96
27
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Cat. No. | Product Name | ||
---|---|---|---|
L7810 | 高溶解性多官能团片段化合物库 | 1159 compounds | |
高溶解性多官能团片段库包含1159 种片段分子 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7202 |
ITE
|
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
ITE 是一种有效的芳烃受体 (AhR) 内源性激动剂,Ki 值为 3 nM。它具有免疫抑制作用。 | |||
T21966 |
MeBIO
|
GSK-3; Aryl Hydrocarbon Receptor; CDK | Cell Cycle/Checkpoint; Immunology/Inflammation; PI3K/Akt/mTOR signaling; Stem Cells |
MeBIO 是一种芳烃受体激动剂,对 GSK-3 和 CDK1/CyclinB 的 IC50 分别为 44 和 55 μM。 MeBIO 不影响 GSK-3β。 | |||
T1960 |
YL-109
|
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
YL-109是一种抗肿瘤剂,可以通过芳烃受体 AhR 信号传导诱导 Hsp70 相互作用蛋白 (CHIP) 表达,具有抑制乳腺癌细胞生长和侵袭性的能力。 | |||
T4608 |
PDM2
|
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
PDM2 是一种有效的选择性芳烃受体 (AhR) 拮抗剂,Ki 为 1.2±0.4 nM。 | |||
T15410 |
GNF351
|
Aryl Hydrocarbon Receptor | Immunology/Inflammation |
GNF351 是芳烃受体 (AhR) 的完全拮抗剂,具有抑制 DRE 依赖性和非依赖性活性的能力。它与结合到 AhR 的光亲和性 AhR 配体竞争,IC50为 62 nM。它在小鼠或人角质形成细胞中的毒性极小。 | |||
T5622 |
BAY-218
AHR antagonist 1 |
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
BAY-218 (AHR antagonist 1) 是一种芳基烃受体(AHR)拮抗剂,在人细胞系中的IC50值为 39.9 nM。 | |||
T20625 |
Prochloraz
咪鲜胺,Sporgon,Prelude |
Estrogen Receptor/ERR; AhR; Androgen Receptor; Antifungal | Endocrinology/Hormones; Immunology/Inflammation; Metabolism; Microbiology/Virology |
Prochloraz (Prelude) 是咪唑类抗真菌剂。Prochloraz 抑制羊毛甾醇的细胞色素 P450 依赖性 14α-脱甲基作用,由此抑制麦角固醇的生物合成,从而导致真菌细胞膜破裂和细胞死亡。它也是雌激素受体和 雄激素受体的拮抗剂,IC50分别为25 μM 和4 μM, 并激活芳烃受体,EC50为1μM。 | |||
T10007 |
1,4-Chrysenequinone
Chrysene-1,4-dione,1,4-屈醌 |
AhR | Immunology/Inflammation; Metabolism |
1,4-Chrysenequinone (Chrysene-1,4-dione) 是多环芳香烃类,是芳烃受体 (AhR) 的激活剂 | |||
T10270 |
BAY 2416964
|
Aryl Hydrocarbon Receptor | Immunology/Inflammation |
BAY 2416964 是一种可口服的芳基烃受体拮抗剂,IC50为 341 nM,可用于研究实体瘤。 | |||
T2448 |
CH-223191
CH 223191 |
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
CH-223191 是一种特异性有效的芳烃受体 (AhR) 拮抗剂,可抑制 TCDD 介导的核转位和 AhR 的 DNA 结合,抑制 TCDD 诱导的荧光素酶活性的 IC50值为 0.03 μM。 | |||
T4607 |
CAY 10465
CAY10465,CAY10465 Exclusive |
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
CAY 10465 是一种选择性和高亲和力的芳香烃受体(AhR)激动剂,Ki 值为 0.2 nM。 | |||
T1831 |
StemRegenin 1
SR1 |
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
StemRegenin 1 (SR1) 是一种芳香烃受体拮抗剂,IC50为 127 nM。 | |||
TQ0257 |
FICZ
6-Formylindolo[3,2-b]carbazole |
Aryl Hydrocarbon Receptor | Immunology/Inflammation |
FICZ (6-Formylindolo[3,2-b]carbazole) 是芳烃受体 (AhR) 的有效芳基激动剂,Kd 值为70 pM。 | |||
T21704 |
5-fluoro 203
5F-203,NSC-703786 |
Others | Others |
5-fluoro 203 (NSC-703786) 是一种细胞毒性分子。它可激活芳香烃受体(AhR) 信号传导,诱导 CYP1A1 的转录,从而形成 DNA 加合物以及细胞周期阻滞。它可以提高活性氧水平,并激活 ERK、p38以及JNK。 | |||
