163
62
3
41
4
Cat. No. | Product Name | ||
---|---|---|---|
L8700 | 铁死亡化合物库 | 779 compounds | |
779 种与铁死亡通路相关的化合物,可用于高通量和高内涵筛选; | |||
L2193 | 抗肝癌化合物库 | 1787 compounds | |
1787 种与肝癌相关的化合物,可以用于抗肝癌药物研发和药理研究; | |||
L5510 | 肝脏毒性化合物库 | 1001 compounds | |
1001 个肝脏毒性化合物的特有集合,可用于高通量、高内涵筛选,是毒理学研究的良好工具; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T83064 |
Anti-hepatic fibrosis agent 2
|
Others | Others |
Fibrosis agent 2为针对Ewing肉瘤断点区域1 (EWSR1) 的特定抗纤维化化合物。 | |||
TD0093 |
Oil Red O
|
Others | Others |
Oil Red O 用于制备染色溶液,可用于检测组织学冷冻切片中的脂质。 | |||
T31976 |
Glymidine sodium
|
Others | Others |
Glymidine sodium 是口服有活性的抗糖尿病药物,也是肝脂肪分解的抑制剂。它通过抑制葡萄糖的形成,也对由于内源性脂质动员抑制而导致的丙酮酸氧化升高具有抑制作用。 | |||
T12490 |
Pitavastatin lactone
|
Others; HMG-CoA Reductase | Metabolism; Others |
Pitavastatin lactone 是 Pitavastatin 在人体中的主要代谢产物。Pitavastatin 是 HMG-CoA 还原酶竞争性抑制剂。 | |||
T13173 |
TMPA
|
Others; AMPK | Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling |
TMPA 是一种核受体 Nur77 和 LKB1 相互作用的拮抗剂。 | |||
T12580 |
PTUPB
|
COX; Epoxide Hydrolase | Immunology/Inflammation; Metabolism; Neuroscience |
PTUPB 是强效的sEH(IC50:0.9 μM)和COX-2(IC50:1.26 μM)的双向抑制剂。 | |||
T4410 |
LM10
|
Others | Others |
LM10 是有效的色氨酸 2,3-双加氧酶的抑制剂。色氨酸 2,3-双加氧酶是一种无关的肝酶,它可通过犬尿氨酸途径降解色氨酸。它对研究癌症疾病具有潜在的研究价值。 | |||
T1403 |
Climbazole
甘宝素,BAY-e 6975 |
Antibiotic; Antifungal | Microbiology/Virology |
Climbazole (BAY-e 6975) 是一种广谱咪唑类抗真菌剂,具有去屑功效。它还是大鼠肝细胞色素 P450 的强诱导剂。 | |||
T5045 |
GSK4112
1,1-Dimethylethyl-N-[(4-chlorophenyl)methyl]-N-[(5-nitro-2-thienyl)methyl])glycinate,SR6452 |
Autophagy | Autophagy |
GSK4112 (SR6452) 是一种 Rev-erbα 激动剂,EC50 为 0.4 μM。它也是一种用于核血红素受体 Rev-erbα 的细胞生物学的小分子化学探针。 | |||
T0462 |
Cilostazol
西洛他唑,OPC 21,OPC 13013 |
PDE; Autophagy | Autophagy; Metabolism |
Cilostazol (OPC 21) 是一种选择性的心血管系统中磷酸二酯酶 3 亚型PDE 3A 的抑制剂,IC50值为 0.2 μM。 | |||
T3124 |
Carbendazim
Bavistin,Carbendazole,多菌灵,Mercarzole |
Antifungal | Microbiology/Virology |
Carbendazim (Mercarzole) 是一种具有抗肿瘤活性的苯并咪唑衍生物,可用于癌症研究。它是一种口服广谱苯并咪唑杀菌剂,可作为真菌疾病研究的杀虫剂。 | |||
T0850 |
Primaquine diphosphate
Primaquine phosphate,磷酸伯氨喹,Primaquine bisphosphate,磷酸伯安喹 |
Antibiotic; Parasite | Microbiology/Virology |
Primaquine diphosphate 是一种合成的 8-氨基喹啉衍生物,具有抗疟特性。它是一种能破坏间日疟原虫和卵形疟原虫肝脏晚期和潜在组织形态的化合物。 | |||
T1410 |
Torsemide
AC-4464,JDL-464,托拉塞米,Torasemide |
Na-K-Cl cotransporter | Membrane transporter/Ion channel |
Torsemide (AC-4464) 是具有口服活性的亨氏环利尿剂,也具有抗醛固酮和血管舒张活性。它可用于研究心力衰竭、肾脏疾病、肝硬化。 | |||
T9195 |
SHR0302
ARQ252 |
Apoptosis; JAK | Angiogenesis; Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
SHR0302 (ARQ252) 是一种具有口服活性的 JAK 抑制剂。它对 JAK1的结合力是 JAK2的 10 倍以上,是 JAK3的 77 倍,是 Tyk2的 420 倍。它抑制JAK1-STAT3磷酸化并诱导肝星状细胞凋亡,具有抗增殖和抗炎作用。 | |||
T8364 |
Mebrofenin
N-(3-溴-2,4,6-三甲基苯基甲酰甲基)乙酰乙酸,SQ 26962 |
Others | Others |
Mebrofenin (SQ 26962) 是一种亚氨基二乙酸 (IDA) ,可用作 Tc-99m 的放射性标记试剂盒。其中Tc-99m Mebrofenin 是一种诊断剂,用于肝胆显像,也是评价肝功能的首选放射性药物。 | |||
T1602 |
Valproic acid sodium salt
丙戊酸钠,Sodium Valproate |
Mitophagy; Gamma-secretase; HIV Protease; GABA Receptor; HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Proteases/Proteasome; Stem Cells |
Valproic acid sodium salt (Sodium Valproate) 是一种HDAC 抑制剂,可抑制HDAC1的活性,诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、偏头痛和双相情感障碍等。 | |||
T2096 |
Framycetin sulfate
Neomycin Sulphate B,硫酸新霉素B,Framycetin sulphate |
Antibacterial; Antibiotic | Microbiology/Virology |
