183
23
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35
7
Cat. No. | Product Name | ||
---|---|---|---|
LF1030 | LC高溶解性片段化合物库 | 9600 compounds | |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T26834 |
BL-1020 Mesylate
CYP-1020 Mesylate |
Dopamine Receptor; GABA Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
BL-1020 Mesylate (CYP-1020 Mesylate) 是一种可口服的 GABA A 受体激动剂和 D2 拮抗剂,可降低多巴胺活性并增强GABAA活性。BL-1020 Mesylate 可用于研究神经分裂、阿尔茨海默症和双向认知障碍。 | |||
T10923 |
CYP17-IN-1
|
P450 | Metabolism |
CYP17-IN-1 是一种有效的 CYP17 口服抑制剂,可抑制大鼠和人类的 CYP17,IC50 分别为 15.8 和 20.1 nM。 | |||
T10922 |
CYP11B2-IN-1
|
P450 | Metabolism |
CYP11B2-IN-1 是一种有效的选择性 CYP11B2 抑制剂,对 CYP11B2 和 CYP11B1 的 IC50 分别为 2.3 nM 和 142 nM。 | |||
T67916 |
CYP4A11/CYP4F2-IN-2
|
P450 | Metabolism |
CYP4A11/CYP4F2-IN-2 是一种有效的和具有口服活性的细胞色素 P450 (CYP) 4A11 和 CYP4F2 的双重抑制剂,IC50 值分别为 140 nM 和 40 nM。CYP4A11/CYP4F2-IN-2可从肝脏和肾脏中提取, 具有治疗肾脏疾病的潜力。 | |||
T72501 |
CYP4A11/CYP4F2-IN-1
|
P450 | Metabolism |
CYP4A11/CYP4F2-IN-1 是一种高效的小分子细胞色素 P450 (CYP) 4A11 和 CYP4F2 抑制剂,对P450 (CYP) 4A11 的 IC50 值为 19 nM,对 CYP4F2 的 IC50 值为 17 nM。CYP4A11/CYP4F2-IN-1 可用于研究肾脏疾病和心脑血管疾病。 | |||
T50011 |
CYP2A6-IN-1
|
Others | Others |
(2-methylpropyl)({[3-(trifluoromethyl)phenyl]methyl})amine 是一种选择性血清素受体激动剂,特异性靶向5-HT2A 和5-HT2C 受体,已被用于研究血清素在各种生理和病理条件下的作用。 | |||
T73040 |
CYP1B1-IN-4
|
P450 | Metabolism |
CYP1B1-IN-4为选择性CYP1B1抑制剂(IC50=0.2 nM),属2,4-二芳基噻唑类化合物。其对细胞的毒性低,且在人类及大鼠肝微粒体中表现出稳定性。 | |||
T73042 |
CYP1B1-IN-5
|
P450 | Metabolism |
CYP1B1-IN-5 是一种具有选择性和高效性的细胞色素 P450 1B1 (CYP1B1) 抑制剂,IC50 为 4.7 nM。CYP1B1-IN-5 可用于研究与代谢相关的疾病。 | |||
T27109 |
CYP1A1 inhibitor 8a
|
Others | Others |
CYP1A1 inhibitor 8a is a potent and selective CYP1A1 inhibitor. It antagonizes B[a]P mediated activation of aromatic hydrocarbon receptor (AhR) in yeast cells, thereby protects human cells from CYP1A1-mediated B[a]P toxicity. | |||
T63496 |
CYP2C9/CYP2C19-IN-1
|
Others | Others |
CYP2C9/CYP2C19-IN-1 是无肝脏毒性和遗传毒性的CYP2C9/CYP2C19强效抑制剂,能够用于研究寨卡病毒 (ZIKV) 感染。 | |||
T63495 |
CYP2C1/CYP2C19-IN-2
|
Others | Others |
CYP2C1/CYP2C19-IN-2 是无肝脏毒性和遗传毒性的CYP2C9/CYP2C19强效抑制剂,能够用于研究寨卡病毒 (ZIKV) 感染。 | |||
T63954 |
CYP3A4-IN-1
|
Others | Others |
CYP3A4-IN-1 是细胞色素 P450 3A4 (CYP3A4) 的有效抑制剂 (IC50: 0.085 μM)。 | |||
T73039 |
CYP1B1-IN-3
|
Others | Others |
CYP1B1-IN-3为选择性CYP1B1抑制剂,其IC50值分别针对CYP1B1、CYP1A1、CYP1A2为6.6, 347.3, >10000 nM。该化合物能够抑制细胞迁移与侵袭,并作用于P-gp、AKT/ERK、FAK/SRC及EMT信号通路。 | |||
T6420 |
BMS-707035
N-[(4-氟苯基)甲基1,6-二氢-5-羟基-1-甲基-6-氧代-2-(四氢-1,1-二氧-2H-1,2-噻嗪-2-基)-4-嘧啶甲酰胺 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
BMS707035是一种 HIV-1 整合酶抑制剂,IC50为15 nM。 | |||
T64249 |
CYP11B1-IN-2
|
Others | Others |
CYP11B1-IN-2 (compound 7aa) 是一种选择性的、口服具有活力的 CYP11B1 抑制剂,能够作用于 human CYP11B1 (IC50: 9 nM) 和 rat CYP11B1 (IC50: 25 nM)。CYP11B1-IN-2 能够用于研究皮质醇过量所致疾病。 | |||
T63337 |
CYP2C19-IN-1
|
Others | Others |
CYP2C19-IN-1 是强效的,无遗传毒性的、无肝脏毒性的 CYP2C19 抑制剂。 CYP2C19-IN-1 能够抑制 RNA 依赖的 RNA 聚合酶 (RdRP) (Ki: 6.16 μM),能够用于研究寨卡病毒 (ZIKV) 感染。 | |||
T61287 |
CYP121A1-IN-1
|
Others | Others |
CYP121A1-IN-1 是一种有效的CYP121A1抑制剂,对抗结核分枝杆菌具有良好的活性 (H37RvMIC90~6.25 μM, ~2.2 μg/mL)。CYP121A1-IN-1 通过抑制 CYP121A1 介导的环(l-酪氨酸-l-酪氨酸)转化为真菌环素,可显著减少真菌环素的产生。 | |||
T64032 |
CYP3A4-IN-3
|
Others | Others |
CYP3A4-IN-3 是特异性的、高度亲和力的细胞色素 P450 3A4 (CYP3A4) (cytochrome P450 3A4 (CYP3A4)) 抑制剂 (IC50: 0.075 μM)。CYP3A4-IN-3 是利托那韦类似物,结构更加简单,且抑制效果是利托那韦的两倍。CYP3A4-IN-3 能够用做抗病毒剂和免疫抑制剂。 | |||
