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T12163N6-(2-Phenylethyl)adenosineP1 receptor,A1AR,derivative,N-6-(2-Phenylethyl)adenosine,Adenosine Recept
N6-(2-Phenylethyl)adenosine is an adenosine derivative and an agonist of adenosine receptors with Ki values of 11.8 nM and 30.1 nM for rat and human A1.
价 格：￥电议型 号：T12163产 地：中国大陆
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T64347ALDH1A3-IN-3ALDH1A3IN3
ALDH1A3-IN-3 (compound 16) is a potent inhibitor of ALDH1A3, with an IC50 of 0.26 μM. ALDH1A3-IN-3 is also a good ALDH3A1 substrate. ALDH1A3-IN-3 can be used for the research of prostate cancer.
价 格：￥电议型 号：T64347产 地：中国大陆
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T8323LolCDE-IN-1antibacterial,inhibit,Bacterial,LolCDEIN1,Inhibitor,LolCDE IN 1,LolCDE
LolCDE-IN-1 is an inhibitor of the Lol proteins (LolCDE) complex. LolCDE-IN-1 shows antibacterial activity.
价 格：￥电议型 号：T8323产 地：中国大陆
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T8722iKIX1antifungal,Inhibitor,drug-resistant,Fungal,CgGal11A,CgPdr1,infection,C. glabrata,iKIX1,inhibit,
iKIX1 is an Pdr1-dependent gene activation. It re-sensitizes drug-resistant C. glabrata to azole antifungals in vitro and in animal models for disseminated and urinary tract C. glabrata infection.
价 格：￥电议型 号：T8722产 地：中国大陆
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T10329anti-TB agent 1antiTB agent 1,anti TB agent 1
anti-TB agent 1 is a potent and orally active anti-tuberculosis agent (MICs: < 2 nM against the Mtb strains H37Rv, rRMP and rINH).
价 格：￥电议型 号：T10329产 地：中国大陆
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T12770RR-11a analog
RR-11a analog is an inhibitor of asparaginyl endopeptidase with IC50s of 4.5 nM, 4.5 nM and 31 nM for AE1 in Trichomonas Vaginalis, AE in Ixodes ricinus and AE in Schistosoma mansoni, respectively.
价 格：￥电议型 号：T12770产 地：中国大陆
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T7697BIX-01294PRMT1,recurrent,Autophagy,H3K9me3,Inhibitor,Cdkn1a,inhibit,p53,Gadd45a,MLKL,Histone Methylt
BIX-01294 is an G9a Histone Methyltransferase inhibitor(IC50 : 1.9 μM).
价 格：￥电议型 号：T7697产 地：中国大陆
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T7948HPGDS inhibitor 2HPGDS inhibitor2,PGE synthase,Inhibitor,inhibit,HPGDS inhibitor-2,HPGDS inhibitor 2
HPGDS inhibitor 2 is a potent, selective hematopoietic prostaglandin D synthase (h-pgds) inhibitor, IC50 = 9.9 nm.
价 格：￥电议型 号：T7948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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T7605Avermectin B1aAntibiotic,Parasite,Inhibitor,Avermectin B-1a,inhibit,Avermectin B1a
Avermectin B1a is a macrocyclic lactone disaccharide anthelmintic agent .
价 格：￥电议型 号：T7605产 地：中国大陆
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T6740Bafilomycin A1Autophagy,Proton Pump,Bafilomycin A 1,Bafilomycin A1,Bafilomycin A-1,Antibiotic,BafA1,
Bafilomycin A1 induces caspase-independent cell death in hepatocellular carcinoma cells via targeting of autophagy and MAPK pathways. Bafilomycin A1 is a vacuolar H+-ATPase inhibitor (IC50: 0.44 nM). It is also found to inhibit autophagy while induces apoptosis.Bafilomycin A1 triggers proliferative potential of senescent cancer cells in vitro and in NOD/SCID mice.
价 格：￥电议型 号：T6740产 地：中国大陆
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T8593RU 249695-HT1B,Serotonin Receptor,fluid,RU 24969,5-HT1A,RU24969,locomotion,Inhibitor,5-HT Receptor,5
RU 24969 is a selective agonist of 5-HT1A and 5-HT1B receptors.
价 格：￥电议型 号：T8593产 地：中国大陆
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T9760IC 86621ATP,Buchwald-Hartwig amination,Inhibitor,IC-86621,IC86621,IC 86621,DSB,antitumor,inhibit,Apo
IC 86621 is a selective and reversible ATP-competitive inhibitor of DNA-PK with an IC50 of 120 nM. IC 86621 increases DNA double-strand break(DSB)-induced antitumor activity with an EC50 of 68 ?M for DNA-PK mediated cellular DSB repair.
价 格：￥电议型 号：T9760产 地：中国大陆
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T8081LC3-mHTT-IN-AN1Autophagosome-tethering compounds,LC3mHTTINAN1,Autophagy,LC3 mHTT IN AN1,ATTECs,Inhib
LC3-mHTT-IN-AN1 is a mHTT-LC3 linker compound that interacts with both mutant huntingtin protein (mHTT) and LC3B. LC3-mHTT-IN-AN1 targeted mHTT to autophagosomes reduces the levels of mHTT in an allele-selective manner in cultured Huntington disease (HD) mouse neurons.
价 格：￥电议型 号：T8081产 地：中国大陆
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TQ0012AZ3451AZ 3451,inhibit,Protease Activated Receptor (PAR),AZ-3451,AZ3451,Thrombin receptors,Inhibitor
AZ3451 is an allosteric antagonist of protease-activated receptor-2 (PAR2, IC50: 23 nM).
价 格：￥电议型 号：TQ0012产 地：中国大陆
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T8136Perospirone hydrochlorideDopamine Receptor,antipsychotic,inhibit,5-HT1A,D2-receptor,SM-9018,5-hydrox
Perospirone hydrochloride is an atypical antipsychotic agent for the treatment of schizophrenia. It also displays affinity towards 5HT1A receptors as a partial agonist.
价 格：￥电议型 号：T8136产 地：中国大陆
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T39705ATG7-IN-1ATG7 IN 1,ATG7IN1,ATG-7-IN-1
ATG7-IN-1 is a selective ATG7 inhibitor with an IC50 of 62 nM.
价 格：￥电议型 号：T39705产 地：中国大陆
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T7406AKR1C3-IN-1AKR-1C3-IN-1,inhibit,AKR1C3IN1,AKR1C3 IN 1,Inhibitor
AKR1C3-IN-1 is a potent and selective inhibitor of AKR1C3(IC50 of 13 nM).
价 格：￥电议型 号：T7406产 地：中国大陆
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T63581-AzakenpaulloneGlycogen synthase kinase-3,1 Azakenpaullone,GSK-3,1-Azakenpaullone,1Azakenpaullone,G
1-Azakenpaullone is a potent and selective GSK-3β inhibitor with IC50 of 18 nM, >100-fold selectivity over CDK1/cyclin B and CDK5/p25.
价 格：￥电议型 号：T6358产 地：中国大陆
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T9685DS-1971ahypersensitivity,thermal,Sodium Channel,hyperalgesia,Na channels,inhibit,Na+ channels,Inhibi
DS-1971a is a highly potent and selective NaV1.7 inhibitor. DS-1971a exhibits a favorable toxicological profile and analgesic effects.
价 格：￥电议型 号：T9685产 地：中国大陆
