635
112
19
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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T39986 |
LOX-IN-3 dihydrochloride
|
Lipoxygenase | Metabolism |
LOX-IN-3 dihydrochloride 是口服有效的赖氨酰氧化酶抑制剂,在纤维化,癌症和/或血管生成方面有研究价值。 | |||
T77528 |
5-LOX-IN-2
|
Apoptosis; Lipoxygenase | Apoptosis; Metabolism |
5-LOX-IN-2 是 一种 5-脂氧合酶抑制剂 (5-LOX )抑制剂,从体外实验测得的IC50 值为 0.33 μM。5-LOX-IN-2 以剂量依赖的方式抑制 5-LOX发挥作用。5-LOX-IN-2 可降低肾癌细胞的细胞活性并诱导凋亡 (apoptosis),可用于研究癌症。 | |||
T65427 |
5-LOX inhibitor
1-(sec-Butyl)-4-(4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)-1H-1,2,4-triazol-5(4H)-one |
Lipoxygenase | Metabolism |
5-LOX inhibitor (1-(sec-Butyl)-4-(4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)-1H-1,2,4-triazol-5(4H)-one) 是伊曲康唑杂质之一,是一种选择性 LOX-5 抑制剂。 | |||
T77677 |
12R-LOX-IN-2
|
Lipoxygenase | Metabolism |
12R-LOX-IN-2 是一种 12R-脂氧合酶 (12R-LOX) 的抑制剂。12R-LOX-IN-2 抑制咪喹莫特 (IMQ) 诱导银屑病角质形成细胞过度增殖,并抑制细胞集落形成。12R-LOX-IN-2 还降低 IMQ 诱导细胞中 Ki67 的蛋白水平和 IL-17A 的 mRNA 表达。12R-LOX-IN-2 可用于牛皮癣和其他皮肤相关炎症性疾病的研究。 | |||
T38006 |
LOX-IN-3
|
Others | Others |
LOX-IN-3, an orally active inhibitor of lysyl oxidase (LOX), holds potential application in the fields of fibrosis, cancer, and angiogenesis research[1]. | |||
T61211 |
5-LOX-IN-1
|
Lipoxygenase | Metabolism |
5-LOX-IN-1 是一种 5-Lipoxygenase(5-LOX)抑制剂(IC50: 2.3 μM)。5-LOX-IN-1 可用于研究癌症。 | |||
T36169 |
15-LOX-1 inhibitor 1
|
Others | Others |
9c(i472) is an inhibitor of 15-lipoxygenase-1 (15-LO-1; IC50 = 0.19 μM).1 It decreases LPS- and IFN-γ-induced NF- B activity in RAW-Blue cells when used at concentrations of 0.2, 1, and 5 μM. 9c(i472) reduces LPS- and IFN-γ-induced increases in Nos2 expression and lipid peroxidation in RAW 264.7 cells when used at a concentration of 5 μM. | |||
T83457 |
12R-LOX-IN-1
|
Others | Others |
12R-LOX-IN-1(Compound 4a)是一种效能为IC50: 28.25 μM的12R-LOX抑制剂。该化合物能够有效抑制Imiquimod诱导的银屑病角质形成细胞的异常增殖和集落形成能力,同时减少活性氧、Ki67、IL-17A、TNF-α和IL-6的生成,适用于抗银屑病研究。 | |||
T78820 |
5-LOX-IN-5
|
Lipoxygenase | Metabolism |
5-LOX-IN-5(Compound 29)作为一种5-LOX抑制剂,拥有56 nM的半抑制浓度(IC50)。它主要被应用于神经退行性疾病的研究领域。 | |||
T8356 |
FPL 62064
|
Lipoxygenase; COX | Immunology/Inflammation; Metabolism; Neuroscience |
FPL 62064 是 5-脂氧合酶和COX 双重抑制剂,具有抗炎活性,对 RBL-1 胞质 5-脂氧合酶和前列腺素合成酶 (环氧化酶) 的IC50值分别为 3.5 和 3.1 μM。 | |||
T62350 |
XO/COX/LOX-IN-1
|
Others | Others |
XO/COX/LOX-IN-1 是一种黄嘌呤氧化酶/环氧酶/脂氧合酶 XO/COX/LOX 的有效抑制剂。XO/COX/LOX-IN-1 能够用于研究炎症、癌症以及代谢性疾病。 | |||
T79158 |
h15-LOX-2 inhibitor 1
|
Lipoxygenase | Metabolism |
h15-LOX-2 inhibitor 1(Comp 105)是一种针对人上皮细胞15-lipoxygenase-2 (h15-LOX-2)的抑制剂,表现出0.34 μM的IC50值。 | |||
T62998 |
COX-2/15-LOX-IN-1
|
Others | Others |
COX-2/15-LOX-IN-1 (Compound 14) 是一种 COX-2 和 15-脂氧合酶 (15-LOX)抑制剂,可作用于 COX-1 (IC50: 10.65 μM)、COX-2 (IC50: 0.075 μM) 和 15-LOX (IC50: 2.98 μM)。COX-2-IN-25 具有抗炎作用。 | |||
T4347 |
ML355
|
Lipoxygenase | Metabolism |
ML355 是一种高选择性12-LOX 抑制剂,IC50=0.34 μM,对其他脂氧化酶和环氧化酶有很好的选择性,具有较好的药物动力学特征。 | |||
T79360 |
COX-2/15-LOX-IN-2
|
Lipoxygenase | Metabolism |
COX-2/15-LOX-IN-2 作为一种效能高的双重抑制剂,对COX-2和15-LOX的IC50值分别为0.065 μM和1.86 μM,显示出显著的抗氧化活性。 | |||
T61674 |
COX-2/5-LOX-IN-1
|
Others | Others |
COX-2/5-LOX-IN-1 (compound 3a), a benzothiophen-2-yl pyrazole carboxylic acid derivative, is a potent and dual inhibitor of COX-2 / 5-LOX. It exhibits superior analgesic and anti-inflammatory properties compared to Celecoxib and Indomethacin. COX-2/5-LOX-IN-1 displays strong inhibitory activity against COX-1, COX-2, and 5-LOX, with IC50 values of 12.13 μM, 0.4 μM, and 4.96 μM, respectively [1]. | |||
T60630 |
COX/5-LOX-IN-1
|
Others | Others |
COX/5-LOX-IN-1 (compound 6b) 是有效的COX/5-LOX 双重抑制剂,具有用于炎症性疾病研究的潜力。COX/5-LOX-IN-1 对于 COX-1、COX-2 和 5-LOX 酶的IC50值分别为 1.07、0.55 和 0.28 μM。 | |||
T61479 |
LOX-IN-3 dihydrochloride monohydrate
|
Others | Others |
LOX-IN-3 dihydrochloride monohydrate (Compound 33) is a lysyl oxidase (LOX) inhibitor with oral activity. It is specifically designed for research purposes in the areas of fibrosis, cancer, and angiogenesis [1]. | |||
T61352 |
COX-2/5-LOX-IN-3
|
Others | Others |
COX-2/5-LOX-IN-3 (compound 5b) is a powerful and dual inhibitor of COX-2 and 5-LOX, with IC50 values of 45.73 μM, 5.45 μM, and 4.33 μM for COX-1, COX-2, and 5-LOX, respectively. This compound, COX-2/5-LOX-IN-3, shows promise for the investigation of inflammatory diseases [1]. | |||
T79362 |
COX-2/15-LOX-IN-4
|
Lipoxygenase | Metabolism |
COX-2/15-LOX-IN-4(compound 5i)是一种针对COX-2和15-LOX的双重抑制剂,其IC50值分别为0.075 μM和1.97 μM。该化合物能有效地阻止LPS诱发的细胞内促炎细胞因子(IL-6, ROS)的产生,表现出明确的抗炎活性。 | |||
T8950 |
CAY10698
|
Lipoxygenase | Metabolism |
CAY10698 是选择性的12-Lipoxygenase (12-LOX)抑制剂,IC50=5.1 μM。它对 5-LOX、15-LOX-1、15-LOX-2 和 COX-1/2 无活性。 | |||
T6243 |
U-73122
U73122 |
Phospholipase; Ferroptosis; Lipoxygenase | Apoptosis; Metabolism |
