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Cat. No. | Product Name | ||
---|---|---|---|
L2510 | 脂代谢化合物库 | 492 compounds | |
492 个脂代谢相关的化合物集合,可用于高通量和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1604L |
Thioredoxin reductase peptide acetate
Thioredoxin reductase peptide acetate(950890-23-0 free base) |
Others | Others |
Thioredoxin reductase peptide acetate(950890-23-0 free base) 对应于硫氧还蛋白还原酶 (TrxR) 中的 53–67 位残基,用于硫氧还蛋白还原酶研究。哺乳动物硫氧还蛋白还原酶 (TR) 催化硫氧还蛋白 (Trx) 的氧化还原活性二硫键的还原,并且在结构和谷胱甘肽还原酶的作用机制,除了 C 末端的 16 个氨基酸延伸部分含有一个罕见的连位硒硫键。 | |||
T14175 |
Aldose reductase-IN-1
AT-001,Caficrestat |
Others; Reductase | Endocrinology/Hormones; Metabolism; Others |
Aldose reductase-IN-1 (AT-001)是醛糖还原酶的高效抑制剂, IC50=为28.9 pM。 | |||
T78342 |
Glutathione reductase
EC 1.6.4.2 |
Others | Others |
Glutathione reductase (EC 1.6.4.2) 是维持还原型谷胱甘肽供应的还原酶。 | |||
TP1604 |
Thioredoxin reductase peptide
|
||
Thioredoxin reductase peptide corresponds to residues 53–67 in thioredoxin reductase (TrxR), used in thioredoxin reductase research.Mammalian thioredoxin reductase (TR) catalyzes the reduction of the redox-active disulfide bond of thioredoxin (Trx) and is | |||
TP1375 |
Thioredoxin reductase peptide TFA
|
||
Thioredoxin reductase peptide TFA corresponds to residues 53-67 in thioredoxin reductase (TrxR), used in thioredoxin reductase research.. | |||
T10636 | 5α-reductase-IN-1 | Others | Others |
5α-reductase-IN-1 is a potent inhibitor of the enzyme 5α-reductase. This compound is primarily employed in research studies to investigate its potential efficacy in treating patterned alopecia. It is commonly used in combination with minoxidil, a well-known treatment for hair loss. | |||
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。 | |||
T61555 |
Aldose reductase-IN-6
|
Others | Others |
Aldose reductase-IN-6 (Compound 3) is a competitive inhibitor of aldose reductase (AR), possessing an IC50 of 3.164 μM and a Ki of 0.018 μM. Notably, Aldose reductase-IN-6 demonstrates no cytotoxicity toward normal cells [1]. | |||
T62951 |
Aldose reductase-IN-2
|
Others | Others |
Aldose reductase-IN-2 (Compound 5f) 是一种醛糖还原酶 (AR) 的有效抑制剂,具有抗氧化作用。Aldose reductase-IN-2 是一种很有前途的抗糖尿病并发症药物。 | |||
T61957 |
Aldose reductase-IN-3
|
Others | Others |
Aldose reductase-IN-3 (Compound 5) 是有效的、中等选择性的醛糖还原酶 (AR) 抑制剂(IC50= 3.99 μM)。醛糖还原酶是参与各种炎症性疾病 (包括败血症) 的分子靶标。Aldose reductase-IN-3在脓毒症中具有研究的潜力。 | |||
T60601 |
Aldose reductase-IN-4
|
Others | Others |
Aldose reductase-IN-4 (comund IIc) 是一种醛糖还原酶的抑制剂,其对ALR1和ALR2的IC50值分别为 11.70 μM 和 0.98 μM。 | |||
T60897 |
Aldose reductase-IN-5
|
Others | Others |
Aldose reductase-IN-5 是一种醛糖还原酶(ALR2)抑制剂,可增强抑制性兴奋性和抗氧化能力的组合,从而延缓糖尿病并发症的进程。 | |||
T22757 |
EBPC
|
Reductase | Endocrinology/Hormones; Metabolism |
EBPC 是醛糖还原酶的选择性抑制剂,其IC50= 47 nM。 | |||
T79520 |
HMG-CoA Reductase-IN-1
|
Others | Others |
HMG-CoA Reductase-IN-1是一种HMG-CoA还原酶抑制剂,显示出高HMGR抑制活性及OATP1B1亲和力,具有pIC50值8.54和pKm值1.98。该化合物适用于高胆固醇血症的研究。 | |||
T16910 |
Sorbinil
|
Reductase | Endocrinology/Hormones; Metabolism |
Sorbinil 是一种醛糖还原酶抑制剂, 在糖尿病及其并发症方面发挥治疗作用。 | |||
T23403 |
Sulindac sulfone
|
Reductase; COX | Endocrinology/Hormones; Immunology/Inflammation; Metabolism; Neuroscience |
Sulindac sulfone 是非甾体抗炎药舒林酸 (sulindac) 的代谢物。 它是醛糖还原酶的抑制剂 (IC50 =367 nM)。 | |||
T14342 |
Atorvastatin lactone
|
HMG-CoA Reductase | Metabolism |
Atorvastatin lactone 是一种 Atorvastatin 的前药。其中 Atorvastatin 是口服具有活力的 3- 羟基 -3- 甲基戊二酰辅酶 A 还原酶抑制剂。 | |||
T6901 |
N6022
|
GSNOR | Metabolism |
N6022 是选择性可逆的S-Nitrosoglutathione reductase 抑制剂,IC50=8 nM。 | |||
T0488 |
Finasteride
非那雄胺,MK-906 |
Reductase | Endocrinology/Hormones; Metabolism |
Finasteride (MK-906) 是 5α-还原酶的竞争性抑制剂,对 II 型 5α-还原酶的IC50为 4.2 nM,对 II 型 5α-还原酶的亲和力是 I 型酶的 100 倍。它可用于研究前列腺增生和雄激素性脱发。 | |||
T10393 |
AT-007
|
Reductase | Endocrinology/Hormones; Metabolism |
AT-007 是口服有效的,中枢神经系统渗透性醛糖还原酶的高效抑制剂, IC50为 100 pM。在 GALT 缺失大鼠中,它降低了有毒的半乳糖醇水平并预防了疾病并发症。 | |||
T1499 |
Dutasteride
GG 745,Avodart,度他雄胺,GI 198745 |
Apoptosis; Reductase | Apoptosis; Endocrinology/Hormones; Metabolism |
Dutasteride (GI 198745) 是一种 5α 还原酶同工酶抑制剂,还可能因其结构域 DHT 相似对雄激素受体产生脱靶效应。 | |||
T5481 |
TRi-1
|
Others | Others |
TRi-1 是不可逆的胞质硫氧还蛋白还原酶1 的特异性抑制剂(IC50:12 nM)。它有抗肿瘤作用,且线粒体毒性很小。 | |||
T17114 |
Tolrestat
托瑞司他,AY-27773 |
Reductase | Endocrinology/Hormones; Metabolism |
Tolrestat (AY-27773) 是一种口服有效的醛糖还原酶抑制剂 (IC50 = 35 nM)。 | |||
T36692 |
Fanotaprim
|
DHFR | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Fanotaprim 是二氢叶酸还原酶的有效抑制剂,抑制 tgDHFR (Toxoplasma gondiiDHFR) 和 hDHFR (human DHFR)的 IC50分别为 1.57 和 308 nM。Fanotaprim 在研究弓形虫病方面具有价值。 | |||
T10339 |
Antitrypanosomal agent 1
|
Parasite | Microbiology/Virology |
Antitrypanosomal agent 1 是一种有效的选择性锥虫硫酮还原酶抑制剂,IC50为 3.3 μM。它抑制谷胱甘肽还原酶,IC50为 64.8 μM,抑制布氏锥虫,EC50为 1 μM。 | |||
T2013 |
Ponalrestat
|
Reductase | Endocrinology/Hormones; Metabolism |
Ponalrestat 是一种口服有效的,选择性的和非竞争性的醛糖还原酶抑制剂,对 ALR2选择性选择性较高,Ki 为 7.7 nM, 对 ALR1 的选择性较弱,Ki 为 60 μM。Ponalrestat 抑制葡萄糖向山梨糖醇的转化。 | |||
T14362 |
AY 9944
|
Others | Others |
AY 9944 是特异性的胆固醇生物合成抑制剂。它抑制 7- 脱氢胆固醇 Δ7- 还原酶 (IC50:13 nM),导致胆固醇不足和 7DHC 积累。在高剂量下,它可在培养的胚胎中抑制固醇 Δ7-Δ8 异构酶,造成胆固醇 8-en-3β-ol 的积累。 | |||
T5195 |
Alrestatin
阿瑞司他丁,AY-22284 |
Reductase | Endocrinology/Hormones; Metabolism |
Alrestatin (AY-22284) 是醛糖还原酶的特异性抑制剂,能够在体外减弱大鼠血管平滑肌中葡萄糖诱导的血管紧张素 II 的产生。 | |||
T8452 |
Dantrolene
|
Others | Others |
Dantrolene 是一种肌肉松弛剂,是人红细胞谷胱甘肽还原酶的非竞争性抑制剂,其Ki 和IC50值分别为 111.6 μM 和 52.3 μM。它是兰尼碱受体拮抗剂及Ca2+信号稳定剂。它可用于研究恶性高热、亨廷顿病、肌肉痉挛和其他神经阻滞剂恶性综合征。 | |||
T1487 |
Fluvastatin sodium
XU 62320 sodium,XU-62-320,氟伐他汀钠,Fluvastatin sodium salt |
Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Fluvastatin sodium (Fluvastatin sodium salt) salt 是羟甲基戊二酰辅酶 A 还原酶的竞争性抑制剂,IC50为 8 nM。它通过依赖 Nrf2 的抗氧化通路保护血管平滑肌细胞免受氧化应激,是一种常用的降胆固醇剂。 | |||
T1458 |
Epalrestat
