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T76788Demcizumab登赛珠单抗OMP 21M18
Demcizumab (OMP 21M18) is an anti-DLL4 monoclonal antibody. Demcizumab is a potent Notch pathway inhibitor. Demcizumab is effective in multiple cancer models, both alone and in combination with chemotherapy agents.
价 格：￥电议型 号：T76788产 地：中国大陆
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T76006Tirzepatide TFA；化合物 Tirzepatide TFATirzepatide TFA(2023788-19-2 free base)|||LY3298176 TFA；Tirzepati
Tirzepatide TFA (LY3298176 TFA), a dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist, is under development for type 2 diabetes treatment [1].
价 格：￥电议型 号：T76006产 地：中国大陆
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T75788α-CGRP(human) TFA；化合物 α-CGRP(human) TFAα-CGRP(human) TFA
α-CGRP(human) TFA is a 37-amino acid regulatory neuropeptide that is extensively located within the central and peripheral nervous system, functioning as a potent vasodilator [1].
价 格：￥电议型 号：T75788产 地：中国大陆
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T74788FtsZ-IN-5；化合物 FtsZ-IN-5FtsZ-IN-5
FtsZ-IN-5 is a potent inhibitor of FtsZ, promoting polymerization while inhibiting its GTPase activity, thereby preventing bacterial division and leading to cell death. It exhibits bactericidal activity without significant induction of bacterial resistance, alongside rapid bactericidal effectiveness. Furthermore, FtsZ-IN-5 demonstrates low hemolytic activity and minimal cytotoxicity towards mammalian cells [1].
价 格：￥电议型 号：T74788产 地：中国大陆
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T72788EGFR/C797S-IN-1；化合物 EGFR/C797S-IN-1EGFR/C797S-IN-1
EGFR/C797S-IN-1 is a potent inhibitor targeting the EGFR-C797S mutation, demonstrated by its IC 50 value of 0.128 ?M. This compound exhibits significant anti-proliferative and anti-tumor effects by inhibiting p-EGFR expression in a dose-dependent manner.
价 格：￥电议型 号：T72788产 地：中国大陆
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T72141Ceftobiprole medocaril sodium；化合物 Ceftobiprole medocaril sodiumBAL5788 sodium；头孢比普酯钠盐|||BAL5788 sodi
Ceftobiprole medocaril sodium (BAL5788) is a parenteral prodrug of Ceftobiprole, a pyrrolidinone cephalosporin administered intravenously. As a broad-spectrum cephalosporin, Ceftobiprole exhibits high in vitro activity against methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant Staphylococci (VRSA), and penicillin-resistant Streptococci. Additionally, it is effective in inhibiting both gram-positive and gram-negative pathogens.
价 格：￥电议型 号：T72141产 地：中国大陆
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T71788Hordenine hydrochloride；化合物 Hordenine hydrochlorideHordenine hydrochloride
Hordenine hydrochloride is a biochemical that inhibits the activity of PDK3, inhibits quorum sensing, and acts as an antibiofilm agent against bacteria.
价 格：￥电议型 号：T71788产 地：中国大陆
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T71355MDL-27788；化合物 MDL-27788MDL-27788
MDL-27788 is a tricyclic inhibitor.
价 格：￥电议型 号：T71355产 地：中国大陆
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T71273CAY10788；化合物 CAY10788CAY10788
CAY10788 is an antagonist of CysLT1 receptor.
价 格：￥电议型 号：T71273产 地：中国大陆
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T70788KST012174 HCl；化合物 KST012174 HClKST012174 HCl
KST012174 is a HIF-1α inhibitor. KST012174 involves in the HIF-1α/p300 protein?protein interaction.
价 格：￥电议型 号：T70788产 地：中国大陆
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T70600BRD-7880；化合物 BRD-7880BRD-7880
BRD-7880 is a potent and highly specific inhibitor of aurora kinases B and C.
价 格：￥电议型 号：T70600产 地：中国大陆
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T69788Daledalin；化合物 DaledalinDaledalin
Daledalin is an antidepressant which was synthesized and trialed for depression in the early 1970s, but was never marketed. It is a selective norepinephrine reuptake inhibitor, with no significant effects on the reuptake of serotonin and dopamine, and no antihistamine or anticholinergic properties.
价 格：￥电议型 号：T69788产 地：中国大陆
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T69704FK788；化合物 FK788FK788
FK788 is a diphenylcarbamate derivative that functions as a highly potent and selective IP agonist.
价 格：￥电议型 号：T69704产 地：中国大陆
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T69617ER-67880；化合物 ER-67880ER-67880
ER-67880 is a novel and potent microtubule inhibitor with potential anticancer activity.
价 格：￥电议型 号：T69617产 地：中国大陆
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T69411CNS-5788；化合物 CNS-5788CNS-5788
CNS-5788 is a potential ischemia-selective N-methyl-D-aspartate (NMDA) receptor ion-channel blocker
价 格：￥电议型 号：T69411产 地：中国大陆
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T69371BMS 378806；化合物 BMS 378806BMS 378806
BMS-378806 is an orally bioavailable HIV-1 inhibitor that interferes with gp120-CD4 interaction.
价 格：￥电议型 号：T69371产 地：中国大陆
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T6915Darolutamide；化合物DarolutamideODM-201|||BAY-1841788；ODM-201|||BAY-1841788
Darolutamide (BAY-1841788) is an androgen receptor (AR) antagonist that blocks AR nuclear translocation (Ki: 11 nM).
价 格：￥电议型 号：T6915产 地：中国大陆
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T68788Ellipticine quinone；化合物 Ellipticine quinoneEllipticine quinone
Ellipticine quinone, also known as NSC-383230, is a Drp1 inhibitor. rpitor1 and Drpitor1a inhibited the GTPase activity of Drp1 without inhibiting the GTPase of dynamin 1. Ellipticine quinone showed greater potency than the current std. Drp1 GTPase inhibitor, mdivi-?1, (IC50 for mitochondrial fragmentation are (0.06, and 10 μM, resp.)?. Ellipticine quinone suppressed lung cancer tumor growth in a mouse xenograft model. Ellipticine quinone also inhibited mitochondrial ROS prodn., prevented mi
价 格：￥电议型 号：T68788产 地：中国大陆
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T67889N-(1-((2-amino-2-oxoethyl)amino)-5-(isopropylamino)-1-oxopentan-2-yl)-1-(19-amino-7-(2-amino-2-oxoet
N-(1-((2-amino-2-oxoethyl)amino)-5-(isopropylamino)-1-oxopentan-2-yl)-1-(19-amino-7-(2-amino-2-oxoethyl)-10-(4-amino-4-oxobutyl)-16-benzyl-13-(sec-butyl)-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaazacycloicosane-4-carbonyl)pyrrolidine-2-carboxamide has a wide range of applications in life science related research.
价 格：￥电议型 号：T67889产 地：中国大陆
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T67888LSamidorphan HCl；沙米多芬盐酸盐Samidorphan HCl（852626-89-2 free base）；Samidorphan HCl（852626-89-2 free base）
Samidorphan HCl is an orally active and highly potent modulator of the opioid system that binds to μ‐opioid, κ‐opioid, and delta-opioid receptors. Samidorphan HCl is a novel μ-opioid receptor antagonist, a partial agonist for k-opioid and delta-opioid receptors. Samidorphan HCl can be used to prevent and treat schizophrenia.
价 格：￥电议型 号：T67888L产 地：中国大陆
