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T7378BRD9539Histone Methyltransferase,chromatin,PRC2,BRD9539,G9a,senescent,BRD-9539,BRD 9539,inhibit,H3K9
BRD9539 is an inhibitor of euchromatin histone methyltransferase 2 (EHMT2), also known as G9a, with an IC50 value of 6.3 μM
价 格：￥电议型 号：T7378产 地：中国大陆
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T7787BMS817378BMS817378,BMS-817378
BMS817378 is a potent and selective inhibitor of MET(IC50 : 1.7 nM).
价 格：￥电议型 号：T7787产 地：中国大陆
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T3046BMY 7378 dihydrochlorideBMY7378 HCl
BMY-7378, α1D-adrenergic receptor antagonist, is a weak partial agonist/antagonist of 5-HT1A receptor.
价 格：￥电议型 号：T3046产 地：中国大陆
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T2699BMS 777607BMS777607；BMS-777607；BMS 817378
BMS-777607 is a Met-related inhibitor for c-Met/Axl/Ron/Tyro3 (IC50: 3.9/1.1/1.8/4.3 nM). BMS-777607 has been investigated for the basic science of Malignant Solid Tumour.
价 格：￥电议型 号：T2699产 地：中国大陆
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T7787BMS817378化合物BMS817378[3-[[4-((2-氨基-3-氯吡啶-4-基)氧基)-3-氟苯基]氨基甲酰基]-5-(4-氟苯基)-4-氧代-4H-吡啶-1-基]甲基磷酸二氢酯
BMS817378 is a potent and selective inhibitor of MET(IC50 : 1.7 nM).
价 格：￥电议型 号：T7787产 地：中国大陆
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T737895(S)-HETE；化合物 5(S)-HETE5(S)-HETE
5(S)-HETE, an endogenous metabolite found in the blood, is utilized in researching Rheumatoid Arthritis, Rhinitis, and Asthma [1] [2].
价 格：￥电议型 号：T73789产 地：中国大陆
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T73785D-Fructose-6-phosphate；化合物 D-Fructose-6-phosphateD-Fructose-6-phosphate
D-Fructose 6-phosphate, an endogenous metabolite found in saliva, holds potential for Lewy Body Dementia research [1] [2].
价 格：￥电议型 号：T73785产 地：中国大陆
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T73783D-Ribofuranose；化合物 D-RibofuranoseD-Ribofuranose
D-Ribofuranose (D-Ribose), an endogenous metabolite found in cerebrospinal fluid, serves as a research tool for studying Ribose 5 Phosphate Isomerase Deficiency and Medium Chain Acyl Co A Dehydrogenase Deficiency [1] [2].
价 格：￥电议型 号：T73783产 地：中国大陆
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T73782Prostaglandin J2；化合物 Prostaglandin J2Prostaglandin J2
Prostaglandin J2 (PGJ2), a derivative of Prostaglandin D2 (PGD2), serves as a potent agonist for PGD2 receptors (DP), exhibiting affinity constants (K i) of 0.9 nM and 6.6 nM for hDP and hCRTH2 receptors, respectively. It activates cyclic AMP production with an EC50 of 1.2 nM, induces oxidative stress, neuronal apoptosis, and promotes the accumulation of ubiquitinated (Ub) proteins. Notably, PGJ2´s neurotoxic properties are implicated in the progression of neurodegenerative diseases such a
价 格：￥电议型 号：T73782产 地：中国大陆
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T7378011β-Hydroxyandrosterone；化合物 11β-Hydroxyandrosterone11β-Hydroxyandrosterone
11β-Hydroxyandrosterone, an 11-oxygenated androgen metabolite, is derived from 11β-hydroxyandrostenedione [1] [2].
价 格：￥电议型 号：T73780产 地：中国大陆
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T7378BRD9539；化合物BRD9539BRD9539
BRD9539 is an inhibitor of euchromatin histone methyltransferase 2 (EHMT2), also known as G9a, with an IC50 value of 6.3 μM
价 格：￥电议型 号：T7378产 地：中国大陆
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T71164CXN37378；化合物 CXN37378CXN37378
CXN37378, also known as NAP, is a potent and selective antagonist for the μ-opioid receptor (MOR). This product has no formal name at the moment. For the convenience of communication, a temporary code name was therefore proposed according to MedKoo Chemical Nomenclature (see web page: https://www.medkoo.com/page/naming).
价 格：￥电议型 号：T71164产 地：中国大陆
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T673783-Bromocinnamic acid, predominantly trans；化合物 3-Bromocinnamic acid, predominantly trans3-Bromocinnam
3-Bromocinnamic acid, predominantly trans is a useful organic compound for research related to life sciences and the catalog number is T67378.
价 格：￥电议型 号：T67378产 地：中国大陆
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T37378Propofol β-D-Glucuronide；Propofol β-D-GlucuronidePropofol β-D-Glucuronide
Propofol β-D-glucuronide is a metabolite of propofol sulfate , a short-acting anesthetic agent. [1] [2] The metabolite is generated through the glucuronidation of propofol by uridine diphosphate glucuronosyltransferases. Propofol metabolism appears to occur more rapidly in women than men. [1]
价 格：￥电议型 号：T37378产 地：中国大陆
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T3046BMY 7378 dihydrochloride；化合物BMY 7378 dihydrochlorideBMY7378 HCl；BMY7378 HCl
BMY 7378 dihydrochloride (BMY7378 HCl) , α1D-adrenergic receptor antagonist, is a weak partial agonist/antagonist of 5-HT1A receptor.
价 格：￥电议型 号：T3046产 地：中国大陆
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T27378FR-193879；化合物 T27378FR193879；FR193879
FR-193879 is an efficacious cephem derivative, it has extremely potent therapeutic efficacy against H. pylori.
价 格：￥电议型 号：T27378产 地：中国大陆
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T2699BMS 777607；化合物BMS-777607BMS777607|||BMS-777607|||BMS 817378；BMS777607|||BMS-777607|||BMS 817378
BMS 777607 (BMS 817378) is a Met-related inhibitor for c-Met/Axl/Ron/Tyro3 (IC50: 3.9/1.1/1.8/4.3 nM). BMS-777607 has been investigated for the basic science of Malignant Solid Tumour.
价 格：￥电议型 号：T2699产 地：中国大陆
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T17378Ald-Ph-amido-C2-nitrate；化合物 T17378Ald-Ph-amido-C2-nitrate
Ald-Ph-amido-C2-nitrate (Example XXIVb) is a thiazolidine derivative primarily employed as a noncleavable ADC linker[1].
价 格：￥电议型 号：T17378产 地：中国大陆