T13276 |
VAF347
4-(3-氯苯基)-N-[4-(三氟甲基)苯基]嘧啶-2-胺 |
Aryl Hydrocarbon Receptor | Immunology/Inflammation |
VAF347 是细胞可渗透且高度亲和力的芳烃受体激动剂,可诱导AhR 信号传导,具有抗炎作用。它抑制颗粒单核细胞 (GM 期) 前体中 CD14+CD11b+单核细胞的发育。 | |||
T2623 |
PD98059
PD 98059 |
ERK; Aryl Hydrocarbon Receptor; MEK; Autophagy | Autophagy; Immunology/Inflammation; MAPK |
PD98059 是一种 MEK 抑制剂,抑制 MEK1 和 MEK2 (IC50=2/50 μM),具有非 ATP 竞争性。PD98059 也是一种 AHR 的配体而起拮抗作用。PD98059 可以抑制细胞自噬。 | |||
T2148 |
Carbidopa monohydrate
Carbidopa Hydrate,S(-)-Carbidopa,卡比多巴水合物 |
Decarboxylase; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism; Others |
Carbidopa monohydrate (S(-)-Carbidopa) 是一种外周型脱羧酶抑制剂,可用于帕金森病的研究。它是一种选择性芳香烃受体 (AhR) 调节剂。它抑制胰腺癌细胞和肿瘤生长。 | |||
T0640 |
Benzyl butyl phthalate
BBP,邻苯二甲酸丁苄酯,1,2-benzenedicarboxylic acid,butyl phenylmethyl ester,Butyl benzyl phthalate |
Others; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Others |
Benzyl butyl phthalate (1,2-benzenedicarboxylic acid) 是邻苯二甲酸酯的一员,可激活乳腺癌细胞中的芳香烃受体,刺激 SPHK1/S1P/S1PR3 信号传导,促进转移性乳腺癌干细胞的形成。它通过上调 Zeb1 的表达,可引起血管瘤细胞的迁移和侵袭。 | |||
T3389 |
Antitumor agent-21
TRX818 |
Others | Others |
Antitumor agent-21 (TRX818) 是一种具有潜在的抗癌、抗炎、抗增殖、抗激素作用和抑制血管生成拟态作用的芳基-喹啉衍生物。 | |||
T2707 |
Pifithrin-α hydrobromide
Pifithrin hydrobromide,Pifithrin-α (PFTα) HBr,Pifithrin-α,PFTα,PFTα hydrobromide |
Ferroptosis; Aryl Hydrocarbon Receptor; p53 | Apoptosis; Immunology/Inflammation |
Pifithrin-α hydrobromide (Pifithrin-α hydrobromide) 是一种 p53 抑制剂,可抑制 p53 反应基因的 p53 依赖性反式激活。它也是芳烃受体的激动剂。 | |||
T0790 |
Carbaryl
1-naphthyl methylcarbamate,甲萘威,Sevin |
AChR | Neuroscience |
Carbaryl (1-naphthyl methylcarbamate) 可作为一种杀虫剂。 | |||
T13012 |
Stearyldiethanolamine
PEG-2 Stearamine,2,2'-(Octadecylazanediyl)diethanol,2,2'-(Octadecylimino)diethanol |
Others | Others |
Stearyldiethanolamine (2,2'-(Octadecylazanediyl)diethanol) 可用于抗菌无纺布和抗菌保鲜膜的研究。 | |||
T13662 | Diarylalkane derivative 1 | Others | Others |
Diarylalkane derivative 1 is used for the research of pancreatitis. | |||
T76448 |
Arylomycin A2
|
||
Arylomycin A2,一种脂肽I型信号肽酶(SPase I)抑制剂抗生素(antibiotic),具有抗菌作用。 | |||
T31481 |
Diisostearyl adipate
|
Others | Others |
Diisostearyl adipate can be used for skin care. | |||
T82293 |
Glutaryl coenzyme A lithium
|
Others | Others |
Glutaryl coenzyme A lithium为Glutaryl coenzyme A的衍生物,后者为一重要内源性代谢物。该化合物常应用于HMG-CoA及Glutaryl coenzyme A相关实验。 | |||
T22268 |
Benzyldimethylstearylammonium chloride
Benzyldimethylstearylammonium Chloride Hydrate,十八烷基二甲基苄基氯化铵 |
Others | Others |
Benzyl dimethyl stearyl ammonium chloride hydrate is a kind of mild smell chemical | |||
T73752 |
Glutarylcarnitine lithium
|