T64037 |
CYP3A4-IN-2
|
Others | Others |
CYP3A4-IN-2 是细胞色素 P450 3A4 (CYP3A4) (cytochrome P450 3A4 (CYP3A4)) 的特异性抑制剂 (IC50: 0.055 μM)。CYP3A4-IN-2 是利托那韦类似物,与利托那韦相比,其 R2 侧基的疏水性更高,抑制作用更强。CYP3A4-IN-2 能够作为免疫抑制剂及抗病毒剂。 | |||
T78204 |
CYP11A1-IN-1
|
Others | Others |
CYP11A1-IN-1(化合物30)是一种针对CYP11A1的抑制剂,其IC50为201-2000 nM。该化合物主要应用于类固醇受体研究,尤其适用于雄激素受体依赖性疾病,例如前列腺癌的研究。 | |||
T61082 |
CYP1B1-IN-2
|
Others | Others |
CYP1B1-IN-2 (compound 9j) is a highly potent and selective inhibitor of CYP1B1, a cytochrome P450 enzyme. It exhibits an IC50 value of 0.52 nM [1]. | |||
T60723 |
CYP1B1-IN-1
|
Others | Others |
CYP1B1-IN-1 (Compound 9e) 是细胞色素 P450 1B1 (CYP1B1) 的选择性抑制剂 (IC 50 = 0.49 nM)。 | |||
T64154 |
CYP51/HDAC-IN-1
|
Others | Others |
CYP51/HDAC-IN-1 是一种口服具有活力的、有效的、双重 CYP51/HDAC 抑制剂。CYP51/HDAC-IN-1 能够抑制重要的毒力因子,可下调相关耐药基因的表达。CYP51/HDAC-IN-1 对热带念珠菌病和隐球菌性脑膜炎都表现出有效的治疗作用。 | |||
T79739 |
CYP51/PD-L1-IN-2
|
Others | Others |
CYP51/PD-L1-IN-2(compound L20)是一种具有抗真菌活性的喹唑啉化合物。它作为CYP51(IC50:0.263 μM)和PD-L1(IC50:0.017 μM)的双重抑制剂,能够在细胞周期的早期引发真菌细胞凋亡。CYP51/PD-L1-IN-2进一步显著降低IL-2、NLRP3、NF-κBp65等蛋白水平,触发线粒体损伤及ROS积累,终致真菌细胞裂解和死亡。 | |||
T79740 |
CYP51/PD-L1-IN-3
|
Others | Others |
CYP51/PD-L1-IN-3(compound L21)是一种具有抗真菌活性的喹唑啉化合物。作为CYP51(IC50: 0.205 μM) 和PD-L1(IC50: 0.039 μM) 的双重抑制剂,它能够引发真菌细胞在细胞周期早期的凋亡。此外,CYP51/PD-L1-IN-3 还能显著降低IL-2、NLRP3、NF-κBp65 蛋白的细胞内水平,并诱导线粒体损害及ROS 聚集,进而导致真菌细胞的裂解与死亡。 | |||
T78902 |
CYP51/PD-L1-IN-4
|
Others | Others |
CYP51/PD-L1-IN-4(化合物14a-2)是一种高效的双靶点抑制剂,其IC50值针对CYP51为0.17 μM,针对PD-L1为0.021 μM。该化合物在体外展现出卓越的抗真菌和抗耐药真菌能力,适用于真菌感染的研究。 | |||
T79738 |
CYP51/PD-L1-IN-1
|
Others | Others |
CYP51/PD-L1-IN-1(compound L11)是一种具有抗真菌活性的喹唑啉化合物,作为CYP51(IC50: 0.884 μM)和PD-L1(IC50: 0.083 μM)的双重抑制剂,能够在细胞周期早期引发真菌细胞的凋亡。该化合物还能有效减少IL-2、NLRP3、NF-κBp65等蛋白的细胞内水平,诱导线粒体损伤及ROS积聚,进而导致真菌细胞的破裂和死亡。 | |||
T74519 |
PROTAC CYP1B1 degrader-1
|
PROTACs | PROTAC |
PROTACCYP1B1 degrader-1 (Compound 6C) 是一种 α-萘黄酮嵌合衍生物,能够通过靶向 CYP1B1降解消除细胞色素 P450 (CYP)1B1 介导的耐药性,对 CYP1B1 和 CYP1A2 的 IC50分别为 95.1 和 9838.6 nM。PROTACCYP1B1 Degrader-1 可用于研究 CYP1B1过表达的前列腺癌。 | |||
T20968 |
CyPPA
|
Potassium Channel; Dopamine Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
CyPPA 是hSK2和hSK3的阳性调节剂,其EC50值分别为 5.6 μM 和14 μM。它对 hSK1 和 hIK 通道无活性。 | |||
T6814 |
Cyproheptadine hydrochloride
Periactin hydrochloride,Anarexol,盐酸赛庚啶,Cyproheptadine HCl,Nuran |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Cyproheptadine hydrochloride (Periactin hydrochloride) 是一种 5-HT2A 受体拮抗剂,具有抗抑郁和抗血清素作用。它具有抗血小板活性,可用于血栓栓塞性疾病的研究。 | |||
T1025 |
Tranylcypromine (2-PCPA) hydrochloride
反苯环丙胺盐酸盐,Tranylcypromine (2-PCPA) HCl,SKF-385 HCl |
Histone Demethylase; MAO | Chromatin/Epigenetic; Metabolism; Neuroscience |
Tranylcypromine (2-PCPA) hydrochloride (SKF-385 HCl) 是一种单胺氧化酶抑制剂,对治疗重度抑郁症、心境恶劣障碍和非典型抑郁症有效。 | |||
T0174 |
Cyproheptadine hydrochloride sesquihydrate
Peritol,盐酸赛庚啶半水合物,Periactin hydrochloride,Cyproheptadine hydrochloride,赛庚啶盐酸盐 |
5-HT Receptor; Histone Methyltransferase; Histamine Receptor | Chromatin/Epigenetic; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Cyproheptadine hydrochloride sesquihydrate (Peritol) 是一种抗组胺剂,也是血清素和组胺2拮抗剂。 | |||
T1167 |
Cyproterone acetate
Androcur,醋酸环丙氯地孕酮,Cyproterone 17-O-acetate,醋酸环丙孕酮 |
Androgen Receptor | Endocrinology/Hormones |
Cyproterone acetate (Cyproterone 17-O-acetate) 是能够抗雄激素(IC50=7.1 nM) 和孕激素合成的类固醇。它与 progesteron 和糖皮质激素受体有亲和力。 | |||