Framycetin sulfate (Neomycin Sulphate B) 是一种氨基糖苷类抗生素,是 RNase P 裂解活性抑制剂,Ki 为 35 μM。它抑制锤头状核酶,Ki 值为 13.5 μM,可用于肝性脑病和肠致病性大肠杆菌感染的研究。 | |||
T6474 |
Divalproex Sodium
Valproate semisodium,Epival,双丙戊酸钠 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Divalproex Sodium (Valproate semisodium) 结合并抑制 γ-氨基丁酸 (GABA) 转氨酶,其抗惊厥活性可通过增加 GABA 脑浓度和抑制分解 GABA 或阻止 GABA 再摄取到神经胶质和神经末梢的酶来发挥。它也是一种 HDAC 抑制剂。由丙戊酸钠和丙戊酸组成,具有抗惊厥和抗癫痫活性。 Divalproex 还可以通过抑制电压敏感的钠通道来抑制重复的神经元放电。 | |||
T6595 |
Moexipril hydrochloride
莫昔普利盐酸盐,Moexipril HCl,RS-10085,SPM 925,CI-925 |
Apoptosis; RAAS | Apoptosis; Endocrinology/Hormones |
Moexipril hydrochloride (Moexipril HCl) 是一种有口服活性的,不含巯基的血管紧张素转化酶抑制剂,可治疗高血压和充血性心力衰竭。 | |||
T10409 |
ATX inhibitor 5
|
PDE | Metabolism |
ATX inhibitor 5 是一种有效且具有口服活性的 autotaxin (ATX) 抑制剂(IC50 : 15.3 nM),可降低 CCl4 诱导的肝纤维化水平,具有抗肝纤维化作用,。 | |||
T60004 |
SRI-37330
|
Others | Others |
SRI-37330 抑制胰高血糖素的分泌和功能,减少肝葡萄糖的产生,并逆转肝脂肪变性。 | |||
T13600 |
CDD3505
4-nitro-1-trityl-1H-imidazole |
P450 | Metabolism |
CDD3505 (4-nitro-1-trityl-1H-imidazole) 能够诱导肝CYP3A 的活动,增强高密度脂蛋白胆固醇的水平。 | |||
T13601 |
CDD3506
1-TRITYL-1H-IMIDAZOL-4-AMINE |
P450 | Metabolism |
CDD3506 (1-TRITYL-1H-IMIDAZOL-4-AMINE) 能够诱导肝CYP3A 的活动,增强高密度脂蛋白胆固醇的水平。 | |||
T30577 |
BRD0418
BRD 0418,BRD-0418 |
Others | Others |
BRD0418作为 TRIB1表达的上调因子,导致肝脏脂蛋白代谢从脂肪生成到清除的重新编程。 | |||
T4508 |
Glycyl-L-Histidyl-L-Lysine
|
Others | Others |
Glycyl-L-Histidyl-L-Lysine 是一种肝细胞生长因子和一种合成的肝营养剂,可刺激肝红细胞生成因子的产生。 | |||
T60033 |
SBI993
|
Others | Others |
SBI993 是 SBI-477 的类似物,可用作生物标志物来确认 MondoA 靶基因在体内表达的预期作用。 SBI993 降低肌肉 TAG 水平和肝脂肪变性。 | |||
T19694 |
Hydronidone
F351,F-351,F 351 |
Others | Others |
Hydronidone (F-351) 是一种 pyridine 衍生物。Hydronidone 对肝纤维化具有潜在的治疗作用。 | |||
T19783 |
Dehydroabiethylamine
NSC-2955,NSC 2955,Dehydroabietylamine,NSC2955,Leelamine free base,Leelamine,脱氢松香胺 |
P450; PDK | Metabolism; PI3K/Akt/mTOR signaling |
Dehydroabiethylamine (NSC-2955) 是肝脏 CYP2B 活性的诱导剂。 Dehydroabiethylamine 抑制丙酮酸脱氢酶激酶 (PDK) 和细胞内胆固醇转运,具有抗肿瘤活性。 | |||
T37184 |
CX08005
2-[(2-tetradecoxyphenyl)carbamoyl]benzoic acid |
Phosphatase | Metabolism |
CX08005 是一种蛋白酪氨酸磷酸酶 1B 抑制剂,可减轻与非酒精性脂肪肝相关的肝脏脂质蓄积和微循环障碍。 | |||
T6807 |
Citiolone
Thioxidrene,Citiolase,西替沃酮 |
Others | Others |
Citiolone (Thioxidrene) 是硫醇衍生药物,可作为粘液溶解剂,用于治疗某些肝脏疾病。 | |||
T27460 |
GSK2324
GSK-2324,GSK 2324 |
FXR | Metabolism |
GSK2324 是一种有效的 FXR 激动剂,通过减少脂肪酸合成的吸收和选择性减少来控制肝脂质,可用于治疗非酒精性脂肪肝。 | |||
T16844 |
Sarmazenil
R-154513,Ro 15-3505 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Sarmazenil (Ro 15-3505) 是苯二氮卓受体部分反向激动剂,具有促惊厥作用,可用于研究慢性肝性脑病 (HE) 。 | |||
T7428 |
SBI-115
|
GPCR19 | GPCR/G Protein |
SBI-115 是TGR5 (GPCR19)拮抗剂,对 TGR5 降低多囊性肝病的肝囊肿形成具有抑制作用。 | |||
T15779 |
LP-533401 hydrochloride
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
LP-533401 hydrochloride 是不能穿过血脑屏障的外周 Tph 抑制剂,抑制5-羟色胺合成,可用于研究牙周病和肝脂肪变性。 | |||
T15379 |
GGsTop
Nahlsgen |
Others | Others |
GGsTop is a non-toxic and irreversible inhibitor of γ glutamyl transpeptidase (GGT) (Ki: 170 μM for Human GGT). GGsTop protects hepatic ischemia-reperfusion injury in the rat model. GGsTop shows Kons of 150±10 and 51±3 /(M·s) against E.coli GGT and human GGT, respectively. | |||
T14875 |
Indocyanine green
Cardiogreen,IC Green,Foxgreen,吲哚菁绿 |
Others | Others |
Indocyanine green (Cardiogreen) 是低毒性荧光剂,普遍用于医学诊断,包括确定心输出量,肝功能和肝血流量,以及用于眼科血管造影。 | |||
T0299 |
Lactitol monohydrate
D-Lactitol monohydrate,单水合乳糖醇 |