U-73122 (U73122) 是一种磷脂酶 C 和 5-脂氧合酶抑制剂,对磷脂酶 C 的 IC50值约为 1-2.1 µM。它是一种 PLC 抑制剂,可减少激动剂诱导的血小板和 PMN 中的 Ca2+ 增加。 | |||
T61910 |
COX-2/5-LOX-IN-2
|
Others | Others |
COX-2/5-LOX-IN-2 是苯并噻吩-2-基吡唑羧酸衍生物。COX-2/5-LOX-IN-2 (5b) 对COX-2和5-LOX 均有抑制作用。COX-2/5-LOX-IN-2 抑制 COX-1、COX-2 和 5-LOX 的IC50s 分别为 5.40、0.01 和 1.78 μM。COX-2/5-LOX-IN-2 显示出超过塞来昔布和吲哚美辛的镇痛和抗炎活性。 | |||
T79361 |
COX-2/15-LOX-IN-3
|
Lipoxygenase | Metabolism |
COX-2/15-LOX-IN-3 (compound 5k) 为COX-2/15-LOX的一种双重抑制剂,具有分别为0.075 μM和1.97 μM的IC50值。该化合物能显著抑制LPS诱导的细胞产生促炎细胞因子(IL-6, ROS和NO),表明其具备显著的抗炎活性。 | |||
T9108 |
BI-0115
|
Lipoxygenase | Metabolism |
BI-0115 是LOX-1的选择性抑制剂,其IC50值为 5.4 µM,可以阻止细胞摄取氧化低密度脂蛋白。它通过形成同源二聚体配体结合域的二聚体来触发受体抑制。 | |||
T16503 |
PF-4191834
PF-04191834 |
Lipoxygenase | Metabolism |
PF-4191834 是 5-Lipoxygenase (5-LOX) 的非铁螯合和非氧化还原抑制剂,IC50 为 229 nM。 PF-4191834 对 5-LOX 的特异性比 12-LOX 和 15-LOX 高约 300 倍,并且对环氧合酶没有活性。 PF-4191834 可用于炎症和疼痛的研究。 | |||
T6568 |
Licofelone
利克飞龙,ML-3000 |
Apoptosis; Lipoxygenase; COX | Apoptosis; Immunology/Inflammation; Metabolism; Neuroscience |
Licofelone (ML-3000) 是一种 COX/LOX 双重抑制剂,IC50分别为 0.21和0.18 μM,有潜力研究骨关节炎,具有抗炎和抗增殖作用。它可诱导细胞凋亡,减少促炎性白三烯和前列腺素的产生。 | |||
T21746 |
Terameprocol
tetramethyl Nordihydroguaiaretic Acid,EM-1421 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Terameprocol (EM-1421) 是 Nordihydroguaiaretic acid 的合成衍生物,是非选择性脂氧合酶抑制剂。 | |||
T7540 |
2,5-Di-tert-butylhydroquinone
BHQ,2,5-二特丁基对苯二酚 |
Calcium Channel; Lipoxygenase; COX | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience |
2,5-Di-tert-butylhydroquinone (BHQ) 是一种有效和选择性的内质网 Ca2+-ATPase 抑制剂,可调节5-LO 以及COX-2活性,IC50分别为 1.8 和 14.1 μM。 | |||
T10098 |
PGS-IN-1
KME-4 |
Lipoxygenase; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism |
PGS-IN-1 (KME-4)是一种前列腺素合成酶抑制剂,IC50=0.28 μM。它也可抑制5-脂肪氧合酶的活性,IC50=1.05 μM。 | |||
T27026 |
CJ-13,610
CJ 13610,CJ-13610 |
Lipoxygenase | Metabolism |
CJ-13,610 是一种具有口服活性的非氧化还原型 5-脂氧合酶 (5-LOX) 抑制剂。 CJ-13,610 抑制白三烯 B4 的生物合成并调节巨噬细胞中 IL-6 mRNA 的表达。 | |||
T21902 |
ML351
|
Lipoxygenase | Metabolism |
ML351 是一种高度特异的15-LOX-1抑制剂,其 IC50=200 nM。它对 T1D 非肥胖糖尿病小鼠模型的血糖异常和β细胞氧化应激有抑制作用。它对相关同工酶 (5-LOX、血小板 12-LOX、15-LOX-2、绵羊 COX-1 和人 COX-2) 表现出良好的选择性(>250倍)。 | |||
T22398 |
Phenidone
菲尼酮,1-phenyl-3-pyrazolidinone |
Lipoxygenase; COX | Immunology/Inflammation; Metabolism; Neuroscience |
Phenidone (1-phenyl-3-pyrazolidinone) 是可口服发环氧化酶和脂氧合酶双重抑制剂,可改善实验性自身免疫性脑脊髓炎大鼠的瘫痪,降低自发性高血压大鼠的血压,可用作照片显像剂。 | |||
T8794 |
4-MMPB
15-Lipoxygenase Inhibitor 1 |
Apoptosis; Others; Lipoxygenase | Apoptosis; Metabolism; Others |
4-MMPB (15-Lipoxygenase Inhibitor 1) 是一种选择性15-脂氧合酶抑制剂,其 IC50值为 18 μM,具有前列腺癌的研究潜力。它对大豆 15-脂氧合酶和人 15-脂氧合酶-1 的 IC50 分别为 19.5 μM 和 19.1 μM。 | |||
T0477 |
Zileuton
Abbott 64077,齐留通,A 64077 |
Ferroptosis; Lipoxygenase; COX | Apoptosis; Immunology/Inflammation; Metabolism; Neuroscience |
Zileuton (A 64077) 是羟基脲的合成衍生物,是一种选择性的5-脂氧合酶抑制剂,具有平喘特性。 | |||
T6576 |
Malotilate
Malotilatum,NKK 105,马洛替酯,Kantec |
Lipoxygenase | Metabolism |
Malotilate (Kantec) 是一种抗纤维化物质,是一种口服活性的促肝药,可选择性抑制5-lipoxygenase (5-LOX)(IC50=4.7 μM)。它通过降低肝脏乙醛水平并防止转铁蛋白保留在肝细胞中,从而预防了酒精-吡唑肝炎中肝细胞损伤的发展。 | |||
T5200 |
Indirubin-3'-monoxime
靛玉红-3' -单肟,Indirubin-3'-oxime |
GSK-3; Lipoxygenase; CDK | Cell Cycle/Checkpoint; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells |
Indirubin-3'-monoxime (Indirubin-3'-oxime) 是一种有效的 GSK3β 抑制剂,IC50值为 22 nM。它对 CDK5/p25、CDK1/cyclin B 和CDk2/cyclin E 也有作用,IC50值分别为 100、180 和 250 nM。 | |||
T7724 |
Tepoxalin
RWJ-20485,RWJ20485,ORF20485,替泊沙林,ORF-20485,RWJ 20485,ORF 20485 |
Lipoxygenase; COX | Immunology/Inflammation; Metabolism; Neuroscience |
Tepoxalin (RWJ 20485) 是有效的5-脂氧合酶和环氧合酶抑制剂,表现出强大的抗炎活性和较小的胃肠道刺激性。 | |||
T6893 |
MK-886
MK886,L 663536 |
Apoptosis; Leukotriene Receptor; COX; PPAR; FLAP | Apoptosis; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
MK-886 (L 663536)是一种细胞可渗透的,具有口服活性的 FLAP (IC50为 30 nM) 和白三烯生物合成 (完整白细胞和人全血中的IC50分别为 3 nM 和 1.1μM) 的抑制剂。它也是一种非竞争性PPARα拮抗剂,可以诱导细胞凋亡。 | |||
T67908 |
ThioLox
|
Lipoxygenase | Metabolism |
ThioLox 是一种竞争性 15-脂氧合酶-1 (15-LOX-1) 抑制剂(IC50值为12 μM)。ThioLox 显示抗炎和神经保护特性。具有抗炎和神经保护作用,对谷氨酸毒性有很强的保护作用。 | |||
T1412 |
Loxapine succinate
Daxolin,Loxapac,Cloxazepin,Loxapine succinate salt,丁二酸洛沙平,琥珀酸洛沙平 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Loxapine succinate (Loxapac) 是D2/D4多巴胺受体,5-羟色胺受体抑制剂,用于精神分裂症。 | |||
T2312 |
Loxiglumide
CR-1505,氯谷胺 |
cholecystokinin | GPCR/G Protein |
Loxiglumide (CR-1505) 是一种缩胆囊素受体拮抗剂。 | |||
T1031 |
Cloxacillin sodium monohydrate
Cloxacillin Sodium,Bactopen,氯唑西林钠一水合物 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cloxacillin sodium monohydrate (Cloxacillin Sodium) 有抗菌作用,对Staphylococcus aureus25923 的最小抑菌浓度为256 mg/L。 | |||
T9319 |
Tosufloxacin
