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Search Results for " cytochrome p450 "

Targets Recommended: Others

267

抑制剂 & 化合物

60

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13

同位素标记化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T25283	Cytochrome P450 2C9 Cyp2C9,Human cytochrome P450 2C9,Cytochrome P 450 2C9,S-Mephenytoin 4-hydroxylase	Others	Others
	Cytochrome P450 2C9 is a cytochrome P-450 subtype that possesses specificity for acidic xenobiotics. It oxidizes a wide range of important clinical drugs under the categories of nonsteroidal anti-inflammatory agents, anticoagulants, hypoglycemic agents, a
T17022	Tebuconazole	P450; Antifungal	Metabolism; Microbiology/Virology
	Tebuconazole 是一种农用唑类杀菌剂，可抑制 CYP51，对白色念珠菌 CYP51 和truncated Homo sapiens CYP51 的IC50分别为 0.9 和 1.3 μM。
T21482	Uniconazole	P450; ROS Kinase	Metabolism; Tyrosine Kinase/Adaptors
	Uniconazole 是植物生长调节剂，能够抑制细胞色素 P450 707As (Ki=68 nM)。他是分解脱落酸的酶家族成员，能够抑制赤霉素和甾醇的生物合成。
TP2238	Cytochrome P450 CYP1B1 (190-198) [Homo sapiens]	Others	Others
	Cytochrome P450 CYP1B1 (190-198) [Homo sapiens] is a peptide from Cytochrome c, which is a small heme protein found loosely associated with the inner membrane of the mitochondrion. Cytochromes c from certain eukaryotes, including plants and fungi but not higher animals, contains methylated lysine residues at specific positions1. Cytochrome c is a required cofactor for Apaf-1 function2.
T10953	Dafadine-A	P450	Metabolism
	Dafadine-A 是dafadine 的类似物，是C. elegans DAF-9 细胞色素P450抑制剂，同时对哺乳动物的CYP27A1具有抑制作用。
T7410	Furafylline 呋拉茶碱,呋喃茶碱	P450	Metabolism
	Furafylline 是有选择性的人细胞色素P450IA2抑制剂(IC50:0.07 μM)。
T21529	(S)-Mephenytoin	Others	Others
	(S)-Mephenytoin 是一种抗惊厥剂。(S)-Mephenytoin 作为细胞色素 P450 (CYP) 同种型 CYP2C19 的底物，可用于分析细胞色素 P450 代谢。
T27617	Inz-1	P450	Metabolism
	Inz-1 是一种有效的真菌特异性线粒体细胞色素 bc1 抑制剂，对酵母和人类的 IC50 分别为 8.092 和 45.320 μM。 Inz-1 可逆转氟康唑或其他三唑类抗真菌药对致病性真菌白色念珠菌的耐药性。
T1650	Chlorzoxazone Paraflex,Chlorzoxazon,氯唑沙宗	P450; Potassium Channel	Membrane transporter/Ion channel; Metabolism
	Chlorzoxazone (Chlorzoxazon) 是作用于中枢的肌肉松弛剂, 可用于肌肉痉挛的研究。
T11991	Mefentrifluconazole	P450; Antifungal	Metabolism; Microbiology/Virology
	Mefentrifluconazole 是一种有效的、选择性的和具有口服活性的真菌 CYP51 (Kd= 0.5 nM) 抑制剂，但对人芳香酶的抑制活性较低，IC50值为0.92 μM。它是一种新型唑类衍生物，用作农用广谱抗真菌剂。
T14841	BVT948	Phosphatase; P450; Histone Methyltransferase	Chromatin/Epigenetic; Metabolism
	BVT948 是一种蛋白酪氨酸磷酸酶抑制剂，还可以抑制赖氨酸甲基转移酶 SETD8 (KMT5A) 和几种细胞色素 P450 (P450) 同工型。
T16412	Oteseconazole VT-1161	P450; Antifungal	Metabolism; Microbiology/Virology
	Oteseconazole (VT-1161) 是一种口服有效的抗真菌剂，结合并抑制白色念球菌的 CYP51，Kd 值小于 39 nM。
T80057	Cytochrome P450 reductase	Others	Others
	Cytochrome P450reductase，一种NADPH-细胞色素还原酶，发挥作用于促进芳香酶构象，以最适合底物结合。
T6260	AMG-208 AMG 208	P450; c-Met/HGFR	Metabolism; Tyrosine Kinase/Adaptors
	AMG-208 是一种选择性的、口服有活性的c-Met/RON 双抑制剂，对c-Met 的IC50为 9 nM。他也是CYP3A4抑制剂(IC50:32 μM)。它具有抗癌作用。
T6216	Abiraterone 阿比特龙,CB-7598	P450	Metabolism
	Abiraterone (CB-7598) 是不可逆的CYP17A1抑制剂，具有抗雄激素作用，抑制细胞色素 p450 酶 CYP17 的 17α-羟化酶 (IC50:2.5 nM) 和 17,20-裂合酶 (IC50:15 nM) 活性。
T7618	Pyributicarb TSH-888,稗草畏	P450	Metabolism
	Pyributicarb (TSH-888) 是氨基甲酸酯型除草剂，能够有效激活CYP3A4基因及人类孕烷 X 受体。
T1491	Atovaquone Atavaquone,阿托伐醌	Others; P450; Dehydrogenase; Antibiotic; Parasite	Metabolism; Microbiology/Virology; Others
	Atovaquone (Atavaquone) 是具有口服活性的选择性寄生虫线粒体细胞色素bc1复合物的抑制剂。它抑制人类和P. falciparum 细胞色素bc1活性，IC50值分别为 460 nM 和 2.0 nM。它有抗疟作用，有潜力用于疟疾、弓形体病、肺孢子虫肺炎和巴贝斯虫病的相关研究。
T3585	TMS (E)-2,3',4,5'-tetramethoxystilbene,2,3',4,5'-Tetramethoxystilbene	P450	Metabolism
	TMS (2,3',4,5'-Tetramethoxystilbene) 是一种白藜芦醇的甲基化衍生物，也是具有选择性的CYP1B1竞争性抑制剂，其IC50=6 nM，Ki=3 nM。它对 CYP1A1 (IC50:300 nM) 及 CYP1A2 (IC50:3.1 μM) 的抑制作用较小。它具有抗癌作用。
T7788	2-Phenyl-2-(1-piperidinyl)propane	Others	Others
	2-Phenyl-2-(1-piperidinyl)propane 是一种具有可逆性、选择性的人 CYP2B6抑制剂，其 IC50为 5.1 μM，Ki 为 5.6。它对 CYP2D6 、CYP3A 均有抑制作用，且 IC50值分别为74 μM、200 μM。
T1403	Climbazole 甘宝素,BAY-e 6975	Antibiotic; Antifungal	Microbiology/Virology
	Climbazole (BAY-e 6975) 是一种广谱咪唑类抗真菌剂，具有去屑功效。它还是大鼠肝细胞色素 P450 的强诱导剂。
T9043	AS1810722	P450; STAT	JAK/STAT signaling; Metabolism; Stem Cells
	AS1810722 是口服有效的STAT6抑制剂，IC50为 1.9 nM。它是一种稠合双环嘧啶衍生物，对有良好的CYP3A4抑制作用，具有用于过敏性疾病，如哮喘和特应性疾病的研究潜力。
T4190	Ticlopidine PCR 5332,Ticlid,噻氯匹定	ATPase; Adiponectin receptor	GPCR/G Protein; Membrane transporter/Ion channel
	Ticlopidine (PCR 5332) 是抗血栓前药。它是CYP2C19人肝细胞色素的抑制剂，抑制 CYP2C9 及 CYP3A4。他是变构CD39的非竞争性抑制剂，能够阻断 NTPDase 同工酶，对NTPDase2和NTPDase3的IC50分别为 170 µM 和 149 µM。
T12171	Nampt-IN-5	P450; NAMPT	Metabolism
	Nampt-IN-5 是烟酰胺磷酸核糖基转移酶抑制剂。它可抑制 A2780 和 COR-L23 细胞，IC50值分别为 0.7 nM 和 3.9 nM。它还抑制 CYP3A4 活性。
T4188	SDZ285428 SDZ285-428	P450; Parasite; Antifungal	Metabolism; Microbiology/Virology
	SDZ285428 是一种CYP51抑制剂。
T4498	Stiripentol 斯利潘托,BCX2600,Diacomit	P450	Metabolism
	Stiripentol (BCX2600) 是抗惊厥剂，对 CYP3A4 (非竞争性) 及 CYP2C19 (竞争性地) 介导的 CLB 向 N-desmethylclobazam (NCLB) 的 N-去甲基化具有抑制作用。
T2196	Fipronil 氟虫腈,Fluocyanobenpyrazole,Termidor	P450; GluCls; GABA Receptor	Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience
	Fipronil (Fluocyanobenpyrazole) 是昆虫GABA 受体的选择性拮抗剂，可抑制蟑螂神经元中谷氨酸盐引起的脱敏和非脱敏。在分离的大鼠肝微粒体中，它诱导细胞色素 P450 (CYP) 亚型CYP1A1/2、CYP2B1/2和CYP3A1/2的活性。