Others | Others |
Lactitol monohydrate (D-Lactitol monohydrate) 是一种乳果糖的糖类似物,是一种糖醇,用作替代甜味剂。有用于便秘和肝性脑病的研究潜力。。 | |||
T19399 |
L-Ornithine L-aspartate
Ornithine Aspartate,L-鸟氨酸 L-天冬氨酸 |
Others | Others |
L-Ornithine L-aspartate (Ornithine Aspartate) 由鸟氨酸和天冬氨酸组成。它能够减少血氨浓度,并消除与肝硬化相关的肝性脑病的症状。 | |||
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)。 | |||
T12174 |
Naphthoquine phosphate
|
Parasite | Microbiology/Virology |
Naphthoquine phosphate 是一种具有口服活性的广谱4-氨基喹啉类抗疟化合物,可能影响病毒进入和进入后复制。Naphthoquine phosphate 具有肝血管中心毒性,常与青蒿素一起使用来治疗疟疾。 | |||
T25458 |
Golexanolone
Golexanolonum,Golexanolona,GR-3027 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Golexanolone (Golexanolona) 是一种新的 GABA-A 受体调节类固醇拮抗剂,可减少外周炎症和神经炎症,并改善慢性高氨血症大鼠的认知和运动功能,可用于研究肝性脑病。 | |||
T35373L |
Bulevirtide (Myrcludex B) acetate
|
HBV | Microbiology/Virology |
Bulevirtide (Myrcludex B) acetate 是一种病毒粒子进入抑制剂,可阻断病毒粒子的肝细胞进入途径,即肝钠/牛磺胆酸盐协同转运多肽 (NTCP) 受体。它可用于 HBV 和 HDV 感染研究。 | |||
T14387 |
AZD9898
|
Leukotriene Receptor | GPCR/G Protein |
AZD9898 是一种白三烯-C4 合成酶抑制剂,IC50 为 0.28 nM。 AZD9898 可用于哮喘研究。 AZD9898 减轻 GABA 结合和肝毒性信号。 | |||
T40598 |
Norethindrone acetate
19-Norethindroneacetate |
Estrogen Receptor/ERR; Progesterone Receptor | Endocrinology/Hormones; Others |
Norethindrone acetate (19-Norethindroneacetate) 是一种雌性激素,对青少年月经和肝腺瘤有抑制作用,常与孕激素联合使用,可用于研究子宫内膜异位症。 | |||
T9186 |
Ervogastat
PF-06865571 |
Transferase | Metabolism |
Ervogastat (PF-06865571) 是一种有效且耐受性良好的二酰基甘油酰基转移酶 2 抑制剂。 Ervogastat 可降低非酒精性脂肪性肝炎 (NASH) 中的脂肪变性和肝脏甘油三酯水平。 | |||
T23097 |
O-1602
O1602,O 1602 |
Cannabinoid Receptor; Calcium Channel | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism |
O-1602 是一种新型 GPR55 激动剂,是一种非典型大麻素,与中枢神经系统和肥胖有关,是治疗膀胱炎的候选化合物。O-1602通过小鼠GPR55 的 PI3激酶/ Akt / SREBP-1c信号传导促进肝脂肪变性。O-1602以GPR3非依赖性方式诱导Hep55B细胞中的细胞内钙升高。 | |||
T36126 |
TMP-153
|
Acyltransferase | Metabolism |
TMP-153 是一种新型高效的 ACAT 抑制剂,对动物肠道和肝脏 ACAT 的 IC50 值为 5-10 nM。TMP-153 具有降胆固醇作用,可抑制大鼠和仓鼠的胆固醇吸收并降低血浆胆固醇。 | |||
T6552 |
Istradefylline
伊曲茶碱,KW-6002 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Istradefylline (KW-6002) 是选择性的可口服的腺苷 A2A 受体拮抗剂,可用于研究药物滥用、睡眠障碍、肝损伤、帕金森病和不安腿综合征等的治疗和基础科学的试验。 | |||
T25285 |
Dalvastatin
RG-12561,RG 12561,RG12561 |
HMG-CoA Reductase | Metabolism |
Dalvastatin (RG-12561) 是一种可口服的 HMG-CoA 还原酶和降胆固醇合成的抑制剂。Dalvastatin 竞争性地抑制大鼠肝脏HMG-CoA还原酶,IC50值为3.4 nmol / l。 Dalvastatin 在在大鼠实验中,抑制肝切片中的胆固醇生物合成,ED50值为0.9。 | |||
T15549 |
Icosabutate
NST-4016,PRC-4016 |
Others | Others |
Icosabutate (NST-4016) 是一种具有口服活性的二十碳五烯酸的衍生物,可抑制 NASH 的肝脏炎症和纤维化,可改善他汀类药物治疗的残留高甘油三酯血症患者的心血管风险状况,降低甘油三脂,可用于研究肝纤维化和动脉粥样硬化。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7992 |
4-Hydroxyflavanone
|
NO Synthase | Immunology/Inflammation |
4-Hydroxyflavanone 是一种黄酮的合成类似物,是 SREBP 成熟和脂质合成的抑制剂。它具有研究肝脏脂肪变性及血脂异常的潜力。 | |||
T3888 |
Scopolin
Murrayin,东莨菪甙,Scopoloside,东莨菪苷 |
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Scopolin (Scopoloside) 是从拟南芥根中分离出来的香豆素,可通过激活SIRT1介导的信号级联反应减轻了肝脂肪变性。 | |||
T3858 |
macranthoidin A
灰毡毛忍冬皂苷甲,金银花 |
Others | Others |
Macranthoidin A 是一种具有口服活性的、提取于金银花中的皂苷。它对四氯化碳,对乙酰氨基酚和镉所致的肝损伤具有保护作用,对耳巴豆油的溶胀具有明显的抑制作用。 | |||
T0746 |
Orotic acid
乳清酸,Vitamin B13,6-Carboxyuracil |
Nucleoside Antimetabolite/Analog; Dehydrogenase; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Orotic acid (Vitamin B13) 是一种嘧啶核苷酸和 RNA 生物合成的前体,从线粒体二氢乳清酸脱氢酶 (DHODH) 中释放,通过细胞质 UMP 合酶转化为 UMP。它可引起大鼠肝脂肪变性和肝肿大,是尿素循环异常的常规新生儿筛查中的一种测量指标。 | |||