Others | Others |
Glutarylcarnitine lithium 丙二酸尿症和 I 型戊二酸尿症的重要诊断代谢物。 | |||
T34714 |
Stearylbetaine
NSC 36343,NSC-36343,NSC-9859,NSC 9859,NSC36343 |
Others | Others |
Stearylbetaine is a bioactive chemical. | |||
T34713 |
Stearyl tyrosine
Stearyl-tyrosine,Stearyltyrosine |
Others | Others |
Stearyl tyrosine is an immunoadjuvants, long-chain stearyl ester of amino acids and peptides. | |||
T34957 |
Tristearyl citrate
|
Others | Others |
Tristearyl citrate is a bioactive chemical. | |||
T19912 |
Distearyl thiodipropionate
NSC65493,NSC-65493,NSC 65493 |
Others | Others |
Distearyl thiodipropionate is an agent of biochemical. | |||
T31948 |
Glutarylleucine
Glutaryl-L-leucine |
Others | Others |
Glutarylleucine is a bioactive chemical. | |||
T76163 |
Arylsulfatase
|
Others | Others |
Arylsulfatase 是原核生物和真核生物的一类酶。Arylsulfatase 是一种硫酸酯酶,常用于生化研究。 | |||
T10106 |
3-arylisoquinolinamine derivative
|
Others | Others |
3-arylisoquinolinamine derivative is a compound with antitumor activity. | |||
T65655 |
Stearyl gallate
|
Others | Others |
Stearyl gallate 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 T65655,CAS号为 10361-12-3。 | |||
T34712 |
Stearyl caprate
Octadecyl decanoate |
Others | Others |
Stearyl caprate is a biochemicla. | |||
T22036 |
Arylquin 1
|
Others | Others |
Arylquin 1 是一种前列腺-凋亡-反应-4(Par-4)促分泌剂,靶向波形蛋白诱导 Par-4 分泌。Arylquin 1 通过诱导溶酶体膜通透性 (LMP) 诱导癌细胞非凋亡性细胞死亡。 | |||
T9658 |
DCZ3301
NPS ALX Compound 4a hydrochloride(1:1)(299433-10-6 Free base) |
Others | Others |
DCZ3301是一种新的芳基胍抑制剂。 | |||
T8980 |
SGA360
|
Aryl Hydrocarbon Receptor | Immunology/Inflammation |
SGA360 是选择性芳烃 (Ah) 受体调节剂。 它具有抗炎特性。 | |||
T84322 |
N-[(4-methylphenyl)carbamothioyl]-2-nitrobenzamide
|
Others | Others |
N-[(4-methylphenyl)carbamothioyl]-2-nitrobenzamide 可用于 N-aryl-N'-(o-nitrobenzoyl)thiourea derivatives 的合成以及相关研究。 | |||
T12071 |
MKC9989
|
IRE1 | Cell Cycle/Checkpoint |
MKC9989 是一种羟基芳基醛 (HAA) 的抑制剂,抑制 IRE1α的 IC50值在 0.23 到 44 μM 之间。 | |||
T19446 |
N-Boc-O-tosyl hydroxylamine
|
Others | Others |
N-Boc-O-tosyl hydroxylamine 是高效的、安全的芳基和烷基胺 N-氨基化的氮源。 | |||
T9704 |
1-Ethynylpyrene
|
P450 | Metabolism |
1-Ethynylpyrene 是有效的细胞色素P450 1A1, 1A2和2B1抑制剂,抑制的IC50分别为 0.18,0.32 和 0.04 μM。 | |||
T10269 |
AHR antagonist 2
|
Aryl Hydrocarbon Receptor | Immunology/Inflammation |
AHR antagonist 2 是芳基烃受体的拮抗剂。 人 AHR 和小鼠 AHR 的 IC50 分别为 0.885 和 2.03 nM。 | |||
T5103 |
AKOS B018304
(5E)-5-(2-硝基苯亚甲基)-2-硫代-四氢噻唑-4-酮 |
Others; Antiviral | Immunology/Inflammation; Others |
AKOS B018304 是芳基衍生物,能够在para位置进行极性替换。AKOS B018304 是一种基孔肯雅病毒抑制剂. | |||
T5541 |
PDM11
1-[2-(4-Chloro-phenyl)-vinyl]-3,5-diMeth,PDM 11 |
AhR | Immunology/Inflammation; Metabolism |