T0168 |
Estradiol (cypionate)
Depofemin,环戊丙酸雌二醇,Estradiol cypionate |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Estradiol cypionate (Depofemin) 是一种 Estradiol 的 17β-环戊丙酸酯,能够作用于雌激素受体。抑制ET-1的合成。 | |||
T77698 |
hCYP3A4 Fluorogenic substrate 1
|
Others; COX | Immunology/Inflammation; Neuroscience; Others |
hCYP3A4 Fluorogenic substrate 1 是邻苯二甲酰亚胺衍生物,对 COX 表现出低活性。 | |||
T7942 |
Tranylcypromine hemisulfate
Tranylcypromine Sulfate,Tranylcypromine (hemisulfate),反苯环丙胺半硫酸盐 |
Histone Demethylase; MAO; Monoamine Oxidase | Chromatin/Epigenetic; Metabolism; Neuroscience |
Tranylcypromine hemisulfate (Tranylcypromine Sulfate) 是单胺氧化酶(MAO) 和赖氨酸特异性去甲基化酶 1 (LSD1) 的抑制剂,可用于研究抑郁症和子宫内膜异位症。 | |||
T15033 |
Cyproconazole
|
Antibacterial | Microbiology/Virology |
Cyproconazole 是一种三唑类杀菌剂,在农业上用于保护作物免受多种真菌病原体的侵害。 | |||
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. | |||
T131586 |
1,2-Dehydro-alpha-cyperone
|
Others | Others |
1,2-Dehydro-alpha-cyperone 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T131586。 | |||
T31154 |
Cypridina luciferin
|
Others | Others |
Cypridina luciferin is a bioactive chemical. | |||
T36501 |
CYPMPO
RR 071 |
Others | Others |
CYPMPO is a free radical spin trap with excellent trapping capabilities toward hydroxyl and superoxide radicals in biological and chemical systems. Decay of the superoxide adduct of CYPMPO proceeds in an apparent first order fashion with half-lives of 15 and 51 minutes in a UV-illuminated hydrogen peroxide solution and a hypoxanthine/xanthine oxidase system, respectively. CYPMPO traps superoxide radicals generated by bovine neutrophils as effectively as DEPMPO.[1] The high melting point (126°C),... | |||
T74965 |
CypE-IN-1
|
Others | Others |
CypD-IN-1 是一种有效的亚型选择性亲环蛋白 E (CypE) 抑制剂。CypD-IN-1 具有 CypE 亲和力,IC50和 Ki 值分别为 0.013 μM 和 0.072 μM。CypD-IN-1 可用于多种疾病的研究,如氧化应激、神经退行性疾病、肝病、衰老、自噬和糖尿病。 | |||
T79914 |
Tranylcypromine
SKF 385 |
Monoamine Oxidase | Neuroscience |
Tranylcypromine (SKF 385)为一种高效的单胺氧化酶抑制剂。 | |||
T79283 |
hCYP1B1-IN-1
|
Others | Others |
hCYP1B1-IN-1 (compound B18)为高效的hCYP1B1抑制剂(IC50=3.6 nM),同时亦为芳香烃受体拮抗剂。该化合物展现优秀的代谢稳定性与细胞膜渗透性,能有效抑制MCF-7细胞迁移。 | |||
T79343 |
hCYP3A4-IN-1
|
Others | Others |
hCYP3A4-IN-1(化合物C6)是一种经口服时具有活性的hCYP3A4抑制剂,其对hCYP3A4的IC50值在人肝微粒体(HLM)为43.93 nM,在CHO-3A4稳定转染细胞系中为153.00 nM。hCYP3A4-IN-1通过竞争性抑制机制,有效抑制CYP3A4催化的N-乙基-1,8-萘二甲酰亚胺(NEN)羟基化反应,其Ki值为30.00 nM。 | |||
T73099 |
Etbicyphat
Trimethylopropane phosphate |
Others | Others |
Etbicyphat (Trimethylopropane phosphate)作为一种GABA(A)受体竞争性拮抗剂展现出显著效果。通过诱发海马体CA1神经元的类似癫痫的活动并与GABA(A)-benzodiazepine受体结合,Etbicyphat的作用机制得到了阐述。 | |||
T33627 |
Nematocyphol
|
Others | Others |
Nematocyphol is a triterpenoid from Euphorbia nematocypha hand-mazz. | |||
T26117 |
Rolicyprine
RMI 83027,RMI-83027,RMI83,027,RMI 83,027,RMI-83,027 |
Others | Others |
Rolicyprine is an antidepressant. | |||
T20787 |
Cyphenothrin
S-2703,Gokilaht,S2703,S 2703 |
Others | Others |
Cyphenothrin, a synthetic pyrethroid insecticide, is effective against cockroaches that have developed resistance to carbamate and organophosphorous insecticides. | |||
T71997 |
CypD-IN-29
|
Others | Others |
CypD-IN-29 is a non-peptidic inhibitor of cyclophilin D as a neuroprotective agent in Aβ-induced mitochondrial dysfunction. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
