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T1149Fenofibrate；非诺贝特Procetofen|||Lipanthyl|||Lipantil；Procetofen|||非诺贝特|||Lipanthyl|||Lipantil
Fenofibrate (Lipanthyl) is a peroxisome proliferator receptor alpha agonist. Fenofibrate is a synthetic phenoxy-isobutyric acid derivate and prodrug with antihyperlipidemic activity.
价 格：￥电议型 号：T1149产 地：中国大陆
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T11465Lenacapavir；化合物LenacapavirGS-6207；GS-6207
Lenacapavir (GS-6207) is a potent capsid-targeting inhibitor of HIV replication. Lenacapavir shows anti-HIV activity with an EC50 of 100 pM in MT-4 cells.
价 格：￥电议型 号：T11465产 地：中国大陆
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T1141Fenbendazole；芬苯达唑Fenbendazol|||Phenbendasol|||Panacur；Fenbendazol|||苯硫咪唑|||芬苯达唑|||Phenbendasol|||Pan
Fenbendazole (Fenbendazol) is an antinematodal benzimidazole used in veterinary medicine.
价 格：￥电议型 号：T1141产 地：中国大陆
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T11353LGallopamil hydrochloride；化合物Gallopamil hydrochlorideMethoxyverapamil hydrochloride；Methoxyverapamil
Gallopamil hydrochloride (Methoxyverapamil hydrochloride) is an antagonist of phenylalkylamine calcium. Gallopamil hydrochloride can be used in antiarrhythmic and vasodilator studies.
价 格：￥电议型 号：T11353L产 地：中国大陆
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T11353Gallopamil；戈洛帕米Methoxyverapamil；Methoxyverapamil|||戈洛帕米
Gallopamil (Methoxyverapamil) inhibits acid secretion in a concentration-dependent manner with an IC50 of 10.9 μM. Gallopamil is a potent antiarrhythmic and vasodilator agent. Gallopamil (Methoxyverapamil), a methoxy derivative of Verapamil, is a phenylalkylamine calcium antagonist.
价 格：￥电议型 号：T11353产 地：中国大陆
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T11317FPA-124；化合物 T11317FPA-124
FPA-124, a cell-permeable copper complex and selective Akt inhibitor with an IC50 of 0.1 μM, engages the pleckstrin homology (PH) and kinase domains of Akt, inducing apoptosis.
价 格：￥电议型 号：T11317产 地：中国大陆
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T1123Camptothecin喜树碱NSC-100880|||Campathecin|||喜树碱|||(S)-(+)-Camptothecin|||CPT
Camptothecin (CPT) belongs to the alkaloid group of natural products and is a specific DNA topoisomerase I (Topo I) inhibitor (IC50=679 nM) with specificity. Camptothecin has antitumor activity and induces apoptosis.
价 格：￥电议型 号：T1123产 地：中国大陆
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T11212EPAC 5376753；化合物EPAC 53767535-{[5-(2,4-dichlorophenyl)furan-2-yl]methylidene}-2-thioxodihydropyrimid
EPAC 5376753 is an allosteric inhibitor of EPAC1 with an IC50 of 4 ?M in Swiss 3T3 cells.
价 格：￥电议型 号：T11212产 地：中国大陆
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T11199Endothelial lipase inhibitor-1；内皮脂酶抑制剂-1Endothelial lipase inhibitor-1
Endothelial lipase inhibitor-1 is a potent endothelial lipase inhibitor with an IC50 of 49 nM.
价 格：￥电议型 号：T11199产 地：中国大陆
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T11186EMPA；化合物EMPAEMPA
EMPA is a selective, high-affinity and reversible antagonist of orexin OX2 receptor(human and rat OX2-HEK293 membranes with KD values of 1.1 and 1.4 nM respectively)
价 格：￥电议型 号：T11186产 地：中国大陆
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T11172EIPA hydrochloride；化合物 T11172L593754 hydrochloride|||MH 12-43 hydrochloride；L593754 hydrochloride|||
EIPA hydrochloride also inhibits Na+/H+-exchanger (NHE) and macropinocytosisEIPA hydrochloride (L593754 hydrochloride) is a TRPP3 channel inhibitor with an IC50 of 10.5 μM.
