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T10542Bifeprunox；化合物 T10542Bifeprunox
Bifeprunox is a potent partial agonist of dopamine D2-like and 5-HT1A receptor (pEC50: 6.37 for hippocampus 5-HT1A; pKis: 7.19 and 8.83 for cortex 5-HT1A and striatum D2). It is an antipsychotic for the research of schizophrenia.
价 格：￥电议型 号：T10542产 地：中国大陆
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T10541Bicyclomycin benzoate；化合物 T10541FR2054；FR2054|||CS-6253
Bicyclomycin benzoate, an antibiotic, exhibits activity against a broad spectrum of Gram-negative/Gram-positive bacteria.
价 格：￥电议型 号：T10541产 地：中国大陆
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T10540BIBP3226 TFA；化合物 T10540BIBP3226 TFA
BIBP3226 TFA is an effective and selective antagonist of neuropeptide Y Y1 (NPY Y1) and neuropeptide FF (NPFF) receptor (Kis: 1.1, 79, and 108 nM for rNPY Y1, hNPFF2, and rNPFF).
价 格：￥电议型 号：T10540产 地：中国大陆
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T10539BIBO3304 TFA；化合物BIBO3304 TFABIBO3304 TFA
BIBO3304 TFA is an effective, orally active, and selective neuropeptide Y (NPY) Y1 receptor antagonist (IC50:0.38 and 0.72 nM for the human and the rat Y1 receptor).
价 格：￥电议型 号：T10539产 地：中国大陆
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T10530BF 227；化合物 T10530BF 227
BF 227 is a candidate for an amyloid imaging probe for PET (Ki: 4.3 nM for Aβ1-42 fibrils).
价 格：￥电议型 号：T10530产 地：中国大陆
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T1053Mebeverine hydrochloride；盐酸麦皮凡林Colofac Hydrochloride|||Duspatalin Hydrochloride|||Duspatal Hydrochlo
Mebeverine hydrochloride (Colofac Hydrochloride), a β-phenylethylamine derivative, is a potent α1 repector inhibitor, relaxing the muscles in and around the gut.
价 格：￥电议型 号：T1053产 地：中国大陆
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T10529BF-168化合物 T10529BF168|||BF 168
BF-168 is a candidate probe for PET and specifically recognizes both neuritic and diffuse plaques (Ki: 6.4 nM for Aβ1-42).
价 格：￥电议型 号：T10529产 地：中国大陆
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T10526β-NF-JQ1；化合物β-NF-JQ1β-NF-JQ1
β-NF-JQ1 is a PROTAC that recruits aryl hydrocarbon receptor E3 (AhR E3) ligase to target proteins. β-NF-JQ1 uses β-NF as an AhR ligand to target bromodomain (BRD)-containing proteins and induce AhR and BRD protein interactions. β-NF-JQ1 shows potent anticancer activity associated with protein knockdown activity. .
价 格：￥电议型 号：T10526产 地：中国大陆
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T10515Anti-Heart Failure Agent 1；化合物 T10515Anti-Heart Failure Agent 1
Anti-Heart Failure Agent 1 is an orally available compound suitable for the treatment of heart failure without inducing vomiting, nausea, and restlessness.
价 格：￥电议型 号：T10515产 地：中国大陆
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T10514FR252384；化合物 T10514FR252384
FR252384 is an antagonist of the neuropeptide Y-Y5 receptor (IC50: 2.3 nM).
价 格：￥电议型 号：T10514产 地：中国大陆
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T10511Anti-hypertensive sulfonanilide 1；化合物 T10511Anti-hypertensive sulfonanilide 1
Anti-hypertensive sulfonanilide 1 is an antihypertensive compound.
价 格：￥电议型 号：T10511产 地：中国大陆
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T10509Xanthine oxidase-IN-1；黄嘌呤氧化酶IN14-(3-Cyano-5,6-difluoroindol-1-yl)-2-hydroxybenzoic acid；4-(3-Cyano-5
Xanthine oxidase-IN-1 is an effective inhibitor of xanthine oxidase with an IC50 value of 6.5 nM. It plays a central role in purine catabolism through the degradation of bioactive nucleotides facilitated by nucleic acid and nucleotide intermediates.
价 格：￥电议型 号：T10509产 地：中国大陆
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T10501YM158 free base；化合物 T10501YM-57158；YM-57158
YM158 free base is a potent and selective antagonist of TXA2 and LTD4 receptor (pA2s: about 8.81 and 8.87).
价 格：￥电议型 号：T10501产 地：中国大陆
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T10495LBefiradol化合物 T10495LNLX-112|||F13640
Befiradol (NLX-112) is an agonist of 5-HT1A receptor.
价 格：￥电议型 号：T10495L产 地：中国大陆
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T10483Lisaftoclax；化合物LisaftoclaxBcl-2/Bcl-xl inhibitor 1|||APG-2575；Bcl-2/Bcl-xl inhibitor 1|||APG-2575
Lisaftoclax (Bcl-2/Bcl-xl inhibitor 1) is an oral dual inhibitor of Bcl-2 and Bcl-xl, with IC50 values of 2 nM and 5.9 nM for Bcl-2 and Bcl-xl, respectively. Lisaftoclax is used to treat chronic lymphocytic leukemia (CLL) by inhibiting the action of the BCL-2 protein, which promotes the death of leukemia cells.
价 格：￥电议型 号：T10483产 地：中国大陆
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T10482LBB-Cl-Amidine hydrochloride化合物 T10482LBB-Cl-Amidine hydrochloride (1802637-39-3 free base)
BB-Cl-Amidine hydrochloride is an inhibitor of peptidylarginine deminase (PAD) [1].
价 格：￥电议型 号：T10482L产 地：中国大陆
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T10472LBay 65-1942 free base；化合物 T10472LBay 65-1942 free base
Bay 65-1942 free base is an inhibitor of ATP-competitive and selective IKKβ.
价 格：￥电议型 号：T10472L产 地：中国大陆
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T10472Bay 65-1942 (R form)；化合物 T10472Bay 65-1942 R form；Bay 65-1942 R form
Bay 65-1942 R form is the less active R-form of Bay 65-1942. Bay 65-1942 is a selective and ATP-competitive IKKβ inhibitor.
价 格：￥电议型 号：T10472产 地：中国大陆
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T10468Elimusertib hydrochloride(1876467-74-1 free base)；化合物 Elimusertib hydrochlorideBAY-1895344 hydrochlo
Elimusertib hydrochloride(1876467-74-1 free base) (BAY-1895344 hydrochloride) is a effective, orally available and selective ATR inhibitor with anti-tumor activity.
价 格：￥电议型 号：T10468产 地：中国大陆
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T10463LBax inhibitor peptide V5 acetate；化合物T10463LBax inhibitor peptide V5 acetate（579492-81-2 free base)；B
Bax inhibitor peptide V5 acetate (Bax inhibitor peptide V5 acetate（579492-81-2 free base)) is a Bax-mediated apoptosis inhibitor, used for cancer treatment.
价 格：￥电议型 号：T10463L产 地：中国大陆