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。 | |||
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。 | |||
T5709 |
Cyperotundone
|
Others | Others |
Cyperotundone 是分离自 Nagarmotha (Cyperus rotundus) 中的一种倍半萜。 | |||
T5S1981 |
alpha-Cyperone
(+)-α-Cyperone,α-香附酮,α-Cyperone |
Others; Endogenous Metabolite | Metabolism; Others |
alpha-Cyperone (α-Cyperone) 与 IL-6, Cox-2, Cdc42, Nck-2, Rac1 的表达下调相关,从而能够抑制炎症反应。 | |||
TN4438 |
Ligucyperonol
|
Others | Others |
Ligucyperonol exhibits significant activities on protecting muscle cells from mild to moderate oxidative stress. | |||
TN5681 |
Cypellocarpin C
Camaldulenside,桉叶苷 |
||
Cypellocarpin C shows potent in vitro antitumor-promoting activity, it also can suppress an in vivo two-stage carcinogenesis induced with nitric oxide and TPA on mouse skin. | |||
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。 | |||
T2761 |
Naringin dihydrochalcone
Naringin DC,柚皮苷二氢查尔酮,柚皮甙二氢查尔酮 |
P450; NF-κB | Metabolism; NF-κB |
Naringin dihydrochalcone (Naringin DC) 是一种新型甜味剂,是来自柚皮苷的一种人工甜味剂。它也是一种CYP enzymes 的抑制剂。 | |||
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。 | |||
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。 | |||
T2876 |
Flavone
2-Phenyl-4-benzopyron,黄酮,2-Phenyl-4-chromone,2-Phenylchromone |
NOS; Endogenous Metabolite | Immunology/Inflammation; Metabolism |
Flavone (2-Phenyl-4-chromone) 是内源性代谢产物的一种。 | |||
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。 | |||
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。 | |||
T3S0860 |
Gitogenin
|
UGT | Metabolism |
Gitogenin 是一种从Tribulus longipetalus 整株中分离出来的天然类固醇,是一种 UDP-葡萄糖醛酸转移酶 1A4 (UGT1A4) 和 α-葡萄糖苷酶的选择性抑制剂,其IC50分别为 0.69 µM (使用三氟拉嗪为底物) 和 37.2 μM,对人类主要细胞色素 P450 亚型的活性无抑制作用。 | |||
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。 | |||
T13520 |
6-Hydroxymelatonin
|
Others | Others |
6-Hydroxymelatonin is a primary metabolic of Melatonin, which is metabolized by CYP 1A2. | |||
TN4130 | Germacrone 4,5-epoxide | gp120/CD4; IL Receptor; P450 | Immunology/Inflammation; Metabolism |
(4S,5S)-(+)-Germacrone-4,5-epoxide inhibits certain subtypes of cytochrome P450 (CYP). | |||
T82305 |
Glucoarabin
|
||
Glucoarabin是一种硫代葡萄糖苷,具备生物活性。在Hepa1c1c7细胞内,Glucoarabin的水解产物能够上调NQO1,而对细胞色素P450 (CYP) 1A1的活性无显著作用。 | |||
T40859 |
5-Hydroxy-8-methoxypsoralen
5-Hydroxyxanthotoxin,5-Hydroxy-8-methoxypsoralen |
Others | Others |
5-Hydroxy-8-methoxypsoralen (5-Hydroxyxanthotoxin) is a metabolite derived from Xanthotoxin, which acts as a potent tricyclic furocoumarin suicide inhibitor of CYP (cytochrome P-450). It is employed as an agent for the treatment of psoriasis, eczema, vitiligo, and certain cutaneous Lymphomas, in combination with phototherapy involving exposure to sunlight. | |||
T36472 |
Tetrahydro-11-deoxy Cortisol
|
Others | Others |
Tetrahydro-11-deoxy cortisol (THS) is the primary urinary metabolite of 11-deoxycortisol. Urinary excretion of THS is elevated in patients with 11β-hydroxylase deficiency, a condition resulting from mutations in the cytochrome P450 (CYP) isoform CYP11B1. Urinary levels of THS are also elevated in patients with adrenocortical carcinoma (ACC) and adrenocortical adenoma (ACA) but are higher in patients with ACC compared to ACA. | |||
TN7505 |
Thujopsene
NSC 44707 |
Others | Others |
