Compound E - 搜索结果 | AbMole中文官网

找到约 38 条 “Compound E” 相关结果（用时 0.178 秒）

目录号	产品名称	中文名称	靶点
M2238	Dorsomorphin (Compound C) dihydrochloride	Dorsomorphin (Compound C) dihydrochloride	AMPK
	BML-275 2HCl; Compound C 2HCl
	Dorsomorphin (BML-275)二盐酸盐是一种有效的，可逆的AMPK选择性抑制剂，K_i为109 nM，Dorsomorphin还对BMP有抑制作用。
M5534	Cortisone	可的松	GCR
	17-Hydroxy-11-dehydrocorticosterone; Kendall's compound E
	Cortisone是一种用于治疗感染或过敏的激素药物
M7043	NPS ALX Compound 4a dihydrochloride	NPS ALX Compound 4a dihydrochloride	Others
	NPS ALX Compound 4a dihydrochloride is a potent and selective 5-HT ₆ antagonist.
M9505	Compound E	Compound E	Gamma-secretase/Beta-secretase
	GSI-XXI; γ-secretase inhibitor XXI; γ-Secretase-IN-1
	Compound E 是一种可透过细胞的强效选择性γ-分泌酶（γ-secretase）和Notch抑制剂。
M11655	ChemBridge-5126190	ChemBridge化合物-5126190	Screening Compounds and Building Blocks
	3,7-dihydro-1H-purine-2,6-dione (5126190)
	ChemBridge特有类药化合物/先导化合物-5126190，由AbMole（奥默生物）独家提供。具体售价货期请咨询AbMole（奥默生物）。运费额外计算。
M12301	ChemBridge-5713492	ChemBridge化合物-5713492	Screening Compounds and Building Blocks
	1-(2-chloro-4-nitrophenyl)-4-[(5-methyl-3-phenyl-4-isoxazolyl)carbonyl]piperazine (5713492)
	ChemBridge特有类药化合物/先导化合物-5713492，由AbMole（奥默生物）独家提供。具体售价货期请咨询AbMole（奥默生物）。运费额外计算。
M12806	ChemBridge-6881166	ChemBridge化合物-6881166	Screening Compounds and Building Blocks
	4-[(2-{[1-(4-ethylphenyl)-2,4,6-trioxotetrahydro-5(2H)-pyrimidinylidene]methyl}phenoxy)methyl]benzoic acid (6881166)
	ChemBridge特有类药化合物/先导化合物-6881166，由AbMole（奥默生物）独家提供。具体售价货期请咨询AbMole（奥默生物）。运费额外计算。
M20547	Rabeprazole Related Compound E	Rabeprazole Related Compound E	Proton Pump
	Rabeprazole thioether; Rabeprazole Sulfide
	Rabeprazole Related Compound E是 Rabeprazole 的活性代谢产物，同时也是一种具有口服活性的质子泵抑制剂，能通过与胃壁细胞中的 (H+/K+)-ATPase 相互作用来抑制胃酸分泌。此外，Rabeprazole Related Compound E 还能显著抑制幽门螺旋杆菌的活性，可用于各种消化系统疾病的相关研究。
M20688	B-Raf inhibitor 1 (Compound 13) dihydrochloride	B-Raf inhibitor 1 (Compound 13) dihydrochloride	Raf
	B-Raf inhibitor 1 (Compound 13) is a type IIA Raf inhibitor which bind to the DFG-out conformation with ki of 1 nM,1 nM,and 0.3 nM for B-Raf(WT), B-Raf(V600E) and C-Raf, respectively.
M21681	Compound 48/80 trihydrochloride	Compound 48/80 trihydrochloride	Phospholipase
	C48/80 trihydrochloride
	Compound 48/80 trihydrochloride 作为选择性肥大细胞激活剂广泛用于动物和组织模型。Compound 48/80 作用于肥大细胞膜，刺激三聚体 G 蛋白，并通过磷脂酶 C 和 D 途径诱导脱颗粒。
M2608	Kobe0065	Kobe0065	Ras
	Kobe0065 is a novel and effective small-molecule compound inhibiting Ras–Raf interaction by SBDD, exhibits potent activity to competitively inhibit the binding of H-Ras·GTP to c-Raf-1 RBD with a Ki value of 46 ± 13 μM.
M2896	OAC1	OAC1	Others
	OAC1 (Oct4-activating compound 1)是一种有效的 Oct4 激活剂，能激活 Oct4 和 Nanog 启动子，促进诱导多功能干细胞 (iPSC) 的形成，以及通过上调 HOXB4 表达激活 OCT4。此外，OAC1 还能增加Oct4-Nanog-Sox2 三联体和 TET1 的转录，并可通过提高效率和缩短重编程时间，促进细胞的重编程。
M4088	Ginsenoside Compound-K	人参皂苷CK	COX
	Ginsenoside K; Ginsenoside C-K
	Ginsenoside Compound-K(人参皂苷CK)是一种 Ginsenoside Rb1 细菌代谢物，通过抑制诱生型一氧化氮合酶 (iNOS) 和 COX-2，从而发挥抗炎作用。
M4902	Chloroxine	克氯辛；氯喔星	Antibiotic
	Chloroxine is a synthetic antibacterial compound that is effective in the treatment of dandruff and seborrheic dermatitis when incorporated in a shampoo.
M4924	Dehydroacetic acid	脱氢乙酸	Antibiotic
	Biocide 470F
	Dehydroacetic acid is an organic compound, classified as a pyrone derivative and is used mostly as a fungicide and bactericide.
M4961	CB72666407	CB72666407	mTOR
	Pyrimidine substituted purine compounds as kinase (S) inhibitors.
M4987	Procyanidin B4	Procyanidin B4	Others
	A series of dimeric procyanidins (1-9) and some related polyphenols (10-15) were chosen as model compounds in a comparative investigation for various biological activities in order to obtain structure-activity relationships.
M5007	Hexyl Chloroformate	己基甲酸氯	Others
