100
3
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19781 |
Clomazone
Gamit,FMC 57020,Command,异恶草松,Dimethazone,Magister |
Others | Others |
Clomazone (Magister) 是一种能够用于控制棉花,豌豆,南瓜,大豆,地瓜,烟草的一年生草和阔叶杂草的广谱抗菌剂。 | |||
T7770 |
Ethylhexyl Triazone
Octyl triazone,乙基己基三嗪酮 |
Others | Others |
Ethylhexyl Triazone (Octyl triazone) 是一种紫外线-B 化学过滤剂,可用作商业防晒剂。 | |||
T1622 |
Rosiglitazone maleate
BRL 49653C,BRL 49653,马来酸罗格列酮 |
Ferroptosis; TRP/TRPV Channel; PPAR; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
Rosiglitazone maleate (BRL 49653) 是一种选择性PPARγ激活剂,具有抗糖尿病特性和潜在抗肿瘤活性。它也是TRP 通道调节剂,可抑制 TRPM2、TRPM3 的活性,激活 TRPC5。 | |||
T22708 |
Darglitazone
CP-86325 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Darglitazone (CP-86325) 是一种噻唑烷二酮,是口服有效的PPAR-γ选择性激动剂。Darglitazone 可以有效控制血糖和脂质代谢,在 II 型糖尿病中有研究价值。 | |||
T0334 |
Rosiglitazone
BRL49653,罗格列酮 |
Ferroptosis; TRP/TRPV Channel; PPAR; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
Rosiglitazone (BRL49653) 是一种 PPARγ 激动剂、TRPC5 激活剂和 TRPM3 抑制剂,具有口服活性。Rosiglitazone 也是一种降糖剂,是噻唑烷二酮类胰岛素增敏剂。 | |||
T27841 |
Lobeglitazone Sulfate
CKD501 Sulfate,CKD501,CKD-501 Sulfate,CKD 501 Sulfate,CKD 501,CKD-501,Lobeglitazone Sulfate. trade name Duvie, Chong Kun Dang |
NOD | Immunology/Inflammation; NF-κB |
Lobeglitazone Sulfate(CKD-501 Sulfate) 是一种新型噻唑烷二酮,具有抗炎活性,抑制LPS诱导的NLRP3炎症小体活化和肝脏炎症,可用于研究 2 型糖尿病 (T2DM)。 | |||
T7877 |
Thiacetazone
氨硫脲,Diazam,Thioacetazone,Neustab,Neotibil |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Thiacetazone (Diazam) 是一种氨基硫脲抗结核剂,也是一种具有口服活性抗生素。它具有抗菌作用,可抑制结核分枝杆菌 H37Rv 的生长,MIC 值为 0.1 μg/mL。 | |||
T5010 |
Propyphenazone
Isopropylantipyrine,Propyphenazone (4-Isopropylantipyrine),异丙安替比林,Isopropylphenazone,4-Isopropylantipyrine,Isopropyrine |
COX | Immunology/Inflammation; Neuroscience |
Propyphenazone (4-Isopropylantipyrine) 是吡唑啉酮衍生物,具有消炎、止痛和解热活性。基于 Propyphenazone 的类似物可作为前药和选择性 cyclooxygenase-2 抑制剂。 | |||
T9132 |
Emorfazone
依莫法宗,PH011085 |
Others | Others |
Emorfazone (PH011085) 具有抗伤害作用。 | |||
T19710 |
Ciglitazone
Ciglitazona,U 63287,ADD3878,ADD-3878,U-63287,ADD 3878 |
Apoptosis; p38 MAPK; PPAR | Apoptosis; DNA Damage/DNA Repair; MAPK; Metabolism |
Ciglitazone (ADD 3878) 是一种强效和选择性的PPARγ激动剂(EC50:3μM)和口服降糖药。Ciglitazone 抑制th17细胞的增殖和分化,降低胰岛素水平、血管内皮生长因子的产生和血压,诱导胃癌细胞的细胞周期停止。Ciglitazone 能诱导负鼠肾上皮细胞的凋亡,激活p38 MAPK 和凋亡诱导因子(AIF)的核转位。 Ciglitazone 在肥胖症和高血糖症的动物模型中表现出降血糖活性。 | |||
T67743 |
4-Pyridinecarboxaldehyde, 2-(2-pyridinyl)hydrazone, [C(E)]-
|
Others | Others |
4-Pyridinecarboxaldehyde, 2-(2-pyridinyl)hydrazone, [C(E)]-是混合配体配位聚合物[Zn4(bdc)4(ppmh)2(H2O)]n 的配体。 | |||
T0214 |
Pioglitazone
U 72107,吡格列酮,匹格列酮 |