Thujopsene, a sesquiterpene found in T. dolabrata, exhibits a wide range of biological activities. It inhibits Na+/K+-ATPase and cytochrome P450 (CYP) isoform CYP2B6 with IC50 values of 25.9 µg/ml and Ki of 0.8 µM, respectively. Additionally, thujopsene demonstrates antimicrobial efficacy against both Gram-positive and Gram-negative bacteria, such as S. aureus, M. luteus, and S. typhimurium, with MICs ranging from 25-50 µg/ml. It also suppresses antigen-induced β-hexosaminidase release in IgE-se... | |||
T37810 |
6',7'-Epoxybergamottin
|
Others | Others |
6'7'-Epoxybergamottin is a furanocoumarin found in grapefruit. It is a potent inhibitor of the cytochrome P450 (CYP) isoform CYP3A4 with an IC50 value of 0.30 ppm in a cell-free assay, 0.33 μM in HL7 human liver cells, and 0.22 μM in S9 human intestine cells. It has been studied in the context of drug interactions with grapefruit constituents. It is found in grapefruit juice at concentrations of 0.1-7.4 μM and inhibits the transport of talinolol , a permeability glycoprotein (P-gp/ABCB1) transpo... |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-00156 |
Cyclophilin F Protein, Human, Recombinant (His)
peptidylprolyl isomerase F,CYP3,Cyp-D,... |
Human | HEK293 Cells |
Cyclophilin F Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 20.3 kDa and the accession number is A0A024QZS4. | |||
TMPY-01593 |
Cyclophilin A Protein, Mouse, Recombinant (His)
peptidylprolyl isomerase A (cyclophilin A),Cphn,CyP... |
Mouse | E. coli |
Cyclophilin A Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 18.8 kDa and the accession number is P17742. | |||
TMPY-03413 |
PPIL2 Protein, Human, Recombinant (aa 280-457, His)
UBOX7,Cyp-60,CYP60,CYC4,peptidylprolyl iso... |
Human | E. coli |
PPIL2, is an enzyme that belongs to the cyclophilin family. The cyclophilins are peptidylprolyl isomerases and are highly conserved ubiquitous. They play an important role in protein folding, immunosuppression by cyclosporin A, and infection of HIV-1 virions. PPIL2 interacts with the proteinase inhibitor eglin c and is localized in the nucleus. It contains 1 PPIL2 cyclophilin-type domain and 1 U-box domain. PPIL2 accelerate the folding of proteins. It catalyzes the cis-trans isomerization of pro... | |||
TMPY-06723 |
Cyp c 1 Protein, Common carp, Recombinant
|
Common carp | E. coli |
Cyp c 1 Protein, Common carp, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 12.5 kDa. | |||
TMPY-01380 |
Cyclophilin B Protein, Human, Recombinant (His)
CYPB,peptidylprolyl isomerase B (cyclophilin B),HEL... |
Human | HEK293 Cells |
PPIB is identified as a candidate gene for OI-IX. Osteogenesis imperfecta (OI) is an inherited disorder of connective tissue typically caused by defects in either COL1A1 or COL1A2. A number of other genes causative of this disorder have been found, including PPIB, which forms one subunit of the prolyl 3-hydroxylase enzyme complex. Patients with OI caused by PPIB mutation should have appropriate early and regular management of their hearing. | |||
TMPJ-00676 |
PPIH Protein, Human, Recombinant (His)
Peptidyl-Prolyl Cis-Trans Isomerase H,Rotamase H,PPIase H,Sm... |
Human | E. coli |