	The Carbonochloridic acid,hexyl ester, belongs to the following product categories: (1)Acid Halides; (2)Carbonyl Compounds; (3)Organic Building Blocks. It has the systematic name of hexyl carbonochloridate.
M6285	Glutaminase C-IN-1	Glutaminase C-IN-1	Glutaminase
	Compound 968
	Glutaminase C-IN-1 (Compound 968) 是一种Glutaminase C变构抑制剂。
M7400	Teijin compound 1	Teijin compound 1	Others
	Teijin compound 1 is a potent CCR2b antagonist.
M7838	8-Hydroxy-2′-deoxyguanosine	8-Hydroxy-2′-deoxyguanosine	Metabolite/Endogenous Metabolite
	A marker compound typically indicative of DNA damage associated with mutagenesis and carcinogenesis.
M7946	Naloxone methiodide	Naloxone methiodide	Others
	Quaternary salt of naloxone that, like the parent compound, is a nonselective antagonist at opioid receptors.
M8161	SE 175	SE 175	Others
	An organic nitrate compound that acts as an NO donor in vivo following reductive transformation of the nitrate group to nitric oxide.
M8166	Sulindac sulfide	硫化舒林酸	Others
	Sulindac sulfide is a non-steroidal anti-inflammatory compound with a preference for COX-1; it is an inhibitor of Ras activation of Raf-1.
M8211	Triacetyl resveratrol	乙酰化白藜芦醇	STAT
	Triacetyl resveratrol displays superior bioavailability to the parent compound, resveratrol.
M8246	GPR35 Agonist, Compound 10	GPR35 Agonist, Compound 10	Others
	GPR35 agonist Compound 10 is a GPR35 agonist the binds with higher affinity than other known agonists, such as kynurenic acid and zaprinast.
M8609	MM-206	MM-206	Others
	MM-206 is a cell-permeable, non-cytotoxic naphthalene sulfonamide compound effectively inhibits STAT3 DNA-binding activity (IC₅₀ = 2.
M8635	Displurigen	Displurigen	Others
	Displurigen is a cell-permeable, phenylthiochromen-4-one derived compound that disrupts the pluripotency of human embryonic stem cells by targeting HSPA8/HSC70 and affects its binding to Oct4.
M8639	STK16-IN-1	STK16-IN-1	Others
	STK16-IN-1 is a cell-permeable pyrrolonaphthyridinone compound that acts as an ATP-competitive inhibitor against NAK (Numb Associated Kinase) family serine/threonine kinase STK16 (IC₅₀/substrate = 0.
M8640	SW044248	SW044248	Topoisomerase
	SW044248 is a cell permeable, indolotriazine-based compound that selectively inhibits topoisomerase 1 (Top 1), but not Top 2, catalyzed DNA decatenation in a manner distinct from that of camptothecin (Cat.
M8647	Raptinal	Raptinal	Caspase
	Raptinal is a cell-permeable bifluorene-dicarbaldehyde compound that acts as a rapid activator of mitochondrial pathway-mediated intrinsic apoptosis.
M8668	MI-4F	MI-4F	Others
	MI-4F is mesoionic compound that exhibits potent anticancer activity against multiple cancer cell lines and in vivo.
M8706	NSC57969	NSC57969	Others
	NSC57969 is a MDR-selective compound that exhibits a robust Pgp-dependent toxic activity across diverse cancer cell lines.
M8717	PBOX-6	PBOX-6	Others
	PBOX-6 belongs to a group of tubulin-targeting pyrrolo-1,5-benzoxazepine (PBOX) compounds that potently induce apoptosis in a wide spectrum of cancer cells, including those originating from the four main types of leukemia.
M8723	PBOX-15	PBOX-15	Others
	PBOX-15 belongs to a group of tubulin-targeting pyrrolo-1,5-benzoxazepine (PBOX) compounds that potently induce apoptosis in a wide spectrum of cancer cells, including those originating from the four main types of leukemia.
M8884	Febantel	非班太尔	Parasite
	Rintal, Combotel
	Febantel is a veteran anthelmintic (wormer) compound belonging to the chemical class of the benzimidazoles.
M9031	6-Methylcoumarin	6-Methylcoumarin	Others
	Toncarine
	6-Methylcoumarin belongs to the class of organic compounds known as coumarins and derivatives.
M9461	Oxyclozanide	氯羟柳胺；五氯柳胺；羟氯柳苯胺	Anti-infection
	五氯柳胺Oxyclozanide is a salicylanilide anthelmintic compound, which acts by uncoupling oxidative phosphorylation in flukes.

信号通路

产品类型

AbMole

服务与支持

技术资源

联系我们