ONO2235,依帕斯他,依帕司他 |
Reductase | Endocrinology/Hormones; Metabolism |
Epalrestat (ONO2235) 是醛糖还原酶抑制剂,在长期治疗中具有良好的耐受性。 它可以有效改善糖尿病神经病变的相关症状并延缓疾病的进展,特别是在微血管病变有限且血糖控制良好的患者中。 | |||
T6450 |
Clinofibrate
克利贝特,S-8527,Lipoclin |
HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
Clinofibrate (Lipoclin) 是一种降脂剂,可抑制羟甲基戊二酰辅酶 A 还原酶。它用于控制血液中的高胆固醇和甘油三酯水平。 | |||
T22229 |
Acid Yellow 36
Metanil Yellow,酸性黄36 |
Others | Others |
Acid Yellow 36 (Metanil Yellow) 是一种偶氮染料和 pH 指示剂,当 pH 值从 1.2 到 2.3 时,发生由红色到黄色的颜色转变。它是 P-450 特异性同工酶和胞浆酶的双功能诱导剂,可用于皮革、造纸和纺织工业。 | |||
T38684 |
AKR1C3-IN-4
AKR1C3-IN-4 |
NADPH | Metabolism |
AKR1C3-IN-4 是醛酮还原酶 1C3 (AKR1C3) 选择性抑制剂,IC50为 0.56 μM。它在去势抵抗性前列腺癌中有研究的价值。 | |||
T0297 |
Clofarabine
Clofarex,氯法拉滨,克罗拉滨,Evoltra,Clolar |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Clofarabine (Clofarex) 是一种核糖核苷酸还原酶抑制剂,IC50值为65 nM。它是核苷类似物,可用于癌症研究。 | |||
T8003 |
Methotrexate disodium
|
Apoptosis; Dehydrogenase; DNA/RNA Synthesis; Antifolate; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Methotrexate disodium 是一种叶酸类似物代谢抑制剂,具有免疫抑制剂和抗肿瘤特性,用于类风湿关节炎和研究多种癌症。 | |||
T14864 |
Caracemide
NSC-253272,卡醋胺 |
Others; DNA/RNA Synthesis; Antibacterial | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Caracemide (NSC-253272) 抑制大肠杆菌的核糖核苷酸还原酶。 Caracemide 可用于抗癌研究。 | |||
T6994 |
SR12813
SR-12813,SR 12813,GW 485801 |
HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
SR12813 (GW 485801) 是一种人孕烷X 受体激动剂,还是一种 3-羟基-3-甲基-戊二酰辅酶 A 还原酶抑制剂,IC50值为 0.85 μM。 | |||
T35317 |
Zopolrestat
CP 73850,CP73850,CP-73850,唑泊司他,Zopolrestatum |
Reductase | Endocrinology/Hormones; Metabolism |
Zopolrestat (CP 73850) 是口服有效的醛糖还原酶抑制剂,IC50为3.1 nM。Zopolrestat (CP 73850) 在糖尿病并发症方面有研究的价值。 | |||
T3693 |
DHFR-IN-3
7-bromoquinazoline-2,4-diamine,7-溴-2,4-二氨基喹唑啉 |
Others; DHFR | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Others |
DHFR-IN-3 (7-bromoquinazoline-2,4-diamine) 是一种二氢叶酸还原酶 (DHFR) 抑制剂。 | |||
T3157 |
COH29
RNR Inhibitor COH29 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
COH29 (RNR Inhibitor COH29) 是一种口服可用的芳香族取代噻唑,是人类核糖核苷酸还原酶 (RNR) 的抑制剂,具有潜在的抗肿瘤活性。它抑制核糖核苷酸还原酶的IC50为 16 μM。 | |||
T12092 |
Monacolin J
Antibiotic MB 530A,Lovastatin diol lactone,辛伐他汀内酯二醇 |
HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
Monacolin J (Antibiotic MB 530A) 是一种胆固醇生物合成抑制剂,抑制 HMG-CoA 还原酶的活性。 | |||
T15568 |
Imirestat
Alcon 1576,AL 1576,咪瑞司他,HOE 843 |
Reductase | Endocrinology/Hormones; Metabolism |
Imirestat (HOE 843) 是=aldose reductase 的抑制剂,在糖尿病中有研究价值。 | |||
T6120 |
Pralatrexate
Folotyn,10-炔丙基-10-去氮杂氨基蝶呤,10-Propargyl-10-deazaaminopterin,普拉曲沙 |
Apoptosis; DHFR; Antifolate; TAM Receptor | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Tyrosine Kinase/Adaptors |
Pralatrexate (10-Propargyl-10-deazaaminopterin) 是一种抗叶酸剂,也是二氢叶酸还原酶抑制剂,Ki 值为 13.4 pM。它具有抗肿瘤活性,可研究复发/难治性 T 细胞淋巴瘤。它是叶酰聚谷氨酸合成酶的底物,具有改善的细胞摄取和保留能力。 | |||
T3116 |
Atorvastatin hemicalcium salt
Lipitor,Atorvastatin hemicalcium,Atorvastatin Calcium,CI-981,阿托伐他汀钙,Sortis |
Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Atorvastatin hemicalcium salt (Atorvastatin Calcium) 是一种口服有效的 HMG-CoA 还原酶抑制剂 ,可用作降低胆固醇的药物。它抑制人 SV-SMC 增殖和侵袭,IC50分别为 0.39 μM 和 2.39 μM。 | |||
T1676 |
Rosuvastatin
罗伐他汀,ZD 4522,瑞舒伐他汀 |
Potassium Channel; HMG-CoA Reductase; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Rosuvastatin (ZD 4522) 是一种抗血脂药,可竞争性抑制羟甲基戊二酰辅酶 A 还原酶,用于降低血浆胆固醇水平和预防心血管疾病。它降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go 相关基因电流,IC50为 195 nM,延迟心脏复极化,延长动作电位持续时间和校正 QT 间期间隔。 | |||
T2534 |
Pitavastatin calcium
P-872441,nisvastatin,itavastatin,Pitavastatin hemicalcium,匹伐他汀钙,NK-104 |
Apoptosis; Mitophagy; Endogenous Metabolite; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Pitavastatin calcium (NK-104) 是一种羟甲基戊二酰-CoA 还原酶抑制剂。它在 HepG2 细胞中抑制乙酸合成胆固醇的IC50为 5.8 nM。它是高效的肝细胞低密度脂蛋白胆固醇受体诱导剂。具有抗癌活性。 | |||
T1510 |
Rosuvastatin calcium
ZD 4522 Calcium,ZD4522,Rosuvastatin hemicalcium,瑞舒伐他汀钙 |
Potassium Channel; HMG-CoA Reductase; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Rosuvastatin calcium (ZD4522) 是肝羟甲基戊二酰辅酶 A 还原酶的选择性和竞争性抑制剂,具有抗血脂活性。它降低成熟 hERG 的表达以及热休克蛋白 70 与 hERG 蛋白的相互作用,还降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go 相关基因电流,延迟心脏复极化,来延长动作电位持续时间和校正 QT 间期间隔。 | |||
T1485 |
Methotrexate
NCI-C04671,WR19039,Amethopterin,甲氨蝶呤,CL14377 |
Apoptosis; Dehydrogenase; DNA/RNA Synthesis; Antifolate; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Methotrexate (WR19039) 是一种叶酸类似物,一种二氢叶酸还原酶 DHFR 的抑制剂。Methotrexate 具有抗代谢、抗肿瘤和免疫抑制等活性,常用于类风湿关节炎和多种肿瘤的研究。 | |||
T20765 |
Atorvastatin
阿托伐他汀,阿伐他汀 |
HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
Atorvastatin 是一种具有口服活性的 HMG-CoA 还原酶抑制剂,通过激活肝细胞色素p450加快代谢,具有有效降低血脂的能力。Atorvastatin 以 IC50 值分别为 0.39 μM 和 2.39 μM 来抑制人 SV-SMC 细胞的增殖和侵袭。Atorvastatin 与氯吡格雷同时服用两种可能会导致患者血栓事件增加。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN2601 |
12-O-Methylcarnosic acid
|
Reductase | Endocrinology/Hormones; Metabolism |
12-O-Methylcarnosic acid 是分离自小叶丹参的丙酮提取物的一种二萜肉桂酸,可抑制 5α-还原酶 (5α-reductase) 活性,IC50为 61.7 μM。它抑制 LNCaP 细胞的增殖。它具有抗微生物活性、抗氧化和抗癌活性。 | |||
T6S2384 |
Poliumoside
|
Reductase | Endocrinology/Hormones; Metabolism |
Poliumoside 是从 Brandisia hancei 的茎和叶中分离出来的咖啡酰化的苯丙烷糖苷。Poliumoside 能够抑制晚期糖基化终产物的形成和大鼠晶状体醛糖还原酶,IC50分别为 19.69 和 8.47 μM。Poliumoside 具有抗炎和抗氧化特性。 | |||
T8115 |
Menthofuran
|
Others | Others |
Menthofuran 是一种天然产品。 | |||
T3378 |
Alpha-Estradiol
α-雌二醇,Alfatradiol,雌二醇,17α-Estradiol,Epiestrol,Epiestradiol |
Estrogen/progestogen Receptor; Reductase; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Alpha-Estradiol (Epiestradiol) 是一种雌性激素,可抑制5α-reductase,在雄原性脱发的研究中有潜力。 | |||
TN1733 |
Hesperetin 7-O-glucoside
|
Anti-infection; Antibacterial; HMG-CoA Reductase | Metabolism; Microbiology/Virology |
Hesperetin 7-O-glucoside 是通过 Hesperidin 的酶促转化产生的一种人 HMG-CoA 还原酶抑制剂,具有降压作用,可抑制幽门螺杆菌的生长。 | |||
TN6715 |