T1149	Fenofibrate Procetofen,非诺贝特,Lipanthyl,Lipantil	P450; PPAR; Autophagy	Autophagy; DNA Damage/DNA Repair; Metabolism
	Fenofibrate (Lipanthyl) 是一种选择性PPARα激动剂，EC50为 30 μM。它是一种合成的苯氧基异丁酸衍生物和前药，具有抗高血脂活性。它抑制细胞色素 P450 亚型, 对CYP2C19、CYP2B6、CYP2C9、CYP2C8和CYP3A4的IC50分别为 0.2、0.7、9.7、4.8 和 142.1 μM。
T13601	CDD3506 1-TRITYL-1H-IMIDAZOL-4-AMINE	P450	Metabolism
	CDD3506 (1-TRITYL-1H-IMIDAZOL-4-AMINE) 能够诱导肝CYP3A 的活动，增强高密度脂蛋白胆固醇的水平。
T0922	Zoxazolamine NSC 24995,Contrazole,氯苯恶唑胺,苯并恶唑胺	Others	Others
	Zoxazolamine (NSC-24995) 是排尿酸和肌肉松弛剂，被广泛用于药物测试，可作为啮齿动物细胞色素 P-450 活性变化的方便指标。
T6215	Abiraterone Acetate Zytiga,乙酸阿比特龙酯,CB7630	P450	Metabolism
	Abiraterone Acetate (CB7630) 是一种具有口服活性的、不可逆的 CYP17A1选择性抑制剂，具有抗雄激素作用。它是 Abiraterone 的前药。
T1434	Clarithromycin A-56268,克拉霉素	P450; ribosome; MRP; Antibacterial; Antibiotic; Autophagy	Autophagy; Immunology/Inflammation; Metabolism; Microbiology/Virology
	Clarithromycin (A-56268) 具有广谱的抗菌活性。它抑制 CYP3A4催化的三唑仑 α-羟基化，IC50(Ki) 值为 56 (43) μM。它抑制 HERG 钾电流。它可削弱连接 hERG1 和 PI3K 的信号通路影响自噬流。
T7370	Talarozole R115866,他拉罗唑	Others; P450; Retinoid Receptor; Autophagy	Autophagy; Metabolism; Others
	Talarozole (R115866) 是一种口服性全反式维甲酸代谢阻断剂，可抑制 CYP26A1 和 CYP26B1，IC50 分别为 5.4 和 0.46 nM。它用于治疗痤疮、牛皮癣和其他角化疾病。
T2088	APD668 APD 668	GPR; P450; Potassium Channel	Endocrinology/Hormones; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism
	APD668 是选择性的，口服有效的GPR119激动剂，对hGPR119和rGPR119的EC50分别为 2.7 nM 和 33 nM。它对除CYP2C9(Ki=0.1 μM) 以外的五种主要 CYP 亚型均无明显抑制作用。它可用于脂肪性肝炎和糖尿病的研究。
T14186	17-ODYA 17-十八炔酸,Alkynyl Stearic Acid	Others; PROTAC Linker	Others; PROTAC
	Alkynyl Stearic Acid 是 CYP450 ω-羟化酶抑制剂。它能够抑制与花生四烯酸孵育的大鼠肾皮质微粒体形成 20-HETE 、dihydroxyeicosatrienoic acids、epoxyeicosatrienoic acids。它可以改善异丙肾上腺素诱导的培养心肌细胞凋亡和坏死。
T21425	Mephenytoin Mesantoin,Methoin,Insulton,Phenantoin,美芬妥因,Methylphenetoin	P450	Metabolism
	Mephenytoin (Phenantoin) 是 CYP2C19 及 CYP2B6 的底物，是一种抗惊厥剂。
T13600	CDD3505 4-nitro-1-trityl-1H-imidazole	P450	Metabolism
	CDD3505 (4-nitro-1-trityl-1H-imidazole) 能够诱导肝CYP3A 的活动，增强高密度脂蛋白胆固醇的水平。
T2397	Topiroxostat 托匹司他,FYX-051	P450; ROS; Xanthine Oxidase	Immunology/Inflammation; Metabolism
	Topiroxostat (FYX-051) 是一种有效的口服黄嘌呤氧化还原酶 (XOR) 抑制剂，IC50=5.3 nM，Ki=5.7 nM。它还表现出弱的CYP3A4抑制活性 (18.6%)。它有用于高尿酸血症的研究潜力。
T3610	Ranitidine 雷尼替丁,HSDB 3925,Ranitidin	P450; Antibacterial; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience
	Ranitidine (HSDB 3925) 是一种选择性的，具有口服活性的组胺 H2 受体拮抗剂，IC50为 3.3 μM。它还一种是CYP2C19和CYP2C9的弱抑制剂，可抑制胃液分泌。
T0865	Ranitidine Hydrochloride AH19065,盐酸雷尼替丁	P450; Antibacterial; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience
	Ranitidine Hydrochloride (AH19065) 是一种具有口服活性的组胺 H2 受体选择性拮抗剂，IC50为 3.3 μM。它还是一种CYP2C19和CYP2C9的弱抑制剂，可抑制胃液分泌。
T9054	RO6889678	HBV	Microbiology/Virology
	RO6889678 是高效的 HBV 衣壳结构抑制剂，其吸收、分布、代谢和排泄特征较为复杂。它可通过 CYP3A4 介导的氧化作用进行代谢，以及通过 UDP-葡萄糖醛酸基转移酶 UGT1A3 和 UGT1A1 介导的直接葡萄糖醛酸化作用进行代谢。它是一种诱导剂，可作用于人肝细胞中 CYP3A4 和共调节蛋白。
T6246	Cobicistat Tybost,GS-9350,考西司他	P450; HIV Protease	Metabolism; Microbiology/Virology; Proteases/Proteasome
	Cobicistat (GS-9350) 是一种细胞色素酶P450 3A 的选择性抑制剂，IC50值为30-285 nM。它是一种药代动力学增强剂，可增强抗 HIV 药物的吸收。
T0679	Ketoconazole R-41400,Xolegel,(±)-Ketoconazol,酮康唑,Extina	NADPH-oxidase; P450; Hydroxylase; Antifungal; Ras	GPCR/G Protein; Immunology/Inflammation; MAPK; Metabolism; Microbiology/Virology
	Ketoconazole (R-41400) 是一种咪唑类抗真菌剂，也是一种 CYP3A4 抑制剂。
T1540	Doxepin hydrochloride Toruan,Doxepin HCl,Aponal,Novoxapin,盐酸多塞平	P450; Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; AChR; Norepinephrine; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience
	Doxepin hydrochloride (Aponal) 是一种可口服的三环抗抑郁剂，是选择性组胺受体 H1拮抗剂。它也是 CYP450抑制剂，抑制 CYP450 2C19和 CYP450 1A2。
T19526	Pradefovir mesylate Pradefovir mesilate,Remofovir mesylate,Hepavir B,甲磺酸帕拉德福韦	P450	Metabolism
	Pradefovir mesylate (Hepavir B) 是一种肝脏 CYP3A4 底物。在人肝微粒体中，Pradefovir 能够转化为 9-[2-(磷酸甲氧基)乙基]腺嘌呤，其Km=60 μM。
T7699	AZD7325 AZD-7325	P450; GABA Receptor	Membrane transporter/Ion channel; Metabolism; Neuroscience
	AZD7325 (AZD-7325) 是具有口服活性的α2和α3受体正向别构调节剂，Ki 分别是 0.3 和 1.3 nM。它是中等 CYP1A2和强效 CYP3A4诱导剂，有用于焦虑和 dravet 综合征相关的研究潜力。
T21507	7-Ethoxyresorufin Resorufin ethyl ether,乙氧基试卤灵	P450; NO Synthase	Immunology/Inflammation; Metabolism
	7-Ethoxyresorufin (Resorufin ethyl ether) 是细胞色素 P450 (尤其是CYP1A1) 的荧光底物和竞争性抑制剂，同时对 NO 合酶具有抑制作用。
T0765	Fomepizole Antizol-Vet,4-甲基吡唑,甲吡唑,4-Methylpyrazole,Antizol	P450; CAT; AChR	Metabolism; Neuroscience; oxidation-reduction
	Fomepizole (4-Methylpyrazole) 是细胞色素 P450 (CYP2E1) 抑制剂。它是乙醇脱氢酶 (alcohol dehydrogenase) 竞争性抑制剂。它能够阻断甲醇和乙二醇进一步转化为有毒代谢产物。它具有成为乙二醇或甲醇中毒的解毒剂的潜力。
T8937	Soticlestat TAK-935,OV935	P450	Metabolism
	Soticlestat (OV935) 是一种首创的、口服有活性的胆固醇 24-羟化酶 (cholesterol 24-hydroxylase, CH24H) 选择性抑制剂。它可用于研究癫痫综合征。
T1290	Oxiconazole nitrate 硝酸奥昔康唑,Ro 13-8996	Others; Antibiotic; Antifection; Antifungal	Microbiology/Virology; Others
	Oxiconazole nitrate (Ro 13-8996) 是广谱抗真菌药物，抑制T. tonsurans 和T.rubrum 的生长，MIC90值分别为 0.25 和 0.5 μg/mL。
T1415	Gemfibrozil 吉非罗齐,CI-719,Jezil,Decrelip,Lopid	P450; Adrenergic Receptor; PPAR	DNA Damage/DNA Repair; GPCR/G Protein; Metabolism; Neuroscience
	Gemfibrozil (CI-719) 是一种PPAR-α激活剂，可作为降脂药。它也是P450非选择性抑制剂，对 CYP2C9、2C19、2C8 和 1A2 的Ki 值分别为 5.8、24、69 和 82 μM。