价 格：￥电议型 号：T11172产 地：中国大陆
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T11122DUPA(OtBu)-OH化合物DUPA(OtBu)-OH(S)-5-叔丁氧基-4-(3-((S)-1,5-二-叔丁氧基-1,5-二氧代-2-戊基)脲啶)-5-氧代戊酸
DUPA(OtBu)-OH is a DUPA precursor. DUPA is used as the targeting moiety to actively deliver Docetaxel (DTX) for treatment of Prostate-Specific Membrane Antigen (PSMA) expressing prostate cancer. PSMA has a high affinity for DUPA(Ki = 8 nM).
价 格：￥电议型 号：T11122产 地：中国大陆
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T11114Duloxetine metabolite Para-Naphthol Duloxetine；度洛西汀代谢物Para-Naphthol duloxetine；度洛西汀代谢物|||Para-Naphth
Para-Naphthol Duloxetine is a serotonin-norepinephrine reuptake inhibitor (SNRI),is a metabolite of Duloxetine.
价 格：￥电议型 号：T11114产 地：中国大陆
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T1111Pralidoxime Chloride吡啶醛肟甲氯2-PAM chloride|||吡啶醛肟甲氯|||2-Pyridinealdoxime methochloride|||2-PAM (chlori
Pralidoxime Chloride (2-PAM chloride) is a useful agent in the treatment of organophosphate poisoning. Pralidoxime binds to organophosphate-inactivated acetylcholinesterase, used to combat poisoning by organophosphates or acetylcholinesterase inhibitors (nerve agents).
价 格：￥电议型 号：T1111产 地：中国大陆
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T11086DOTAP chloride；(2,3-二油氧基丙基)三甲基氯化铵1,2-Dioleoyl-3-trimethylammonium-propane chloride；(2,3-二油氧基丙基)三甲基氯化
DOTAP chloride (1,2-Dioleoyl-3-trimethylammonium-propane chloride) is a useful and effective cationic lipid transfection DNA(plasmids, BacMIDs) and modified nucleic acids (antisense oligonucleotides) without the use of auxiliary lipids.
价 格：￥电议型 号：T11086产 地：中国大陆
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T11079NMI 8739；化合物NMI 8739n-docosahexaenoyl dopamine|||Dha-DA conjugate；n-docosahexaenoyl dopamine|||Dha-D
NMI 8739 (n-docosahexaenoyl dopamine) is an agonist of D2 autoreceptor. NMI 8739 reduces NO production and elicits concentration-dependent suppression of CCL-20, MCP-1 and IL-6 release.
价 格：￥电议型 号：T11079产 地：中国大陆
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T11077Dopamine D2 receptor antagonist-1；多巴胺D2受体拮抗剂-1Dopamine D2 receptor antagonist-1
Dopamine D2 Receptor Antagonist-1 functions as a negative allosteric modulator (NAM) of the dopamine D2 receptor (D2R), demonstrating sub-millimolar affinity.
价 格：￥电议型 号：T11077产 地：中国大陆
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T11060DMAPT；化合物DMAPTDimethylamino Parthenolide；Dimethylamino Parthenolide
DMAPT (Dimethylamino Parthenolide) is a water-soluble analogue of Parthenolide (PTL). It is an orally active NF-κB inhibitor with an LD50 of 1.7 μM on primary acute myeloid leukemia cells.
价 格：￥电议型 号：T11060产 地：中国大陆
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T1104Paromomycin Sulfate；硫酸巴龙霉素Aminosidine sulfate|||Paromomycin sulfate salt；Aminosidine sulfate|||Parom
Paromomycin binds specifically to the RNA oligonucleotide at the A site of bacterial 30S ribosomes, thereby causing misreading and premature termination of translation of mRNA and inhibition of protein synthesis followed by cell death. Paromomycin Sulfate (Aminosidine sulfate) is the sulfate salt form of paromomycin, a structural derivative of neomycin, an aminoglycoside antibiotic with amebicidal and bactericidal effects against predominantly aerobic gram-negative bacteria.
价 格：￥电议型 号：T1104产 地：中国大陆
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T10990Dehydrocorydaline chloride盐酸脱氢紫堇碱盐酸脱氢紫堇碱|||13-Methylpalmatine chloride
Dehydrocorydaline chloride (13-Methylpalmatine chloride) is an alkaloid with anti-inflammatory and anti-cancer activity. Can improve the activation of p38 MAPK.
价 格：￥电议型 号：T10990产 地：中国大陆