tosufloxacin tosilate,托氟沙星,Ozex,7-(3-Aminopyrrolidin-1-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid |
Others | Others |
Tosufloxacin (Ozex) 是一种喹诺酮类抗菌剂,是茶碱代谢的有效抑制剂。 | |||
T15777 |
Loxoribine
RWJ 21757,7-Allyl-8-oxoguanosine,洛索立宾 |
Influenza Virus; TLR | Immunology/Inflammation; Microbiology/Virology |
Loxoribine (RWJ 21757) 是一种鸟苷类似物,是一种口服生物可利用的选择性 Toll 样受体 (TLR) 7 激动剂。 具有抗病毒和抗肿瘤活性。它是一种新型的强效免疫刺激剂,具有较广谱的免疫生物学活性。 | |||
T22456 |
Voreloxin hydrochloride
SNS-595 hydrochloride,Vosaroxin,(3S-反式)-1,4-二氢-7-[3-甲氧基-4-(甲基氨基)-1-吡咯烷基]-4-氧代-1-(2-噻唑基)-1,8-萘啶-3-羧酸单盐酸盐 |
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
Voreloxin hydrochloride (SNS-595 hydrochloride) 是一种新型拓扑异构酶 II 抑制剂,能够诱导 DNA 双链断裂,阻滞 G2 期,引起细胞凋亡。 | |||
T1293 |
Gatifloxacin
BMS 206584-01,PD 135432,CG5501,BMS-206584,AM-1155,加替沙星 |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Gatifloxacin (CG5501) 是一种具有广谱抗菌活性的氟喹诺酮类抗生素。它可抑制大肠杆菌 DNA 解旋酶 (IC50=0.109 μg/ml) 和细菌 II 型拓扑异构酶(IC50=13.8 μg/ml)。在动物模型中,它有抗细菌性结膜炎作用。 | |||
T0826 |
Meloxicam
美洛昔康,Movalis,Mobic,Metacam |
Apoptosis; COX; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Neuroscience |
Meloxicam (Metacam) 是一种非甾体类抗炎剂,抑制COX 的活性,对 COX-2 和 COX-1 的IC50值分别为 0.49 µM 和 36.6 µM。 | |||
T5323 |
Toloxatone
托洛沙酮,MD 69276 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Toloxatone (MD 69276) 是可逆的单胺氧化酶 A (MAOA) 抑制剂,是一种抗抑郁剂。 | |||
T6919 |
Omaveloxolone
RTA-408 |
Apoptosis; Others; Nrf2; STING | Apoptosis; Immunology/Inflammation; Others |
Omaveloxolone (RTA-408) 是一种抗氧化炎症调节剂,可激活Nrf2并抑制一氧化氮。它通过抑制 STING 依赖的 NF-κb 信号通路,来抑制破骨细胞的生成。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6S0413 |
Pectolinarigenin
柳穿鱼黄素,Pectolinaringenin |
Others; Lipoxygenase; COX | Immunology/Inflammation; Metabolism; Neuroscience; Others |
Pectolinarigenin (Pectolinaringenin) 是 COX-2/5-LOX 的双重抑制剂,可抑制炎症病变中类花生酸的形成,具有抗炎活性。 | |||
T3399 |
Psoralidin
|
Others; Estrogen/progestogen Receptor; Reactive Oxygen Species; Lipoxygenase; Gamma-secretase; Akt; COX; Antibacterial | Cytoskeletal Signaling; Endocrinology/Hormones; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; NF-κB; Others; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells |
Psoralidin 是COX-2和5-LOX 的抑制剂,有抗癌,抗菌和抗炎作用。它显著下调NOTCH1信号传导,还极大地诱导活化氧产生。 | |||
T8260 |
4',5-Dihydroxyflavone
|
Lipoxygenase; Glucosidase | Metabolism |
4',5-Dihydroxyflavone 是大豆 LOX-1,Ki=102.6 μM。它也是一种酵母 α-葡萄糖苷酶抑制剂,IC50=66 μM。 | |||
TQ0180 |
Chebulagic acid
|
SARS-CoV; Influenza Virus; Lipoxygenase; COX | Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience |
Chebulagic acid 是从 Terminalia chebula Retz 中分离出来的一种 COX-LOX 双重抑制剂,有抗炎和抗感染作用。它抑制 SARS-CoV-2病毒的复制,EC50值为 9.76 μM。它还是 M2(S31N)抑制剂和抗流感病毒剂。 | |||
T8002 |
3-Hydroxycoumarin
|
Lipoxygenase | Metabolism |
3-hydroxycoumarin 是一种 15-LOX-1的有效氧化还原抑制剂,近期被证明能保护海胆生殖细胞免受紫外线 B 的损伤。 | |||
T2807 |
Caffeic Acid
|
Lipoxygenase; Endogenous Metabolite; TRP/TRPV Channel | Membrane transporter/Ion channel; Metabolism |
Caffeic acid 是5-脂氧合酶和 TRPV1离子通道的双重抑制剂。 | |||
TN5634 |
Aureusidin
Auresudidin,金鱼草素,Auresidin |
Antioxidant; Reactive Oxygen Species; Lipoxygenase | Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction |
Aureusidin (Auresidin) 具有抗氧化和脂氧合酶抑制活性,具有抗炎作用。 | |||
TN2330 |
Phenethyl ferulate
Caffeic Acid 3-Methyl Phenethyl Ester,阿魏酸苯乙酯,阿魏酸苯乙醇酯 |
Lipoxygenase; COX | Immunology/Inflammation; Metabolism; Neuroscience |
Phenethyl ferulate (Caffeic Acid 3-Methyl Phenethyl Ester) 对化学诱导的结肠癌具有化学预防特性,可增强偶氮甲烷诱导的结肠肿瘤的细胞凋亡。 它抑制环氧合酶(COX) 和 5-脂氧合酶 (5-LOX) ,IC50 值分别为 4.35 和 5.75 μM。 | |||
T5714 |
5-O-Demethylnobiletin
5-DEMETHYLNOBILETIN,去甲基川陈皮素 |
Leukotriene Receptor; Lipoxygenase | GPCR/G Protein; Metabolism |
5-O-Demethylnobiletin (5-DEMETHYLNOBILETIN) 是从黄芪中分离出的多甲氧基黄酮,具有抗炎活性,可通过直接抑制 5-LOX 发挥作用,IC50为 0.1 μM。 | |||
T5759 |
S-(+)-Marmesin
(+)-Marmesin,异紫花前胡内酯,(S)-Marmesin,marmesin |
Lipoxygenase; COX | Immunology/Inflammation; Metabolism; Neuroscience |
S-(+)-Marmesin (marmesin) 是一种从木橘成熟树皮中分离得到的香豆素,具有 COX-2/5-LOX 双重抑制活性。 | |||
TJS2190 |
Nordihydroguaiaretic acid
去甲二氢愈创木酸,NDGA,Dihydronorguaiaretic Acid |
Antioxidant; Ferroptosis; Lipoxygenase; Autophagy | Apoptosis; Autophagy; Metabolism; oxidation-reduction |
Nordihydroguaiaretic acid (NDGA) 是从极叉开拉瑞阿提取出的一种天然产物,是脂氧合酶抑制剂,具有抗氧化和清除自由基的特性。 | |||
T3S0153 |
Xanthatin
苍耳亭,叶黄制菌素 |
Apoptosis; VEGFR; Lipoxygenase; Wnt/beta-catenin; Antibacterial | Angiogenesis; Apoptosis; Cytoskeletal Signaling; Metabolism; Microbiology/Virology; Stem Cells; Tyrosine Kinase/Adaptors |
Xanthatin 是一种从Xanthium strumarium 叶子中提取的天然产物,可诱导细胞凋亡。它抑制布鲁氏菌的IC50值为 2.63 μg/ mL,对寄生虫特异性锥虫硫磷还原酶具有不可逆的弱抑制作用。它通过抑制PGE2的合成和 5-脂氧合酶的活性而显示出抗炎活性。 | |||
TN1097 |
β-Boswellic acid
Beta-boswellic acid,β-乳香酸 |
Lipoxygenase; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