7-Ketocholesterol
|
Others | Others |
7-Ketocholesterol 是胆固醇的代谢物。 | |||
T5S1131 |
Ganoderic acid C6
灵芝酸C6 |
Others | Others |
Ganoderic acid C6 是醛糖还原酶活性的抑制剂。 | |||
T1207 |
Lovastatin
MK-803,洛伐他汀,Mevinolin |
Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Lovastatin (MK-803) 是一种 HMG-CoA 还原酶抑制剂,用于降低胆固醇。 | |||
T0683 |
Mevastatin
Compactin,ML236B,美伐他汀 |
Apoptosis; Antibacterial; Antibiotic; HMG-CoA Reductase; Autophagy; Lipid | Apoptosis; Autophagy; Metabolism; Microbiology/Virology |
Mevastatin (ML236B) 是他汀类 HMG-CoA 还原酶抑制剂。它是一种降脂药,可诱导细胞凋亡,将癌细胞阻滞在 G0/G1期。它还可增加内皮型一氧化氮合酶的 mRNA 和蛋白质水平。它有抗肿瘤活性,用于心血管疾病的研究。 | |||
T0725 |
Isoliquiritigenin
异甘草素,ISL,Isoliquiritigen,GU17 |
Apoptosis; Influenza Virus; Reductase; Autophagy | Apoptosis; Autophagy; Endocrinology/Hormones; Metabolism; Microbiology/Virology |
Isoliquiritigenin (ISL) 是从光果甘草根中分离得到的一种黄酮类天然产物,具有抗肿瘤的活性。它抑制流感病毒复制,EC50为 24.7 μM,还能抑制 aldose reductase 的活性,IC50值为 320 nM。 | |||
T1664 |
Meglutol
Dicrotalic acid,3-Hydroxy-3-methylglutaric acid,美格鲁托 |
Endogenous Metabolite; HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
Meglutol (3-Hydroxy-3-methylglutaric acid) 是一种抗血脂剂,可降低胆固醇、甘油三酯、血清 β-脂蛋白和磷脂。它抑制胆固醇生物合成中的限速酶羟甲基戊二酰辅酶 A 还原酶的活性。 | |||
TN1438 |
beta-Amyrin acetate
beta-香树脂醇乙酸酯 |
Antioxidant; HMG-CoA Reductase; Epoxide Hydrolase; Antifungal | Metabolism; Microbiology/Virology; oxidation-reduction |
beta-Amyrin acetate 抑制 HMG-CoA 还原酶 (HMGCR) 和 sEH 活性,IC50 为 3.4 μM。 beta-Amyrin acetate 具有抗炎、抗真菌、抗氧化和抗高血脂活性。 | |||
T0687 |
Simvastatin
辛伐他汀,MK-0733,MK 733 |
Apoptosis; Mitophagy; Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Simvastatin (MK 733) 是一种 HMG-CoA 还原酶抑制剂 (Ki=0.2 nM),具有口服活性。Simvastatin 具有降血脂活性,可以抑制肝脏产生胆固醇,还可以用于预防心血管疾病。 | |||
T0672 |
Pravastatin sodium
CS-514 Sodium,普伐他汀钠,CS-514 (sodium) |
Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Pravastatin sodium (CS-514 (sodium)) 是一种 HMG-CoA 还原酶抑制剂,抑制甾醇合成,IC50 为 5.6 μM。 | |||
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。 | |||
T3801 |
(Rac)-Byakangelicin
白当归素,Bjacangelicin,Bjakangelicin,Biacangelicin,7H-Furo[3,2-g][1]benzopyran-7-one, 9-(2,3-dihydroxy-3-methylbutoxy)-4-methoxy-,Byakangelicin |
Others | Others |
(Rac)-Byakangelicin (7H-Furo[3,2-g][1]benzopyran-7-one, 9-(2,3-dihydroxy-3-methylbutoxy)-4-methoxy-) 是一种 Byakangelicin 的外消旋体,主要分离自 Angelica 属中。其中 Byakangelicin 是醛糖还原酶抑制剂(IC50:6.2 μM),可用作抗肿瘤剂。 | |||
TN1661 |
Ganoderic acid C2
灵芝酸 C2 |
Reductase; Histamine Receptor; Immunology/Inflammation related | Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Ganoderic acid C2 是分离自灵芝的一种三萜化合物, 具有潜在的抗肿瘤生物活性,以及抗组胺、抗衰老和细胞毒性作用。它对rat lens aldose reductase 具有很高的抑制活性,IC50为 3.8 µM。 | |||
TN1016 |
Kukoamine A
|
NF-κB; Lipoxygenase; DNA/RNA Synthesis; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; NF-κB |
Kukoamine A 是一种天然的精胺衍生物,具有抗癌、抗高血压、细胞保护、抗氧化和抗炎活性。它是锥虫硫磷还原酶抑制剂,Ki 值为 1.8 μM。 | |||
T5372 |
L-SelenoMethionine
L-(+)-Selenomethionine,L-硒代蛋氨酸 |
Apoptosis; Amino Acids and Derivatives; Endogenous Metabolite | Apoptosis; Metabolism |
L-SelenoMethionine (L-(+)-Selenomethionine) 是 Selenomethionine 的 L-异构体,是硒的主要天然食物形式。它是一种癌症化学预防剂,可以增加谷胱甘肽过氧化物酶的表达,还可以通过饮食补充降低癌症的发生率并诱导癌细胞凋亡。 | |||
T3329 |
4',7-Dimethoxyisoflavone
4',7-二甲氧基异黄酮,Dimethoxydaidzein,Daidzein dimethyl ether |
Endogenous Metabolite; Antifungal | Metabolism; Microbiology/Virology |
4',7-Dimethoxyisoflavone (Daidzein dimethyl ether) 是从阔荚合欢中分离的黄酮类化合物,有抗真菌作用,可抑制大鼠前列腺睾酮5α-还原酶。 | |||
TN1975 |
Neosmitilbin
Neoastilbin,新落新妇苷 |
Others | Others |
Neosmitilbin (Neoastilbin) 分离于 Garcinia mangostana。它能够有效抑制晶状体醛糖还原酶的活性,可能具有抗氧化和抗炎作用。 | |||
T5S0543 |
Isocurcumenol
|
Apoptosis; Estrogen Receptor/ERR; Reductase | Apoptosis; Endocrinology/Hormones; Metabolism |
Isocurcumenol 是从莪术中分离得到的一种天然产物,是一种ERα抑制剂,对 DLA 和 KB 癌细胞的IC50分别为 99.1 µg/mL 和 178.2 µg/mL,具有抗肿瘤活性。 | |||
T10183 |
6-Methoxytricin
|
Reductase | Endocrinology/Hormones; Metabolism |
6-Methoxytricin 是从积雪草中分离的黄酮类化合物,是醛糖还原酶 (AR) 和晚期糖基化终产物 (AGE) 的抑制剂,抑制生物细胞中的T细胞增殖和活化。 | |||
TN1656 |
Ganoderenic acid A
灵芝烯酸A,灵芝烯酸 A |
Others | Others |
Ganoderenic acid A 是三萜类化合物。它对 CCl4 诱导的肝损伤具有保护作用。它是β-葡萄糖醛酸酶抑制剂。 | |||
T3S0507 |
Homovanillic acid
Homovaniuic acid,Vanilacetic acid,高香草酸,Vanillacetic acid |
Others; Endogenous Metabolite | Metabolism; Others |
Homovanillic acid (Vanillacetic acid) 是一种多巴胺代谢物,它与乳糜泻、生长激素缺乏、芳香族氨基酸脱羧酶缺乏症以及脂联素还原酶缺乏症相关。 | |||
T7730 |
Aminopterin
APGA,氨基蝶呤,4-Aminofolic acid |
Antifolate | Cell Cycle/Checkpoint |
Aminopterin (4-Aminofolic acid) 是叶酸的 4-氨基衍生物,是叶酸拮抗剂,具有抗癌和免疫抑制活性,用于研究儿童白血病。它催化叶酸还原为四氢叶酸,竞争性抑制二氢叶酸还原酶,Ki 值为 3.7 pM。 | |||
TN5845 |
Neochlorogenic acid methyl ester
5-O-Caffeoylquinic acid methyl ester,Methyl 3-caffeoylquinate,GIP (1-39) acetate(725474-97-5 Free base),Methyl neochlorogenate,新绿原酸甲酯 |
Antioxidant; HBV | Microbiology/Virology; oxidation-reduction |
Neochlorogenic acid methyl ester (5-O-Caffeoylquinic acid methyl ester) 来源于毛蒿和黑色苦莓(Aronia melanocarpa)果实。Neochlorogenic acid methyl ester 显示出抗 HBV 活性、抗氧化活性和醌还原酶活性,CD 为 6.7 μM。 | |||
T6S0840 |
Engeletin
Dihydrokaempferol 3-rhamnoside,黄杞苷 |
NF-κB; Reductase | Endocrinology/Hormones; Metabolism; NF-κB |
Engeletin (Dihydrokaempferol 3-rhamnoside) 是一种黄酮苷类物质,从hymenaea martiana 中获得,抑制NF-κB 信号通路的激活,具有抗炎、缓解疼痛、消肿、利尿、抗菌等作用。 | |||
T8072 |
S-Methyl-L-cysteine
S-甲基-L-半胱氨酸,S-Methylcysteine |
Antioxidant; Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction |
S-Methyl-L-cysteine (S-Methylcysteine) 是一种催化抗氧化系统中甲硫氨酸硫氧化物还原酶 A 的作用底物,是一种天然产物,具有抗氧化、神经保护及减肥的功效。 | |||
T5S1026 |
Apigenin-7-glucuronide
Apigenin 7-O-glucuronide,芹菜素-7-葡萄糖醛酸 |
MMP | Proteases/Proteasome |
Apigenin-7-glucuronide (Apigenin 7-O-glucuronide) 能够抑制基质金属蛋白酶的活性,其对 MMP-3 (IC50:12.87 μM),MMP-8 (IC50:22.39 μM),MMP-9 (IC50:17.52 μM),MMP-13 (IC50:0.27 μM)。 | |||
TN2030 |
P-Hydroxyphenethyl trans-ferulate