T2718 |
Palmatine chloride
|
Others; Indoleamine 2,3-Dioxygenase (IDO); Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Metabolism; Others |
Palmatine chloride 是口服具有活力的不可逆 IDO-1抑制剂。它能够减轻结肠损伤,预防肠道菌群失调和调节色氨酸分解代谢,并改善 DSS 诱发的结肠炎。 | |||
T0700 |
Ursodeoxycholic acid
熊去氧胆酸,UDCA,Ursodiol |
Potassium Channel; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism |
Ursodeoxycholic acid (UDCA)是一种有效的肝脏特异性脂肪酸转运蛋白 5 (FATP5) 抑制剂,通过 FATP5 依赖性方式抑制原代肝细胞摄取长链脂肪酸。Ursodeoxycholic acid 能够抑制胆固醇的吸收,用于溶解胆结石,并具有研究与肥胖相关的脂肪肝疾病的潜力。 | |||
T19081 |
1,3-Dithiane
1,3-Dithian,M-DITHIANE,1,3-Dithiacyclohexane,1,3-二噻烷 |
Anti-infection; Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology |
1,3-Dithiane (1,3-Dithian) 是一种受保护的甲醛阴离子等价物,可用作有用的标记合成子。它是在煮熟的牛肉提取物中发现的含硫美拉德反应产物 。 | |||
T5S0802 |
Palmatine
巴马汀,Berbericinine,Burasaine |
Indoleamine 2,3-Dioxygenase (IDO); AChR; AChE; Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Metabolism; Neuroscience |
Palmatine (Burasaine) 是口服具有活力的、不可逆IDO-1抑制剂。它可以减轻结肠损伤,预防肠道菌群失调和调节色氨酸分解代谢,从而改善DSS (Dextran Sulphate Sodium Salt) 诱发的结肠炎。它有用于结肠炎的研究潜力。 | |||
T3999 |
D(+)-Galactosamine hydrochloride
D-半乳糖胺盐酸盐,D-氨基半乳糖盐酸盐,D-Galactosamine HCl |
Others | Others |
D(+)-Galactosamine hydrochloride (D-Galactosamine HCl) 是一种被证实的实验毒素,它能够产生自由基及UTP 核苷酸的消耗导致肝损伤,中毒剂量会造成肾功能不全,而肾功能衰竭通常和终末期肝损伤有关。脂多糖/D-Galactosamine 诱导的急性肝损伤是一种已知的暴发性肝衰竭动物模型。 | |||
T3271 |
Orotic acid zinc
乳清酸锌二水合物,Orotic acid zinc salt dihydrate,Zinc Orotate |
Nucleoside Antimetabolite/Analog; Others; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Others |
Orotic acid zinc (Zinc Orotate) 是一种嘧啶核苷酸和 RNA 生物合成的前体,从线粒体二氢乳清酸脱氢酶 (DHODH) 中释放,通过细胞质 UMP 合酶转化为 UMP。它可引起大鼠肝脂肪变性和肝肿大,是尿素循环异常的常规新生儿筛查中的一种测量指标。 | |||
T7064 |
Valproic Acid
Sodium valproate,2-Propylpentanoic Acid,丙戊酸,VPA,Depakine,2-Propylvaleric Acid |
Mitophagy; Gamma-secretase; HIV Protease; GABA Receptor; Sodium Channel; HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Proteases/Proteasome; Stem Cells |
Valproic Acid (2-Propylpentanoic Acid) 是一种 HDAC 抑制剂,可抑制 HDAC1 活性,诱导 HDAC2 降解,具有口服活性。Valproic Acid 可以用于癫痫和躁郁症的研究。 | |||
T29078 |
Ursodeoxycholic acid sodium
UDCA Na,UDCA sodium,Sodium Ursodeoxycholate,熊去氧胆酸钠盐,Ursodiol sodium,Ursodeoxycholic Acid (sodium salt),Ursodeoxycholate sodium |
FXR; Endogenous Metabolite; GPCR19 | GPCR/G Protein; Metabolism |
Ursodeoxycholic acid sodium (Sodium Ursodeoxycholate) 是一种天然存在的次级胆汁酸,具有抗炎和细胞保护活性。Ursodeoxycholic acid sodium 作为信号分子,通过与胆汁酸激活受体相互作用发挥其作用,包括 G 蛋白偶联胆汁酸受体 5 (TGR5) 和法尼醇 X 受体 (FXR)。 | |||
TWA2417 |
Sodium taurocholate
牛黄胆酸钠(牛胆酸钠,牛胆酸钠盐,牛磺膽酸鈉,牛磺胆酸钠,牛磺胆酸钠盐,牛胆酸钠水合物,水合牛磺胆酸钠,牛胆酸钠(混合物),牛黄胆酸钠(水合),牛磺胆酸钠(标准品)),Taurocholate Sodium |
Others | Others |
Sodium taurocholate (Taurocholate Sodium) hydrate 具有显著的生物学效应,例如通过上调 VEGF-A 的表达抑制肝动脉结扎所致的胆道损伤。对免疫系统具有一定的调节作用。 | |||
TN6751 |
1-HEXACOSANOL
|
NPC1L1; AMPK | Chromatin/Epigenetic; Membrane transporter/Ion channel; PI3K/Akt/mTOR signaling |
1-HEXACOSANOL 激活 AMPK 和肝脏自噬并抑制 SREBP2,导致降胆固醇活性和肝脏脂肪变性的改善。 | |||
PDK0060 |
Pseudotropine
|
Others | Others |
Pseudotropine 是一种植物生物碱,是 Tropane 的衍生物。 | |||
T2136 |
Geniposidic Acid
京尼平甙酸,京尼平苷酸 |
Apoptosis; Others; Endogenous Metabolite | Apoptosis; Metabolism; Others |
Geniposidic acid 是一种环烯醚萜苷,用于治疗黄疸、炎症和肝脏疾病,具有辐射保护和抗癌活性。 | |||
TN1599 |
Eburicoic acid
Eburicoicacid,MFCD00238594,ZINC4655149,齿孔菌酸 |