β-Boswellic acid (Beta-boswellic acid) 是从乳香的树胶脂中分离出来的一种天然产物。它是 5-脂氧合酶(5-LO) 产物形成的非还原型抑制剂,其直接与 5-LO 相互作用或阻断其易位。具有抗癌、抗肿瘤和抗高血脂活性。 | |||
T3384 |
Wedelolactone
蟛蜞菊内酯,IKK Inhibitor II |
Apoptosis; NF-κB; Lipoxygenase; Caspase | Apoptosis; Metabolism; NF-κB; Proteases/Proteasome |
Wedelolactone (IKK Inhibitor II) 是来自旱莲草的一种天然产物,通过阻断 IκBα 的磷酸化和降解来抑制细胞中 NF-κB 介导的基因转录,具有抗癌,抗炎和抗氧化活性。 | |||
TN1255 |
3-O-Acetyl-11-hydroxy-beta-boswellic acid
|
Lipoxygenase | Metabolism |
3-O-Acetyl-11-hydroxy-beta-boswellic acid 是 5-脂氧合酶抑制剂。 | |||
TN1182 |
11-Keto-beta-boswellic acid
11-Keto-beta-boswellic acid,11-酮基-BETA-乳香酸 |
Leukotriene Receptor; NF-κB; Lipoxygenase | GPCR/G Protein; Metabolism; NF-κB |
11-Keto-beta-boswellic acid 是来自乳香的一种五环三萜酸,具有抗炎活性和剂量依赖性心脏保护作用,主要是由于抑制5-脂氧合酶、白三烯、NF-κB 的激活和肿瘤坏死因子 α 的产生。 | |||
T6567 |
Levofloxacin
Levaquin,Cravit,Tavanic,Fluoroquinolone,左氧氟沙星,(-)-Ofloxacin |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Levofloxacin (Fluoroquinolone) 是合成的氟喹诺酮类抗生素,有抑制细菌DNA 旋转酶的超螺旋活性的作用,能阻止DNA 复制。 | |||
T1121 |
Podofilox
鬼臼毒素,Podophyllotoxin,(+)-Shikonin |
Microtubule Associated; Topoisomerase | Cytoskeletal Signaling; DNA Damage/DNA Repair |
Podofilox ((+)-Shikonin) 是从八角莲中分离的一种木脂素,是微管组装和 DNA 拓扑异构酶 II 抑制剂。它对皮肤和粘膜有很强的刺激性,具有角质溶解作用,可用于治疗疣和角化病,具有潜在的抗肿瘤特性。 | |||
T1276 |
Danofloxacin mesylate
甲磺酸达氟沙星,CP 76136-27 |
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Danofloxacin mesylate (CP 76136-27) 是一种兽医用氟喹诺酮类抗菌素。 | |||
T4S1658 |
Benzoyloxypaeoniflorin
苯甲酰氧化芍药苷,Benzoyloxypeoniflorin,苯甲酰氧芍药苷 |
NF-κB; Tyrosinase | NF-κB; Proteases/Proteasome |
Benzoyloxypaeoniflorin (Benzoyloxypeoniflorin) 是一种酪氨酸酶抑制剂,分离于Paeonia suffruticosa 的根,对mushroom tyrosinase 的 IC50为 0.453 mM。它是一种NF-κB 抑制剂,它通过对血小板聚集和凝血的抑制作用,有助于改善血液循环。 | |||
TN1343 |
8-Geranyloxypsoralen
8-香叶草氧基补骨脂素 |
Anti-infection; P450; BACE | Metabolism; Microbiology/Virology; Neuroscience |
8-Geranyloxypsoralen 是一种呋喃香豆素,分离自葡萄柚,是 P450 3A4 的有效抑制剂(IC50:3.93 μM)。 | |||
T5744 |
7-Prenyloxycoumarin
7-(异戊烯基氧基)香豆素,Nsc267697,7-O-Prenylumbelliferone,7-异戊烯氧基香豆素 |
Antifungal | Microbiology/Virology |
7-Prenyloxycoumarin (Nsc267697) 是一种 Heracleum dissectum 的天然产物,对乳腺癌具有预防和治疗作用。 | |||
T1549 |
Raloxifene hydrochloride
LY156758 hydrochloride,盐酸雷洛昔芬,Raloxifene HCl,LY139481 hydrochloride,Keoxifene hydrochloride,LY156758 (Keoxifene) HCl |
Estrogen Receptor/ERR; Others; MAO; Estrogen/progestogen Receptor; Autophagy | Autophagy; Endocrinology/Hormones; Metabolism; Neuroscience; Others |
Raloxifene hydrochloride (LY156758 hydrochloride) 是一种选择性且可口服的雌激素受体调节剂,用于预防绝经后妇女的骨质疏松症。它对骨骼和胆固醇代谢具有雌激素激动作用,但对乳腺和子宫组织具有完全的雌激素拮抗作用。 | |||
T8384 |
Gatifloxacin hydrochloride
AM-1155 (hydrochloride),BMS-206584 (hydrochloride),PD135432 (hydrochloride),加替沙星盐酸盐 |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Gatifloxacin hydrochloride (AM-1155 hydrochloride) 是一种氟喹诺酮类抗生素,有广谱抗菌活性。它可抑制大肠杆菌 DNA 解旋酶 (IC50=0.109 μg/ml)和细菌 II 型拓扑异构酶(IC50=13.8 μg/ml) 。它在动物模型中,可研究细菌性结膜炎。 | |||
T8130 |
Ciprofloxacin hydrochloride monohydrate
Oftacilox,Ciprofloxacin hydrochloride hydrate,Bay-09867 hydrochloride monohydrate,环丙沙星盐酸盐一水合物,Ceprimax,盐酸环丙沙星(一水物),Ciloxan |
Antibacterial; Antibiotic | Microbiology/Virology |
Ciprofloxacin hydrochloride monohydrate (Bay-09867 hydrochloride monohydrate) 是一种具有高效抗菌活性的氟喹诺酮类抗生素。 | |||
TN1025 |
3,29-O-Dibenzoyloxykarounidiol
|
Others | Others |
3,29-O-Dibenzoyloxykarounidiol 是一种苯甲酸三萜烯酯,从 Momordica grosvenori 果实中提取。它能够抑制肿瘤启动子 TPA 诱导的 EB 病毒早期抗原活化。 | |||
T8046 |
Tosufloxacin tosylate hydrate
Tosufloxacin p-Toluenesulfonate Hydrate,A-61827 tosylate hydrate,对甲苯磺酸妥舒沙星水合物,T-3262 Tosylate Hydrate |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Tosufloxacin tosylate hydrate (A-61827 tosylate hydrate) 是一个氟喹诺酮类抗菌剂。 | |||
T1306 |
Norfloxacin
氟哌酸,MK-0366,诺氟沙星 |
DNA gyrase; Topoisomerase; Endogenous Metabolite; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Norfloxacin (MK-0366) 是广谱抗生素,能通过结合DNA 旋转酶抑制革兰氏阳性和阴性菌。 | |||
TN5613 |
3α-Cinnamoyloxy-9β,17-dihydroxy-ent-kaur-15-en-19-oic acid
ent-3β-Cinnamoyloxy-9α,17-dihydroxykaur-15-en-19-oic acid |
||
3α-Cinnamoyloxy-9β,17-dihydroxy-ent-kaur-15-en-19-oic acid 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5613,CAS号为 2186648-60-0。 | |||
TN5303 |
14β,16β-Dihydroxy-3β-(β-D-glucopyranosyloxy)-5α-bufa-20,22-dienolide
|
||
14β,16β-Dihydroxy-3β-(β-D-glucopyranosyloxy)-5α-bufa-20,22-dienolide 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5303,CAS号为 1323952-04-0。 | |||
TN5555 |
7α-Galloyloxysweroside
|
||
7α-Galloyloxysweroside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5555,CAS号为 2222365-76-4。 | |||
TN5683 |
Ethyl 4-(rhamnosyloxy)benzylcarbamate
|
||
Ethyl 4-(rhamnosyloxy)benzylcarbamate 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5683,CAS号为 208346-80-9。 | |||
T83233 |
8-Hydroxy-9-isobutyryloxy-10-(2-methylbutanoyl)thymol
|
||