化合物

Cytochrome P450 2C9

Cat.No: T25283

Synonym: Cyp2C9,Human cytochrome P450 2C9,Cytochrome P 450 2C9,S-Mephenytoin 4-hydroxylase

Target: Others

Cat.No: T17022

Target: P450, Antifungal

Cat.No: T21482

Target: P450, ROS Kinase

Cytochrome P450 CYP1B1 (190-198) [Homo sapiens]

Cat.No: TP2238

Target: Others

Cat.No: T10953

Target: P450

Cat.No: T7410

Synonym: 呋拉茶碱,呋喃茶碱

Target: P450

(S)-Mephenytoin

Cat.No: T21529

Target: Others

Cat.No: T27617

Target: P450

Cat.No: T1650

Synonym: Paraflex,Chlorzoxazon,氯唑沙宗

Target: P450, Potassium Channel

Mefentrifluconazole

Cat.No: T11991

Target: P450, Antifungal

Cat.No: T14841

Target: Phosphatase, P450, Histone Methyltransferase

Cat.No: T16412

Synonym: VT-1161

Target: P450, Antifungal

Cytochrome P450 reductase

Cat.No: T80057

Target: Others

Cat.No: T6260

Synonym: AMG 208

Target: P450, c-Met/HGFR

Cat.No: T6216

Synonym: 阿比特龙,CB-7598

Target: P450

Cat.No: T7618

Synonym: TSH-888,稗草畏

Target: P450

Cat.No: T1491

Synonym: Atavaquone,阿托伐醌

Target: Others, P450, Dehydrogenase, Antibiotic, Parasite

Cat.No: T3585

Synonym: (E)-2,3',4,5'-tetramethoxystilbene,2,3',4,5'-Tetramethoxystilbene

Target: P450

2-Phenyl-2-(1-piperidinyl)propane

Cat.No: T7788

Target: Others

Cat.No: T1403

Synonym: 甘宝素,BAY-e 6975

Target: Antibiotic, Antifungal

Cat.No: T9043

Target: P450, STAT

Cat.No: T4190

Synonym: PCR 5332,Ticlid,噻氯匹定

Target: ATPase, Adiponectin receptor

Cat.No: T12171

Target: P450, NAMPT

Cat.No: T4188

Synonym: SDZ285-428

Target: P450, Parasite, Antifungal

Cat.No: T4498

Synonym: 斯利潘托,BCX2600,Diacomit

Target: P450

Cat.No: T2196

Synonym: 氟虫腈,Fluocyanobenpyrazole,Termidor

Target: P450, GluCls, GABA Receptor

Cat.No: T1149

Synonym: Procetofen,非诺贝特,Lipanthyl,Lipantil

Target: P450, PPAR, Autophagy

Cat.No: T13601

Synonym: 1-TRITYL-1H-IMIDAZOL-4-AMINE

Target: P450

Cat.No: T0922

Synonym: NSC 24995,Contrazole,氯苯恶唑胺,苯并恶唑胺

Target: Others

Abiraterone Acetate

Cat.No: T6215

Synonym: Zytiga,乙酸阿比特龙酯,CB7630

Target: P450

Cat.No: T1434

Synonym: A-56268,克拉霉素

Target: P450, ribosome, MRP, Antibacterial, Antibiotic, Autophagy

Cat.No: T7370

Synonym: R115866,他拉罗唑

Target: Others, P450, Retinoid Receptor, Autophagy

Cat.No: T2088

Synonym: APD 668

Target: GPR, P450, Potassium Channel

Cat.No: T14186

Synonym: 17-十八炔酸,Alkynyl Stearic Acid

Target: Others, PROTAC Linker

Cat.No: T21425

Synonym: Mesantoin,Methoin,Insulton,Phenantoin,美芬妥因,Methylphenetoin

Target: P450

Cat.No: T13600

Synonym: 4-nitro-1-trityl-1H-imidazole

Target: P450

Cat.No: T2397

Synonym: 托匹司他,FYX-051

Target: P450, ROS, Xanthine Oxidase

Cat.No: T3610

Synonym: 雷尼替丁,HSDB 3925,Ranitidin

Target: P450, Antibacterial, Histamine Receptor

Ranitidine Hydrochloride

Cat.No: T0865

Synonym: AH19065,盐酸雷尼替丁

Target: P450, Antibacterial, Histamine Receptor

Cat.No: T9054

Target: HBV

Cat.No: T6246

Synonym: Tybost,GS-9350,考西司他

Target: P450, HIV Protease

Cat.No: T0679

Synonym: R-41400,Xolegel,(±)-Ketoconazol,酮康唑,Extina

Target: NADPH-oxidase, P450, Hydroxylase, Antifungal, Ras

Doxepin hydrochloride

Cat.No: T1540

Synonym: Toruan,Doxepin HCl,Aponal,Novoxapin,盐酸多塞平

Target: P450, Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor, AChR, Norepinephrine, Histamine Receptor

