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T27759KY1022；化合物 T27759KY1022
KY1022 is a ras destabilizer. KY1022 targets the Wnt/?-catenin pathway and inhibits development of metastatic colorectal cancer.
价 格：￥电议型 号：T27759产 地：中国大陆
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T27758KW-7158；化合物 T27758KW 7158；KW 7158
KW-7158, a potassium channel activator, is used potentially for the treatment of urinary urgency and frequency.
价 格：￥电议型 号：T27758产 地：中国大陆
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T27757Kv1.5-IN-IIII；化合物 T27757Kv1.5INIIII|||Kv1.5INIV|||Compound IIII|||Kv1.5IN4|||Compound 4；Kv1.5INIIII|
Kv1.5-IN-IIII is a potent inhibitor of Kv1.5.
价 格：￥电议型 号：T27757产 地：中国大陆
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T27756KUNG94；化合物 T27756KUNG 94|||KUNG-94；KUNG 94|||KUNG-94
KUNG94 is a potent and selective inhibitor of Glucose regulated protein 94 (Grp94) (IC50 = 8 nM), the endoplasmic reticulum resident of the 90 kDa heat shock protein (Hsp90) family.
价 格：￥电议型 号：T27756产 地：中国大陆
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T27755KUNG38；化合物 T27755KUNG-38|||KUNG 38；KUNG-38|||KUNG 38
KUNG38 is a purine-based inhibitor of Grp94.
价 格：￥电议型 号：T27755产 地：中国大陆
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T27754KUL-7211；化合物 T27754KUL7211|||KUL 7211；KUL7211|||KUL 7211
KUL-7211 is an β2 and β3 adrenergic receptor agonist. KUL-7211 is a potent ureteral relaxant with a relatively small hypotensive effect.
价 格：￥电议型 号：T27754产 地：中国大陆
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T27753KT-362 fumarateKT-362富马酸盐KT 362|||KT362|||KT-362
KT-362 fumarate is a novel compound that acts as an antagonist of calcium channels, potassium channels and sodium channels.KT-362 fumarate causes vasodilation by affecting intracellular calcium mobilization in atrial muscle cells.KT-362 fumarate has a relaxing effect on femoral and basilar artery strips in rabbits.
价 格：￥电议型 号：T27753产 地：中国大陆
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T27752KT109化合物 T27752KT-109|||KT 109
KT109 is a selective inhibitor of DAGLβ (IC50 = 42 nM). KT109-treated wild-type mice displayed reductions in LPS-induced allodyni as well as in DAGL-β (-/-) micea. Repeated KT109 administration prevented the expression of LPS-induced allodynia, without evidence of tolerance. Intraplantar injection of KT109 into the LPS-treated paw, but not the contralateral paw, reversed the allodynic responses. KT109 also reversed allodynia in the CCI and CINP models and lacked discernible side effects (e.g. an
价 格：￥电议型 号：T27752产 地：中国大陆
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T27751KSK-120；化合物 T27751KSK120|||KSK 120；KSK120|||KSK 120
KSK-120 is a potent Chlamydia trachomatis inhibitor, it targets the glucose-6-phosphate (G-6P) metabolism pathway of Chlamydia trachomatis.
价 格：￥电议型 号：T27751产 地：中国大陆
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T27750KSJ0001；化合物 T27750KSJ-0001|||KSJ 0001；KSJ-0001|||KSJ 0001
KSJ0001, a HBV virus inhibitor, inhibits HBV replication in transfected Huh7 cells.
价 格：￥电议型 号：T27750产 地：中国大陆
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T2775Baicalin；黄芩苷Baicalein 7-O-β-D-glucuronide；黄芩苷|||黄岑苷|||Baicalein 7-O-β-D-glucuronide
Baicalin (Baicalein 7-O-β-D-glucuronide) is a prolyl endopeptidase inhibitor isolated from scutellaria baicalensis, with antioxidant, anti-tumor, anti-HIV properties.
价 格：￥电议型 号：T2775产 地：中国大陆
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T2774LLycorine hydrochloride monohydrate；化合物 T2774LLycorine hydrochloride monohydrate
Lycorine hydrochloride monohydrate is a bioactive chemical.
价 格：￥电议型 号：T2774L产 地：中国大陆
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T27749KRP-297；化合物 T27749KRP297|||MK-0767|||L410198|||L 410198；KRP297|||MK-0767|||L410198|||L 410198
KRP297 is a PPAR agonist potentially for the treatment of type 2 diabetes and dyslipidemia.
价 格：￥电议型 号：T27749产 地：中国大陆
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T27748LKRP-199 sodium；化合物KRP-199钠盐KRP-199 sodium(221164-28-9 Free base)；KRP-199 sodium(221164-28-9 Free bas
KRP-199 sodium sodium is highly potent and selective for AMPA-R in vitro and exhibits good neuroprotection in vivo.
价 格：￥电议型 号：T27748L产 地：中国大陆
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T27748KRP-199；化合物 T27748KRP-199
KRP-199, a highly potent and selective antagonist for the AMPA receptors, exhibits good neuroprotective effects in vivo.
价 格：￥电议型 号：T27748产 地：中国大陆
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T27747KRP-109；化合物 T27747KRP 109|||KRP109；KRP 109|||KRP109
KRP-109, a neutrophil elastase (NE) inhibitor, acts by decreasing expression of TGF-? Signal Related Genes.
价 格：￥电议型 号：T27747产 地：中国大陆
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T27746KRP-101；化合物 T27746KRP 101；KRP 101
KRP-101, a PPARɑ agonist, is used potentially for the treatment of diabetes and hyperlipidaemia.
价 格：￥电议型 号：T27746产 地：中国大陆
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T27745KRN 5500；化合物 T27745SPK-241|||NSC-650426|||SPK241|||KRN-5500|||NSC650426|||KRN5500；SPK-241|||NSC-6504
KRN 5500, a derivative of the nucleoside antibiotic spicamycin, has a wide range of antitumor activity against human cancer cell lines.
价 格：￥电议型 号：T27745产 地：中国大陆
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T27744KRM-II-81；化合物 T27744KRM-II81|||KRM-II 81；KRM-II81|||KRM-II 81
KRM-II-81 is a γ-Aminobutyric Acid Type A (GABAA) Receptor Ligand. KRM-II-81 exhibits improved anxiolytic-like effects in a mouse marble burying assay and a rat Vogel conflict test.
价 格：￥电议型 号：T27744产 地：中国大陆
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T27743KRH-594 free acid；化合物 T27743WK14922K|||WK-1492|||WK-14922K|||WK1492；WK14922K|||WK-1492|||WK-14922K||
KRH-594 is a potent, specific and insurmountable AT1 receptor antagonist. KRH-594 ameliorates hyperlipidaemia and nephropathy in diabetic spontaneously hypertensive rats. KRH-594 prevents end-organ damage in stroke-prone spontaneously hypertensive/Izm rats.
价 格：￥电议型 号：T27743产 地：中国大陆