8-Hydroxy9,10-diisobutyryloxy-thymol 是从Inula sericophylla中提取的有效萜类化合物。 | |||
T83516 |
(Z)-2-Angeloyloxymethyl-2-butenoic
|
||
(Z)-2-Angeloyloxymethyl-2-butenoic acid 是 An anthriscus sylvestris Hoffm. 根部的一种天然产物。 | |||
T83558 |
(3S,4aS,10aS)-3-(Acetyloxy)-2,3,4,4a,10,10a-hexahydro-6-hydroxy-1,1,4a-trimethyl-7-(1-methylethyl)-9(1H)-phenanthrenone
|
||
(3S,4aS,10aS)-3-(Acetyloxy)-2,3,4,4a,10,10a-hexahydro-6-hydroxy-1,1,4a-trimethyl-7-(1-methylethyl)-9(1H)-phenanthrenone(化合物3)是从丹参(Salvia miltiorrhiza)根提取的棕榈酸盐。该化合物展现出抗癌活性,对于不同的人类癌症细胞系具有显著的抑制效果,其DC50值分别为:HeLa细胞系25.5 μg/mL、HepG2细胞系37.5 μg/mL以及OVCAR-3细胞系30.2 μg/mL。 | |||
TN2938 |
3-Hydroxy-3-acetonyloxindole
|
Others | Others |
3-Hydroxy-3-acetonyloxindole是一种天然产物,属于萝藦科牛奶菜属,其产品编号为 TN2938,CAS号为 33417-17-3。3-Hydroxy-3-acetonyloxindole可用作对照参考。 | |||
TN3294 |
8alpha-(2-Methylacryloyloxy)hirsutinolide 13-O-acetate
|
NADPH-oxidase; P450; MAO | Immunology/Inflammation; Metabolism; Neuroscience |
8alpha-(2-Methylacryloyloxy)hirsutinolide 13-O-acetate shows inhibitory activity toward CYP2A6 and MAO-A and MAO-B enzymes. | |||
TN5862 |
8-Hydroxy-9,10-diisobutyryloxythymol
|
||
8-Hydroxy-9,10-diisobutyryloxythymol 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5862,CAS号为 22518-08-7。 | |||
TN3302 |
8 beta-(4-Acetoxy-5-hydroxytigloyloxy)costunolide
|
Others | Others |
8 beta-(4-Acetoxy-5-hydroxytigloyloxy)costunolide 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3302,CAS号为 109770-86-7。 | |||
TN3301 |
8beta-(2-Hydroxy-2-methyl-3-oxobutyryloxy)glucozaluzanin C
|
Others | Others |
8beta-(2-Hydroxy-2-methyl-3-oxobutyryloxy)glucozaluzanin C 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3301,CAS号为 93395-31-4。 | |||
TN2627 |
14beta-Benzoyloxy-2-deacetylbaccatin VI
|
Others | Others |
14beta-Benzoyloxy-2-deacetylbaccatin VI是一种天然产物,属于红豆杉科红豆杉属,其产品编号为 TN2627,CAS号为 705973-69-9。14beta-Benzoyloxy-2-deacetylbaccatin VI可用作对照参考。 | |||
T38658 |
3-(β-D-Glucopyranosyloxy)-1,6-dihydroxy-2-methyl-9,10-anthracenedione
|
Others | Others |
3-(β-D-Glucopyranosyloxy)-1,6-dihydroxy-2-methyl-9,10-anthracenedione, also known as an anthraquinone, has been specifically extracted from Rubia cordifolia. | |||
T38657 |
2-Naphthalenecarboxylic acid, 4-(D-glucopyranosyloxy)-1-hydroxy-3-(3-hydroxy-3-methylbutyl)-, methyl ester
|
Others | Others |
2-Naphthalenecarboxylic acid, 4-(D-glucopyranosyloxy)-1-hydroxy-3-(3-hydroxy-3-methylbutyl)-, methyl ester (compound 3) is a naturally occurring substance found in the dried roots of Rubia cordifolia. | |||
TN6331 | 3β-(4-Hydroxybenzoyloxy)-21β,29-dihydroxyserrat-14-en-24-oic acid | ||
3β-(4-Hydroxybenzoyloxy)-21β,29-dihydroxyserrat-14-en-24-oic acid 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6331,CAS号为 1217268-13-7。 | |||
TN6207 | 7-(6'R-hydroxy-3',7'-dimethylocta-2',7'-dienyloxy)coumarin | ||
7-(6'R-hydroxy-3',7'-dimethylocta-2',7'-dienyloxy)coumarin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6207,CAS号为 118584-19-3。 | |||
TN5375 |
1β,10β-Epoxy-6β-isobutyryloxy-9-oxofuranoeremophilane
|
||
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane is a natural product from Ligularia fischeri. | |||
TN3277 |
8-Geranyloxy-5,7-dimethoxycoumarin
|
Others | Others |
8-Geranyloxy-5,7-dimethoxycoumarin是一种天然产物,属于芸香科飞龙掌血属,其产品编号为 TN3277,CAS号为 1228175-65-2。8-Geranyloxy-5,7-dimethoxycoumarin可用作对照参考。 | |||
TN2987 |
3Alaph-Tigloyloxypterokaurene L3
|
Others | Others |
3Alaph-Tigloyloxypterokaurene L3 is a natural product from Wedelia trilobata. | |||
TN3295 |
8alpha-(2-Methylacryloyloxy)hirsutinolide
|
Others | Others |
8alpha-(2-Methylacryloyloxy)hirsutinolide 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3295,CAS号为 188293-70-1。 | |||
TN2849 |
3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid
|
Antifection | Microbiology/Virology |
2-O-beta-d-Glucosyloxy-4-methoxybenzenepropanoic acid[3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid] exhibits glutathione S-transferase (GST) inhibitory and antifungal activities. | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01968 |
LOX Protein, Human, Recombinant (His & MBP)
LOX,Protein-lysine 6-oxidase,Lysyl oxidase |
Human | Baculovirus Insect Cells |
LOX Protein, Human, Recombinant (His & MBP) is expressed in Baculovirus. | |||
TMPH-03359 |
LOX Protein, Rat, Recombinant (His)
Lysyl oxidase,Protein-lysine 6-oxidase,Lox |
Rat | E. coli |
Responsible for the post-translational oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin. Regulator of Ras expression. May play a role in tumor suppression. Plays a role in the aortic wall architecture. LOX Protein, Rat, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 33.0 kDa and the accession number is P16636. | |||
TMPH-02863 |
LOX Protein, Mouse, Recombinant (His & Myc)