反式-阿魏酸对羟基苯乙酯 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
p-Hydroxyphenethyl trans-ferulate 具有抗高血糖 (酵母α-葡萄糖苷酶,IC5019.24 ± 1.73 µmol L-1),抗氧化,抗炎活性,也具有抗癌特性和血清素能特性。 | |||
T14128 |
Adenosylcobalamin
Cobamamide,Coenzyme B12,腺苷钴胺,AdoCbl |
Endogenous Metabolite | Metabolism |
Adenosylcobalamin (AdoCbl) 是一种 Vitamin B12的特性形式,其中 Vitamin B12 是是甲基丙二酰 CoA 突变酶的辅助因子。 | |||
TN2122 |
Quercetin 3-gentiobioside
Quercetin-3-gentiobioside |
Reductase | Endocrinology/Hormones; Metabolism |
Quercetin 3-gentiobioside (Quercetin-3-gentiobioside) 是一种AR 和 AGE 形成的抑制剂,可从 A. iwayomogi 中提取。Quercetin 3-gentiobioside 对醛糖还原酶 (AR) 的生物活性和晚期糖基化终产物 (AGEs) 的形成具有抑制作用。 | |||
T3665 |
Tectoridin
射干苷,Shekanin |
Estrogen Receptor/ERR; Reductase | Endocrinology/Hormones; Metabolism |
Tectoridin (Shekanin) 是分离自 Maackia amurensis 中的异黄酮,是一种植物雌激素,能够激活雌激素和甲状腺激素受体。它通过 ER 依赖性基因组途径和 GPR30 依赖性非基因组途径发挥雌激素作用。 | |||
T4717 |
25-Hydroxycholesterol
25-羟基胆固醇,25-羟基胆甾醇 |
Others; Endogenous Metabolite; HMG-CoA Reductase | Metabolism; Others |
25-Hydroxycholesterol 是胆固醇的代谢产物,由巨噬细胞响应 Toll 样受体激活而分泌。它有效抑制 B 细胞产生 IgA,EC50约为 65 nM。 | |||
TN2111 |
Prunin
Naringenin 7-0-glucoside,柚皮素-7-O-葡萄糖苷 |
Phosphatase; Anti-infection; Virus Protease | Metabolism; Microbiology/Virology |
Prunin (Naringenin 7-0-glucoside) 是一种人肠道病毒 A71 抑制剂。它抑制蛋白酪氨酸磷酸酶 1B,IC50值为 5.5 μM。 | |||
TN2272 |
Tigloylgomisin H
|
Nrf2 | Immunology/Inflammation |
Tigloylgomisin H 是分离自S. chinensis 果实中的木酚素。Tigloylgomisin H 能诱导小鼠肝癌细胞 Hepa1c1c7 中醌还原酶活性。Tigloylgomisin H 是单功能诱导剂,通过 Nrf2-ARE 途径特异性上调 II 期解毒酶 NQO1。Tigloylgomisin H 是潜在的肝癌预防剂。 | |||
T5S1988 |
Isorhamnetin-3-O-glucoside
Isorhamnetin-3-O-beta-D-Glucoside,异鼠李素-3-O-葡萄糖苷 |
Others | Others |
Isorhamnetin-3-O-glucoside (Isorhamnetin-3-O-beta-D-Glucoside) 是一种天然化合物,广泛存在于蔬菜和水稻中,经消化后可在肠道菌群中代谢。 | |||
T5813 |
BYAKANGELICIN
|
Reductase | Endocrinology/Hormones; Metabolism |
Byakangelicin 是发现于当归根中的一种活性化合物,可作为调节剂,改善各种活性化合物 (Umb,Cur 和 Dox) 的脑积累,增强研究效果。它提高所有PXR 靶基因 (如MDR1) 的表达,并广泛的诱导药物-药物相互作用。它可抑制性激素的作用,可能会增加内源激素的分解代谢。 | |||
TN1037 |
Groenlandicine
|
Topoisomerase | DNA Damage/DNA Repair |
Groenlandicine 是来自黄连的一种原小檗碱生物碱,能诱导拓扑异构酶 I 介导的 DNA 裂解。它对人类重组醛糖还原酶(HRAR)具有中度的抑制作用,IC50值为 154.2 μM。 | |||
T6102 |
2'-acetylacteoside
|
Antioxidant; Reductase | Endocrinology/Hormones; Metabolism; oxidation-reduction |
2'-Acetylacteoside 是一种苯乙醇苷类化合物,分离自来江藤中,可抑制自由基诱导的红细胞溶血,具有清除自由基的作用。 | |||
T2S1635 |
3-Isomangostin
|
MTH1 | DNA Damage/DNA Repair |
3-Isomangostin 可从莽吉柿壳中提取的一种天然产物,是一种乙酰胆碱酯酶选择性抑制剂,也是一种有效的人醛糖还原酶抑制剂,IC50 为 3.48 uM。它抑制 MutT 同源物 1 (MTH1),IC50 为 52 nM。它具有清除自由基、抗疟原虫和抗癌的活性。 | |||
TL0008 |
Gigantol
|
Wnt/beta-catenin; Glucosidase | Cytoskeletal Signaling; Metabolism; Stem Cells |
Gigantol 是一种联苄基化合物,从几种药用兰花中获得,是一种Wnt/β-catenin 通路抑制剂,具有抗肿瘤活性。 | |||
T4918 |
DL-Glyceraldehyde
Glyceric aldehyde,DL-甘油醛晶体 |
Reductase | Endocrinology/Hormones; Metabolism |
DL-Glyceraldehyde (Glyceric aldehyde) 是由酶甘油醛脱氢酶的作用产生的,该酶使用 NADP 作为辅因子将甘油转化为甘油醛。它是一种高活性化合物,可以修饰和交联蛋白质。 | |||
T19365 |
Hydroxypyruvic acid
3-Hydroxypyruvic acid,β-Hydroxypyruvic acid |
Others | Others |
Hydroxypyruvic acid is an intermediate in the metabolism of glycine, serine, and threonine. It is a substrate for serine-pyruvate aminotransferase and glyoxylate reductase/hydroxypyruvate reductase. | |||
TN6514 |
2-Carboxybenzaldehyde
|
||
The major peak of 2-Carboxybenzaldehyde reductase activity in human liver co-purifies with hAFAR protein. Sulphydryl substances and some proteins play important roles in preserving the molecular and catalytic properties of 2-Carboxybenzaldehyde reductase. | |||
TN5183 |
Triptocalline A
|
Others | Others |
Triptocalline A shows an inhibitory effect on rat lens aldose reductase. | |||
T81570 |
Paecilaminol
FKI-0550 |
||
Paecilaminol (FKI-0550) 为一种高效的 NADH 富马酸还原酶 (NADH-fumarate reductase) 抑制剂,其对蛔虫 (Ascaris suum) NADH 富马酸还原酶展现了 5.1 μM 的 IC50 值。 | |||
T19576 |
Tetrahydrocortisone
|
Others | Others |
Tetrahydrocortisone, a stress-induced hormone and a urinary metabolite of Cortisone, originates from the reduction of Cortisone facilitated by 5-reductase. | |||
T39435 |
Myrciacetin
|
Others | Others |
Myrciacetin, a flavonoid derived from Rhododendron dauricum, exhibits inhibitory activity against rat lens aldose reductase, as demonstrated by an IC50 value of 13 μM. | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00288 |
Adrenodoxin reductase Protein, Bovine, Recombinant (His)
Ferredoxin reductase,Adrenodoxin reductase... |
Bovine | P. pastoris (Yeast) |
Serves as the first electron transfer protein in all the mitochondrial P450 systems including cholesterol side chain cleavage in all steroidogenic tissues, steroid 11-beta hydroxylation in the adrenal cortex, 25-OH-vitamin D3-24 hydroxylation in the kidney, and sterol C-27 hydroxylation in the liver. Adrenodoxin reductase Protein, Bovine, Recombinant (His) is expressed in yeast with N-10xHis tag. The predicted molecular weight is 52.8 kDa and the accession number is P08165. | |||
TMPH-01224 |
Dihydrofolate reductase Protein, Human, Recombinant (His)
DHFR,Dihydrofolate reductase |
Human | E. coli |
Key enzyme in folate metabolism. Contributes to the de novo mitochondrial thymidylate biosynthesis pathway. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. Binds its own mRNA and that of DHFR2. | |||
TMPH-00658 |
NAD(P)H-flavin reductase Protein, E. coli, Recombinant (His)
Riboflavin reductase [NAD(P)H],Ferrisiderophore |
E. coli | E. coli |
Catalyzes the reduction of soluble flavins by reduced pyridine nucleotides. | |||
TMPH-00287 |
Adrenodoxin reductase Protein, Bovine, Recombinant (E. coli, His)
Ferredoxin--NADP(+) reductase,ADXR,NADPH:adrenodoxi... |
Bovine | E. coli |
