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T8162Cannabidivarininhibit,Cannabidivarin,Inhibitor,GWP-42006,非拟精神病药大麻素,GWP42006,GWP 42006
Cannabidivarin is a potent inhibitor against gamma 2 subunit of GABAA receptors. it may serve as a novel drug with definite control over childhood absence epilepsy.
价 格：￥电议型 号：T8162产 地：中国大陆
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TN1420Bacopaside Iinhibit,Inhibitor,Bacopaside I
Bacopaside I is a saponin isolated from Bacopa monniera. Bacopaside I is a modulator of Aquaporin-1 channel, has neuroprotective functions, it has anti-Alzheimer´s disease, it ameliorates cognitive impairment in APP/PS1 mice via immune-mediated clearance of α2-amyloid,exbibits antioxidant properties and free radical scavenging capacity and exerts antidepressant-like effect.
价 格：￥电议型 号：TN1420产 地：中国大陆
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T7420ValifenalateIR-5885,Inhibitor,Valifenalate,inhibit,IR 5885,Bacterial
Valifenalate is antifungal agent, effective against various types of mildew
价 格：￥电议型 号：T7420产 地：中国大陆
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T6828ZL0420inhibit,Epigenetic Reader Domain,(E/Z)-ZL0420,BRD4,airway inflammation,immune response genes,Z
ZL0420 is a potent and selective bromodomain-containing protein 4 ( BRD4 ) inhibitor with nanomolar binding affinities to bromodomains (BDs) of BRD4. ZL0420 has IC 50 values of 27 nM against BRD4 BD1 and 32 nM against BRD4 BD2.
价 格：￥电议型 号：T6828产 地：中国大陆
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T62420P2Y2R/GPR17 antagonist 1
P2Y2R/GPR17 antagonist 1 (Compound 14m) is a dual P2Y2R and GPR17 antagonist. P2Y2R/GPR17 antagonist 1 shows IC50 values of 3.17 ?M and 1.67 ?M against P2Y2R and GPR17, respectively. P2Y2R/GPR17 antagonist 1 shows excellent metabolic stability in human liver microsomes.
价 格：￥电议型 号：T62420产 地：中国大陆
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T9689M4205factor,M-4205,receptor,M4205,cell,CD117,growth,inhibit,mast/stem,mutations,SCFR,c-Kit,M 4205,In
M4205 is an inhibitor of c-Kit exhibiting high activity on c-Kit mutations in exons 11, 13, 17.
价 格：￥电议型 号：T9689产 地：中国大陆
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T7277SB 242084Serotonin Receptor,SB 242084,inhibit,5-HT Receptor,Inhibitor,SB-242084,5-hydroxytryptamine
SB 242084 dihydrochloride hydrate is a psychoactive drug and research chemical which acts as a selective antagonist for the 5HT2C receptor.
价 格：￥电议型 号：T7277产 地：中国大陆
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T22420(S)-Viloxazine Hydrochloride
(S)-Viloxazine Hydrochloride, the S-isomer of Viloxazine. Viloxazine is a selective norepinephrine reuptake inhibitor (NRI) that can be used as an antidepressant.
价 格：￥电议型 号：T22420产 地：中国大陆
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T6420BMS-707035BMS 707035,HIV-1 integrase strand transfer,HIV,Human immunodeficiency virus,antiviral,BMS7
BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.
价 格：￥电议型 号：T6420产 地：中国大陆
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T7392RevefenacinRevefenacin,TD4208,TD 4208,inhibit,Muscarinic acetylcholine receptor,Inhibitor,mAChR,GSK
Revefenacin is a mAChR antagonist has a high affinity on M3 receptor( Ki : 0.18 nM),and potentially useful for the treatment of respiratory disease.
价 格：￥电议型 号：T7392产 地：中国大陆
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T6549Isepamicin sulfateSch 21420,Sch21420,inhibit,Antibiotic,Inhibitor,Bacterial,Isepamicin,Sch-21420,Ise
Isepamicin Sulphate, an aminoglycoside antibacterial with good activity against strains producing type I 6-acetyltransferase, inhibits bacterial protein synthesis by targeting the bacterial 30S ribosomal subunit.
价 格：￥电议型 号：T6549产 地：中国大陆
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T6619Desmethyl Erlotinib hydrochlorideDesmethyl Erlotinib hydrochloride,CP 373420,inhibit,CP-373420,Inhib
OSI-420 (Desmethyl Erlotinib, CP-473420) is an active metabolite of erlotinib which is an orally active EGFR tyrosin kinase inhibitor with IC50 of 2 and 20 nM for human EGFR and EGFR autophosphorylation in tumor cells.
价 格：￥电议型 号：T6619产 地：中国大陆
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T9420prifinium bromideMuscarinic acetylcholine receptor,Prifinium,prifinium bromide,Inhibitor,Anti-spasmo
Prifinium bromide is a quaternary ammon antimuscarinic. It inhibits hyperkinesia of the digestive organs and urinary tract and has a spasmolytic action.
价 格：￥电议型 号：T9420产 地：中国大陆
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T6328Desmethyl ErlotinibO-Desmethyl Erlotinib；OSI-420；CP-473420
OSI-420 is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM).
价 格：￥电议型 号：T6328产 地：中国大陆
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T6283Wortmannin渥曼青霉素；KY-12420；SL-2052
Wortmannin is the first described PI3K inhibitor with IC50 of 3 nM, with little selectivity within the PI3K family. Also blocks autophagosome formation and potently inhibits DNA-PK/ATM with IC50 of 16 nM and 150 nM.
价 格：￥电议型 号：T6283产 地：中国大陆
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T5420Cycloguanil hydrochlorideChloroguanide Triazine；环氯胍盐酸盐
Cycloguanil is an active metabolite of the antimalarial compound proguanil. It acts as an inhibitor of dihydrofolate reductase (Kis: 0.3 and 1.5 nM for Plasmodium and human forms, respectively).
价 格：￥电议型 号：T5420产 地：中国大陆
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T44204-Hydroxytamoxifen(Z)-4-hydroxy Tamoxifen；trans-4-Hydroxytamoxifen；ICI 79280；4-羟基他莫昔芬
4-Hydroxytamoxifen is a selective estrogen receptor modulator (SERM).
价 格：￥电议型 号：T4420产 地：中国大陆
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T4290Preladenant瑞德南特；SCH-420814
Preladenant is an orally bioavailable antagonist of the adenosine A2A receptor (Ki: 1.1 nM) and has >1000-fold selectivity over all other adenosine receptors.
价 格：￥电议型 号：T4290产 地：中国大陆
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T4209TAK-659 hydrochlorideTAK-659
TAK-659 is a potent and selective inhibitor of spleen tyrosine kinase (SYK) with an IC50 value of 3.2 nM. It is selective against most other kinases, but potent toward both SYK and FLT3.
价 格：￥电议型 号：T4209产 地：中国大陆