Antioxidant; TNF; NOS; NO Synthase; CCR; Immunology/Inflammation related | Apoptosis; Immunology/Inflammation; Microbiology/Virology; oxidation-reduction |
Eburicoic acid (ZINC4655149) 具有抗炎和抗氧化活性,从而保护肝脏免受 CCl4 引起的肝损伤,可用于抗肝癌研究。 | |||
T5261 |
(E)-Oct-2-enoic acid
trans-2-Octenoic acid,2-Octenoate,2-辛烯酸,2-Octenoic acid |
Others; Endogenous Metabolite | Metabolism; Others |
(E)-Oct-2-enoic acid (2-Octenoate) 是内源性代谢产物的一种。 | |||
T36831 |
9-Oxononanoic Acid
9-ONA |
Phospholipase; CPT | Metabolism |
9-Oxononanoic Acid是一种氧化脂肪酸,由亚油酸自氧化形成,它能提高磷脂酶 A2(PLA2)的活性,并增加离体人体血浆中血栓素 B2 的生成。9-Oxononanoic Acid 能减少肝脏新脂肪酸的合成,并提高大鼠肝脏肉碱棕榈酰转移酶(β-氧化的标志物)的活性。 | |||
T0799 |
Lactulose
Duphalac,4-O-β-D-Galactopyranosyl-D-fructose,D-Lactulose,Lactulosum,乳果糖 |
Others | Others |
Lactulose (Lactulosum) 是一种不易吸收的糖,一般给药 8 到 12 小时后开始发挥药效,但可能需要两天时间改善便秘。它可用于便秘和肝性脑病的研究。 | |||
TN1675 |
Gardenin B
栀子黄素B |
Apoptosis; ROS; Caspase; NO Synthase | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Gardenin B 是从Baccharis scandens 中分离出的一种黄酮类天然产物。它对肺、乳腺、结肠、肝和白血病细胞系以及角质形成细胞具有优异的抗增殖活性。 | |||
T3924 |
Astragaloside II
黄芪皂苷 II,Astrasieversianin VIII |
TGF-beta/Smad | Stem Cells |
Astragaloside II (Astrasieversianin VIII) 是一种分离自黄芪中的天然化合物。 | |||
T21383 |
D-Thyroxine
Dethyrona,Detyroxin,Dextroid,Dextrothyroxine;Biotirmone,Dextroxin,Biotirmone,Debetrol,Dextrothyroxine |
Others | Others |
D-Thyroxine (Dextroxin) 是一种甲状腺激素,对 TSH 的分泌具有抑制作用,可用于研究高胆固醇血症。 | |||
TN2359 |
Iristectorigenin B
Iristectrigenin B |
Liver X Receptor | Metabolism |
Iristectorigenin B (Iristectrigenin B) 是一种有效的肝脏 X 受体 (LXR) 调节剂,是从 Belamcanda chinensis 中分离的小分子化合物。Iristectrigenin B 可促进巨噬细胞 RAW 1.1 细胞中 ABCA264 和 ABCG7 的表达。 | |||
T75636 |
(E/Z)-Squalene
(E/Z)-Super Squalene,(E/Z)-AddaVax |
Others | Others |
(E/Z)-Squalen 调节细胞内活性氧化物质 (ROS) 的产生,并呈浓度和时间依赖性引起细胞凋亡和坏死 。(E/Z)-Squalene ((E/Z)-AddaVax) 在肝脏中积累并降低肝脏胆固醇和甘油三酯。 | |||
T0687 |
Simvastatin
辛伐他汀,MK-0733,MK 733 |
Apoptosis; Mitophagy; Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Simvastatin (MK 733) 是一种 HMG-CoA 还原酶抑制剂 (Ki=0.2 nM),具有口服活性。Simvastatin 具有降血脂活性,可以抑制肝脏产生胆固醇,还可以用于预防心血管疾病。 | |||
T4916 |
D-Glucaric acid potassium
D-Saccharic acid potassium salt,Glucosaccharic acid,D-葡萄糖二酸单钾盐,Glucaric Acid |
Others; Endogenous Metabolite | Metabolism; Others |
D-Glucaric acid potassium (D-Saccharic acid potassium salt) 是内源性代谢产物的一种。 | |||
TWO2727 |
Propane-1,2,3-triyl tripalmitate
Palmitic Triglyceride,Tripalmitin,Tripalmitoylglycerol,Glycerol Tripalmitate,三棕榈酸甘油酯 |
Others; Endogenous Metabolite | Metabolism; Others |
Propane-1,2,3-triyl tripalmitate (Glycerol Tripalmitate) 是内源性代谢产物的一种。 | |||
T4713 |
Phosphorylcholine chloride calcium salt tetrahydrate
Phosphocholine chloride calcium salt tet,胆碱磷酸氯化钙四水,CalciuM Phosphorylcholine Tetrahydrate |
Others; Endogenous Metabolite | Metabolism; Others |
Phosphorylcholine chloride calcium salt tetrahydrate (Phosphocholine chloride calcium salt tet) 是内源性代谢产物的一种。 | |||
T4S0797 |
Berberine
小檗碱,Berberin,Umbellatine,黄连素 |
Reactive Oxygen Species; Topoisomerase; Endogenous Metabolite; Antibacterial; Antibiotic; Autophagy | Autophagy; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Berberine (Umbellatine) 属于生物碱类天然产物,可以激活 AMPK、抑制 DNA 拓扑异构酶、诱导 ROS 生成。Berberine 具有抗肿瘤、抗菌、降血糖、降血脂等生物学活性。 | |||
T2909 |
Fraxetin
7,8-dihydroxy-6-methoxy coumarin,秦皮素,弗拉西汀 |
Apoptosis; Others | Apoptosis; Others |