Serves as the first electron transfer protein in all the mitochondrial P450 systems including cholesterol side chain cleavage in all steroidogenic tissues, steroid 11-beta hydroxylation in the adrenal cortex, 25-OH-vitamin D3-24 hydroxylation in the kidney, and sterol C-27 hydroxylation in the liver. Adrenodoxin reductase Protein, Bovine, Recombinant (E. coli, His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 55.8 kDa and the accession number is ... | |||
TMPH-00625 |
FMN reductase Protein, E. coli, Recombinant (His)
FMN reductase,ssuE,FMN reductase (NADPH),S... |
E. coli | Baculovirus Insect Cells |
Catalyzes an NADPH-dependent reduction of FMN, but is also able to reduce FAD or riboflavin. | |||
TMPH-00608 |
Dihydrofolate reductase Protein, E. coli, Recombinant (His)
Dihydrofolate reductase,folA,tmrA |
E. coli | E. coli |
Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. | |||
TMPH-03535 |
Dihydrofolate reductase Protein, S. aureus, Recombinant (His & Myc)
DHFR,Dihydrofolate reductase,folA |
Staphylococcus aureus | E. coli |
Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. Dihydrofolate reductase Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 25.6 kDa and the accession number is P99079. | |||
TMPH-03581 |
Dihydrofolate reductase Protein, S. epidermidis, Recombinant (His)
dfrC,folA1,Dihydrofolate reductase,folA,DHFR |
Staphylococcus epidermidis | E. coli |
Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. Dihydrofolate reductase Protein, S. epidermidis, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 22.0 kDa and the accession number is P0C0P1. | |||
TMPH-00683 |
TMAO reductase 1 Protein, E. coli O157:H7, Recombinant (His & Myc)
Trimethylamine-N-oxide reductase 1,torA |
E. coli | E. coli |
Reduces trimethylamine-N-oxide (TMAO) into trimethylamine; an anaerobic reaction coupled to energy-yielding reactions. | |||
TMPH-00007 |
HMGCR Protein, Human, Recombinant (His)
HMGCR,3-hydroxy-3-methylglutaryl-coenzyme A reductase |
Human | E. coli |
Catalyzes the conversion of (3S)-hydroxy-3-methylglutaryl-CoA (HMG-CoA) to mevalonic acid, the rate-limiting step in the synthesis of cholesterol and other isoprenoids, thus plays a critical role in cellular cholesterol homeostasis. HMGCR is the main target of statins, a class of cholesterol-lowering drugs. | |||
TMPJ-00937 |
RRM2 Protein, Human, Recombinant (His)
RRM2,RR2,Ribonucleotide Reductase Small Subunit,Rib... |
Human | HEK293 Cells |
Ribonucleoside-Diphosphate Reductase Subunit M2 (RRM2) belongs to the ribonucleoside diphosphate reductase small chain family. The reductase of RRM2 catalyzes the formation of deoxyribonucleotides from ribonucleotides. Synthesis of the encoded protein (M2) is regulated in a cell-cycle dependent fashion. RRM2 supplies the precursors essential for DNA synthesis. RRM2 catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides. Phosphorylation on Ser-20 relieves the in... | |||
TMPH-02686 |
GLXR Protein, Mouse, Recombinant (His & SUMO)
Grhpr,Glyoxylate reductase/hydroxypyruvate redu... |
Mouse | E. coli |
Enzyme with hydroxy-pyruvate reductase, glyoxylate reductase and D-glycerate dehydrogenase enzymatic activities. Reduces hydroxypyruvate to D-glycerate, glyoxylate to glycolate oxidizes D-glycerate to hydroxypyruvate. | |||
TMPH-00218 |
DHCR7 Protein, Bovine, Recombinant (His)
DHCR7,7-dehydrocholesterol reductase,Sterol Delta(7... |
Bovine | E. coli |
7-dehydrocholesterol reductase of the cholesterol biosynthetic pathway reducing the C7-C8 double bond of cholesta-5,7-dien-3beta-ol (7-dehydrocholesterol/7-DHC) and cholesta-5,7,24-trien-3beta-ol, two intermediates in that pathway. DHCR7 Protein, Bovine, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 55.8 kDa and the accession number is Q5E9J5. | |||
TMPH-03020 |
MTR Protein, Mycobacterium tuberculosis, Recombinant (His & Myc & SUMO)
mtr,Mycothione reductase,Mycothiol-disulfide re... |
Mycobacterium tuberculosis | E. coli |
Catalyzes the NAD(P)H-dependent reduction of mycothione (the oxidized disulfide form of mycothiol) to mycothiol. | |||
TMPH-00578 |
NrdD Protein, E. coli, Recombinant (His)
nrdD,Class III ribonucleoside-triphosphate reductase |
E. coli | E. coli |
Catalyzes the conversion of ribonucleotides into deoxyribonucleotides, which are required for DNA synthesis and repair. NrdD Protein, E. coli, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 84.0 kDa and the accession number is P28903. | |||
TMPJ-00813 |
QDPR Protein, Human, Recombinant (His)
Dihydropteridine Reductase,QDPR,DHPR,HDHPR,Quinoid ... |
Human | HEK293 Cells |
Dihydropteridine reductase, also known as HDHPR and Quinoid dihydropteridine reductase, QDPR and DHPR, belongs to the short-chain dehydrogenases/reductases (SDR) family. QDPR exists as a homodimer. QDPR is part of the pathway that recycles a substance called tetrahydrobiopterin, also known as BH4 and tryptophan hydroxylases. The regeneration of this substance is critical for the proper processing of several other amino acids in the body. Tetrahydrobiopterin also helps produce certain chemicals i... | |||
TMPH-03196 |
PYCR Protein, Mycobacterium tuberculosis, Recombinant (His & Myc)
PCA reductase,Pyrroline-5-carboxylate reductase... |
Mycobacterium tuberculosis | E. coli |
Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline. PYCR Protein, Mycobacterium tuberculosis, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 37.6 kDa and the accession number is P9WHU7. | |||
TMPJ-01009 |
BLVRA Protein, Human, Recombinant (His)
Biliverdin reductase A,BVR,BVR A,BLVR,BLVRA,Biliver... |
Human | E. coli |