Pradefovir mesylate

Cat.No: T19526

Synonym: Pradefovir mesilate,Remofovir mesylate,Hepavir B,甲磺酸帕拉德福韦

Target: P450

Cat.No: T7699

Synonym: AZD-7325

Target: P450, GABA Receptor

7-Ethoxyresorufin

Cat.No: T21507

Synonym: Resorufin ethyl ether,乙氧基试卤灵

Target: P450, NO Synthase

Cat.No: T0765

Synonym: Antizol-Vet,4-甲基吡唑,甲吡唑,4-Methylpyrazole,Antizol

Target: P450, CAT, AChR

Cat.No: T8937

Synonym: TAK-935,OV935

Target: P450

Oxiconazole nitrate

Cat.No: T1290

Synonym: 硝酸奥昔康唑,Ro 13-8996

Target: Others, Antibiotic, Antifection, Antifungal

Cat.No: T1415

Synonym: 吉非罗齐,CI-719,Jezil,Decrelip,Lopid

Target: P450, Adrenergic Receptor, PPAR

Cat. No.	Product Name	Target	Signaling Pathways
T6S1894	Linderane	P450	Metabolism
	Linderane 分离自 Lindera strychnifolia，能够不可逆的抑制 cytochrome P450 2C9。它具有抗痉挛及缓解疼痛的功能。
T3818	Fraxinol	Others; P450	Metabolism; Others
	Fraxinol 是一种分离自半边莲中的化合物。
T8038	7-Ethoxy-4-Methylcoumarin	Others	Others
	7-Ethoxy-4-Methylcoumarin 具有独特气味的芳香化合物。它被认为是细胞中酶的抑制剂，已被用于酶抑制的研究，并已被用于研究各种药物对人体的影响。
T3696	polygalaxanthone III	Others; P450	Metabolism; Others
	Polygalaxanthone III 提取自远志polygala tenuifolia wild，可抑制CYP450酶。它能够抑制由 CYP2E1 催化的氯唑沙宗 6-羟基化(IC50:50.56μM)。
T5594	Cedrol	P450; Antifungal	Metabolism; Microbiology/Virology
	Cedrol 是一种雪松烷倍半萜类叔醇，抑制细胞色素 P450 (CYP) 异构体 CYP2B6 和 CYP3A4，Kis 分别为 0.9 和 3.4 μM，具有抗炎，抗脓毒，抗痉挛，滋补，收敛，利尿，杀虫和抗真菌活性。
T3669	Curcumenol (+)-Curcumenol,莪术醇	P450	Metabolism
	Curcumenol ((+)-Curcumenol) 提取具有药用价值的 Curcuma zedoaria，是高效的 CYP3A4抑制剂(IC50=12.6 μM)，具有神经抗肿瘤、保护、抗炎、和保肝的作用。它在 LPS 刺激的 BV-2 小胶质细胞中，抑制 Akt 介导的 NF-κB 活化及 p38 MAPK 信号通路。
T7970	7-Ethoxycoumarin	Others	Others
	7-Ethoxycoumarin 是细胞色素 P450(CYP) 的底物，现已被应用于多种 CYP 的功能表征。
T2854	Phillyrin Forsythin,连翘苷	P450; Influenza Virus; AMPK	Chromatin/Epigenetic; Metabolism; Microbiology/Virology; PI3K/Akt/mTOR signaling
	Phillyrin (Forsythin) 是从连翘中分离出来的一种天然产物，具有抗甲型流感病毒的活性，以及抗菌和消炎作用。
TQ0191	Dihydromethysticin 二氢麻醉椒素,(+)-Dihydromethysticin	P450	Metabolism
	Dihydromethysticin ((+)-Dihydromethysticin) 是一种卡伐内酯，发现于 Piper methysticum 中。，它能够显著诱导 CYP3A23 的活性。
TN1650	Friedelin 软木三萜酮,无羁萜	P450; NOS; Caspase; Prostaglandin Receptor	Apoptosis; GPCR/G Protein; Immunology/Inflammation; Metabolism; Proteases/Proteasome
	Friedelin 是分离自 Maytenus ilicifolia(Mart) 的叶子。它是 CYP3A4的非竞争性抑制剂，其 IC50和 Ki 分别为10.79 μM 和 6.16 μM，也是 CYP2E1的竞争性抑制剂，其 IC50和 Ki 分别为 22.54 μM 和 18.02 μM。
T0595	Naringin Naringoside,柚皮苷	Mitophagy; P450; Endogenous Metabolite; Autophagy	Autophagy; Metabolism
	Naringin (Naringoside) 是一种黄烷酮糖苷，有抗氧化活性、降血脂、抗癌和抑制细胞色素P450酶的药理作用。
T5S2343	Acetylshikonin 乙酰紫草素,Acetyl shikonin	Others; P450; AChE	Metabolism; Neuroscience; Others
	Acetylshikonin 来源于紫草根，具有抗癌、抗炎作用。它是一种 AChE 抑制剂，具有很强的抗凋亡活性。它是一种非选择性的细胞色素 P450抑制剂，对所有 P450 亚型抑制的 IC50值范围为 1.4-4.0 μM。
T2926	Schizandrin A	P450; Virus Protease; Autophagy	Autophagy; Metabolism; Microbiology/Virology
	Schisandrin A 是一种从东方药物五味子中提取的主要有效成分，抑制 CYP3A 活性，IC50 分别为 6.60 μM 和 Ki 为 5.83 μM。
T5778	5,7-DIMETHOXYFLAVONE	Anti-infection; P450	Metabolism; Microbiology/Virology
	5,7-Dimethoxyflavone 是一种 Kaempferia parviflora 的主要成分，具有抗肿瘤、抗肥胖及抗炎活性。它对细胞色素 P450 (CYP) 3As 具有抑制作用，也是抗乳腺癌蛋白 (BCRP) 抑制剂。
T3149	Salvianolic Acid C 丹酚酸C,丹酚酸 C	Others; P450	Metabolism; Others
	Salvianolic acid C 属于天然产物，是一种细胞色素 P4502C8(CYP2C8) 和细胞色素 P4502J2(CYP2J2) 的抑制剂 (Ki=4.82/5.75 μM)，具有非竞争性。Salvianolic Acid C 具有抗新冠病毒活性。
TN1078	Seneciphylline 千里光菲灵碱,千里光非灵	P450; GST	Metabolism; oxidation-reduction
	Seneciphylline 是一种有毒的吡咯烷核生物碱，存在于千里光植物中。它显著增加了环氧水合酶和谷胱甘肽-S-转移酶的特性，但导致细胞色素 P-450 和相关单加氧酶特性的抑制。
T3668	Galangin Norizalpinin,高良姜素,3,5,7-Trihydroxyflavone	ERK; P450; NF-κB; Autophagy	Autophagy; MAPK; Metabolism; NF-κB
	Galangin (Norizalpinin) 是芳烃受体的激动剂/拮抗剂，并且还显示对 CYP1A1 活性的抑制作用。
T2770	Gentiopicroside Gentiopicrin,龙胆苦甙,龙胆苦苷	P450; HCV Protease	Metabolism; Microbiology/Virology; Proteases/Proteasome
	Gentiopicroside (Gentiopicrin) 是天然环烯醚萜苷，具有抗炎和抗氧化活性。它抑制P450的活性，对 CYP2A6 的 IC50和 Ki 值分别为 61 µM 和 22.8 µM，
T3776	Rhapontigenin 丹叶大黄素,Protigenin	P450; Antibacterial; Antifungal	Metabolism; Microbiology/Virology
	Rhapontigenin (Protigenin) 是一种基于机制的选择性细胞色素 P450 1A1 (IC50: 400 nM) 灭活剂。它是一种芳烃羟化酶，可激活作为致癌物质的多环芳烃。它是白藜芦醇的天然类似物，具有抗癌，抗氧化剂，抗真菌和抗菌活性。
T1704	Diosmetin Luteolin 4-methyl ether,香叶木素	P450; Trk receptor	Metabolism; Tyrosine Kinase/Adaptors
	Diosmetin (Luteolin 4-methyl ether) 是一种天然类黄酮，能够抑制人CYP1A 酶活性，在HepG2细胞的IC50值为40 μM。
T5786	TETRAHYDROPIPERINE 四氢胡椒碱,Cosmoperine	P450; TRP/TRPV Channel	Membrane transporter/Ion channel; Metabolism
	Tetrahydropiperine (Cosmoperine) 是胡椒碱的环己基类似物，也是一种天然芳基戊酰胺，从Piper longum 分离得到。它对细胞色素 P450 (CYP) 同工型 CYP1A1/芳基烃羟化酶 (AHH；IC50=23 µM)具有抑制作用。
T2143	Bergapten 5-Methoxypsoralen,佛手柑内酯,香柑内酯	P450; Autophagy	Autophagy; Metabolism
	Bergapten (5-Methoxypsoralen) 是白芷中的一种香豆素，也是一种补骨脂素，可抑制细胞复制。
T5S0669	Bergamottin 5-Geranoxypsoralen,Bergamotine,Bergaptin,佛手柑素	P450	Metabolism
	Bergamottin (5-Geranoxypsoralen) 是竞争性CYP1A1抑制剂(Ki:10.703 nM)。
T7938	Quinidine 奎尼丁,奎宁树	Parasite	Microbiology/Virology
	Quinidine 是一种抗心律失常剂，也是 K+通道的有效阻断剂，其 IC50值为 19.9 μM。它是一种选择性细胞色素 P450db 的有效抑制剂，也可研究疟疾。
T8079	α-Terpinyl acetate 乙酸松油酯,Terpinyl Acetate	Others; P450	Metabolism; Others
	α-Terpinyl acetate 是一种单萜酯，分离自 Laurus nobilis L.精油。它是P450 2B6的竞争性底物，与其活性部位结合的Kd 值为 5.4 μM 。
T11218	ε-Viniferin epsilon-Viniferin,Epsilon-白藜芦醇脱氢二聚体	P450	Metabolism
	ε-Viniferin (epsilon-Viniferin) 提取自 Vitis vinifera，是 Resveratrol 的二聚体，能够抑制 CYP 家族,其 Ki=0.5~20 μM，具有抗氧化作用。
T3401	Ginsenoside F1 人参皂苷 F1,20(S)-Ginsenoside F1	P450; Endogenous Metabolite	Metabolism
	Ginsenoside F1 (20(S)-Ginsenoside F1) 是一种 Ginsenoside Rg1 的酶促修饰衍生物，它竞争性抑制CYP3A4，对 CYP2D6 具有较弱的抑制作用。
T3797	Isosilybin Isosilybinin,Isosilibinin,异水飞蓟宾,Silymarin,Silybin B,Q-100795	P450	Metabolism