Ferroptosis; PPAR | Apoptosis; DNA Damage/DNA Repair; Metabolism |
Pioglitazone (U 72107) 是一种胰岛素增敏剂和噻唑烷二酮,适用于治疗 2 型糖尿病。它是一种选择性PPARγ激动剂,高亲和力结合到 PPARγ 配体结合域,作用于人和鼠 PPARγ的EC50分别为 0.93 和 0.99 μM。 | |||
T4639 |
Azemiglitazone
MSDC 0602 |
Mitochondrial Metabolism; mTOR | Metabolism; PI3K/Akt/mTOR signaling |
Azemiglitazone (MSDC 0602) 是一种 PPARγ 保留的噻唑烷二酮类药物 (TZD),与能够线粒体丙酮酸载体 (MPC) 相互作用并抑制其活性,降低 pparγ 介导的副作用的风险,有用于 2 型糖尿病研究的潜能。 | |||
T0435 |
Sulfinpyrazone
(+/-)-Sulfinpyrazone,G-28315,苯磺保泰松,NSC 75925 |
COX | Immunology/Inflammation; Neuroscience |
Sulfinpyrazone (NSC-75925) 是一种口服有效的尿酸剂,具有抗血栓和血小板抑制作用。它可作用于慢性和间歇性痛风性关节炎。 | |||
T1432 |
Phenylbutazone
Butazolidine,保泰松 |
COX | Immunology/Inflammation; Neuroscience |
Phenylbutazone (Butazolidine) 是是非甾体类抗炎药,前列腺素 H 合酶过氧化物酶的还原辅助因子,可诱导肌肉盲样蛋白 1 表达,有用于强直性脊柱炎的研究潜力。 | |||
T0980 |
Nifenazone
尼芬那宗,Niapyrin,Nicodone,烟酰氨基比林,Nicazane |
COX | Immunology/Inflammation; Neuroscience |
Nifenazone (Nicodone) 是吡唑类试剂,可用于研究各种风湿性疾病。 | |||
T5314 |
pyridoxal isonicotinoyl hydrazone
吡哆醛异烟酰肼,PIH |
Others | Others |
pyridoxal isonicotinoyl hydrazone (PIH) 是亲脂的三价铁螯合剂,具有高铁螯合特性。 | |||
T0897 |
Nitrofurazone
NFZ,呋喃西林,Nitrofural,Furacilin |
Dehydrogenase; Antibacterial; Glutathione reductase; Antibiotic | Metabolism; Microbiology/Virology; oxidation-reduction |
Nitrofurazone (Furacilin) 是一种抗生素。 | |||
T26613L |
Ambazone
Ambazon,Primal,安巴腙 |
Others | Others |
Ambazone (Primal) 被发现对小鼠和大鼠的各种可移植肿瘤具有活性。 | |||
T35617 |
Mitoguazone
MGBG,Methyl-GAG |
Apoptosis; HIV Protease | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Mitoguazone (Methyl-GAG) 是一种可透过血脑屏障的选择性的 S-腺苷-蛋氨酸脱羧酶 (S-adenosyl-methionine decarboxylase) 抑制剂,可破坏多胺的生物合成。Mitoguazone 是一种具有抗肿瘤活性的合成多羰基衍生物,可抑制 HIV DNA 整合到单核细胞和巨噬细胞中的细胞 DNA 中,诱导细胞凋亡 (apoptosis)。Mitoguazone 具可用于预防急性白血病,霍奇金淋巴瘤和非霍奇金淋巴瘤。 | |||
T6646 |
Rosiglitazone hydrochloride
盐酸罗格列酮,BRL-49653 HCl,Rosiglitazone HCl |
Ferroptosis; TRP/TRPV Channel; PPAR; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
Rosiglitazone hydrochloride (BRL-49653 HCl) 是一种降血糖药物,通过与脂肪细胞中的 PPAR 受体结合来刺激胰岛素分泌。它对 PPARγ1、PPARγ2 和 PPARγ 的EC50值分别为 30 nM、100 nM 和 60 nM。它也是TRPC5的激活剂和TRPM3的抑制剂。 | |||
T6437 |
Cefoperazone
头孢哌酮,Cefob,Medocef |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefoperazone (Medocef) 是一种半合成的头孢菌素,有抗菌活性。 | |||
T1650 |
Chlorzoxazone
Paraflex,Chlorzoxazon,氯唑沙宗 |
P450; Potassium Channel | Membrane transporter/Ion channel; Metabolism |
Chlorzoxazone (Chlorzoxazon) 是作用于中枢的肌肉松弛剂, 可用于肌肉痉挛的研究。 | |||
T3170 |
Troglitazone
CS-045,Romozin,Rezulin,Romglizone,Noscal,Prelay,曲格列酮 |
Apoptosis; Ferroptosis; PPAR; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism |
Troglitazone (Romglizone) 是一种 PPARγ 激动剂,具有抗炎和抗肿瘤活性。 | |||
T0214L |
Pioglitazone hydrochloride
U-72107E,AD 4833,U 72107A,Pioglitazone HCl,匹格列酮盐酸盐 |
Ferroptosis; PPAR | Apoptosis; DNA Damage/DNA Repair; Metabolism |
Pioglitazone hydrochloride (AD 4833) 是一种选择性PPARγ激动剂,高亲和力结合到 PPARγ 配体结合域。作用于人和鼠 PPARγ,EC50分别为 0.93 和 0.99 μM。它是一种口服活性噻唑烷二酮的盐酸盐,具有抗糖尿病特性和潜在的抗肿瘤活性。 | |||
T7722 |
Feprazone
Prenazone,非普拉宗,DA 2370,DA2370,DA-2370 |
Others | Others |
Feprazone (DA-2370) 具有抗炎和抗脂肪生成特性。 Feprazone 可用于治疗关节和肌肉疼痛的研究。 | |||
T15581 |
Inolitazone
RS5444,Efatutazone,CS-7017,伊诺他酮 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Inolitazone (RS5444) 是一种高亲和力PPARγ激动剂。在体外,Inotazone 显示生长抑制的IC50约为0.8 nM。 | |||
T28454 |
Proquazone
Proquazona,Arthrex,Proquazonum,Biarison,普罗喹宗 |
Others | Others |
Proquazone (Arthrex) 是一种非甾体抗炎药。 | |||
T1218 |
Cefoperazone sodium salt
CP 52640-2,头孢哌酮钠,Cefoperazone sodium |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefoperazone sodium salt (CP 52640-2) 是一种半合成的头孢菌素,具有广谱抗菌活性。 | |||
T68046 |
Ciproquazone
|
Others | Others |
Ciproquazone 具有镇痛活性,可用于治疗脊柱炎。 | |||
T60272 |
Isatin-β-thiosemicarbazone
IBT |
HSV | Microbiology/Virology |
Isatin-β-thiosemicarbazone 是一种有效的单纯疱疹病毒 (HSV) 抑制剂。Isatin-β-thiosemicarbazone 在对 HSV-1 和 HSV-2 都具有抑制作用,表现出抗病毒活性。Isatin-β-thiosemicarbazone 是一种有效的抗痘病毒剂 (anti-poxvirus)可用用于治疗猴痘病毒、正痘病毒和牛痘病毒。 | |||
T7710 |
MOFEBUTAZONE
|
Others | Others |
Mofebutazone 抑制前列腺素和白三烯的免疫释放。 | |||
T26613 | Ambazone hydrate | ||
Ambazone hydrate has anti-cancer activity. | |||
T69083 | Nitraquazone | ||
Nitraquazone is a phosphodiesterase inhibitor | |||
T20669 |
Bentazone
苯达松,BAS 351-07H,EPA Pesticide Chemical Code 275200 |
||
Paicaotan is a heterocyclic herbicide. It can removal broadleaf weeds and sedge in the soybean field. | |||
T15580 |
Inolitazone dihydrochloride
RS5444 dihydrochloride,CS-7017 dihydrochloride,Efatutazone dihydrochloride |
PPAR | DNA Damage/DNA Repair; Metabolism |
Inolitazone dihydrochloride 一种有效的、高亲和力的 PPARγ 激动剂,其生物活性的体现依赖于 PPARγ(IC50:0.8 nM),对细胞生长具有抑制作用。Inolitazone dihydrochloride 加强细胞周期激酶抑制剂p21 WAF1/CIP1的作用。 | |||
T72177 |
Oxyphenbutazone monohydrate
羟布宗一水合物 |
||
Oxyphenbutazone monohydrate 是一种保泰松 (Phenylbutazone) 代谢物,具有抗炎作用。Oxyphenbutazone monohydrate 是一种具有口服活性的非选择性 COX 抑制剂。Oxyphenbutazone monohydrate 能选择性地杀死不复制的结核分枝杆菌 (Mycobaterium tuberculosis)。 | |||
T40874 |
2-Nitrobenzaldehyde semicarbazone 13C,15N2
2-Nitrobenzaldehyde semicarbazone 13C,15N2 |
||
2-Nitrobenzaldehyde semicarbazone (13C, 15N2) is utilized in the LC-MS/MS method for semicarbazide analysis. | |||
T39152 |
4-Hydroxyphenylbutazone
|