PDM11 (1-[2-(4-Chloro-phenyl)-vinyl]-3,5-diMeth) 是抗氧化剂白藜芦醇的衍生物。它在白藜芦醇活性测定中不活跃。它对辐射分解产生的羟基自由基引发的亚油酸胶束氧化没有明显的保护作用。 | |||
T10325 |
ANI-7
|
Chk | Cell Cycle/Checkpoint |
ANI-7是芳香烃受体(AhR)途径的激活剂。ANI-7抑制多种癌症细胞的生长,并有效且选择性地抑制MCF-7乳腺癌症细胞的生长(GI50:0.56μM)。 | |||
T3637 |
Pifithrin-β hydrobromide
Cyclic PFT-α,PFT-β,Cyclic Pifithrin-α hydrobromide,Pifithrin-β,PFT β (hydrobromide) |
Ferroptosis; p53 | Apoptosis |
Pifithrin-β hydrobromide (Cyclic PFT-α) 是一种 p53 的抑制剂,可逆地阻断 p53 依赖性转录激活和细胞凋亡。IC50值为23 μM。 | |||
T10526 |
β-NF-JQ1
|
Others; PROTACs | Others; PROTAC |
β-NF-JQ1是一种PROTAC,可将芳烃受体E3 (AhR E3) 连接酶招募到目标蛋白上。β-NF-JQ1使用β-NF 作为AhR 配体靶向含溴odomain(BRD)的蛋白,诱导AhR 和BRD 蛋白相互作用。β-NF-JQ1显示出与蛋白敲除活性相关的强大的抗癌活性 。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1451 |
Brevifolincarboxylic acid
|
AhR; Aryl Hydrocarbon Receptor; Glucosidase | Immunology/Inflammation; Metabolism |
Brevifolincarboxylic acid 是从头状蓼中分离得到的一种天然产物,抑制芳烃受体(AhR)。它是一种 α-葡萄糖苷酶抑制剂,IC50 为 323.46 μM。 | |||
T6795 |
Carbidopa
卡比多巴,(S)-(-)-Carbidopa,Lodosyn |
Decarboxylase; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism; Others |
Carbidopa (Lodosyn) 是一种选择性芳香烃受体(AhR)调节剂,是外周型脱羧酶抑制剂,抑制胰腺癌细胞和肿瘤生长,可用于帕金森病的研究。 | |||
T5786 |
TETRAHYDROPIPERINE
四氢胡椒碱,Cosmoperine |
P450; TRP/TRPV Channel | Membrane transporter/Ion channel; Metabolism |
Tetrahydropiperine (Cosmoperine) 是胡椒碱的环己基类似物,也是一种天然芳基戊酰胺,从Piper longum 分离得到。它对细胞色素 P450 (CYP) 同工型 CYP1A1/芳基烃羟化酶 (AHH;IC50=23 µM)具有抑制作用。 | |||
T4928 |
L-Kynurenine
L-犬尿氨酸,(S)-Kynurenine |
AhR; Aryl Hydrocarbon Receptor; Endogenous Metabolite | Immunology/Inflammation; Metabolism |
L-Kynurenine ((S)-Kynurenine) 是L-色氨酸的代谢物,是芳香烃受体激动剂,可抑制同种异体 T 细胞增殖并增加恶性 U87 神经胶质瘤细胞侵入胶原基质。 | |||
T0878 |
Diosmin
Venosmine,Diosmil,Barosmin,地奥司明,地奥司明(7-芸香糖甙) |
Aryl Hydrocarbon Receptor; Norepinephrine | Immunology/Inflammation; Neuroscience |
Diosmin (Venosmine) 是在各种柑橘类水果中发现的类黄酮,也是芳烃受体激动剂,有增强血管壁的作用。 | |||
T4644 |
Tapinarof
GSK2894512,Benvitimod,苯烯莫德,WBI 1001 |
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
Tapinarof (Benvitimod) 是一种从发光杆菌中提取的天然产物,可消除炎症。它是芳烃受体 (AhR) 激动剂,EC50为 13 nM。 | |||
TN2883 |
3',4'-Dimethoxyflavone
|
Others; PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair; Others |
3',4'-Dimethoxyflavone 是类黄酮化合物的参考标准,类黄酮化合物具有多种药用活性。 | |||
T4939 |
Indole-3-pyruvic acid
3-(3-吲哚基)-2-氧代丙酸,3-(3-Indolyl)-2-oxopropanoic acid |
Others | Others |
Indole-3-pyruvic acid (3-(3-Indolyl)-2-oxopropanoic acid) 是一种参与Indole-3-acetic acid 生物合成的化合物,Indole-3-acetic acid 是一种植物激素,在调节生长和对环境变化的反应中起重要作用。 | |||
T5281 |
Skatole
粪臭素,Scatole,3-Methylindole,3-Methylindole,3-甲基吲哚,3-Methyl-1H-indole,beta-Methylindole |
