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Cat. No. | Product Name | Target | Signaling Pathways |
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T11092 |
DPBQ
ZINC1620467,2,3-Diphenylbenzo[g]quinoxaline-5,10-dione |
p53 | Apoptosis |
DPBQ (ZINC1620467) 是一种 p53 的激活剂。DPBQ 以多倍体特异性方式激活并诱导凋亡 (apoptosis),但不会抑制拓扑异构酶或结合 DNA。 | |||
T71861 |
Sulfonyl quinoxaline 1
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Sulfonyl quinoxaline 1 is an inhibitor of RhoG-hepcidin uptake. | |||
T26249 |
TANDEM (quinoxaline)
Tandem |
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TANDEM (quinoxaline) is a synthetic analog of antibiotics quinoxaline. | |||
T78422 |
2,3-Di(furan-2-yl)quinoxaline
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2,3-Di(furan-2-yl)quinoxaline (Compound 5)为喹诺啉类化合物, 赋予蓝色荧光。该化合物展现出良好的细胞渗透性,并在微摩尔浓度(1.5 μM)下展现出充分的亮度。 | |||
T8459 |
DNQX disodium salt
DNQX Disodium |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
DNQX disodium salt 是一种选择性、强竞争性的非 NMDA 谷氨酸受体 (non-NMDA glutamate receptor) 拮抗剂 (对 AMPA、kainate 和 NMDA 受体的 IC50分别为 0.5、2 和 40 μM),是一种喹恶啉衍生物。 | |||
T64832 | (S,S)-2,3-Bis(t-butylmethylphosphino)quinoxaline | ||
(S,S)-2,3-Bis(t-butylmethylphosphino)quinoxaline 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 T64832。 | |||
T66640 |
2,3-Bis((R)-tert-butyl(methyl)phosphino)quinoxaline
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2,3-Bis((R)-tert-butyl(methyl)phosphino)quinoxaline 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 T66640,CAS号为 866081-62-1。 | |||
T7304 |
DNQX
二硝基喹酮,FG 9041 |
GluR; iGluR | Membrane transporter/Ion channel; Neuroscience |
DNQX (FG 9041) 是喹恶啉衍生物,是一种选择性和强竞争性的非 NMDA 谷氨酸受体拮抗剂,对 AMPA、kainate 和 NMDA 受体的IC50分别为 0.5、2 和 40 μM。 | |||
T35681 |
MeIQx
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MeIQx (MeIQx) is a food-derived carcinogen that has been found in high temperature-cooked fish and meats.1It is activated by hydroxylation and subsequent O-acetylationviathe cytochrome P450 (CYP) isoform CYP1A2 and N-acetyltransferase 2, respectively, in UV5 cells expressing the human enzymes to a metabolite that reacts with DNA to form adducts.2MeIQx (200 and 400 ppm in the diet) induces tumor formation in rats.3 | |||
T67023 | (6bR,10aS)-3-Methyl-2,3,6b,7,8,9,10,10a-octahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline | ||
(6bR,10aS)-3-Methyl-2,3,6b,7,8,9,10,10a-octahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline 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 T67023,CAS号为 313368-85-3。 | |||
T67021 |
(6bR,10aS)-Ethyl 3-methyl-2,3,6b,7,10,10a-hexahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline-8(9H)-carboxylate
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(6bR,10aS)-Ethyl 3-methyl-2,3,6b,7,10,10a-hexahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline-8(9H)-carboxylate 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 T67021,CAS号为 313369-26-5。 | |||
T67022 | (6bR,10aS)-Ethyl 3-methyl-2-oxo-2,3,6b,7,10,10a-hexahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline-8(9H)-carboxylate | ||
(6bR,10aS)-Ethyl 3-methyl-2-oxo-2,3,6b,7,10,10a-hexahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline-8(9H)-carboxylate 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 T67022,CAS号为 313369-25-4。 | |||
T1177 |
Sulfaquinoxaline
磺胺喹恶啉,Avicocid,磺胺喹噁啉,Sulphaquinoxaline,Sulfabenzpyrazine |
Others; Antibacterial; Antibiotic; Parasite | Microbiology/Virology; Others |
Sulfaquinoxaline (Sulfabenzpyrazine) 是一种兽用抗菌剂,对革兰氏阴性菌和革兰氏阳性菌均有活性。它能用于预防球虫病和细菌感染。 | |||
T14953 |
Chloroquinoxaline sulfonamide
NSC-339004,Chloroquinoxaline |
Topoisomerase | DNA Damage/DNA Repair |
Chloroquinoxaline sulfonamide is a topoisomerase II alpha/beta poison. It is used to control coccidiosis in poultry, rabbit, sheep, and cattle. | |||
T0917 |
Sulfaquinoxaline sodium salt
