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T11264FAPI-4；化合物 T11264FAPI-4
Api-4 is a fibroblast activated protein (FAP) inhibitor used in cancer research.
价 格：￥电议型 号：T11264产 地：中国大陆
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T11263FAPI-2；化合物 T11263FAPI-2
Fapi-2 is a fibroblast activated protein (FAP) inhibitor used in cancer research.
价 格：￥电议型 号：T11263产 地：中国大陆
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T11215Episilvestrol；化合物 T11215Episilvestrol
Episilvestrol is a specific eIF4A-targeting translation inhibitor, with antitumor activity. Episilvestrol is a derivative of silvestrol, isolated from the fruits and twigs of Aglaia silvestris.
价 格：￥电议型 号：T11215产 地：中国大陆
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T11214EPI-589；化合物 T11214EPI-589
EPI-589, a quinone derivative and oxidoreductase enzyme inhibitor, is considered safe and well tolerated, showing promise for the treatment of amyotrophic lateral sclerosis (ALS).
价 格：￥电议型 号：T11214产 地：中国大陆
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T11204ENS-163 phosphate；化合物 T11204Sandoz ENS 163 phosphate|||ENS 213-163|||Thiopilocarpine phosphate；Sando
Ens-163 phosphate is a muscarinic M1 receptor agonist. It is selective.
价 格：￥电议型 号：T11204产 地：中国大陆
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T11160EGFR-IN-5；化合物EGFR-IN-5EGFR-IN-5|||inhibit|||Epidermal growth factor receptor|||HER1|||ErbB-1|||Inhib
EGFR-IN-5 is a selective inhibitor of EGFR. The IC50s for EGFR, EGFR(L858R), EGFR(L858R/T790M), and EGFR(L858R/T790M/C797S) are 10.4, 1.1, 34, 7.2 nM, respectively.
价 格：￥电议型 号：T11160产 地：中国大陆
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T1114Ciclopirox olamine；环吡酮乙醇胺盐Ciclopirox ethanolamine；环吡酮乙醇胺盐|||环吡司胺|||Ciclopirox ethanolamine
Ciclopirox olamine is a broad-spectrum antifungal agent with additional antibacterial and anti-inflammatory activities.
价 格：￥电议型 号：T1114产 地：中国大陆
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T11129LDuvelisib (R enantiomer) hydrochloride；杜韦利西布R对映体盐酸盐IPI-145 R enantiomer HCl|||Duvelisib (R enantiome
Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) is a PI3K inhibitor. Duvelisib (R enantiomer) hydrochloride is the less active enantiomer of Duvelisib.
价 格：￥电议型 号：T11129L产 地：中国大陆
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T11129Duvelisib (R enantiomer)化合物Duvelisib R entiomerDuvelisib R enantiomer|||IPI-145 R enantiomer|||INK11
Duvelisib R enantiomer (IPI-145 R enantiomer) is an enantiomer of Duvelisib with lower activity. Duvelisib is a PI3K inhibitor.
价 格：￥电议型 号：T11129产 地：中国大陆
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T11122-(Hydroxymethyl)pyridine吡啶甲醇吡啶甲醇|||Piconol
2-(Hydroxymethyl)pyridine (Piconol) is used as an organic synthesis and medicinal chemistry intermediate for the synthesis of the stimulant laxative bisacodyl, and as a pyridinol with hypoglycemic activity.
价 格：￥电议型 号：T1112产 地：中国大陆
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T11093DPPH；2,2-联苯基-1-苦基肼基2,2-Diphenyl-1-picrylhydrazyl；2,2-联苯基-1-苦基肼基|||2,2-Diphenyl-1-picrylhydrazyl
DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a cell-permeable, stable free radical that is commonly used to evaluate the ability of compounds to act as free radical scavengers or hydrogen donors and to measure the antioxidant activity of tissue extracts
价 格：￥电议型 号：T11093产 地：中国大陆
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T11080Dopropidil；多普吡地Dopropidil
Dopropidil is a new anti-angina pectoris calcium regulator, which has intracellular calcium antagonist activity and anti-ischemic effects in various predicted animal models.