AhR; p38 MAPK; Aryl Hydrocarbon Receptor; Endogenous Metabolite; Antibacterial; Autophagy; Antifungal | Autophagy; Immunology/Inflammation; MAPK; Metabolism; Microbiology/Virology |
Skatole (3-Methyl-1H-indole) 是由肠道菌群产生的,通过激活芳基烃受体和 p38调节肠上皮细胞功能。 | |||
T2947 |
Indole-3-carbinol
吲哚-3-甲醇,I3C,3-Indolemethanol,3-吲哚甲醇,Indole-3-Methanol |
E1/E2/E3 Enzyme; NF-κB; Aryl Hydrocarbon Receptor; Endogenous Metabolite; p53 | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB; Ubiquitination |
Indole-3-carbinol (I3C) 是樟子松中的一种天然产物,是可口服的硫代葡萄糖苷葡糖苷酶裂解产物。它是芳烃受体 (AhR) 的激动剂,可抑制 NF-κB 和 IκBα 激酶活化。 | |||
T5802 |
Stearyl glycyrrhetinate
|
Antiviral; Antibacterial | Immunology/Inflammation; Microbiology/Virology |
Stearyl glycyrrhetinate 是甘草提取物中的主要成分之一,具有抗菌作用,对金黄色葡萄球菌菌株的 MIC 大于 256 mg/L。 | |||
T19340 |
Glutarylcarnitine
O-glutaroyl-L-carnitine |
Endogenous Metabolite | Metabolism |
Glutarylcarnitine (O-glutaroyl-L-carnitine) 是大多数串联质谱新生儿筛查计划中监测的丙二酸尿症和谷草酸尿症 I 型的诊断代谢物。 | |||
TN6363 |
Tsaokoarylone
|
||
Tsaokoarylone 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 TN6363,CAS号为 811471-20-2。 | |||
TN4433 |
Licoarylcoumarin
|
cAMP; HIV Protease; Antifection | GPCR/G Protein; Microbiology/Virology; Proteases/Proteasome |
Licoarylcoumarin is a strong inhibitor of adenosine 3',5'-cyclic monophosphate (cAMP) phosphodiesterase. Licoarylcoumarin has antibacterial effects on the VRE strains; it has anti-HIV activity, and it has inhibitory effects on xanthine oxidase. | |||
TN2028 |
p-Coumaryl alcohol
|
Others | Others |
p-Coumaryl alcohol derivatives have antioxidant activity. | |||
TN7326 |
8'-O-(3-hydroxy-3-methylglutaryl)-8'-hydroxyabscisic acid
|
Others | Others |
TN3842 |
Diarylcomosol III
|
Others | Others |
Diarylcomosol III shows inhibitory effects on melanogenesis in B16 melanoma cells, it is a promising therapeutic agent for the treatment of skin disorders. | |||
T83542 |
(E)-p-Coumaryl alcohol
(E)-p-Hydroxycinnamyl alcohol |
||
(E)-p-Coumaryl alcohol,一种香豆素的代谢产物,从高良姜和红景天中分离,具显著的细胞毒性,应用于炎症研究。 | |||
T81506 |
Petunidin-3-O-(6-O-p-coumaryl)-5-O-diglucoside
|
||
Petunidin-3-O-(6-O-p-coumaryl)-5-O-diglucoside 是葡萄中可分离提取的天然产物。 | |||
T8281 |
(R)-Sulforaphane
L-Sulforaphane,(R)-1-异硫氰酰-4-(甲基亚磺酰)丁烷 |
Nrf2 | Immunology/Inflammation |
L-Sulforaphane 是高效的Keap1/Nrf2/ARE途径诱导剂。与 S-异构体相比,它对大鼠肝脏和肺部的致癌解毒酶系统的诱导能力更强。 | |||
T83321 |
4-Demethyldeoxypodophyllotoxin
|
Chk | Cell Cycle/Checkpoint |
4-Demethyldeoxypodophyllotoxin 是一种来自 Podophyllum peltatum 根部的芳基四氢萘木酚素类化合物,具有抗癌活性,可调节 MCF-7乳腺癌细胞中的Chk-2信号通路。 | |||
T3776 |
Rhapontigenin
丹叶大黄素,Protigenin |
P450; Antibacterial; Antifungal | Metabolism; Microbiology/Virology |
Rhapontigenin (Protigenin) 是一种基于机制的选择性细胞色素 P450 1A1 (IC50: 400 nM) 灭活剂。它是一种芳烃羟化酶,可激活作为致癌物质的多环芳烃。它是白藜芦醇的天然类似物,具有抗癌,抗氧化剂,抗真菌和抗菌活性。 | |||