Human Biliverdin reductase A (BLVRA) is belonged to the Gfo/Idh/MocA family and Biliverdin reductase subfamily. BLVRA is an enzyme that in humans is encoded by the BLVRA gene. BLVRA plays an important role in reducing the gamma-methene bridge of the open tetrapyrrole, biliverdin IX alpha, to bilirubin with the concomitant oxidation of a NADH or NADPH cofactor. BLVRA acts on biliverdin by reducing its double-bond between the pyrrole rings into a single-bond. It accomplishes this using NADPH + H+ ... | |||
TMPH-01761 |
Neuroglobin Protein, Human, Recombinant (His & SUMO)
Nitrite reductase,Neuroglobin,NGB |
Human | E. coli |
Neuroglobin Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 32.9 kDa and the accession number is Q9NPG2. | |||
TMPH-03191 |
NirS Protein, Pseudomonas stutzeri, Recombinant (His & Myc)
Nitrite reductase,Cytochrome oxidase,Hydroxylamine ... |
Pseudomonas stutzeri | E. coli |
N/A. NirS Protein, Pseudomonas stutzeri, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 56.0 kDa and the accession number is P24040. | |||
TMPH-03008 |
ENR Protein, Mycobacterium tuberculosis, Recombinant (His)
FAS-II enoyl-ACP reductase,Enoyl-ACP reductase<... |
Mycobacterium tuberculosis | E. coli |
ENR Protein, Mycobacterium tuberculosis, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 32.6 kDa and the accession number is P9WGR0. | |||
TMPY-03617 |
GMPR Protein, Human, Recombinant (His)
GMPR1,guanosine monophosphate reductase |
Human | E. coli |
GMPR, also known as GMPR1, belongs to the IMPDH/GMPR family.This familyofenzymesincludesIMP dehydrogenaseandGMP reductase. These enzymes are involved inpurine metabolism and adopt aTIM barrelstructure. GMPR is an enzyme that catalyzes the irreversible and NADPH-dependent reductive deamination of GMP to IMP. GMPR functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides. | |||
TMPH-00564 |
FabG Protein, E. coli, Recombinant (His & Myc)
Beta-Ketoacyl-acyl carrier protein reductase,fabG,B... |
E. coli | E. coli |
Catalyzes the NADPH-dependent reduction of beta-ketoacyl-ACP substrates to beta-hydroxyacyl-ACP products, the first reductive step in the elongation cycle of fatty acid biosynthesis. | |||
TMPY-00354 |
MSRB3 Protein, Human, Recombinant (hFc)
methionine sulfoxide reductase B3,DFNB74 |
Human | HEK293 Cells |
MSRB3 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 43.7 kDa and the accession number is Q8IXL7-1. | |||
TMPY-00538 |
MSRB3 Protein, Human, Recombinant (His)
methionine sulfoxide reductase B3,DFNB74 |
Human | HEK293 Cells |
MSRB3 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 18.4 kDa and the accession number is Q8IXL7-2. | |||
TMPH-02174 |
PYCR1 Protein, Human, Recombinant (His & SUMO)
pyrroline-5-carboxylate reductase |
Human | E. coli |
PYCR1 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli with N-terminal 6xHis-SUMO tag. The predicted molecular weight is 33.7 kDa. Accession number: Q8TBX0 | |||
TMPY-03867 |
CBR3 Protein, Human, Recombinant (His)
SDR21C2,carbonyl reductase 3,hCBR3,HEL-S-25 |
Human | E. coli |
CBR3, also known as hCBR3, belongs to the short-chain dehydrogenases/reductases (SDR) family. CBR3 is expressed in ovary, pancreas, intestine, colon, kidney, brain, thymus, lung, heart, liver, spleen, leukocyte, prostate and testis. It is a monomeric NADPH-dependent oxidoreductase and is closely linked to another carbonyl reductase gene – CBR1. CBR3 catalyzes the reduction of a large number of biologically and pharmacologically active carbonyl compounds to their corresponding alcohols. It has lo... | |||
TMPH-02198 |
TXNRD2 Protein, Human, Recombinant (His & SUMO)
TR-beta,Thioredoxin reductase 2, mitochondrial,Thio... |
Human | E. coli |
Involved in the control of reactive oxygen species levels and the regulation of mitochondrial redox homeostasis. Maintains thioredoxin in a reduced state. May play a role in redox-regulated cell signaling. | |||
TMPH-02797 |
NQO1 Protein, Mouse, Recombinant (His)
Quinone reductase 1,NAD(P)H dehydrogenase [quinone]... |
Mouse | P. pastoris (Yeast) |
The enzyme apparently serves as a quinone reductase in connection with conjugation reactions of hydroquinons involved in detoxification pathways as well as in biosynthetic processes such as the vitamin K-dependent gamma-carboxylation of glutamate residues in prothrombin synthesis. NQO1 Protein, Mouse, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 32.8 kDa and the accession number is Q64669. | |||
TMPH-03536 |
FabI Protein, S. aureus, Recombinant (His & SUMO)
Enoyl-[acyl-carrier-protein] reductase [NADPH] FabI... |
Staphylococcus aureus | E. coli |
Catalyzes the reduction of a carbon-carbon double bond in an enoyl moiety that is covalently linked to an acyl carrier protein (ACP). Involved in the elongation cycle of fatty acid which are used in the lipid metabolism. FabI Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 44.0 kDa and the accession number is Q6GI75. | |||
TMPH-02794 |
Myoglobin Protein, Mouse, Recombinant (E. coli, His & Myc)
Nitrite reductase MB,Mb,Pseudoperoxidase MB,Myoglob... |
Mouse | E. coli |
Myoglobin Protein, Mouse, Recombinant (E. coli, His & Myc) is expressed in E. coli. | |||
TMPY-02438 |
AKR1B1 Protein, Human, Recombinant (His)
ALDR1,AR,ADR,aldo-keto reductase family 1, member B... |
Human | E. coli |
Aldose reductase (AKR1B1) belongs to the aldo/keto reductase superfamily. AKR1B1 is a NADPH-dependent aldo-keto reductase best known as the rate-limiting enzyme of the polyol pathway. Expression of AKR1B1 was the highest in lens and retina. It is the first enzyme in the polyol pathway through which glucose is converted to sorbitol which is important for the function of various organs in the body, and has been implicated in the etiology of diabetic complications. AKR1B1 is quite abundant in the c... | |||
TMPY-02461 |
AKR1A1 Protein, Human, Recombinant (His)
DD3,ALDR1,HEL-S-6,aldo-keto reductase family 1, mem... |
Human | E. coli |
