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T3168MN-64；化合物MN64MN64；MN64
MN-64 is a tankyrases inhibitor, showed 6 nM potency against tankyrase 1, isoenzyme selectivity, and Wnt signaling inhibition.
价 格：￥电议型 号：T3168产 地：中国大陆
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T30260AZD-5672；化合物AZD-5672AZD 5672|||AZD5672|||UNII-61XQN688TW；AZD 5672|||AZD5672|||UNII-61XQN688TW
AZD-5672 is an antagonist of CCR5 with an IC50 of 0.32 nM. AZD-5672 inhibits hERG cardiac ion channel binding and P-gp-mediated digoxin transport with IC50s of 7.3 μM and 32 μM. AZD-5672 can be used in studies about rheumatoid arthritis.
价 格：￥电议型 号：T30260产 地：中国大陆
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T29158WIN 62,577；化合物 T29158WIN62,577|||WIN-62,577；WIN62,577|||WIN-62,577
WIN 62,577 is a allosteric antagonist of mAChR.
价 格：￥电议型 号：T29158产 地：中国大陆
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T28977Tilisolol HCl；化合物 T28977Tilisolol, trade name Selecal|||N 696|||N-696|||N696；Tilisolol, trade name S
Tilisolol is a nonselective blocker of beta-adrenergic. Tilisolol hydrochloride dilates coronary arteries through an ATP-sensitive K(+)-channel opening mechanism in dogs.
价 格：￥电议型 号：T28977产 地：中国大陆
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T26683AUTEN-67；化合物 T26683Autophagy enhancer 67|||MTMR14 inhibitor|||AUTEN67；Autophagy enhancer 67|||MTMR14
AUTEN-67 is a specific inhibitor of MTMR14 and autophagy enhancer with potent antiaging and neuroprotective effects. AUTEN-67 also delays the onset and decreases the severity of Huntington´s disease.
价 格：￥电议型 号：T26683产 地：中国大陆
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T26266TH-162；化合物 T26266L-PIA|||(R)?-PIA|||(R)?- PIA|||(R)?-?PIA|||L-2-N6-(Phenylisopropyl)adenosine；L-PIA|
TH-162, also known as (R)?-?PIA and Adenosine, N-(1-methyl-2-phenylethyl)-, (R)-, is an agonist of the A1 adenosine receptor. Affinity for adenosine receptors is approx. 100× that of the (+)-isomer.
价 格：￥电议型 号：T26266产 地：中国大陆
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T26237Sulisatin；化合物 T26237DAN 603|||Laxitex|||DAN603|||Sulisatinum|||DAN-603；DAN 603|||Laxitex|||DAN603|||
Sulisatin is a laxative drug. It is hydrolyzed in the large intestine by the intestinal flora to its diphenyl derivative, BHMI, which is responsible for the laxative activity of the drug.
价 格：￥电议型 号：T26237产 地：中国大陆
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T25109ARN-6039；化合物 T25109ARN 6039|||ARN6039；ARN 6039|||ARN6039
ARN-6039 is an orally available inverse agonist of RORγ for Autoimmune Neuroinflammatory Demyelinating Disease. The activity of ARN-6039 against RORγ was demonstrated in a RORγ-activated IL-17A Prom/LUCPorter assay in HEK 293 cells (360 nM) and in IL-17 release from CD4+T cell assays (220 nM).
价 格：￥电议型 号：T25109产 地：中国大陆
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T24605PDE5-IN-6c；化合物 T24605PDE5 inhibitor 6c|||PDE5IN6c；PDE5 inhibitor 6c|||PDE5IN6c
PDE5-IN-6c is a potent and selective inhibitor of PDE5A1.
价 格：￥电议型 号：T24605产 地：中国大陆
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T2223Kinetin；激动素6-Furfuryladenine|||N6-Furfuryladenine；激动素|||6-Furfuryladenine|||6-糠氨基嘌呤|||N6-Furfurylade
Kinetin (N6-Furfuryladenine), a type of cytokinin, has plant growth regulation effects.