	Isosilybin (Isosilibinin) 是一种类黄酮，来源于乳蓟；能够抑制CYP3A4诱导(IC50:74 μM)。
T3736	Olivetol 橄榄醇,5-Pentylresorcinol,5-n-Amylresorcinol,3,5-二羟基戊苯	Cannabinoid Receptor; P450; IκB/IKK	GPCR/G Protein; Metabolism; NF-κB
	Olivetol (5-n-Amylresorcinol) 是天然多酚类化合物，存在于地衣中，或由一些昆虫产生。它竞争性地抑制大麻素受体CB1和CB2，抑制 CYP2C19 (IC50=15.3 μM;Ki=7.21 μM) 和 CYP2D6 (IC50=2.71 μM;Ki=2.87 μM) 的活性。
T2S1434	Bergaptol 5-Hydroxyfuranocoumarin,4-Hydroxybergapten,5-羟基-6,7-呋喃并香豆素,5-Hydroxypsoralen	P450	Metabolism
	Bergaptol (4-Hydroxybergapten) 是CYP3A4酶脱苄基作用的抑制剂(IC50:24.92 uM)，具有抗癌、抗增殖作用。
TJS1159	Chrysosplenetin 猫眼草黄素,Chrysosptertin B	P450; Ferroptosis; P-gp	Apoptosis; Membrane transporter/Ion channel; Metabolism; Neuroscience
	Chrysosplenetin 是青蒿和其他几种中草药中的一种多甲氧基化黄酮类天然产物，抑制 P-gp 活性并逆转由青蒿素诱导的上调的 P-gp 和 MDR1 水平。
T3735	Tetrahydrocurcumin Sabiwhite,Tetrahydrodiferuloylmethane,四氢姜黄素,HZIV 81-2,Tetrahydro Curcumin	P450; Endogenous Metabolite; Autophagy	Autophagy; Metabolism
	Tetrahydrocurcumin (HZIV 81-2) 是从姜黄中发现的一种天然产物，是姜黄素的主要代谢产物，可抑制 CYP2C9和 CYP3A4，具有很强的抗氧化和心脏保护作用。
T1011	Itraconazole 伊曲康唑,R51211	P450; Hedgehog/Smoothened; Antibiotic; Autophagy; Antifungal	Autophagy; GPCR/G Protein; Metabolism; Microbiology/Virology; Stem Cells
	Itraconazole (R51211) 属于三唑类天然产物，是一种抗真菌剂，具有口服活性。Itraconazole 是一种 Hedgehog 信号通路拮抗剂，一种 oxysterol-binding protein (OSBP) 抑制剂，也是一种细胞色素 P-450 依赖性酶的抑制剂。
TN6848	Piperonylic acid 胡椒酸,2H-1,3-benzodioxole-5-carboxylic acid	P450	Metabolism
	Piperonylic acid (2H-1,3-benzodioxole-5-carboxylic acid) 是一种具有亚甲二氧基活性的天然分子，与反式肉桂酸结构相似，可作为选择性反式肉桂酸 4-羟化酶的灭活剂。
T1548	Methoxsalen NCI-C55903,8-甲氧基补骨脂素,Xanthotoxin,8-Methoxypsoralen,8-MOP,甲氧沙林	P450; DNA	DNA Damage/DNA Repair; Metabolism
	Methoxsalen (NCI-C55903) 是一种呋喃香豆素化合物，是P450抑制剂。它具有补充骨脂的作用，能够用于湿疹、牛皮癣、白癜风及一些暴露在阳光下的皮肤淋巴瘤的研究
T7132	(Rac)-Brassinazole BRASSINAZOLE,3-(4-氯苯基)-1-甲基-1-苯基-2-(1,2,4-三唑-1-基)-1-丙醇,(Rac)-芸苔素唑	P450	Metabolism
	(Rac)-Brassinazole 是三唑型化合物，是油菜素甾醇 (BR) 生物合成抑制剂。它能够增强 CYP90B 在 BR 生物合成中的抑制作用。
T7056	Dronedarone 决奈达隆,SR 33589	P450; Potassium Channel; Calcium Channel; Sodium Channel; Adrenergic Receptor; AChR; Autophagy	Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience
	Dronedarone (SR 33589) 是一种胺碘酮类似物，对治疗心房颤动可能有效。它是CYP3A4的底物和中度抑制剂。它是多种离子电流的有效阻滞剂，通过非竞争性结合到肾上腺素能受体显示出抗肾上腺素能的效果。
T3811	Ginsenoside C-K 20(S)-人参皂苷 C-K,Ginsenoside compound K,Ginsenoside K,人参皂苷 C-K	P450; cell cycle arrest; COX; NO Synthase	Cell Cycle/Checkpoint; Immunology/Inflammation; Metabolism; Neuroscience
	Ginsenoside C-K (Ginsenoside K) 是 Ginsenoside Rb1 的细菌代谢物，可通过抑制诱生型一氧化氮合酶和COX-2来发挥抗炎作用。它在人肝微粒体中抑制CYP2C9和CYP2A6活性，IC50分别为 32.0±3.6 和 63.6±4.2 μM。
T2878	Ginsenoside Rd Panaxoside Rd,Sanchinoside Rd,人参皂苷Rd,人参皂苷 Rd,Gypenoside VIII	P450; Calcium Channel; NF-κB; COX; Endogenous Metabolite	Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB
	Ginsenoside Rd (Gypenoside VIII) 抑制 TNFα 诱导的NF-κB 转录活性，还抑制COX-2和iNOSmRNA 的表达。它抑制CYP2D6、CYP1A2、CYP3A4和CYP2C9，也抑制Ca2+内流，有可能抑制或阻止肿瘤生长。
T2175	Apigenin C.I. Natural Yellow 1,4',5,7-Trihydroxyflavone,NSC 83244,金银花,Apigenol,芹菜素,LY 080400	P450; Autophagy	Autophagy; Metabolism
	Apigenin (LY 080400) 属于黄酮类天然产物，是一种 CYP2C9 抑制剂 (Ki=2 μM)，具有竞争性。Apigenin 可以减少焦虑，影响免疫健康，调节激素，被用作镇静剂、温和的镇痛剂和安眠剂。
T6S0923	Hypericin Hypericine,金丝桃素,Cyclosan	Apoptosis; Antiviral; Influenza Virus; Tyrosine Kinases; Antibacterial; PKC	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; Microbiology/Virology; Tyrosine Kinase/Adaptors
	Hypericin (Cyclosan) 是贯叶连翘的提取物，有抗菌、抗病毒、抗肿瘤和抗抑郁作用。
T5582	β-Apo-8'-carotenal ψ-胡萝卜醛,trans-β-apo-8'-carotenal,BETA-阿朴-8'-胡萝卜醛,Apocarotenal	Others; P450	Metabolism; Others
	β-Apo-8'-carotenal (Apocarotenal) 是一种存在于许多蔬菜、水果中的维生素原 A 类胡萝卜素，是大鼠CYP1A1和CYP1A2的诱导剂。
T8125	Quinidine sulfate dihydrate 硫酸奎尼宁,硫酸奎尼丁二水合物,Chinidin Sodium,β-quinine Sodium,Pitayine Sodium,Quinidine sulfate	P450	Metabolism
	Quinidine sulfate dihydrate (Pitayine Sodium) 是抗心律失常剂，能够阻断 K+通道(IC50:19.9 μM)。它是细胞色素 P450db 的选择性抑制剂，可用于研究疟疾。
T6S1917	Schisandrol B Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B	P450; Reactive Oxygen Species; Autophagy	Autophagy; Immunology/Inflammation; Metabolism; NF-κB
	Schisandrol B (Besigomsin) 是华中五味子的主要活性成分，具有保肝、抗炎、抗糖尿病和抗氧化的作用。它抑制活性氧的产生，也抑制 P-糖蛋白和CYP3A 的活性。
T0671	2-Naphthol Betanaphthol,β-萘酚,乙萘酚	Others; Endogenous Metabolite	Metabolism; Others
	2-Naphthol 是一种 naphthalene 的代谢物，由细胞色素 P450 亚型 (CYP 1A1，CYP 1A2，CYP 2A1，CYP 2E1 和 CYP 2F2) 催化而成。2-Naphthol 具有细胞毒性。
T11680	Isoasatone A	P450	Metabolism
	Isoasatone A 是一种具有抗虫作用的天然产物，分离自Heterotropa takaoiM。它作用于细胞色素 P450 单加氧酶和谷胱甘肽转移酶，产生抗S. litura 作用。
Fr13756	Isonicotinic acid	Endogenous Metabolite; Drug Metabolite	Metabolism
	Isonicotinic acid 是 Isoniazid 的代谢产物。Isoniazid 通过肼解转化为 Isonicotinic acid。 Isoniazid 向 Isonicotinic acid 的生物转化可以通过细胞色素 P450 酶催化。
T0610	Piceatannol 白皮杉醇,trans-Piceatannol,Astringenin	Apoptosis; Serine/threonin kinase; PKA; Syk; PKC; Autophagy	Angiogenesis; Apoptosis; Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism; Tyrosine Kinase/Adaptors
	Piceatannol (Astringenin) 是一种Syk 抑制剂，可降低由 TNF 诱导的 iNOS 表达，可研究急性肺损伤。它是存在于各种水果和蔬菜中天然存在的多酚二苯乙烯，可诱导细胞自噬和凋亡，具有抗癌和抗炎特性。
T1153	Trimethoprim NIH 204,BW 56-72,甲氧苄啶,NSC-106568	DHFR; DNA/RNA Synthesis; Antifolate; Antibacterial; Antibiotic	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology
	Trimethoprim (NSC-106568) 是抑菌抗生素，也是具有口服活性的二氢叶酸还原酶抑制剂。它对多种革兰氏阳性和革兰氏阴性需氧细菌具有活性，可用于尿路感染，肺孢子菌肺炎和志贺氏菌病的研究。
T2940	6-Hydroxyflavone 6-羟基黄酮,6-HF	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	6-Hydroxyflavone (6-HF) 是天然存在的黄酮化合物，具有抗炎作用。它对牛血红蛋白糖基化具有抑制作用。它能激活 AKT、ERK 1/2、JNK 信号通路，有效促进成骨细胞分化。它能抑制 LPS 诱导的 NO 的产生。
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天然产物