Aldehyde reductase (AKR1A1) is a member of the aldo-keto reductase superfamily, which consists of more than 40 known enzymes and proteins that includes variety of monomeric NADPH-dependent oxidoreductases, such as aldehyde reductase. Aldehyde reductase has wide substrate specificities for carbonyl compounds. These enzymes are implicated in the development of diabetic complications by catalyzing the reduction of glucose to sorbitol. Aldehyde reductase possess a structure with a beta-alpha-beta fo... | |||
TMPY-03287 |
RRM1 Protein, Human, Recombinant (His & GST)
ribonucleotide reductase M1,R1,RR1,RIR1 |
Human | Baculovirus Insect Cells |
RRM1 is a subunit of ribonucleoside-diphosphate reductase which is constituted by two subunits. Ribonucleoside-diphosphate reductase is an enzyme essential for the production of deoxyribonucleotides prior to DNA synthesis in S phase of dividing cells. RRM1 is one of several genes located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocort... | |||
TMPH-00725 |
NarG Protein, E. coli, Recombinant (His & Myc)
narG,Quinol-nitrate oxidoreductase subunit alpha,Re... |
E. coli | E. coli |
The nitrate reductase enzyme complex allows E.coli to use nitrate as an electron acceptor during anaerobic growth. The alpha chain is the actual site of nitrate reduction. | |||
TMPH-02795 |
Myoglobin Protein, Mouse, Recombinant (His & Myc)
Mb,Nitrite reductase MB,Myoglobin,Pseudoperoxidase ... |
Mouse | HEK293 Cells |
Serves as a reserve supply of oxygen and facilitates the movement of oxygen within muscles. Myoglobin Protein, Mouse, Recombinant (His & Myc) is expressed in HEK293 mammalian cells with N-10xHis and C-Myc tag. The predicted molecular weight is 21.9 kDa and the accession number is P04247. | |||
TMPY-01812 |
Enoyl-ACP Reductase Protein, E. coli, Recombinant (His)
b1288,JW1281,gts,ECK1283,qmeA,envM |
E. coli | E. coli |
Enoyl-ACP reductase, also known as NADH-dependent enoyl-ACP reductase and FABI, is a cell inner membrane and peripheral membrane protein which belongs to theshort-chain dehydrogenases/reductases (SDR) family and FabI subfamily. Microorganisms produce many kinds of antibiotics which function in an antagonistic capacity in nature where they have much competition. Bacterial FAS provides essential fatty acids for use in the assembly of key cellular components. Among them, FABI is an enoyl-ACP... | |||
TMPH-01747 |
FDXR Protein, Human, Recombinant (His & SUMO)
Ferredoxin--NADP(+) reductase,NADPH:adrenodoxin oxi... |
Human | E. coli |
Serves as the first electron transfer protein in all the mitochondrial P450 systems including cholesterol side chain cleavage in all steroidogenic tissues, steroid 11-beta hydroxylation in the adrenal cortex, 25-OH-vitamin D3-24 hydroxylation in the kidney, and sterol C-27 hydroxylation in the liver. FDXR Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 61.6 kDa and the accession number is P22570. | |||
TMPY-02519 |
BLVRB Protein, Human, Recombinant (His)
HEL-S-10,biliverdin reductase B,FLR,BVRB,SDR43U1 |
Human | E. coli |
Biliverdin reductase (hBVR) is a serine/threonine kinase that catalyzes reduction of the heme oxygenase (HO) activity product, biliverdin, to bilirubin. BVR consists of an N-terminal dinucleotide-binding domain (Rossmann-fold) and a C-terminal domain that contains a six-stranded β-sheet that is flanked on one face by several α-helices. The C-terminal and N-terminal domains interact extensively, forming the active site cleft at their interface. Biliverdin reductase (BVR) catalyzes the last step i... | |||
TMPH-02498 |
AKR1C3 Protein, Mouse, Recombinant (His & Myc)
Aldo-keto reductase family 1 member C13 |
Mouse | E. coli |
Catalyzes the dehydrogenation of 17-beta-hydroxysteroids. May also exhibit significant activity with a variety of cyclic and alicyclic alcohols. Uses both NAD and NADP, but the activity is much greater with NAD than with NADP. AKR1C3 Protein, Mouse, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 44.5 kDa and the accession number is Q8VC28. | |||
TMPH-03408 |
NirK Protein, Rhizobium sullae, Recombinant (His)
nirK,Cu-NIR,Copper-containing nitrite reductase |
Rhizobium sullae | E. coli |
NirK Protein, Rhizobium sullae, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 40.8 kDa and the accession number is Q60214. | |||
TMPY-02527 |
p53R2 Protein, Human, Recombinant (His)
P53R2,MTDPS8A,MTDPS8B,ribonucleotide reductase M2 B... |
Human | E. coli |
Ribonucleoside reductase subunit M2B, also known as RRM2B or p53R2, is an enzyme belonging to the iron-dependent ribonucleotide reductase (RNR) enzyme family which is essential for DNA synthesis. Ribonucleotide reductase (RNR) is an enzyme that catalyzes the formation of deoxyribonucleotides from ribonucleotides and plays a critical role in regulating the total rate of DNA synthesis so that DNA to cell mass is maintained at a constant ratio during cell division and DNA repair. RRM2B is a phospho... | |||
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-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. | |||
TMPH-00553 |
Fructose 5-dehydrogenase [NADP(+)] Protein, Erwinia citreus, Recombinant (His & KSI)
Fructose 5-dehydrogenase [NADP(+)],5-ketofructose reduct... |
Erwinia citreus | E. coli |
Fructose 5-dehydrogenase [NADP(+)] Protein, Erwinia citreus, Recombinant (His & KSI) is expressed in E. coli. | |||
TMPH-02476 |
HMGCR Protein, Mouse, Recombinant (His)
Hmgcr,3-hydroxy-3-methylglutaryl-coenzyme A reductase |
Mouse | E. coli |
Catalyzes the conversion of (3S)-hydroxy-3-methylglutaryl-CoA (HMG-CoA) to mevalonic acid, the rate-limiting step in the synthesis of cholesterol and other isoprenoids, thus plays a critical role in cellular cholesterol homeostasis. HMGCR Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 20.4 kDa and the accession number is Q01237. | |||