Fraxetin (7,8-dihydroxy-6-methoxy coumarin) 是从秦皮中分离出来的一种天然产物,可诱导细胞凋亡,具有抗肿瘤、抗氧化作用和抗炎作用。 | |||
TCS1772 |
Dehydroabietic acid
Dehydroabietate,脱氢松香酸 |
Antifection | Microbiology/Virology |
Dehydroabietic acid (Dehydroabietate) 是 EBV-EA 活化抑制剂。 它是食物衍生化合物,可通过降低血浆葡萄糖、胰岛素水平、血浆甘油三酯 (TG) 和肝 TG 水平来治疗肥胖相关疾病。它的衍生物在动物模型中表现出抗分泌和抗胃蛋白酶作用。 | |||
T0186 |
Docetaxel trihydrate
RP-56976 (Trihydrate),RP56976 (NSC 628503) Trihydrate,多西他赛三水合物 |
Apoptosis; BCL; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Docetaxel trihydrate (RP-56976 Trihydrate) 是一种抗肿瘤试剂,抑制微管解聚的IC50值为 0.2 μM。它是紫杉醇的半合成类似物,能减弱 bcl-2 和 bcl-xL 基因表达的影响。它阻滞G2/M 细胞周期,导致细胞凋亡。 | |||
T5248 |
(R)-3-Hydroxybutanoic acid
|
Others; Endogenous Metabolite | Metabolism; Others |
(R)-3-Hydroxybutanoic acid 是一种代谢物,在 3-羟基丁酸脱氢酶催化下由乙酸乙酯转化而成。它可以作为营养来源和抗生素、维生素和信息素的前体。 | |||
T3414 |
Morroniside
莫诺苷,奎宁树 |
Apoptosis; MMP; Pyroptosis | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Morroniside 通过抑制神经元凋亡和 MMP9/2 的表达从而发挥神经保护作用,可作为 db/db 小鼠肝脏炎症反应和脂质代谢的调节剂。它通过抑制高血糖和氧化应激表现出对糖尿病肾损伤和人脐静脉内皮细胞的保护作用。 | |||
T6S0221 |
Eriocitrin
eriodictyol 7-rutinoside,圣草次甙,Eriodictyol-7-O-Rutinoside,Eriodictioside,圣草次甙;圣草次苷,Eriodictyol glycoside |
Apoptosis; Carbonic Anhydrase | Apoptosis; Metabolism |
Eriocitrin (Eriodictyol-7-O-Rutinoside) 是从柠檬中分离出来的一种黄酮类天然产物,是强效的抗氧化剂。它通过激活线粒体涉及的内在信号传导途径来触发细胞凋亡。它通过上调 p53、cyclin A、cyclin D3 和 CDK6 使 S 期细胞周期停滞,从而抑制肝癌细胞的增殖。 | |||
T10196 |
7α-Hydroxy-4-cholesten-3-one
7-hydroxy-4-cholesten-3-one |
Others | Others |
7α-Hydroxy-4-cholesten-3-one 是一种可穿过血脑屏障的胆汁酸前体,可作为肝胆汁酸合成的指标。7α-Hydroxy-4-cholesten-3-one 是一种孕烷 X 受体 (PXR) 激动剂。7α-Hydroxy-4-cholesten-3-one 可用于研究与胆汁酸生物合成缺陷有关的疾病。 | |||
T5S0896 |
Loureirin A
龙血素 A,龙血素A |
Akt; PI3K | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
Loureirin A 是一种黄酮类物质,从龙血树中分离得到,能够降低Akt 的磷酸化,具有抗血小板聚集作用。 | |||
T6S1917 |
Schisandrol B
Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B |
P450; Reactive Oxygen Species; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; NF-κB |
Schisandrol B (Besigomsin) 是华中五味子的主要活性成分,具有保肝、抗炎、抗糖尿病和抗氧化的作用。它抑制活性氧的产生,也抑制 P-糖蛋白和CYP3A 的活性。 | |||
T5S0106 |
Peimisine
贝母辛,Ebeiensine |
RAAS; AChR | Endocrinology/Hormones; Neuroscience |
Peimisine (Ebeiensine) 非竞争性拮抗气管平滑肌 M 受体,抑制 Ach 引起的平滑肌收缩。它兴奋 β 受体和拮抗内钙释放,促进一氧化氮释放,可舒张气管平滑肌,有平喘作用。 | |||
TN2063 |
Physalin B
NSC-287088 |
Apoptosis; NF-κB; Akt; PI3K; Nrf2; NOD | Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; PI3K/Akt/mTOR signaling |
Physalin B 是茄科植物的主要活性化合物之一,具有广泛的生物活性,可用于治疗炎症湿疹和疱疹等疾病。Physalin B 通过激活 PI3K/Akt 通路抑制 NF-κB 和 NLRP3,从而改善脂多糖诱导的急性肺损伤造成的炎症反应。Physalin B 通过激活 Nrf2 通路抑制 PDGF-BB 诱导的 VSMC 增殖、迁移和表型转化。Physalin B 通过抑制 LAP2α-HDAC1 介导的胶质瘤相关癌基因 1 的去乙酰化和肝星状细胞活化来发挥抗肿瘤活性。 | |||
T20524 |
Lasiocarpine
7-Angelyleuropine,(-)-Lasiocarpine,Europine 7-angelate,AI3-51770 |
Others | Others |
Lasiocarpine is a pyrrolizidine alkaloid, it has acute cytotoxicity in human and hepatic cell lines. | |||
T28021 |
meso-Dihydroguaiaretic acid
|
||
meso-Dihydroguaiaretic acid is an LXR-α antagonist, it inhibits hepatic lipid accumulation by activating AMP-activated protein kinase in human HepG2 cells. | |||
TMA1409 |
cis-Mulberroside A
|
TNF; NOS | Apoptosis; Immunology/Inflammation |
cis-Mulberroside A shows high analgesic and anti-inflammatory activities, it can protect mice against ethanol-induced hepatic damage. | |||
T11513 |
Gum arabic
Arabic gum,阿拉伯胶 |
Others | Others |
