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T15192Eact；化合物EactEact
Eact is a selective and potent TMEM16A activator. It directly activates the TRPV1 channels in sensory nociceptors. Which also produces itch, acute nociception and thermal hypersensitivity.
价 格：￥电议型 号：T15192产 地：中国大陆
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T15191PROTAC ERRα ligand 1；化合物PROTAC ERRα ligand 1PROTAC ERRα ligand 1
PROTAC ERRα ligand 1 is an α (ERRα) antagonist of estrogen-related receptor (IC50s of 0.04 and 2.8 μM for ERRα and ERRγ, respectively).
价 格：￥电议型 号：T15191产 地：中国大陆
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T15190L(S,R,S)-AHPC-PEG4-NH2；化合物T15190LVHL Ligand-Linker Conjugates 4|||E3 ligase Ligand-Linker Conjugates
(S,R,S)-AHPC-PEG4-NH2 (VHL Ligand-Linker Conjugates 4) is a synthetic E3 ligase ligand-linker conjugate comprising a VHL ligand based on (S,R,S)-AHPC and a 4-unit PEG linker.
价 格：￥电议型 号：T15190L产 地：中国大陆
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T15190(S,R,S)-AHPC-PEG4-NH2 hydrochloride；化合物 T15190E3 ligase Ligand-Linker Conjugates 7|||VH032-PEG4-NH2
(S, R, S)-AHPC-PEG4-NH2 hydrochloride is a chemically synthesized conjugate consisting of an E3 ligase ligand-linker, incorporating the VHL ligand based on (S, R, S)-AHPC, and a 4-unit PEG linker, which are specifically designed for use in PROTAC technology.
价 格：￥电议型 号：T15190产 地：中国大陆
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T15189Thalidomide-O-amido-C4-N3；化合物Thalidomide-O-amido-C4-N3E3 ligase Ligand-Linker Conjugates 18|||Cerebl
Thalidomide-O-amido-C4-N3 (Cereblon Ligand-Linker Conjugates 4) is an E3 ligase ligand-linker conjugate incorporating the Thalidomide-based cereblon ligand and a linker.
价 格：￥电议型 号：T15189产 地：中国大陆
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T15188E-?6123；化合物 T15188E-?6123
E-6123 is an antagonist of platelet-activating factor (PAF) receptor.
价 格：￥电议型 号：T15188产 地：中国大陆
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T15187E-5324；化合物 T15187E-5324
E-5324 is potent cholesterol acyltransferase (ACAT) inhibitor (IC50s: 44 to 190 nM).
价 格：￥电议型 号：T15187产 地：中国大陆
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T15186(E)-4-Hydroxytamoxifen；(E)-4-羟基他莫昔芬(E)-4-Hydroxytamoxifen
(E)-4-Hydroxytamoxifen is a less active isomer of (Z)-4-hydroxytamoxifen and also is an estrogen receptor modulator.
价 格：￥电议型 号：T15186产 地：中国大陆
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T15185Lucitanib；德立替尼E-3810；E-3810|||德立替尼
Lucitanib (E-3810) is a novel VEGFR and FGFR inhibitor. It potently and selectively inhibits VEGFR1, VEGFR2, VEGFR3, FGFR1 and FGFR2 (IC50s: 7 nM, 25 nM, 10 nM, 17.5 nM, and 82.5 nM, respectively).
价 格：￥电议型 号：T15185产 地：中国大陆
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T15184E 2012化合物E 2012(E)-1-[(1S)-1-(4-氟苯基)乙基]-3-[3-甲氧基-4-(4-甲基-1H-咪唑-1-YL)亚苄基]哌啶-2-酮
E2012 is a γ-secretase modulator (GSM). E2012 inhibits 3β-hydroxysterol Δ24-reductase (DHCR24) at the final step in the cholesterol biosynthesis. E 2012 aims at Alzheimer´s disease by reduction of amyloid β-42, and induces cataract following repeated doses in the rat.
价 格：￥电议型 号：T15184产 地：中国大陆
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T15183Dynarrestin；化合物DynarrestinDynarrestin
Dynarrestin is a cytoplasmic dynein 1 and 2 aminothiazole inhibitor that reversibly inhibits dynein 1-driven microtubule sliding in vitro and intracellular dynein 1 and 2-dependent processes without affecting ATP hydrolysis and interfering with ciliogenesis .
价 格：￥电议型 号：T15183产 地：中国大陆
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T15182DW-1350；化合物 T15182DW-1350
DW-1350 is an antagonist of LTB4 receptor.
价 格：￥电议型 号：T15182产 地：中国大陆
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T15181DuP-697；化合物DuP-697DuP-697
DuP-697 is an irreversible and specific inhibitor of COX-2 with IC50 values of 10 nM and 800 nM for human COX-2 and COX-1. DuP-697 shows antiproliferative activity with an IC50 of 42.8 nM. DuP-697 exhibits antiangiogenic, anti-inflammatory, antipyretic and apoptotic effects.
价 格：￥电议型 号：T15181产 地：中国大陆
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T15180Duocarmycin A；化合物 T15180Duocarmycin A
Duocarmycin A, an antitumor antibiotic, is a DNA alkylator and efficiently alkylates adenine N3 at the 3′ end of AT-rich sequences in the DNA. Duocarmycin A, as a chemotherapeutic agent, results in HLC-2 cells typically apoptotic changes.
价 格：￥电议型 号：T15180产 地：中国大陆
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T1518Olmesartan Medoxomil；奥美沙坦酯CS 866|||Benicar；奥美沙坦酯|||CS 866|||Benicar
Olmesartan Medoxomil (Benicar) is an angiotensin II type 1 receptor blocker that is used to manage hypertension.
价 格：￥电议型 号：T1518产 地：中国大陆
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T1517LBenserazide；化合物 T1517LRo-44602|||Ro44602|||Ro 44602|||Serazide；Ro-44602|||Ro44602|||Ro 44602|||Seraz
Benserazide is an inhibitor of dopa decarboxylase. It is often given with levodopa in the treatment of Parkinson´s to prevent the conversion of levodopa to dopamine in the periphery, thereby increasing the amount that reaches the central nervous system and reducing the required dose.
价 格：￥电议型 号：T1517L产 地：中国大陆
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T15179DTSSP Crosslinker；化合物DTSSP CrosslinkerDTSSP Crosslinker
DTSSP Crosslinker is a cleavable ADC linker and can be used to synthesize antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15179产 地：中国大陆
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T15178dTRIM24；化合物dTRIM24dTRIM24
dTRIM24 is a selective bifunctional TRIM24 degradation agent based on PROTAC technology, consisting of the ligands von Hippel-Lindau and TRIM24.
价 格：￥电议型 号：T15178产 地：中国大陆
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T15176DSS Crosslinker；双琥珀酰亚胺辛二酸酯DSS Crosslinker
DSS Crosslinker is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).It is a homobifunctional crosslinker that is cell membrane permeable. DSS crosslinker has amine-reactive NHS esters at both ends of an 8-atom (11.4 angstrom) spacer arm that are used to conjugate proteins. DSS crosslinker can be used to conjugate or crosslink intracellular proteins.
价 格：￥电议型 号：T15176产 地：中国大陆
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T15175DSP Crosslinker；化合物DSP CrosslinkerDSP Crosslinker
DSP Crosslinker is a cleavable ADC linker, used in antibody-drug conjugates (ADCs) synthesis[1].
价 格：￥电议型 号：T15175产 地：中国大陆