价 格：￥电议型 号：T11080产 地：中国大陆
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T11078Deschloroclozapine；氯氮平杂质Deschloroclozapine
Deschloroclozapine, a metabolite of Clozapine, is a highly potent muscarinic DREADDs agonist. Deschloroclozapine binds to DREADD receptor subtypes hM3Dq and hM4Di with Ki of 6.3 and 4.2 nM, respectively.
价 格：￥电议型 号：T11078产 地：中国大陆
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T10991Dehydronitrosonisoldipine；化合物DehydronitrosonisoldipineDehydronitrosonisoldipine
Dehydronitrosonisoldipine is an inhibitor of sterile α and TIR motif-containing 1 and can be used in studies about neurodegenerative disorders. Dehydronitrosonisoldipine inhibits axon degenration and the Vincristine-activated cADPR production in neurons.
价 格：￥电议型 号：T10991产 地：中国大陆
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T10989Dehydroaripiprazole；化合物DehydroaripiprazoleOPC-14857|||DM-14857；OPC-14857|||DM-14857
Dehydroaripiprazole (DM-14857) is the active metabolite of aripiprazole. Aripiprazole is an antipsychotic drug, which is metabolized by CYP3A4 and CYP2D6 and mainly forms dehydroaripiprazole. Dehydroaripiprazole has antipsychotic activity equivalent to aripiprazole.
价 格：￥电议型 号：T10989产 地：中国大陆
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T10979DCPIB；化合物DCPIBDCPIB
DCPIB, a known specific and potent inhibitor of volume-regulated anion channels (VRAC),DCPIB displayed superior selectivity toward TRESK with an IC50 of 0.14 μM, demonstrating at least 100-fold higher affinity over TREK1/TRAAK channels.
价 格：￥电议型 号：T10979产 地：中国大陆
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T10961Darenzepine；达仑西平Darenzepine
Darenzepine is a muscarinic receptor inhibitor.
价 格：￥电议型 号：T10961产 地：中国大陆
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T10943D-(-)-Lactic acid；D-乳酸(R)-2-Hydroxypropionic acid；(R)-2-Hydroxypropionic acid|||D-乳酸
D-(-)-Lactic acid is a normal intermediate in sugar fermentation (oxidation, metabolism). It is identified as a competitive inhibitor of ProDH (proline dehydrogenase) in plants.
价 格：￥电议型 号：T10943产 地：中国大陆
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T10828CK2/PIM1-IN-1；化合物 T10828CK2/PIM1-IN-1
CK2/PIM1-IN-1 is an inhibitor of CK2 and PIM1 (IC50s: 3.787 μM and 4.327 μM). It is developed for the research of proliferative disorders such as cancer, as well as other kinase-associated conditions.
价 格：￥电议型 号：T10828产 地：中国大陆
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T10804CHMFL-PI3KD-317；化合物CHMFL-PI3KD-317CHMFL-PI3KD-317
CHMFL-PI3KD-317 is a highly potent, selective and orally active PI3Kδ inhibitor, with an IC50 of 6 nM, and exhibits over 10-1500 fold selectivity over other class I, II and III PIKK family isoforms, such as PI3Kα (IC50, 62.6 nM), PI3Kβ (IC50, 284 nM), PI3Kγ (IC50, 202.7 nM), PIK3C2A (IC50, >10000 nM), PIK3C2B (IC50, 882.3 nM), VPS34 (IC50, 1801.7 nM), PI4KIIIA (IC50, 574.1 nM) and PI4KIIIB (IC50, 300.2 nM). CHMFL-PI3KD-317 inhibits PI3Kδ-mediated Akt T308 phosphorylation in Raji cells, with an E
价 格：￥电议型 号：T10804产 地：中国大陆
