro. DHCE could inhibit cellular proliferation and induce cell apoptosis in myeloma cells mediated through different mechanisms, possibly through inhibiting the ERK1/2 and IL-6/STAT3 pathways.
价 格：￥电议型 号：T27174产 地：中国大陆
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T27165Diazaborine；化合物 T27165Diazaborine compound 2b18|||Pkf 84.474|||Pkf 84474|||Pkf-84474|||SA-84474；Diaz
Diazaborine inhibits maturation of rRNAs for the large ribosomal subunit. Diazaborine blocks ribosome biogenesis by inhibiting the AAA-ATPase Drg1. Diazaborine treatment causes, within minutes, a rapid redistribution of the protein from the nucleolus to the periphery of the nucleus, which provides a possible explanation for the effect of diazaborine on rRNA processing.
价 格：￥电议型 号：T27165产 地：中国大陆
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T27087Cronidipine；氯硝地平LF 2.0254|||LF-20254|||LF20254|||LF 20254；LF 2.0254|||LF-20254|||LF20254|||LF 20254
Cronidipine (LF 20254), a calcium channel antagonist, is used potentially for the treatment of hypertension and myocardia ischemia.
价 格：￥电议型 号：T27087产 地：中国大陆
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T27027CJ-15208；化合物 T27027CJ15,208|||CJ-15,208|||CJ 15,208.c[Phe-D-Pro-Phe-Trp]；CJ15,208|||CJ-15,208|||CJ 1
CJ-15208 is a potent and selective κ-opioid receptor antagonist from a fungus, Ctenomyces serratus ATCC15502 (IC50 are 47 nM for kappa, 260 nM for mu, and 2,600 nM for delta respectly). In the electrically-stimulated twitch response assay of rabbit vas deferens, CJ-15208 recovered the suppression by a kappa agonist asimadoline with an ED50 of 1.3 microM.
价 格：￥电议型 号：T27027产 地：中国大陆
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T27022Cipralisant maleate；化合物 T27022GT-2331|||Cipralisant maleate. trade name Perceptin|||GT 2331|||GT2331
Cipralisant maleate is a potent, selective Histamine H3 receptor antagonist.
价 格：￥电议型 号：T27022产 地：中国大陆
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T26944Capeserod HCl；化合物 T26944SL-65.0155|||SL-650155|||SL 650155|||SL 65.0155；SL-65.0155|||SL-650155|||SL
Capeserod HCl, a 5-hydroxytriptamine 4 (5-HT4) receptor agonist, is used potentially for the treatment of Alzheimer´s disease.
价 格：￥电议型 号：T26944产 地：中国大陆
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T26943CAP-7.1；化合物 T26943CAP7.1；CAP7.1
CAP-7.1, a DNA topoisomerase inhibitor, is used potentially for the treatment of biliary cancer and non-small cell lung cancer.
价 格：￥电议型 号：T26943产 地：中国大陆
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T26885BO-1158；化合物 T26885BO1158. Antibiotic BO 1158；BO1158. Antibiotic BO 1158
BO-1158 is an antibacteria agent.
价 格：￥电议型 号：T26885产 地：中国大陆
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T26839BM 21.1298；化合物 T26839BM21.1298|||BM-21.1298；BM21.1298|||BM-21.1298
BM 21.1298 is a inhibition of HIV-1 reverse transcriptase.
价 格：￥电议型 号：T26839产 地：中国大陆
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T26818Binedaline；化合物 T26818binodaline. Ixprim|||SCHA 1059|||SCHA1059|||Sgd-Sch-1059|||SCHA-1059；binodaline
Binedaline is a selective norepinephrine reuptake inhibitor with Ki value of 25 nM.
价 格：￥电议型 号：T26818产 地：中国大陆