Peptidyl-Prolyl Cis-Trans Isomerase H (PPIH) belongs to the Cyclophilin-type PPIase family that accelerate the folding of proteins. PPIases can catalyze the cis-trans isomerization of Proline Imidic peptide bonds in oligopeptides. PPIH participates in pre-mRNA splicing. It is a specific component of the complex that includes pre-mRNA processing factors PRPF3, PRPF4, and PRPF18, as well as U4/U5/U6 tri-snRNP. In addition, PPIH has PPIase activity and may play a role as a chaperone mediating the i... | |||
TMPJ-01090 |
PPID Protein, Human, Recombinant (His)
Cyclophilin-40,CYPD,Peptidyl-Prolyl Cis-Trans Isome... |
Human | E. coli |
Peptidyl-Prolyl Cis-Trans Isomerase D (PPID) belongs to the cyclophilin-type PPIase family and PPIase D subfamily. PPID is widely expressed and it contains one PPIase cyclophilin-type domain and three TPR repeats. PPID catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerates the folding of proteins. PPID can bind to the immunosuppressant cyclosporine A and is known that its overexpression suppresses the apoptosis in cancer cells. | |||
TMPH-03297 |
LGALS3BP Protein, Rat, Recombinant (His)
Protein 90K,Mac-2-binding protein,Galectin-3-binding protein... |
Rat | E. coli |
Promotes integrin-mediated cell adhesion. May stimulate host defense against viruses and tumor cells. | |||
TMPH-03017 |
CYP51 Protein, Mycobacterium tuberculosis, Recombinant (His & Myc)
Cytochrome P450-14DM,Sterol 14alpha-demethylase,Sterol 14-al... |
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-02141 |
CYP21A2 Protein, Human, Recombinant (His)
Cytochrome P450 21,CYP21A2,Cytochrome P450-C21B,Cyt... |
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-02140 |
CYP21A2 Protein, Human, Recombinant (E. coli, His)
Cytochrome P-450c21,Cytochrome P450-C21B,CYP21,21-O... |
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-00956 |
Aromatase/CYP19A1 Protein, Human, Recombinant (His)
ARO1,CYP19A1,Estrogen synthase,Cytochrome P450 19A1... |
Human | E. coli |
Aromatase/CYP19A1 Protein, Human, Recombinant (His) is expressed in E. coli. | |||
TMPH-01184 |
CYP2A6 Protein, Human, Recombinant (His & Myc)
CYP2A3,Coumarin 7-hydroxylase,1,4-cineole 2-exo-mon... |
Human | E. coli |
CYP2A6 Protein, Human, Recombinant (His & Myc) is expressed in E. coli. | |||
TMPH-01182 |
CYP1A1 Protein, Human, Recombinant (His)
Cytochrome P450 1A1,Cytochrome P450-C,Cytochrome P450-P1,Cyt... |
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. | |||
TMPY-05321 |
CYP3A4 Protein, Human, Recombinant (His)
P450C3,P450PCN1,CYPIIIA4,CP34,cytochrome P450 famil... |
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-02139 |
CYP17A1 Protein, Human, Recombinant (GST)
Cytochrome P450 17A1,CYPXVII,CYP17A1,C... |
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-01185 |
CYP2C19 Protein, Human, Recombinant (His & Myc)
Cytochrome P450 2C19,(R)-limonene 6-monooxygenase,(S)-limone... |
Human | E. coli |
CYP2C19 Protein, Human, Recombinant (His & Myc) is expressed in E. coli. | |||
TMPJ-01389 |
PPIE Protein, Human, Recombinant (His)
Rotamase E,PPIE,Cyclophilin E,PPIase E,CYP33,Cyclop... |
Human | E. coli |
Peptidyl-prolyl cis-trans isomerase E, also known as Cyclophilin E, Cyclophilin-33, Rotamase E, CYP33, PPIE, is an enzyme which belongs to the cyclophilin-type PPIase family of PPIase E subfamily. PPIE found in all the examined tissues including heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. PPIE contains one PPIase cyclophilin-type domain and one RRM (RNA recognition motif) domain. PPIE accelerates the folding of proteins. It catalyzes the cis-trans isomerization of ... | |||