TN6694 |
5,6-Benzoflavone
β-Naphthoflavone,beta-NF |
Antioxidant | oxidation-reduction |
5,6-Benzoflavone (β-Naphthoflavone) 是芳烃受体的外源配体,可破坏人肝癌 HepG2 细胞中的锌稳态。5,6-Benzoflavone (β-Naphthoflavone) 具有抗炎和抗氧化活性,抑制通过 AKT/Nrf-2/HO-1-NF-kappaB 信号转导轴,抑制 LPS 诱导的炎症,抑制TNF-α诱导的ICAM-1和VCAM-1表达,可用于研究神经退行性疾病。 | |||
T4938 |
Potassium 1H-indol-3-yl sulfate
硫酸吲哚钾盐,Indoxyl sulfate potassium salt,Potassium 3-indoxyl sulfate |
AhR; Endogenous Metabolite | Immunology/Inflammation; Metabolism |
Potassium 1H-indol-3-yl sulfate (Potassium 3-indoxyl sulfate) 是人芳烃受体(AhR)的激动剂。芳烃受体(AhR)最近被发现是免疫炎症条件的病理生理调节剂,Potassium 1H-indol-3-yl sulfate 已被证明是AhR的配体。Potassium 1H-indol-3-yl sulfate 也是膳食蛋白质中色氨酸的代谢物。色氨酸被肠道细菌代谢为吲哚,吲哚被吸收到血液中,然后在肝脏中进一步代谢为硫酸吲哚,通常通过尿液排出体外。在肾功能受损的慢性肾病患者中,Potassium 1H-indol-3-yl sulfate 可作为尿毒症毒素在血清中积累,诱导氧化应激并加速疾病进展。250 μM Potassium 1H-indol-3-yl sulfate 可诱导NF-Κb活化,促进大鼠近端小管细胞TGF-β1和Smad3的表达,与促纤维化活性相关。 | |||
TN6366 |
Lupinalbin A
鲁冰花 |
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Lupinalbin A as the most potent estrogen receptor α- and aryl hydrocarbon receptor agonist in Eriosema laurentii de Wild. (Leguminosae). It exerts anti-inflammatory effects via the inhibition of pro-inflammatory cytokines and blocking of IFN-β/STAT1 pathw | |||
T75433 |
Norisoboldine hydrochloride
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Others | Others |
Norisoboldine hydrochloride是一种口服活性天然芳基烃受体(AhR)激动剂,作为林参中的主要异喹啉类生物碱,适用于类风湿性关节炎和溃疡性结肠炎的研究。 | |||
T73402 |
Flavipin
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Others | Others |
Flavipin 是一种芳香烃受体(Ahr)激动剂,可诱导小鼠 CD4+T 细胞和 CD11b+巨噬细胞表达 Ahr 下游基因。Flavipin 抑制 Arid5a 在 Il23a3'UTR 上的稳定功能,这是一种新发现的靶 mRNA。Flavipin 具有清除 DPPH 自由基的能力,IC50值为7.2 μM,对α-葡萄糖苷酶具有较强的抑制作用,IC50值为 33.8 μM。 |
Cat. No. | Product Name | Species | Expression System |
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TMPH-02916 |
SULT1A1 Protein, Mouse, Recombinant (His & Myc)
Sulfotransferase 1A1,ST1A4,Aryl sulfotransferase,Su... |
Mouse | E. coli |
SULT1A1 Protein, Mouse, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 39.0 kDa and the accession number is P52840. | |||
TMPH-03376 |
SULT1A1 Protein, Rat, Recombinant (His & Myc & SUMO)
Sulfokinase,Aryl sulfotransferase IV,Phenol sulfotr... |
Rat | E. coli |
SULT1A1 Protein, Rat, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10XHis-SUMO and C-Myc tag. The predicted molecular weight is 53.9 kDa and the accession number is P17988. | |||
TMPH-00958 |
AHR Protein, Human, Recombinant (His)
Aryl hydrocarbon receptor,Class E basic helix-loop-... |
Human | E. coli |
AHR Protein, Human, Recombinant (His) is expressed in E. coli. | |||