Cat.No: T6S1894

Target: P450

Cat.No: T3818

Target: Others, P450

7-Ethoxy-4-Methylcoumarin

Cat.No: T8038

Target: Others

polygalaxanthone III

Cat.No: T3696

Target: Others, P450

Cat.No: T5594

Target: P450, Antifungal

Cat.No: T3669

Synonym: (+)-Curcumenol,莪术醇

Target: P450

7-Ethoxycoumarin

Cat.No: T7970

Target: Others

Cat.No: T2854

Synonym: Forsythin,连翘苷

Target: P450, Influenza Virus, AMPK

Dihydromethysticin

Cat.No: TQ0191

Synonym: 二氢麻醉椒素,(+)-Dihydromethysticin

Target: P450

Cat.No: TN1650

Synonym: 软木三萜酮,无羁萜

Target: P450, NOS, Caspase, Prostaglandin Receptor

Cat.No: T0595

Synonym: Naringoside,柚皮苷

Target: Mitophagy, P450, Endogenous Metabolite, Autophagy

Cat.No: T5S2343

Synonym: 乙酰紫草素,Acetyl shikonin

Target: Others, P450, AChE

Cat.No: T2926

Target: P450, Virus Protease, Autophagy

5,7-DIMETHOXYFLAVONE

Cat.No: T5778

Target: Anti-infection, P450

Salvianolic Acid C

Cat.No: T3149

Synonym: 丹酚酸C,丹酚酸 C

Target: Others, P450

Cat.No: TN1078

Synonym: 千里光菲灵碱,千里光非灵

Target: P450, GST

Cat.No: T3668

Synonym: Norizalpinin,高良姜素,3,5,7-Trihydroxyflavone

Target: ERK, P450, NF-κB, Autophagy

Gentiopicroside

Cat.No: T2770

Synonym: Gentiopicrin,龙胆苦甙,龙胆苦苷

Target: P450, HCV Protease

Cat.No: T3776

Synonym: 丹叶大黄素,Protigenin

Target: P450, Antibacterial, Antifungal

Cat.No: T1704

Synonym: Luteolin 4-methyl ether,香叶木素

Target: P450, Trk receptor

TETRAHYDROPIPERINE

Cat.No: T5786

Synonym: 四氢胡椒碱,Cosmoperine

Target: P450, TRP/TRPV Channel

Cat.No: T2143

Synonym: 5-Methoxypsoralen,佛手柑内酯,香柑内酯

Target: P450, Autophagy

Cat.No: T5S0669

Synonym: 5-Geranoxypsoralen,Bergamotine,Bergaptin,佛手柑素

Target: P450

Cat.No: T7938

Synonym: 奎尼丁,奎宁树

Target: Parasite

α-Terpinyl acetate

Cat.No: T8079

Synonym: 乙酸松油酯,Terpinyl Acetate

Target: Others, P450

Cat.No: T11218

Synonym: epsilon-Viniferin,Epsilon-白藜芦醇脱氢二聚体

Target: P450

Cat.No: T3401

Synonym: 人参皂苷 F1,20(S)-Ginsenoside F1

Target: P450, Endogenous Metabolite

Cat.No: T3797

Synonym: Isosilybinin,Isosilibinin,异水飞蓟宾,Silymarin,Silybin B,Q-100795

Target: P450

Cat.No: T3736

Synonym: 橄榄醇,5-Pentylresorcinol,5-n-Amylresorcinol,3,5-二羟基戊苯

Target: Cannabinoid Receptor, P450, IκB/IKK

Cat.No: T2S1434

Synonym: 5-Hydroxyfuranocoumarin,4-Hydroxybergapten,5-羟基-6,7-呋喃并香豆素,5-Hydroxypsoralen

Target: P450

Chrysosplenetin

Cat.No: TJS1159

Synonym: 猫眼草黄素,Chrysosptertin B

Target: P450, Ferroptosis, P-gp

Tetrahydrocurcumin

Cat.No: T3735

Synonym: Sabiwhite,Tetrahydrodiferuloylmethane,四氢姜黄素,HZIV 81-2,Tetrahydro Curcumin

Target: P450, Endogenous Metabolite, Autophagy

Cat.No: T1011

Synonym: 伊曲康唑,R51211

Target: P450, Hedgehog/Smoothened, Antibiotic, Autophagy, Antifungal

Piperonylic acid

Cat.No: TN6848

Synonym: 胡椒酸,2H-1,3-benzodioxole-5-carboxylic acid

Target: P450

Cat.No: T1548

Synonym: NCI-C55903,8-甲氧基补骨脂素,Xanthotoxin,8-Methoxypsoralen,8-MOP,甲氧沙林

Target: P450, DNA

(Rac)-Brassinazole

Cat.No: T7132

Synonym: BRASSINAZOLE,3-(4-氯苯基)-1-甲基-1-苯基-2-(1,2,4-三唑-1-基)-1-丙醇,(Rac)-芸苔素唑

Target: P450

Cat.No: T7056

Synonym: 决奈达隆,SR 33589

Target: P450, Potassium Channel, Calcium Channel, Sodium Channel, Adrenergic Receptor, AChR, Autophagy

Ginsenoside C-K

Cat.No: T3811

Synonym: 20(S)-人参皂苷 C-K,Ginsenoside compound K,Ginsenoside K,人参皂苷 C-K

Target: P450, cell cycle arrest, COX, NO Synthase

Cat.No: T2878

Synonym: Panaxoside Rd,Sanchinoside Rd,人参皂苷Rd,人参皂苷 Rd,Gypenoside VIII

Target: P450, Calcium Channel, NF-κB, COX, Endogenous Metabolite

Cat.No: T2175

Synonym: C.I. Natural Yellow 1,4',5,7-Trihydroxyflavone,NSC 83244,金银花,Apigenol,芹菜素,LY 080400

Target: P450, Autophagy

Cat.No: T6S0923

Synonym: Hypericine,金丝桃素,Cyclosan

Target: Apoptosis, Antiviral, Influenza Virus, Tyrosine Kinases, Antibacterial, PKC

β-Apo-8'-carotenal

Cat.No: T5582

Synonym: ψ-胡萝卜醛,trans-β-apo-8'-carotenal,BETA-阿朴-8'-胡萝卜醛,Apocarotenal

Target: Others, P450

Quinidine sulfate dihydrate

Cat.No: T8125

Synonym: 硫酸奎尼宁,硫酸奎尼丁二水合物,Chinidin Sodium,β-quinine Sodium,Pitayine Sodium,Quinidine sulfate