Gum Arabic, a branched-chain, complex polysaccharide derived from A. Senegal, exhibits antioxidant properties and offers protection against experimental hepatic, renal, and cardiac toxicities. Additionally, it finds application in immunohistochemistry. | |||
T81521 |
Penispidin A
|
||
Penispidin A抑制HepG2细胞内的肝脏脂质积累现象。 | |||
TN6004 |
Deoxycalyciphylline B
|
||
Deoxycalyciphylline B exhibits hepatic toxicity. Deoxycalyciphylline B and Methyl homosecodaphniphyllate show different inhibitory effects on thephenoloxidase (PO) of Spodoptera exigua (Hbner) and the inhibitor concentrations leading to 50% (IC50) activit | |||
TN3517 |
Bisacurone
|
IL Receptor; IκB/IKK; TNF; NF-κB; ROS; Akt; PKC | Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; PI3K/Akt/mTOR signaling |
Bisacurone has anti-oxidant, anti-inflammatory, and anti-metastatic activities, it may have a protective effect against ethanol-induced liver injury by suppressing hepatic oxidation and inflammation. | |||
T38805 |
Euphol acetate
|
Others | Others |
Euphol acetate, a triterpene found in Euphorbia broteri, has demonstrated inhibitory effects on the hepatic transport proteins known as organic anion-transporting polypeptide 1/3 (OATP1B1/3). | |||
T11365 |
Ganodermanontriol
|
Others | Others |
Ganodermanontriol, a sterol derived from Ganoderma lucidum, showcases hepatoprotective activity and possesses anti-inflammatory properties in tert-butyl hydroperoxide (t-BHP)-damaged hepatic cells through the upregulation of HO-1 expression. | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPJ-00479 |
KHK Protein, Human, Recombinant (His)
KHK,Hepatic fructokinase,Ketohexokinase |
Human | HEK293 Cells |
Ketohexokinase, also known as Hepatic fructokinase, is a member of the carbohydrate kinase PfkB family. It exits as a homodimer and most abundant in liver, kidney, gut, spleen and pancreas. Low levels also found in adrenal, muscle, brain and eye.This enzyme catalyzes conversion of fructose to fructose-1-phosphate. It is the first enzyme with a specialized pathway that catabolizes dietary fructose. Defects in KHK are the cause of fructosuria. | |||
TMPH-01585 |
Ketohexokinase/KHK Protein, Human, Recombinant (GST)
Hepatic fructokinase,KHK,Ketohexokinase |
Human | E. coli |
Catalyzes the phosphorylation of the ketose sugar fructose to fructose-1-phosphate. Ketohexokinase/KHK Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 59.7 kDa and the accession number is P50053. | |||
TMPH-02747 |
Ketohexokinase/KHK Protein, Mouse, Recombinant (His)
Ketohexokinase,Khk,Hepatic fructokinase |
Mouse | E. coli |
Ketohexokinase/KHK Protein, Mouse, Recombinant (His) is expressed in E. coli. | |||
TMPY-00419 |
HEPACAM Protein, Human, Recombinant (His)
HEPACAM,MLC2A,hepatic and glial cell adhesion molec... |
Human | HEK293 Cells |
HEPACAM Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 24.5 kDa and the accession number is Q14CZ8-1. | |||
TMPJ-01058 |
ARG2 Protein, Human, Recombinant (His)
ARG2,Kidney-type arginase,Type II arginase,Arginase-2, mitoc... |
Human | E. coli |
Arginase-2 (ARG2) is a member of the arginase family. Arginase is a manganese-containing enzyme which catalyzes the hydrolysis of arginine to ornithine and urea. ARG2 is highly expressed in kidney and prostate, not founded in the liver, heart and pancreas. ARG2 has been implicated in the regulation of the arginine/ornithine concentrations in the cell. ARG2 may take part in the regulation of extra-urea cycle arginine metabolism and in down-regulation of nitric oxide synthesis. The extrahepatic ar... | |||