TMPJ-00586 |
SULT1A2 Protein, Human, Recombinant (His)
STP2,Aryl Sulfotransferase 2,ST1A2,Phenol Sulfotran... |
Human | E. coli |
Sulfotransferase 1A2 (SULT1A2) is a member of the Sulfotransferase 1 family. Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. SULT1A2 is a cytoplasmic protein and exists as a homodimer. SULT1A2 mediates the metabolic activation of carcinogenic N-hydroxyarylamines to DNA binding products and might thus participate as a modulating factor of cancer risk. | |||
TMPH-00957 |
ARNT Protein, Human, Recombinant (His)
Hypoxia-inducible factor 1-beta,Class E basic helix-loop-hel... |
Human | P. pastoris (Yeast) |
ARNT Protein, Human, Recombinant (His) is expressed in Yeast. | |||
TMPY-05911 |
Influenza B (B/Maryland/1959) Hemagglutinin/HA Protein (His)
Harvey rat sarcoma viral oncogene homolog |
Influenza B | HEK293 Cells |
Influenza B (B/Maryland/1959) Hemagglutinin/HA Protein (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 59.7 kDa and the accession number is AAA43701. | |||
TMPY-01709 |
HIF-1 alpha Protein, Human, Recombinant (His)
bHLHe78,HIF-1 α,hypoxia inducible factor 1, alpha subunit (b... |
Human | E. coli |
HIF-1 alpha, also known as HIF1A, contains 1 basic helix-loop-helix (bHLH) domain, 1 PAC (PAS-associated C-terminal) domain, and 2 PAS (PER-ARNT-SIM) domains. It is one of the two subunits of Hypoxia-inducible factor-1 (HIF1). HIF1 is a transcription factor found in mammalian cells cultured under reduced oxygen tension that plays an essential role in cellular and systemic homeostatic responses to hypoxia. HIF1 is a heterodimer composed of an alpha subunit and a beta subunit. The beta subunit has... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMIJ-0060 |
Glutaryl carnitine-d3 HCl
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Glutaryl carnitine-d3 HCl 是 Glutaryl carnitine HCl 的氘代化合物。 | |||
TMIJ-0516 |
Carbaryl-d3
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Carbaryl-d3 是 Carbaryl 的氘代化合物。Carbaryl 的 CAS 号为 63-25-2。Carbaryl 可作为一种杀虫剂。 | |||
T70313 |
Indoxyl Sulfate-d5 potassium salt
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Indoxyl sulfate-d5 is intended for use as an internal standard for the quantification of indoxyl sulfate by GC- or LC-MS. Indoxyl sulfate is a uremic toxin and a metabolite of tryptophan. It is formed via sulfation of indole, an intermediate generated from tryptophan by intestinal bacteria, by the sulfotransferase (SULT) isoform 1A1 variant 2 (SULT1A1*2) in the liver. Indoxyl sulfate activates the aryl hydrocarbon receptor (AhR) in HepG2 40/6 hepatoma cells (EC50 = 12.1 nM in a reporter assay). ... |