TMPH-00097 |
AtAER Protein, Arabidopsis thaliana, Recombinant (His & SUMO)
NADPH-dependent oxidoreductase 2-alkenal reduct... |
Arabidopsis thaliana | E. coli |
AtAER Protein, Arabidopsis thaliana, 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 Q39172. | |||
TMPH-00098 |
AtAER Protein, Arabidopsis thaliana, Recombinant
P1-ZCr,NADPH-azodicarbonyl/quinone reductase,NADPH-... |
Arabidopsis thaliana | E. coli |
AtAER Protein, Arabidopsis thaliana, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 38.1 kDa and the accession number is Q39172. | |||
TMPJ-00955 |
MDH1 Protein, Human, Recombinant (His)
Cytosolic Malate Dehydrogenase,MDH1,MDHA,Diiodophenylpyruvat... |
Human | E. coli |
Malate Dehydrogenase, Cytoplasmic (MDH1) is an enzyme which belongs to the MDH Type 2 sub-family of LDH/MDH superfamily. MDH1 is involved in the Citric Acid Cycle that catalyzes the conversion of Malate into Oxaloacetate (using NAD+) and vice versa. MDH1 should not be confused with Malic Enzyme, which catalyzes the conversion of Malate to Pyruvate, producing NADPH. MDH1 also participates in Gluconeogenesis, the synthesis of Glucose from smaller molecules. Pyruvate in the mitochondria is acted up... | |||
TMPY-02271 |
TRXR1/TXNRD1 Protein, Human, Recombinant (aa 161-647, His)
thioredoxin reductase 1,TR1,TXNR,TR,TRXR1,GRIM-12 |
Human | E. coli |
Thioredoxin reductase 1 (TXNRD1) which is a selenocysteine-containing protein is overexpressed in many malignancies. TXNRD1 plays a key role in regulating cell growth and transformation, and protects cells against oxidative damage. We investigated the association between TXNRD1 polymorphisms and ATDH susceptibility. Moreover, TXNRD1 is an essential selenium-containing enzyme involved in detoxification of reactive oxygen species (ROS) and redox signaling. And genetic variations in TXNRD1 favor th... | |||
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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12488 |
Pitavastatin D4
NK-104 D4 |
Others | Others |
Pitavastatin D4 is deuterium labeled Pitavastatin. Pitavastatin is a potent inhibitor of HMG-CoA reductase. | |||
T10916 |
Cycloguanil D6
Chlorguanide triazine D6 |
Others | Others |
Cycloguanil D6 is a dihydrofolate reductase inhibitor, deuterium-labeled Cycloguanil. | |||
T10915 |
Cycloguanil D6 Nitrate
Chlorguanide triazine D6 Nitrate |
Others | Others |
Cycloguanil D6 Nitrate is a dihydrofolate reductase inhibitor, deuterium-labeled Cycloguanil. | |||
T12757 |
Rosuvastatin D3 Sodium
|
Others | Others |
Rosuvastatin D3 Sodium is deuterium labeled Rosuvastatin, which is a competitive HMG-CoA reductase inhibitor(IC50 of 11 nM). | |||
T19551 |
Rosuvastatin D6 Calcium
|
Others | Others |
Rosuvastatin D6 Calcium is deuterium labeled Rosuvastatin, which is a competitive HMG-CoA reductase inhibitor(IC50 of 11 nM). | |||
T12759 |
Rosuvastatin D6 Sodium
|
Others | Others |
Rosuvastatin D6 Sodium is deuterium labeled Rosuvastatin, which is a competitive HMG-CoA reductase inhibitor(IC50 of 11 nM). | |||
T11306 |
Fluvastatin D6 sodium
XU 62-320 (D6) |
Others | Others |
Fluvastatin sodium is a first fully synthetic, competitive HMG-CoA reductase inhibitor with an IC50 of 8 nM.Fluvastatin D6 sodium is deuterium labeled Fluvastatin sodium. | |||
T10128 |
(3S,5R)-Fluvastatin D6 sodium
(3S,5R)-XU 62-320 D6 |
Others | Others |
(3S,5R)-Fluvastatin D6 sodium is the deuterium-labeled (3S,5R)-Fluvastatin sodium. Fluvastatin is a first fully synthetic, competitive HMG-CoA reductase inhibitor (IC50: 8 nM). | |||
TMIJ-0496 |
Lovastatin-d3
|
||
Lovastatin-d3 是 Lovastatin 的氘代化合物。Lovastatin 的 CAS 号为 75330-75-5。Lovastatin是一种 HMG-CoA 还原酶抑制剂,用于降低胆固醇。 | |||
TMIJ-0225 |
Finasteride-d9
|
||
Finasteride-d9 是 Finasteride 的氘代化合物。Finasteride 的 CAS 号为 98319-26-7。Finasteride 是 5α-还原酶的竞争性抑制剂,对 II 型 5α-还原酶的IC50为 4.2 nM,对 II 型 5α-还原酶的亲和力是 I 型酶的 100 倍。它可用于研究前列腺增生和雄激素性脱发。 | |||
TMIJ-0265 |
Homovanillic Acid-13C-d3
|
||
Homovanillic Acid-13C-d3 是 Homovanillic Acid 的 13C 和氘代化合物。Homovanillic Acid 的 CAS 号为 306-08-1。Homovanillic acid 是一种多巴胺代谢物,它与乳糜泻、生长激素缺乏、芳香族氨基酸脱羧酶缺乏症以及脂联素还原酶缺乏症相关。 | |||
TMIH-0242 |
Fluvastatin-d6 Sodium Salt
|
||
Fluvastatin-d6 Sodium Salt 是 Fluvastatin Sodium Salt 的氘代化合物。Fluvastatin Sodium Salt 的 CAS 号为 93957-55-2。Fluvastatin sodium salt 是羟甲基戊二酰辅酶 A 还原酶的竞争性抑制剂,IC50为 8 nM。它通过依赖 Nrf2 的抗氧化通路保护血管平滑肌细胞免受氧化应激,是一种常用的降胆固醇剂。 | |||
TMIJ-0119 |
Pitavastatin-d4 Sodium Salt
|
||
Pitavastatin-d4 Sodium Salt 是 Pitavastatin Sodium Salt 的氘代化合物。Pitavastatin Sodium Salt 的 CAS 号为 574705-92-3。 | |||
TMID-0057 |
(4-Hydroxy-3-methoxyphenyl)acetic-2,2-d2 Acid
|
||
(4-Hydroxy-3-methoxyphenyl)acetic-2,2-d2 Acid 是 (4-Hydroxy-3-methoxyphenyl)acetic Acid 的氘代化合物。(4-Hydroxy-3-methoxyphenyl)acetic Acid 的 CAS 号为 306-08-1。Homovanillic acid 是一种多巴胺代谢物,它与乳糜泻、生长激素缺乏、芳香族氨基酸脱羧酶缺乏症以及脂联素还原酶缺乏症相关。 | |||
TMIH-0504 |
Rosuvastatin-d6 Calcium Salt
|
||
Rosuvastatin-d6 Calcium Salt 是 Rosuvastatin Calcium Salt 的氘代化合物。Rosuvastatin Calcium Salt 的 CAS 号为 147098-20-2。Rosuvastatin calcium 是肝羟甲基戊二酰辅酶 A 还原酶的选择性和竞争性抑制剂,具有抗血脂活性。它降低成熟 hERG 的表达以及热休克蛋白 70 与 hERG 蛋白的相互作用,还降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go相关基因电流,延迟心脏复极化,来延长动作电位持续时间和校正 QT 间期间隔。 | |||
TMID-0041 |
Menaquinone-9-d7
Vitamin K2-MK9-d7 |
||
Menaquinone-9-d7 是 Menaquinone-9 的氘代化合物。Menaquinone-9 的 CAS 号为 523-39-7。Menaquinone 9 (MK-9) 是一种维生素 K2 类似物,已在包括大肠杆菌在内的各种细菌中发现。Menaquinone 9 对紫外线敏感,可与细菌电子传输链的一种成分可溶性硝酸还原酶结合。 | |||
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。 | |||
TMIJ-0040 |
17alpha-Estradiol-2,4-d2
|
||
17alpha-Estradiol-2,4-d2 是 17alpha-Estradiol 的氘代化合物。17alpha-Estradiol 的 CAS 号为 57-91-0。17α-Estradiol 是一种雌性激素,可抑制5α-reductase,在雄原性脱发的研究中有潜力。 |