Ras excision protein,Protein-lysine 6-oxidase,Lysyl oxidase,... |
Mouse | Baculovirus Insect Cells |
Responsible for the post-translational oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin. Regulator of Ras expression. May play a role in tumor suppression. Plays a role in the aortic wall architecture. | |||
TMPH-01969 |
LOX Protein, Human, Recombinant (His & Myc & SUMO)
Protein-lysine 6-oxidase,LOX,Lysyl oxidase |
Human | E. coli |
Responsible for the post-translational oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin. Regulator of Ras expression. May play a role in tumor suppression. Plays a role in the aortic wall architecture. LOX Protein, Human, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 49.0 kDa and the accession number is P28300. | |||
TMPK-01168 |
LOX-1 Protein, Mouse, Recombinant (His)
LOXIN,LOX-1,CLEC8A,Ox-LDL receptor 1,S... |
Mouse | HEK293 Cells |
LOX-1 is a transmembrane glycoprotein that binds to and internalizes ox-LDL.LOX-1 gene deletion in mice and anti-LOX-1 therapy has been shown to decrease inflammation, oxidative stress and atherosclerosis. LOX-1 deletion also results in damage from ischemia, making LOX-1 a promising target of therapy for atherosclerosis and related disorders. In this article we focus on the different mechanisms for regulation, signaling and the various effects of LOX-1 in contributing to atherosclerosis. | |||
TMPY-02490 |
LOX-1 Protein, Human, Recombinant (His)
LOXIN,SCARE1,SLOX1,LOX1,OLR1,oxid... |
Human | HEK293 Cells |
LOX-1 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 26.5 kDa and the accession number is P78380. | |||
TMPY-03553 |
15 Lipoxygenase 2 Protein, Human, Recombinant
arachidonate 15-lipoxygenase, type B,ALOX15B,15- |
Human | Baculovirus Insect Cells |
15 Lipoxygenase 2 Protein, Human, Recombinant is expressed in Baculovirus insect cells. The predicted molecular weight is 76 kDa and the accession number is AAH35217.1. | |||
TMPY-03462 |
15 Lipoxygenase 2 Protein, Human, Recombinant (His & GST)
ALOX15B,arachidonate 15-lipoxygenase, type B,15- |
Human | Baculovirus Insect Cells |
15 Lipoxygenase 2 Protein, Human, Recombinant (His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 103.7 kDa and the accession number is AAH35217.1. | |||
TMPY-03351 |
LOX-1 Protein, Cynomolgus, Recombinant (His)
oxidized low density lipoprotein (lectin-like) receptor 1,OL... |
Cynomolgus | HEK293 Cells |
LOX-1 Protein, Cynomolgus, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 26.9 kDa and the accession number is G7PJT2. | |||
TMPY-04066 |
LOX-1 Protein, Rat, Recombinant (His)
oxidized low density lipoprotein (lectin-like) receptor 1,Ol... |
Rat | HEK293 Cells |
LOX-1 Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 37.9 kDa and the accession number is O70156. | |||
TMPY-03371 |
LOX-1 Protein, Rat, Recombinant (hFc)
OLR1,Lox1,Oldlr1,oxidized low density lipoprotein (... |
Rat | HEK293 Cells |
LOX-1 Protein, Rat, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 63.9 kDa and the accession number is O70156. | |||
TMPH-00955 |
ALOX12 Protein, Human, Recombinant (His)
Polyunsaturated fatty acid lipoxygenase ALOX12,LOG1... |
Human | E. coli |
ALOX12 Protein, Human, Recombinant (His) is expressed in E. coli. | |||
TMPY-00203 |
LOXL2 Protein, Mouse, Recombinant (His)
1110004B06Rik,4930526G11Rik,9430067E15Rik,lysyl oxidase-like... |
Mouse | HEK293 Cells |
Lysyl oxidase homolog 2, also known as Lysyl oxidase-like protein 2, Lysyl oxidase-related protein 2, Lysyl oxidase-related protein WS9-14 and LOXL2, is a secreted protein that belongs to the lysyl oxidase family. LOXL2 contains four SRCR domains. The lysyl oxidase family is made up of five members: lysyl oxidase (LOX) and lysyl oxidase-like 1-4 ( LOXL1, LOXL2, LOXL3, LOXL4 ). All members share conserved C-terminal catalytic domains that provide for lysyl oxidase or lysyl oxidase-like enzyme act... | |||
TMPH-01630 |
LOXL3 Protein, Human, Recombinant (GST & His)
LOXL3,Lysyl oxidase homolog 3,Lysyl oxidase-like pr... |
Human | E. coli |
LOXL3 Protein, Human, Recombinant (GST & His) is expressed in E. coli expression system with N-6xHis-GST tag. The predicted molecular weight is 55.7 kDa and the accession number is P58215. | |||
TMPH-01628 |
LOXL1 Protein, Human, Recombinant
Lysyl oxidase-like protein 1,Lysyl oxidase homolog 1,LOX... |
Human | E. coli |
Active on elastin and collagen substrates. LOXL1 Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 53.0 kDa and the accession number is Q08397. | |||
TMPH-01629 |
LOXL1 Protein, Human, Recombinant (His)
Lysyl oxidase-like protein 1,LOXL1,Lysyl oxidase ho... |
Human | E. coli |
Active on elastin and collagen substrates. | |||