价 格：￥电议型 号：T2223产 地：中国大陆
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T20832Dimethenamid；化合物 T20832San 682H|||San-682H|||San682H；San 682H|||San-682H|||San682H
Dimethenamid is a chloroacetamide herbicide.
价 格：￥电议型 号：T20832产 地：中国大陆
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T20638Silthiofam；化合物 T20638MON 65500|||Silthiopham|||Latitude|||MON65500|||MON-65500；MON 65500|||Silthioph
Silthiofam is very effective against Gaeumannomyces graminis var. tritici (Ggt), recently it has been widely used for the take-all control in China. Ggt could cause Wheat take-all.
价 格：￥电议型 号：T20638产 地：中国大陆
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T20476Lauroyl lysine；月桂酰赖氨酸N6-Lauroyl-L-lysine；月桂酰赖氨酸|||N6-Lauroyl-L-lysine
Lauroyl lysine (N6-Lauroyl-L-lysine) functions as skin and hair conditioning agents and as surfactants-cleansing agents in personal care products.
价 格：￥电议型 号：T20476产 地：中国大陆
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T19464N6,N6-DimethyladenosineN6,N6-二甲基腺苷N6,N6-二甲基腺苷
N6,N6-Dimethyladenosine is find in mycobacterium bovis Bacille Calmette-Guérin tRNA.
价 格：￥电议型 号：T19464产 地：中国大陆
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T19455H-L-Lys(Poc)-OH HClH-L-Lys(Poc)-OH 盐酸盐N6-((Prop-2-yn-1-yloxy)carbonyl)-L-lysine hydrochloride|||N-Ε-
N-ε-propargyloxycarbonyl-L-lysine hydrochloride (N6-((Prop-2-yn-1-yloxy)carbonyl)-L-lysine hydrochloride) is a modified amino acid for cancer therapy development.
价 格：￥电议型 号：T19455产 地：中国大陆
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T16678PSN632408；化合物 T16678PSN632408
PSN632408 is an optimized agonist of GPR119 receptors that display similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC50: 5.6 and 7.9 uM, respectively).
价 格：￥电议型 号：T16678产 地：中国大陆
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T16578PRN694；化合物 T16578PRN694
PRN694 shows extended target residence time on ITK and RLK, enabling durable attenuation of effector cells in vitro and in vivo. PRN694 is an irreversible, highly selective, and effective covalent interleukin-2-inducible T-cell kinase (ITK) and resting lymphocyte kinase (RLK) dual inhibitor (IC50s: 0.3 nM and 1.4 nM, respectively).
价 格：￥电议型 号：T16578产 地：中国大陆
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T16263N6-Cyclopentyladenosine；N6-环戊基腺苷酸UK-80882|||CPA；UK-80882|||CPA
N6-Cyclopentyladenosine (CPA) is a selective agonist of the adenosine A1 receptor and can be used to mimic the action of the adenosine A1 receptor, with Ki´s of 2.3 nM, 790 nM, and 43 nM for human A1, A2A, and A3 receptors, respectively.N6-Cyclopentyladenosine (CPA) can be used to modulate cellular signaling and neurotransmission and other biological processes. Cyclopentyladenosine (CPA) is used to regulate cell signaling, neurotransmitter release and other biological processes.
价 格：￥电议型 号：T16263产 地：中国大陆
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T15483LEDGIN6；化合物 T15483HIV-1 integrase inhibitor 2；HIV-1 integrase inhibitor 2
HIV-1 integrase inhibitor 2 is used for the treatment of human immunodeficiency virus (HIV) infection.
价 格：￥电议型 号：T15483产 地：中国大陆
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T13214LTRPV4 agonist-1 free base；化合物TRPV4 agonist-1 free baseOUN67600；OUN67600
TRPV4 agonist-1 free base (OUN67600) is an agonist of transient receptor potential vanilloid 4 (TRPV4;EC50 of 60 nM, in the hTRPV4 Ca2+ assay).
价 格：￥电议型 号：T13214L产 地：中国大陆