SQ-Na,磺胺喹恶啉钠盐,Sulfaquinoxaline sodium,磺胺喹啉钠 |
Antibacterial; Antibiotic; Parasite | Microbiology/Virology |
Sulfaquinoxaline sodium salt (SQ-Na) 是一种兽用广谱抗菌剂,有抗革兰氏阴性菌和革兰氏阳性菌活性。Sulfaquinoxaline 能用于预防球虫病和细菌感染。 | |||
T10186 |
6-Quinoxalinecarboxylic acid, 2,3-bis(bromomethyl)-
6-Quinoxalinecarboxylic-acid,-2,3-bis_bromomethyl_-,6-Quinoxalinecarboxylic acid,2,3-bis(bromomethyl)- |
Others | Others |
6-Quinoxalinecarboxylic acid, 2,3-bis(bromomethyl)-, derived from 2,3-Bis(bromomethyl)quinoxaline, displays antibacterial properties. | |||
T61664 |
Benzoquinoquinoxaline
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Benzoquinoquinoxaline (BQQ) is a heterocyclic compound featuring an aminoalkyl side chain. BQQ exhibits preferential binding to DNA triplex structures, intercalating between the bases to stabilize the triplex conformation. Additionally, conjugation of BQQ to 1,10-phenanthroline enables specific binding and cleavage of double-strand DNA at the site where a triplex structure forms [1]. | |||
T41355 |
3-Methyl-2-quinoxalinecarboxylic acid
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T3726 |
Erdafitinib
厄达替尼,JNJ-42756493 |
Apoptosis; FGFR | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
Erdafitinib (JNJ-42756493) 是一种喹喔啉衍生物,是一种具有口服活性的FGFR 家族抑制剂,抑制FGFR1/2/3/4活性的IC50分别为1.2、 2.5、3.0和5.7 nM。 | |||
T8457 |
NPS2390
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GluR | Neuroscience |
NPS2390 是钙敏感受体抑制剂,也是 mGluR1 和 mGluR5 的非竞争性拮抗剂。 | |||
T5111 |
4-Bromomethyl-2-cyanobiphenyl
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Others | Others |
4-Bromomethyl-2-cyanobiphenyl 是一种卤代苯甲腈,用于喹喔啉血管紧张素 II 受体拮抗剂的蛋白质结合研究。 | |||
T6422 |
Brimonidine Tartrate
AGN190342 tartrate,304 tartrate,酒石酸溴莫尼定,AGN190342 (tartrate),UK 14304 (tartrate),UK14304 tartrate |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Brimonidine Tartrate (AGN190342 tartrate) 是一种 alpha2 Adrenergic Receptor (alpha2-AR) 受体激动剂。 | |||
T40635 |
Desoxycarbadox
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Desoxycarbadox, derived from Carbadox, is a quinoxaline-di-N-oxide antibiotic compound. | |||
T70586 | S 2720 | ||
S 2720 is a human immunodeficiency virus type 1 (HIV-1)-specific reverse transcriptase (RT) inhibitor quinoxaline. | |||
T63366 |
Anticancer agent 31
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Anticancer agent 31 是抗癌剂,是1,3-二苯基脲喹喔啉衍生物。Anticancer agent 31 能够将细胞周期阻滞在 S 期,并诱导凋亡 (apoptosis),表现出抗肿瘤作用。 | |||
T70770 |
Cyclazosin Free Base
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Cyclazosin Free Base is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of furoic acid with the secondary amino group of 6,7-dimethoxy-2-[(4aR,8aS)-octahydroquinoxalin-1-yl]quinazolin-4-amine. It has a role as an adenosine A2A receptor antagonist. It is a member of quinazolines, a member of furans, an aromatic ether, a quinoxaline derivative, an aromatic amide and a monocarboxylic acid amide. | |||
T70430 | XK469 | ||
XK489 is a synthetic quinoxaline phenoxypropionic acid derivative with proapoptotic and antiproliferative activities. R(+)XK469 selectively inhibits topoisomerase II-beta, blocks activation of MEK/MAPK signaling kinases, stimulates caspases, and upregulates p53-dependent proteins, including cyclins A and B1, thereby arresting cancer cells in the G2/M phase of the cell cycle. Both R(+) and S(-) isomers of this agent are cytotoxic, although the R-isomer is more potent. | |||
T62511 |
AZ3391
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AZ3391 是一种喹喔啉衍生物,是一种 PARP 的有效抑制剂。其中 PARP 酶家族在许多细胞过程中具有重要作用(如复制、重组、染色质重塑和 DNA 损伤修复)。AZ3391 具有潜力进行中枢神经系统组织中发生的疾病和病症的研究(如大脑和脊髓)。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T19091 |
2-(2',3',4'-Trihydroxybutyl)quinoxaline
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Others | Others |
2-(2',3',4'-Trihydroxybutyl)quinoxaline is a food metabolite. |