TMPH-01084 |
CYP11A1 Protein, Human, Recombinant (His & SUMO)
Cholesterol side-chain cleavage enzyme, mitochondrial,CY... |
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-01183 |
CYP26B1 Protein, Human, Recombinant (His)
Cytochrome P450 26A2,CYP26B1,P450RAI2,Cytochrome P4... |
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 P450-J,4-nitr... |
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-01181 |
CYP11B2 Protein, Human, Recombinant (His & SUMO)
ALDOS,Corticosterone 18-monooxygenase, CYP11B2,Aldo... |
Human | E. coli |
CYP11B2 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli. | |||
TMPH-01186 |
CYP2C9 Protein, Human, Recombinant (His & Myc)
CYP2C10,Cytochrome P450 2C9,S-mephenytoin 4-hydroxy... |
Human | E. coli |
CYP2C9 Protein, Human, Recombinant (His & Myc) is expressed in E. coli. | |||
TMPY-02180 |
CXCL1 Protein, Human, Recombinant (His & NusA)
CA21H,CPS1,CYP21,GRO1,GROa,SCYB1,NAP-3,MGSA-a,P450c... |
Human | E. coli |
CXCL1 Protein, Human, Recombinant (His & NusA) is expressed in E. coli expression system with His and NusA tag. The predicted molecular weight is 65 kDa and the accession number is P09341-1. | |||
TMPY-02026 |
CXCL1 Protein, Human, Recombinant (His & SUMO)
FSP,P450c21B,CYP21B,CAH1,GROa,SCYB1,MGSA,chemokine ... |
Human | E. coli |
CXCL1 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with His and SUMO tag. The predicted molecular weight is 21.3 kDa and the accession number is P09341-1. | |||
TMPY-02868 |
CXCL1 Protein, Human, Recombinant
chemokine (C-X-C motif) ligand 1 (melanoma growth stimulatin... |
Human | E. coli |
CXCL1 Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 7.9 kDa and the accession number is P09341-1. | |||
TMPY-02297 |
ACYP1 Protein, Human, Recombinant (GST)
ACYPE,acylphosphatase 1, erythrocyte (common) type |
Human | E. coli |
ACYP1 Protein, Human, Recombinant (GST) is expressed in E. coli expression system with GST tag. The predicted molecular weight is 38 kDa and the accession number is P07311. | |||
TMPY-02298 |
ACYP2 Protein, Human, Recombinant (GST)
ACYM,acylphosphatase 2, muscle type,ACYP |
Human | E. coli |
Recent genome-wide association studies have identified genetic variants in ACYP2 and WFS1 that are associated with cisplatin-induced ototoxicity. We sought to explore the role of these genetic susceptibility factors to cisplatin-induced ototoxicity in patients with testicular cancer. Telomere length, as a marker of biological aging, has been reported to influence the risk of several age-related diseases, including ischemic stroke. Recent studies have identified the genetic variant within ACYP2 a... | |||
TMPH-00364 |
Pectate lyase 1 Protein, Chamaecyparis obtusa, Recombinant (His & SUMO)
Major pollen allergen Cha o 1,Pectate lyase 1 |
Chamaecyparis obtusa | E. coli |
Has pectate lyase activity. Pectate lyase 1 Protein, Chamaecyparis obtusa, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 54.1 kDa and the accession number is Q96385. | |||
TMPJ-00048 |
CYPA Protein, Mouse, Recombinant
SP18,PPIA,PPIase A,Peptidyl-prolyl cis-trans isomerase A, |
Mouse | E. coli |