TMPH-02774 |
LOXL4 Protein, Mouse, Recombinant (His)
Loxl4,Lysyl oxidase-related protein C,Lysyl oxidase... |
Mouse | E. coli |
May modulate the formation of a collagenous extracellular matrix. LOXL4 Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 85.9 kDa and the accession number is Q924C6. | |||
TMPH-00866 |
ADAMTS14 Protein, Human, Recombinant (His)
A disintegrin and metalloproteinase with thrombospondin moti... |
Human | E. coli |
Has aminoprocollagen type I processing activity in the absence of ADAMTS2. Seems to be synthesized as a latent enzyme that requires activation to display aminoprocollagen peptidase activity. Cleaves lysyl oxidase LOX at a site downstream of its propeptide cleavage site to produce a short LOX form. ADAMTS14 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 40.2 kDa and the accession number is Q8WXS8. | |||
TMPH-01552 |
IRF1 Protein, Human, Recombinant (GST & His)
IRF1,Interferon regulatory factor 1 |
Human | Baculovirus Insect Cells |
Transcriptional regulator which displays a remarkable functional diversity in the regulation of cellular responses. Regulates transcription of IFN and IFN-inducible genes, host response to viral and bacterial infections, regulation of many genes expressed during hematopoiesis, inflammation, immune responses and cell proliferation and differentiation, regulation of the cell cycle and induction of growth arrest and programmed cell death following DNA damage. Stimulates both innate and acquired imm... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMIH-0154 |
Ciprofloxacin-d8
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Ciprofloxacin-d8 是 Ciprofloxacin 的氘代化合物。Ciprofloxacin 的 CAS 号为 85721-33-1。Ciprofloxacin是一种有高抗菌活性的氟喹诺酮类抗生素。 | |||
TMIH-0306 |
Lomefloxacin-d5
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Lomefloxacin-d5 是 Lomefloxacin 的氘代化合物。 | |||
T71984 |
Enrofloxacin-d5
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Enrofloxacin-d5 is intended for use as an internal standard for the quantification of enrofloxacin by GC- or LC-MS. Enrofloxacin is a fluoroquinolone antibiotic. It is active against panels of Campylobacter, E. coli, and Salmonella isolates (mean MIC50s = 0.06, 0.5, and 0.03 µg/ml, respectively). It is also active against equine isolates of L. intracellularis (MICs = 0.125-0.5 µg/ml). Enrofloxacin inhibits bacterial DNA gyrase. In vivo, enrofloxacin (10 mg/kg) increases survival in a mouse model... | |||
TMIJ-0211 |
Loxoprofen-d4
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Loxoprofen-d4 是 Loxoprofen 的氘代化合物。Loxoprofen 的 CAS 号为 68767-14-6。Loxoprofen 是一种非甾体类抗炎药,具有解热作用,可用于缓解疼痛的研究。它是非选择性COX抑制剂,对 COX-1 和 COX-2 的IC50分别为 6.5 和 13.5 μM。 | |||
TMIJ-0158 |
Sitafloxacin-d4
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Sitafloxacin-d4 是 Sitafloxacin 的氘代化合物。Sitafloxacin 的 CAS 号为 127254-12-0。Sitafloxacin (Sitafloxacin anhydrous) 是一种具有口服活性的氟喹诺酮类抗生素,具有广谱的抗菌活性。Sitafloxacin 可用于研究呼吸道感染和尿路感染。 | |||
TMID-0195 |
Levofloxacin-d8
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Levofloxacin-d8 是 Levofloxacin 的氘代化合物。Levofloxacin 的 CAS 号为 100986-85-4。Levofloxacin是合成的氟喹诺酮类抗生素,有抑制细菌DNA旋转酶的超螺旋活性的作用,能阻止DNA复制。 | |||
TMIJ-0293 |
Difloxacin-d3 hydrochlorid (methyl-d3)
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Difloxacin-d3 hydrochlorid (methyl-d3) 是 Difloxacin hydrochlorid 的氘代化合物。Difloxacin hydrochlorid 的 CAS 号为 5522-39-4。 | |||
T11113 |
Duloxetine D3 hydrochloride
(S)-Duloxetine D3 hydrochloride,LY248686 D3 hydrochloride |
Others | Others |
Duloxetine D3 hydrochloride is a serotonin-norepinephrine reuptake inhibitor (SNRI) with a Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD).Duloxetine D3 hydrochloride ((S)-Duloxetine D3 hydrochloride) i | |||
TMIJ-0079 |
N-Carbobenzyloxyglycine-d2
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N-Carbobenzyloxyglycine-d2 是 N-Carbobenzyloxyglycine 的氘代化合物。N-Carbobenzyloxyglycine 的 CAS 号为 1138-80-3。Z-Glycine (Carbobenzoxyglycine) 是一种药物-脂质结合物,旨在促进脑渗透,基于其亲脂性和与生物膜中脂质的相似性。 | |||
TMIJ-0212 |
trans-Hydroxy Loxoprofen-13C-d3
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trans-Hydroxy Loxoprofen-13C-d3 (Mixture of Diastereomers) 是 trans-Hydroxy Loxoprofen 的 13C 和氘代化合物。trans-Hydroxy Loxoprofen 的 CAS 号为 371753-19-4。 | |||
TMIJ-0325 |
Duloxetine-d7 Maleate
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Duloxetine-d7 Maleate 是 Duloxetine Maleate 的氘代化合物。Duloxetine Maleate 的 CAS 号为 116817-86-8。 | |||
TMID-0079 |
Norfloxacin-d8
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Norfloxacin-d8 是 Norfloxacin 的氘代化合物。Norfloxacin 的 CAS 号为 70458-96-7。Norfloxacin是广谱抗生素,能通过结合DNA旋转酶抑制革兰氏阳性和阴性菌。 | |||
TMIH-0398 |
Norfloxacin-d5
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Norfloxacin-d5 是 Norfloxacin 的氘代化合物。 | |||
