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T13592,3-Dihydrobenzofuranyl-5-acetic acid；2,3-二氢苯并呋喃-5-乙酸2,3-Dihydrobenzofuranyl-5-acetic acid
2,3-Dihydro-5-benzofuranacetic Acid is used as Pharmaceutical material and intermeidates.
价 格：￥电议型 号：T1359产 地：中国大陆
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T13559Astragaloside VI；化合物 T13559Astragaloside VI
Astragaloside VI could improve wound healing by activating the EGFR/ERK signaling pathway.
价 格：￥电议型 号：T13559产 地：中国大陆
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T13459(+)-Apogossypol；化合物 T13459Apogossypol|||NSC736630；Apogossypol|||NSC736630
(+)-Apogossypol is an antagonist of pan-BCL-2. (+)-Apogossypol binds to Mcl-1(Bcl-2 and Bcl-xL with EC50s of 2.6, 2.8 and 3.69 μM, respectively).
价 格：￥电议型 号：T13459产 地：中国大陆
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T13413Zoniporide hydrochloride hydrate；化合物 T13413CP-597396 hydrochloride hydrate；CP-597396 hydrochloride h
Zoniporide hydrochloride hydrate is a potent and selective sodium-hydrogen exchanger type 1 (NHE-1) inhibitor. Zoniporide hydrochloride hydrate inhibits human NHE-1 with IC50 of 14 nM.
价 格：￥电议型 号：T13413产 地：中国大陆
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T13409LZK824859 hydrochloride (2271122-53-1 free base)；化合物 T13409LZK824859 hydrochloride；ZK824859 hydrochlo
ZK824859 hydrochloride is an oral available and selective inhibitor of urokinase plasminogen activator (uPA)(IC50s of 79 nM, 1580 nM and 1330 nM for human uPA, tPA, and plasmin, respectively).
价 格：￥电议型 号：T13409L产 地：中国大陆
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T13409ZK824859；化合物 T13409ZK824859
ZK824859 is an oral available and selective inhibitor of urokinase plasminogen activator (uPA)(IC50s of 79 nM, 1580 nM and 1330 nM for human uPA, tPA, and plasmin, respectively).
价 格：￥电议型 号：T13409产 地：中国大陆
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T13400Ziprasidone D8；化合物 T13400CP-88059 D8；CP-88059 D8
Ziprasidone D8 is deuterium labeled Ziprasidone, which is a antagonist of combined 5-HT (serotonin) and dopamine receptor and exhibits potent effects of antipsychotic activity.
价 格：￥电议型 号：T13400产 地：中国大陆
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T13359XPC-6444；化合物 T13359XPC-6444
XPC-6444 is a isoform-selective, and CNS-penetrant inhibitor of NaV1.6 with IC50 of41 nM for hNaV1.6,with anticonvulsant activity.
价 格：￥电议型 号：T13359产 地：中国大陆
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T13330WAY-213613 hydrochloride；化合物WAY-213613 hydrochlorideWAY-213613 hydrochloride (868359-05-1 free base)
WAY-213613 hydrochloride is a potent, selective nonsubstrate reuptake inhibitor of GLT-1/EAAT2 with IC 50 of 85 nM. WAY-213613 hydrochloride inhibits EAAT1 and EAAT3 with IC50 values of 5 and 3.8 microM, respectively. WAY-213613 hydrochloride shows no activity at ionotropic and metabotropic glutamate receptors. It is a potential tool for the elucidation of EAAT2 function and can be used for the research of central nervous system [1] [2].
价 格：￥电议型 号：T13330产 地：中国大陆
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T13320VU591 hydrochloride；化合物VU591 hydrochlorideVU591 hydrochloride
VU591 hydrochloride is a selective renal outer medullary potassium channel (Kir1.1, ROMK) antagonist (IC50：0.24 μM). Thought to block the intracellular pore of the Kir1.1 channel. Exhibits no effect on Kir7.1 at concentrations up to 10 μM; does not inhibit Kir2.1, Kir2.3 or Kir4.1. Displays similar potency to VU 590
价 格：￥电议型 号：T13320产 地：中国大陆
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T13294Veledimex (S enantiomer)；化合物 T13294RG-115932 S enantiome|||INXN-1001 S enantiome；RG-115932 S enantio
Veledimex S enantiomer is the S enantiomer of veledimex. Veledimex is an oral activator ligand for a proprietary gene therapy promoter system and CYP3A4/5 inhibitor.
价 格：￥电议型 号：T13294产 地：中国大陆
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T13293LVeledimex；化合物 T13293LRG-115932|||INXN-1001；RG-115932|||INXN-1001
Veledimex is an oral activator ligand for a proprietary gene therapy promoter system. It is also a moderate inhibitor of and substrate for CYP3A4/5.
价 格：￥电议型 号：T13293L产 地：中国大陆
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T13293Veledimex racemate；化合物 T13293RG-115932 racemate|||INXN-1001 racemate；RG-115932 racemate|||INXN-1001
Veledimex racemate, the racemic form of veledimex, is an orally available, small-molecule ligand that activates the RheoSwitch Therapeutic System.
价 格：￥电议型 号：T13293产 地：中国大陆
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T13285Vatinoxan hydrochloride；化合物 T13285MK-467 hydrochloride|||L-659066 hydrochloride；MK-467 hydrochloride
Vatinoxan hydrochloride is an antagonist of the peripheral α2 adrenergic receptors.
价 格：￥电议型 号：T13285产 地：中国大陆
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T13259URAT1 inhibitor 1；化合物 T13259URAT1 inhibitor 1
URAT1 inhibitor 1 (1g) is an inhibitor of uric acid transporter 1 (URAT1) (IC50: 32 nM), has the potential to treat hyperuricemia associated with gout.
价 格：￥电议型 号：T13259产 地：中国大陆
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T13186LTL02-59 dihydrochloride；化合物 T13186LTL02-59 dihydrochloride
TL02-59 dihydrochloride is an orally active inhibitor of Src-family kinase Fgr (IC50: 0.03 nM).
价 格：￥电议型 号：T13186L产 地：中国大陆
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T13186TL02-59；化合物TL02-59TL02-59
TL02-59 is a selective inhibitor of Fgr in Src-family kinase (IC50 = 0.03 nM). TL02-59 inhibits Lyn and Hck with IC50s of 0.1 nM and 160 nM, respectively. TL02-59 potently suppresses acute myelogenous leukemia cell growth.
价 格：￥电议型 号：T13186产 地：中国大陆
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T13181Tolcapone D7；化合物 T13181Ro 40-7592 D7；Ro 40-7592 D7
Tolcapone D7 is a deuterium-labeled Tolcapone. Tolcapone is a selective and orally active inhibitor of COMT.
价 格：￥电议型 号：T13181产 地：中国大陆
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T131724Compound TBBP03959；化合物 TBBP03959Compound TBBP03959
Compound TBBP03959 is a useful organic compound for research related to life sciences. The catalog number is T131724 and the CAS number is 38419-75-9.
价 格：￥电议型 号：T131724产 地：中国大陆