Peptidyl-prolyl cis-trans isomerase A is a cytoplasm protein which belongs to the cyclophilin-type PPIase family and PPIase A subfamily. Cyclophilins(CyPs) are a family of proteins found in organisms ranging from prokaryotes to humans. These molecules exhibit peptidyl-prolyl isomerase activity, suggesting that they influence the conformation of proteins in cells. Cyclophilin A accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopep... | |||
TMPJ-00798 |
ACYP1 Protein, Human, Recombinant (His)
ACYPE,Acylphosphate phosphohydrolase 1,erythrocyte ... |
Human | E. coli |
ACYP1, also known as Acylphosphatase-1, Acylphosphatase, erythrocyte isozyme, Acylphosphatase, organ-common type isozyme, Acylphosphate phosphohydrolase 1 and ACYPE, is a small cytosolic enzyme which catalyzes the hydrolysis of the carboxyl-phosphate bond of acylphosphates.ACYP1 is a protein which belongs to the acylphosphatase family and contains 1 fibrinogen C-terminal domain. Two isoenzymes have been isolated, called muscle acylphosphatase and erythrocyte acylphosphatase, on the basis of thei... | |||
TMPJ-01049 |
CYPA Protein, Human, Recombinant
Rotamase A,Peptidyl-prolyl cis-trans isomerase A,PPIase A,PP... |
Human | E. coli |
Peptidyl-prolyl cis-trans isomerase A is a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family, which catalyzes the cis-trans isomerization of proline imidic peptide bonds. Cyclophilin A regulate many biological processes, including intracellular signaling, transcription, inflammation, and apoptosis. Cyclophilin is also incorporated into many viruses, including HIV1, where it has been speculated to be involved in functions such as viral assembly and infectivity. The immunosuppressi... | |||
TMPH-01748 |
CYPOR Protein, Human, Recombinant (GST)
NADPH--cytochrome P450 reductase,P450R,CPR,POR,CYPO... |
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-00817 |
Pectate lyase 1 Protein, Hesperocyparis arizonica, Recombinant (His & Myc)
Major pollen allergen Cup a 1,Pectate lyase 1 |
Hesperocyparis arizonica | E. coli |
Has pectate lyase activity. Pectate lyase 1 Protein, Hesperocyparis arizonica, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 42.6 kDa and the accession number is Q9SCG9. | |||
TMPH-02801 |
CYPOR Protein, Mouse, Recombinant (His)
CYPOR,P450R,CPR,NADPH--cytochrome P450 reductase,PO... |
Mouse | E. coli |
CYPOR Protein, Mouse, Recombinant (His) is expressed in E. coli. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIJ-0464 |
trans-Cypermethrin-d6 (dimethyl-d6)
|
||
trans-Cypermethrin-d6 (dimethyl-d6) 是 trans-Cypermethrin 的氘代化合物。trans-Cypermethrin 的 CAS 号为 67375-30-8。alpha-Cypermethrin 是一种合成拟除虫菊酯杀虫剂,用于大规模商业农业应用。 | |||
T12701 |
(rel)-Tranylcypromine D5 hydrochloride
2-Phenylcyclopropylamine D5 hydrochloride |
Histone Demethylase | Chromatin/Epigenetic |
(rel)-Tranylcypromine D5 hydrochloride is a deuterium labeled (rel)-Tranylcypromine hydrochloride. (rel)-Tranylcypromine hydrochloride is an irreversible, nonselective inhibitor of monoamine oxidase (MAO) used in the treatment of depression. | |||
TMIJ-0358 |
2-Naphthol-d8
|
||
2-Naphthol-d8 是 2-Naphthol 的氘代化合物。2-Naphthol 的 CAS 号为 135-19-3。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。 | |||
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... | |||
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... | |||
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。 | |||
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... |