||
4-Hydroxyphenylbutazone, a metabolite of Phenylbutazone, functions as an effective reducing cofactor for the peroxidase activity of prostaglandin H synthase (PHS). Phenylbutazone is a nonsteroidal anti-inflammatory drug (NSAID) known for its efficiency in this role. | |||
T37852 |
Chlorzoxazone N-Glucuronide
|
||
Chlorzoxazone N-glucuronide is a phase II metabolite of the skeletal muscle relaxant chlorzoxazone . Chlorzoxazone N-glucuronide is formed via glucuronidation of chlorzoxazone by the UDP-glucuronosyltransferase (UGT) isoform UGT1A9. | |||
T30946 |
Cintazone
NSC-102825,NSC 102825,NSC102825 |
||
Cintazone is a biochemical. | |||
T19894 |
Phenylbutazone sodium
Sodium phenylbutazone,Sodium butazolidine,Phenylbutazone sodium salt |
||
Phenylbutazone sodium shows the effect of anti-inflammatory. | |||
T19643 |
Cefbuperazone Sodium
T 1982,BMY25182,BMY 25182,T-1982,BMY-25182,T1982 |
||
Cefbuperazone Sodium is a penicillin-binding protein inhibitor. It is used as antibacterials. | |||
T71298 |
Ipenoxazone HCl
|
||
Ipenoxazone HCl is a glutamate receptor antagonist potentially for the treatment of Alzheimer's disease. | |||
T30324 |
Benzaldehyde, m-hydroxy-, (5-nitro-2-pyridyl)hydrazone
|
||
Benzaldehyde, m-hydroxy-, (5-nitro-2-pyridyl)hydrazone is a bioactive chemical. | |||
T29966 |
Ametohepazone
Ametohepazon |
||
Ametohepazone is a biochemical with radiosensitizing action. | |||
T25431 |
Fluproquazone
Tormosyl,46 790,46-790 |
||
Fluproquazone is a quinazolinone derivative with potent antipyretic, analgesic, and anti-inflammatory effects. However, it was withdrawn during development due to liver toxicity. | |||
T19896 |
Phenylbutazone calcium
DA 241,P 241,DA-241,Phenylbutazone calcium salt,DA241 |
||
Phenylbutazone calcium is a calcium derivative of phenylbutazone that has anti-inflammatory effects. | |||
T26003 |
Pyrazinobutazone
DB139,Carudol,DB-139,Ranoroc,DB 139 |
||
Pyrazinobutazone is an antipyrene derivative which possesses anti-inflammatory properties. | |||
T34846 |
Thiazolinobutazone
LAS-11871,LAS 11871,LAS11871,TZB |
||
Thiazolinobutazone is the 2-amino-2-thiazoline salt of phenylbutazone. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2A2509 |
Laurocapram
月桂氮酮,Tranzone,Azone,N-Lauryl caprolactam,N-0252,月桂氮卓酮,N-Dodecylcaprolactam |
Others | Others |
Laurocapram (N-Lauryl caprolactam) 是吸收促进剂,对于亲脂性和亲水性物质都是一种最有效的吸收剂。 | |||
T21164 |
Sulfentrazone
甲磺草胺,FP-846 |
Others | Others |
Sulfentrazone (FP-846) 是苯基三唑啉酮除草剂,能够抑制原卟啉原氧化酶,导致脂质细胞膜破裂,可用于控制某些阔叶和禾本科杂草。 | |||
TN2312 | Xanthiazone | Others | Others |
Xanthiazone is a natural product |