Target: P450

Cat.No: T6S1917

Synonym: Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B

Target: P450, Reactive Oxygen Species, Autophagy

Cat.No: T0671

Synonym: Betanaphthol,β-萘酚,乙萘酚

Target: Others, Endogenous Metabolite

Cat.No: T11680

Target: P450

Isonicotinic acid

Cat.No: Fr13756

Target: Endogenous Metabolite, Drug Metabolite

Cat.No: T0610

Synonym: 白皮杉醇,trans-Piceatannol,Astringenin

Target: Apoptosis, Serine/threonin kinase, PKA, Syk, PKC, Autophagy

Cat.No: T1153

Synonym: NIH 204,BW 56-72,甲氧苄啶,NSC-106568

Target: DHFR, DNA/RNA Synthesis, Antifolate, Antibacterial, Antibiotic

6-Hydroxyflavone

Cat.No: T2940

Synonym: 6-羟基黄酮,6-HF

Target: GABA Receptor

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Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPH-00160	Cytochrome P450 BM-3 Protein, Bacillus megaterium, Recombinant (His & Myc) cyp102A1,Bifunctional cytochrome P450/NADP...	Bacillus megaterium	E. coli
	Cytochrome P450 BM-3 Protein, Bacillus megaterium, Recombinant (His & Myc) is expressed in E. coli.
TMPH-01182	CYP1A1 Protein, Human, Recombinant (His) Cytochrome P450 1A1,Cytochrome	Human	E. coli
	CYP1A1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 63.7 kDa and the accession number is P04798.
TMPH-02140	CYP21A2 Protein, Human, Recombinant (E. coli, His) Cytochrome P-450c21,Cytochrome P450	Human	E. coli
	A cytochrome P450 monooxygenase that plays a major role in adrenal steroidogenesis. Catalyzes the hydroxylation at C-21 of progesterone and 17alpha-hydroxyprogesterone to respectively form 11-deoxycorticosterone and 11-deoxycortisol, intermediate metabolites in the biosynthetic pathway of mineralocorticoids and glucocorticoids. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via...
TMPH-02141	CYP21A2 Protein, Human, Recombinant (His) Cytochrome P450 21,CYP21A2,Cytochrome<...	Human	P. pastoris (Yeast)
	A cytochrome P450 monooxygenase that plays a major role in adrenal steroidogenesis. Catalyzes the hydroxylation at C-21 of progesterone and 17alpha-hydroxyprogesterone to respectively form 11-deoxycorticosterone and 11-deoxycortisol, intermediate metabolites in the biosynthetic pathway of mineralocorticoids and glucocorticoids. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via...
TMPH-01183	CYP26B1 Protein, Human, Recombinant (His) Cytochrome P450 26A2,CYP26B1,P450...	Human	E. coli
	CYP26B1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 63.5 kDa and the accession number is Q9NR63.
TMPH-02618	CYP2E1 Protein, Mouse, Recombinant (His) Cyp2e1,Cytochrome P450 2E1,Cytochrome<...	Mouse	E. coli
	A cytochrome P450 monooxygenase involved in the metabolism of fatty acids. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (NADPH--hemoprotein reductase). Catalyzes the hydroxylation of carbon-hydrogen bonds. Hydroxylates fatty acids specifically at the omega-1 position displaying the highest catalytic activity for saturated fatty acids. May be invo...
TMPH-03017	CYP51 Protein, Mycobacterium tuberculosis, Recombinant (His & Myc) Cytochrome P450-14DM,Sterol 14alpha-demeth...	Mycobacterium tuberculosis	Baculovirus Insect Cells
	Its precise biological substrate is not known. Catalyzes C14-demethylation of lanosterol, 24,25-dihydrolanosterol and obtusifoliol which is critical for ergosterol biosynthesis. It transforms lanosterol into 4,4'-dimethyl cholesta-8,14,24-triene-3-beta-ol.
TMPH-01185	CYP2C19 Protein, Human, Recombinant (His & Myc) Cytochrome P450 2C19,(R)-limonene 6-monoox...	Human	E. coli
	CYP2C19 Protein, Human, Recombinant (His & Myc) is expressed in E. coli.
TMPH-01184	CYP2A6 Protein, Human, Recombinant (His & Myc) CYP2A3,Coumarin 7-hydroxylase,1,4-cineole 2-exo-monooxygenas...	Human	E. coli
	CYP2A6 Protein, Human, Recombinant (His & Myc) is expressed in E. coli.
TMPH-01186	CYP2C9 Protein, Human, Recombinant (His & Myc) CYP2C10,Cytochrome P450 2C9,S-mephenytoin ...	Human	E. coli
	CYP2C9 Protein, Human, Recombinant (His & Myc) is expressed in E. coli.
TMPH-01084	CYP11A1 Protein, Human, Recombinant (His & SUMO) Cholesterol side-chain cleavage enzyme, mitochondrial,CYP11A...	Human	E. coli
	CYP11A1 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 72.1 kDa and the accession number is P05108.
TMPH-03447	ERG11 Protein, S. cerevisiae, Recombinant (GST) Ergosterol biosynthetic protein 11,Cytochrome P...	Saccharomyces cerevisiae	E. coli
	Catalyzes C14-demethylation of lanosterol which is critical for ergosterol biosynthesis. It transforms lanosterol into 4,4'-dimethyl cholesta-8,14,24-triene-3-beta-ol. ERG11 Protein, S. cerevisiae, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 29.1 kDa and the accession number is P10614.
TMPH-02801	CYPOR Protein, Mouse, Recombinant (His) CYPOR,P450R,CPR,NADPH--cytochrome P450...	Mouse	E. coli
	CYPOR Protein, Mouse, Recombinant (His) is expressed in E. coli.
TMPH-02139	CYP17A1 Protein, Human, Recombinant (GST) Cytochrome P450 17A1,CYPXVII,CYP17A1,CYP17...	Human	E. coli
	A cytochrome P450 monooxygenase involved in corticoid and androgen biosynthesis. Catalyzes 17-alpha hydroxylation of C21 steroids, which is common for both pathways. A second oxidative step, required only for androgen synthesis, involves an acyl-carbon cleavage. The 17-alpha hydroxy intermediates, as part of adrenal glucocorticoids biosynthesis pathway, are precursors of cortisol (Probable). Hydroxylates steroid hormones, pregnenolone and progesterone to form 17-alpha hydroxy metabolites, follow...
TMPH-01748	CYPOR Protein, Human, Recombinant (GST) NADPH--cytochrome P450 reductase,P450<...	Human	E. coli
	This enzyme is required for electron transfer from NADP to cytochrome P450 in microsomes. It can also provide electron transfer to heme oxygenase and cytochrome B5. CYPOR Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 102.9 kDa and the accession number is P16435.
TMPH-00956	Aromatase/CYP19A1 Protein, Human, Recombinant (His) ARO1,CYP19A1,Estrogen synthase,Cytochrome P450<...	Human	E. coli
	Aromatase/CYP19A1 Protein, Human, Recombinant (His) is expressed in E. coli.
TMPH-01181	CYP11B2 Protein, Human, Recombinant (His & SUMO) ALDOS,Corticosterone 18-monooxygenase, CYP11B2,Aldosterone s...	Human	E. coli
	CYP11B2 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli.
TMPY-05321	CYP3A4 Protein, Human, Recombinant (His) P450C3,P450PCN1,CYPIIIA4,CP34,cytochro...	Human	E. coli
	CYP3A4 is an important member of the cytochrome P450 enzyme superfamily, with 33 allelic variants. Human cytochrome P450 3A4 (CYP3A4) is an important drug metabolizing enzyme involved in a number of drug-drug and food-drug interactions. Systemic inflammation has been linked to suppressed CYP3A4 activity.
TMPH-00220	Adrenodoxin, mitochondrial Protein, Bovine, Recombinant (His) Hepato-ferredoxin,FDX1,Ferredoxin-1,Adrenodoxin, mitochondri...	Bovine	E. coli
	Essential for the synthesis of various steroid hormones. Participates in the reduction of mitochondrial cytochrome P450 for steroidogenesis. Transfers electrons from adrenodoxin reductase to CYP11A1, a cytochrome P450 that catalyzes cholesterol side-chain cleavage to produce pregnenolone, the precursor of most steroid hormones. Does not form a ternary complex with adrenodoxin reductase and CYP11A1 but shuttles between the two enzymes to transfer electrons. Adrenodoxin, mitochondrial Protein, Bov...