TMIH-0478 |
rac-Duloxetine-d3
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rac-Duloxetine-d3 是 rac-Duloxetine 的氘代化合物。rac-Duloxetine 的 CAS 号为 116817-13-1。 | |||
TMIH-0105 |
Baloxavir-d4
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Baloxavir-d4 是 Baloxavir 的氘代化合物。Baloxavir 的 CAS 号为 1985605-59-1。Baloxavir 是衍生自前药 Baloxavir marboxil,是流感病毒聚合酶 PA 亚基的一流帽依赖性核酸内切酶抑制剂。它抑制病毒 RNA 的转录和复制,具有强大的抗病毒活性。 | |||
TMIJ-0136 |
Moxifloxacin-d4 HCl
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Moxifloxacin-d4 HCl 是 Moxifloxacin HCl 的氘代化合物。Moxifloxacin HCl 的 CAS 号为 186826-86-8。Moxifloxacin Hydrochloride是一种口服有效的 8-甲氧基喹诺酮类抗菌药物,可研究感染性肺炎,急性细菌性鼻窦炎和慢性支气管炎的急性细菌性加重。 | |||
TMID-0194 |
Ofloxacin-d8
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Ofloxacin-d8 是 Ofloxacin 的氘代化合物。Ofloxacin 的 CAS 号为 82419-36-1。Ofloxacin是可抑制细菌DNA旋转酶的一种氟喹诺酮类抗生素。 | |||
TMIJ-0288 |
Danofloxacin-d3
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Danofloxacin-d3 是 Danofloxacin 的氘代化合物。Danofloxacin 的 CAS 号为 112398-08-0。Danofloxacin free base 是一种具有口服活性第三代氟喹诺酮抗菌剂,对大多数革兰氏阴性和革兰氏阳性细菌,支原体和衣原体物种具有广谱的活性,并通过抑制细菌的 DNA 回转酶发挥抗菌作用。它可用于牛,猪和鸡呼吸道疾病的研究。 | |||
TMID-0271 |
Miloxacin-d3
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Miloxacin-d3 是 Miloxacin 的氘代化合物。Miloxacin 的 CAS 号为 37065-29-5。 | |||
TMIH-0364 |
Naloxone-d5
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Naloxone-d5 是 Naloxone 的氘代化合物。 | |||
TMIJ-0015 |
Ciprofloxacin-d8 Hydrochloride
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Ciprofloxacin-d8 Hydrochloride 是 Ciprofloxacin Hydrochloride 的氘代化合物。Ciprofloxacin Hydrochloride 的 CAS 号为 93107-08-5。Ciprofloxacin hydrochloride是一种高抗菌活性的氟喹诺酮类抗生素。 | |||
TMIH-0472 |
Rac Loxoprofen sodium-d3
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Rac Loxoprofen sodium-d3 是 Rac Loxoprofen sodium 的氘代化合物。Rac Loxoprofen sodium 的 CAS 号为 68767-14-6。Loxoprofen 是一种非甾体类抗炎药,具有解热作用,可用于缓解疼痛的研究。它是非选择性COX抑制剂,对 COX-1 和 COX-2 的IC50分别为 6.5 和 13.5 μM。 | |||
TMIJ-0059 |
Moxifloxacin-d4
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Moxifloxacin-d4 是 Moxifloxacin 的氘代化合物。Moxifloxacin 的 CAS 号为 151096-09-2。Moxifloxacin 是一种8-甲氧基喹诺酮类口服有效抗菌药物,用于急性细菌性鼻窦炎,慢性支气管炎的急性细菌性加重和感染性肺炎的研究。 | |||
TMID-0270 |
Pefloxacin-d5
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Pefloxacin-d5 是 Pefloxacin 的氘代化合物。Pefloxacin 的 CAS 号为 70458-92-3。 | |||
T10181 |
6-beta-Naloxol D5 hydrochloride
6β-Naloxol D5 hydrochloride |
Others | Others |
6-beta-Naloxol D5 hydrochloride is a deuterium-labeled opioid antagonist, closely related to naloxone, that serves as an effective compound in the field of chemical research. | |||
TMIH-0305 |
Lomefloxacin-d5 hydrochloride
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Lomefloxacin-d5 hydrochloride 是 Lomefloxacin hydrochloride 的氘代化合物。Lomefloxacin hydrochloride 的 CAS 号为 98079-51-7。Lomefloxacin是一种广谱喹诺酮类抗生素,具有抗菌活性。它可研究支气管炎、尿路感染、结膜炎、外耳炎和中耳炎。 | |||
TMIH-0300 |
Levofloxacin-d3
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Levofloxacin-d3 是 Levofloxacin 的氘代化合物。Levofloxacin 的 CAS 号为 100986-85-4。Levofloxacin是合成的氟喹诺酮类抗生素,有抑制细菌DNA旋转酶的超螺旋活性的作用,能阻止DNA复制。 | |||
TMIH-0406 |
Ofloxacin-d3
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Ofloxacin-d3 是 Ofloxacin 的氘代化合物。 | |||
TMIH-0205 |
Duloxetine-d3 HCl
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Duloxetine-d3 HCl 是 Duloxetine HCl 的氘代化合物。Duloxetine HCl 的 CAS 号为 136434-34-9。Duloxetine hydrochloride 是一种 5-羟色胺-去甲肾上腺素重吸收 (serotonin-norepinephrine reuptake) 抑制剂 (SNRI),Ki=4.6 nM,可用于广泛性焦虑症的研究。 | |||
T11998 |
Meloxicam-d3
Meloxicam D4 |
Others | Others |
Meloxicam D4 is deuterium labeled Meloxicam. Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity,(Target:COX-1; IC50: 36.6 μM ;(Target:COX-2; IC50: 0.49 μM). | |||
TMIJ-0037 |
Sarafloxacin-d8 Hydrochloride
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Sarafloxacin-d8 Hydrochloride 是 Sarafloxacin Hydrochloride 的氘代化合物。Sarafloxacin Hydrochloride 的 CAS 号为 91296-87-6。Sarafloxacin hydrochloride是一种抗菌化合物。 | |||
TMIJ-0213 |
Naloxone-d5 HCl
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Naloxone-d5 HCl 是 Naloxone HCl 的氘代化合物。Naloxone HCl 的 CAS 号为 357-08-4。Naloxone hydrochloride 是一种特异性、没有激动剂活性的opiate拮抗剂。它是 mu、delta 和 kappa 阿片受体的竞争性拮抗剂。 | |||
TMIJ-0300 |
Duloxetine-d7
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Duloxetine-d7 是 Duloxetine 的氘代化合物。Duloxetine 的 CAS 号为 116539-59-4。Duloxetine 是一种 5 羟色胺-去甲肾上腺素重吸收 (serotonin-norepinephrine reuptake) 抑制剂,Ki=4.6 nM,可作用于广泛性焦虑症的研究。 | |||
TMID-0281 |
Moxifloxacin-13C-d3
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Moxifloxacin-13C-d3 是 Moxifloxacin 的 13C 和氘代化合物。Moxifloxacin 的 CAS 号为 151096-09-2。Moxifloxacin 是一种8-甲氧基喹诺酮类口服有效抗菌药物,用于急性细菌性鼻窦炎,慢性支气管炎的急性细菌性加重和感染性肺炎的研究。 |