Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2192 |
Indazole
|
Sodium Channel | Membrane transporter/Ion channel |
Indazole 又称benzpyrazole 或isoindazone,它的衍生物表现出广泛的生物活性,吲哚唑及其衍生物可用于癌症、神经系统疾病、心血管疾病、胃肠道疾病的研究 | |||
T25534 |
Indazole-Cl
Indazole Cl |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
Indazole-Cl 是一种选择性雌激素受体激动剂和选择性雌激素受体调节剂(SERM)。 | |||
T83625 |
iNOS-IN-14
3-bromo-1H-indazole-7-carbonitrile |
NOS | Immunology/Inflammation |
iNOS-IN-14 (3-bromo-1H-indazole-7-carbonitrile) 是一种有效的一氧化氮合酶(NOS)抑制剂,抑制nNOS的NADPH氧化酶活性。 | |||
T22988 |
MK-4827 Racemate
Niraparib Racemate,2-(4-piperidin-3-ylphenyl)indazole-7-carboxamide |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
MK-4827 Racemate (Niraparib Racemate) 是一种选择性 PARP1 和 PARP2 抑制剂,IC50 分别为 3.8 nM 和 2.1 nM,对 PARP3、V-PARP 和 Tank1 的选择性超过 330 倍。 | |||
T28886 |
Suprafenacine
N'-[(E)-(4-methylphenyl)methylidene]-4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide |
Microtubule Associated | Cytoskeletal Signaling |
Suprafenacine (N'-[(E)-(4-methylphenyl)methylidene]-4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide) 是一种细胞渗透性微管去稳定剂,可在 G2/M 期诱导细胞周期停滞和细胞凋亡。 它 与微管结合并抑制秋水仙碱连接处的聚集。 它对癌细胞有选择性,包括耐药癌细胞。 | |||
Fr21265 |
2-Methyl-2H-indazole-3-carboxylic acid
|
||
2-Methyl-2H-indazole-3-carboxylic acid 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 Fr21265,CAS号为 34252-44-3。 | |||
T32417 |
KP1019
FFC14A,KP 1019,indazolium trans-tetrachlorobis(1H-indazole)ruthenate-(III) |
||
KP1019 is now discontinued. | |||
T7474 |
7-Nitroindazole
|
NOS | Immunology/Inflammation |
7-Nitroindazole 是一种具有抗损伤及心血管作用的选择性nNOS 抑制剂,也是评价一氧化氮在中枢神经系统中生物学效应的有效工具。 | |||
T1369 |
1-Methylindazole-3-carboxylic acid
|
Others | Others |
1-Methylindazole-3-carboxylic acid 是一种具有适当沸点的优良溶剂。 | |||
T10107 |
3-Bromo-7-nitroindazole
|
NOS | Immunology/Inflammation |
3-Bromo-7-nitroindazole 是有效的、选择性的神经元型一氧化氮合酶抑制剂,对 eNOS 或诱导型一氧化氮合酶的效果相对较弱。3-Bromo-7-nitroindazole 对全身和大脑中的细胞间信使一氧化氮的合成都有影响。 | |||
T67133 |
6-Hydroxyindazole
|
||
6-Hydroxyindazole 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T67133,CAS号为 23244-88-4。 | |||
T0239 |
Lonidamine
AF1890,氯尼达明,DICA,Diclondazolic Acid |
Apoptosis; Hexokinase; Mitochondrial Metabolism | Apoptosis; Metabolism |
Lonidamine (Diclondazolic Acid) 是一种抗肿瘤药物,是己糖激酶、线粒体丙酮酸载体和质膜单羧酸转运蛋白抑制剂,同时也抑制线粒体复合物 II。 | |||
T8807 |
Benzydamine
|
Others | Others |
Benzydamine 是一种苄基吲唑,具有镇痛、解热和抗炎作用。 Benzydamine 用于减少手术后和创伤后的疼痛和水肿,并促进愈合。 | |||
T64396 |
Antiviral agent 38
|
Antiviral | Immunology/Inflammation |
Antiviral agent 38具有抗菌和抗病毒活性,可用来研究乙肝病毒。 | |||
T28006 |
MDMB-CHMINACA
(S)-MDMB-CHMINACA |
||
MDMB-CHMINACA, an indazole-based synthetic cannabinoid, acts as a potent agonist of the CB1 receptor. | |||
T28310 |
PD 114595
PD-114595,PD114595 |
||
PD 114595 is a Benzothiopyrano-indazole cpd. PD 114595 belongs to a class of DNA complexers, PD 114595 has curative properties against murine solid tumor models. | |||
T19322 |
FKK
|
Others | Others |
FKK is an indazole derivative and also a novel bronchodilator. | |||
T30103 |
APP-CHMINACA
PX-3,PX3 |
||
APP-CHMINACA is a synthetic cannabinoid (CB) featuring a 1-(cyclohexylmethyl)-1H-indazole-3-carboxamide (CHMINACA) base. It displays a 10-fold greater affinity for the central CB1 receptor than that of JWH 018. | |||
T11416 | Glucagon receptor antagonists-5 | Others | Others |
Glucagon receptor antagonists-5 is an orally bioavailable indazole-based glucagon receptor antagonist (Ki: 32 nM). It has potential for the treatment of type 2 diabetes mellitus (T2DM). | |||
T28320 |
PD 121373
PD121373,PD-121373 |
||
PD 121373 is a Benzothiopyrano-indazole cpd. The benzothiopyranoindazoles are potent inhibitors of nucleic acid synthesis, reducing both DNA and RNA synthesis to the same extent at similar concentrations. | |||
T27013 |
CHS-111
CHS 111 |
||
CHS-111 is a benzyl indazole compound. CHS-111 inhibits superoxide anion (O(2)(-)) generation. CHS-111 reduces the fMLP-stimulated PLD activity (IC(50) 3.9±1.2μM). CHS-111 inhibits the interaction of PLD1 with ADP-ribosylation factor (Arf) 6 and Ras homol | |||
T80922 |
Tubulin polymerization-IN-56
|
||
Tubulin polymerization-IN-56(compound 8l),一种吲唑衍生的微管蛋白聚合抑制剂,通过与秋水仙碱位点的相互作用,能够引发细胞周期停滞与细胞凋亡。该化合物还能降低细胞迁移并在体内更有效地抑制肿瘤生长。 | |||
T60793 |
Tubulin inhibitor 26
|
||
Tubulin inhibitor 26 (compound 3c) 是一种吲唑衍生物,是微管蛋白抑制剂,对 HepG2、HCT116、SW620、HT29 和 A549 癌细胞系具有显著的低纳摩尔效力。Tubulin inhibitor 26 抑制G2/M 期肿瘤细胞,并且诱导细胞凋亡。Tubulin inhibitor 26 在体内抑制肿瘤生长,并且不影响小鼠体重。 |