重组蛋白

Cytochrome P450 BM-3 Protein, Bacillus megaterium, Recombinant (His & Myc)

Cat.No: TMPH-00160

Species: Bacillus megaterium

Expression System: E. coli

CYP1A1 Protein, Human, Recombinant (His)

Cat.No: TMPH-01182

Species: Human

Expression System: E. coli

CYP21A2 Protein, Human, Recombinant (E. coli, His)

Cat.No: TMPH-02140

Species: Human

Expression System: E. coli

CYP21A2 Protein, Human, Recombinant (His)

Cat.No: TMPH-02141

Species: Human

Expression System: P. pastoris (Yeast)

CYP26B1 Protein, Human, Recombinant (His)

Cat.No: TMPH-01183

Species: Human

Expression System: E. coli

CYP2E1 Protein, Mouse, Recombinant (His)

Cat.No: TMPH-02618

Species: Mouse

Expression System: E. coli

CYP51 Protein, Mycobacterium tuberculosis, Recombinant (His & Myc)

Cat.No: TMPH-03017

Species: Mycobacterium tuberculosis

Expression System: Baculovirus Insect Cells

CYP2C19 Protein, Human, Recombinant (His & Myc)

Cat.No: TMPH-01185

Species: Human

Expression System: E. coli

CYP2A6 Protein, Human, Recombinant (His & Myc)

Cat.No: TMPH-01184

Species: Human

Expression System: E. coli

CYP2C9 Protein, Human, Recombinant (His & Myc)

Cat.No: TMPH-01186

Species: Human

Expression System: E. coli

CYP11A1 Protein, Human, Recombinant (His & SUMO)

Cat.No: TMPH-01084

Species: Human

Expression System: E. coli

ERG11 Protein, S. cerevisiae, Recombinant (GST)

Cat.No: TMPH-03447

Species: Saccharomyces cerevisiae

Expression System: E. coli

CYPOR Protein, Mouse, Recombinant (His)

Cat.No: TMPH-02801

Species: Mouse

Expression System: E. coli

CYP17A1 Protein, Human, Recombinant (GST)

Cat.No: TMPH-02139

Species: Human

Expression System: E. coli

CYPOR Protein, Human, Recombinant (GST)

Cat.No: TMPH-01748

Species: Human

Expression System: E. coli

Aromatase/CYP19A1 Protein, Human, Recombinant (His)

Cat.No: TMPH-00956

Species: Human

Expression System: E. coli

CYP11B2 Protein, Human, Recombinant (His & SUMO)

Cat.No: TMPH-01181

Species: Human

Expression System: E. coli

CYP3A4 Protein, Human, Recombinant (His)

Cat.No: TMPY-05321

Species: Human

Expression System: E. coli

Adrenodoxin, mitochondrial Protein, Bovine, Recombinant (His)

Cat.No: TMPH-00220

Species: Bovine

Expression System: E. coli

Cat. No.	Product Name	Target	Signaling Pathways
TMIJ-0110	Clarithromycin-13C-d3
	Clarithromycin-13C-d3 是 Clarithromycin 的 13C 和氘代化合物。Clarithromycin 的 CAS 号为 81103-11-9。Clarithromycin 具有广谱的抗菌活性。它抑制CYP3A4催化的三唑仑 α-羟基化，IC50(Ki) 值为 56 (43) μM。它抑制 HERG 钾电流。它可削弱连接 hERG1 和 PI3K 的信号通路影响自噬流。
TMIJ-0135	Abiraterone-d4
	Abiraterone-d4 是 Abiraterone 的氘代化合物。Abiraterone 的 CAS 号为 154229-19-3。Abiraterone 是不可逆的CYP17A1抑制剂，具有抗雄激素作用，抑制细胞色素 p450 酶 CYP17 的 17α-羟化酶 (IC50:2.5 nM) 和 17,20-裂合酶 (IC50:15 nM) 活性。
TMIJ-0239	Cobicistat-d8
	Cobicistat-d8 是 Cobicistat 的氘代化合物。Cobicistat 的 CAS 号为 1004316-88-4。Cobicistat 是一种细胞色素酶P450 3A 的选择性抑制剂，IC50值为30-285 nM。它是一种药代动力学增强剂，可增强抗 HIV 药物的吸收。
TMIJ-0031	Sulfamethoxazole-13C6
	Sulfamethoxazole-13C6 是 Sulfamethoxazole 的 13C 的标记化合物。Sulfamethoxazole 的 CAS 号为 723-46-6。Sulfamethoxazole是磺胺类抗菌素，用于细菌感染。Sulfonamides是对氨基苯甲酸的竞争性拮抗剂。
T71302	Norfluoxetine-d5 HCl
	Norfluoxetine-d5 is intended for use as an internal standard for the quantification of norfluoxetine by GC- or LC-MS. Norfluoxetine is an active metabolite of the antidepressant fluoxetine. It is formed from fluoxetine by the cytochrome P450 (CYP) isoforms CYP2C9, CYP2C19, and CYP3A. Norfluoxetine inhibits serotonin (5-HT) uptake in rat brain synaptosomal membrane preparations (Ki = 44.7 nM) and isolated human platelets (IC50 = ~15 nM). It has been found in the tissues of fish exposed to wastewa...
TMIJ-0326	Cyclosporin A-d4 (Major)
	Cyclosporin A-d4 (Major) 是 Cyclosporin A 的氘代化合物。Cyclosporin A 的 CAS 号为 59865-13-3。Cyclosporine A 是一种能与亲环素结合的抑制剂。根据它的作用机制可作为钙调神经磷酸酶抑制剂、细胞色素 P450 3A4 抑制剂和 P-糖蛋白抑制剂。
TMIJ-0076	Ritonavir-13C-d3
	Ritonavir-13C-d3 是 Ritonavir 的 13C 和氘代化合物。Ritonavir 的 CAS 号为 155213-67-5。Ritonavir 是一种 HIV 蛋白酶抑制剂，可研究 HIV 感染和 AIDS 。它也是SARS-CoV 3CLpro的抑制剂，IC50为 1.61 μM。
T71326	1,3,7-Trimethyluric Acid-d9
	1,3,7-Trimethyluric acid-d9 is intended for use as an internal standard for the quantification of 1,3,7-trimethyluric acid by GC- or LC-MS. 1,3,7-Trimethyluric acid is a derivative of uric acid and a metabolite of caffeine. It is formed from caffeine by the cytochrome P450 isoform CYP3A4. 1,3,7-Trimethyluric acid scavenges hydroxyl radicals in a cell-free assay and inhibits t-butyl hydroperoxide-induced lipid peroxidation by 56.5% in isolated human erythrocyte membranes.
T69758	Flutamide-d7
	Flutamide-d7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 µM, respectively. Flutamide (50 mg/kg per day) reduces tumor growth in a PC-82 mouse xenograft mo...
TMIH-0604	Voriconazole-d3
	Voriconazole-d3 是 Voriconazole 的氘代化合物。Voriconazole 的 CAS 号为 137234-62-9。Voriconazole 是一种三唑类抗真菌剂，可抑制真菌麦角甾醇的生物合成。它特异性抑制由真菌细胞色素 P450 酶介导的 14-α-羊毛甾醇去甲基化作用
TMIH-0457	Proguanil-d6 HCl
	Proguanil-d6 HCl 是 Proguanil HCl 的氘代化合物。Proguanil HCl 的 CAS 号为 637-32-1。Proguanil hydrochloride 是一种双胍类抗疟疾剂，在体内代谢形成环胍。它还是一种二氢叶酸还原酶抑制剂。
T71327	Paraxanthine-d6
	Paraxanthine-d6 is intended for use as an internal standard for the quantification of paraxanthine by GC- or LC-MS. Paraxanthine is an active metabolite of caffeine. It is formed via N3-demethylation of caffeine by the cytochrome P450 (CYP) isoform CYP1A2. Paraxanthine is an adenosine A1 and A2 receptor antagonist. In vivo, paraxanthine increases striatal cGMP and extracellular striatal dopamine levels and locomotor activity, as well as inhibits motor depression induced by the adenosine A1 agoni...
TMID-0116	Carbamazepine-10,11-epoxide-d10 (rings-d10)
	Carbamazepine-10,11-epoxide-d10 (rings-d10) 是 Carbamazepine-10,11-epoxide 的氘代化合物。Carbamazepine-10,11-epoxide 的 CAS 号为 36507-30-9。Carbamazepine 10,11-epoxide是抗惊厥药卡马西平 (carbamazepine) 的活性代谢物。它由卡马西平通过微粒体中的细胞色素 P450 (CYP) 同种型 CYP3A4 和 CYP2C8 形成，微粒体分别由表达 CYP3A4 或 CYP2C8 的 HepG2 细胞制备。它对小鼠最大电击诱发的癫痫发作具有抗惊厥活性。

同位素标记化合物

Clarithromycin-13C-d3

Cat.No: TMIJ-0110

Cat.No: TMIJ-0135

Cat.No: TMIJ-0239

Sulfamethoxazole-13C6

Cat.No: TMIJ-0031

Norfluoxetine-d5 HCl

Cat.No: T71302

Cyclosporin A-d4 (Major)

Cat.No: TMIJ-0326

Ritonavir-13C-d3

Cat.No: TMIJ-0076

1,3,7-Trimethyluric Acid-d9

Cat.No: T71326

Cat.No: T69758

Voriconazole-d3

Cat.No: TMIH-0604

Proguanil-d6 HCl

Cat.No: TMIH-0457

Paraxanthine-d6

Cat.No: T71327

Carbamazepine-10,11-epoxide-d10 (rings-d10)

Cat.No: TMID-0116

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