TMPH-03232 |
HSD17B13 Protein, Rat, Recombinant (His)
Hsd17b13,17-beta-hydroxysteroid dehydrogenase 13,Hepatic... |
Rat | Baculovirus Insect Cells |
N/A. HSD17B13 Protein, Rat, Recombinant (His) is expressed in Baculovirus insect cells with N-6xHis tag. The predicted molecular weight is 32.4 kDa and the accession number is Q5M875. | |||
TMPH-03233 |
HSD17B13 Protein, Rat, Recombinant (E. coli, His)
Short-chain dehydrogenase/reductase 9,Hsd17b13,17-beta-hydro... |
Rat | E. coli |
N/A. HSD17B13 Protein, Rat, Recombinant (E. coli, His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 37.4 kDa and the accession number is Q5M875. | |||
TMPH-02526 |
Arginase-2/ARG2 Protein, Mouse, Recombinant (His & SUMO)
Arginase II,Kidney-type arginase,Type II arginase,Arg2,Argin... |
Mouse | E. coli |
May play a role in the regulation of extra-urea cycle arginine metabolism and also in down-regulation of nitric oxide synthesis. Extrahepatic arginase functions to regulate L-arginine bioavailability to nitric oxid synthase (NOS). Arginine metabolism is a critical regulator of innate and adaptive immune responses. Seems to be involved in negative regulation of the survival capacity of activated CD4(+) and CD8(+) T cells. May suppress inflammation-related signaling in asthmatic airway epithelium.... | |||
TMPH-03248 |
ASGR1 Protein, Rat, Recombinant (His & Myc)
Asialoglycoprotein receptor 1,ASGP-R 1,rHL-1,Asgr1,HL-1,Asgr... |
Rat | HEK293 Cells |
Mediates the endocytosis of plasma glycoproteins to which the terminal sialic acid residue on their complex carbohydrate moieties has been removed. The receptor recognizes terminal galactose and N-acetylgalactosamine units. After ligand binding to the receptor, the resulting complex is internalized and transported to a sorting organelle, where receptor and ligand are disassociated. The receptor then returns to the cell membrane surface. ASGR1 Protein, Rat, Recombinant (His & Myc) is expressed in... | |||
TMPH-02529 |
ASGR2 Protein, Mouse, Recombinant (His & Myc)
ASGPR 2,HL-2,mHL-2,Asgr-2,Hepatic lectin 2,ASGP-R 2... |
Mouse | E. coli |
Mediates the endocytosis of plasma glycoproteins to which the terminal sialic acid residue on their complex carbohydrate moieties has been removed. The receptor recognizes terminal galactose and N-acetylgalactosamine units. After ligand binding to the receptor, the resulting complex is internalized and transported to a sorting organelle, where receptor and ligand are disassociated. The receptor then returns to the cell membrane surface. ASGR2 Protein, Mouse, Recombinant (His & Myc) is expressed ... | |||
TMPH-00845 |
HSD17B13 Protein, Human, Recombinant (His & Myc)
Hepatic retinol/retinal dehydrogenase,Short chain d... |
Human | P. pastoris (Yeast) |
HSD17B13 Protein, Human, Recombinant (His & Myc) is expressed in yeast with N-6xHis and C-Myc tag. The predicted molecular weight is 34.8 kDa and the accession number is Q7Z5P4. | |||
TMPJ-01415 |
ANGPTL4 Protein, Mouse, Recombinant (hFc)
Angptl4,HFARP,Fasting-induced adipose factor,Fiaf,Secreted p... |
Mouse | HEK293 Cells |
Angiopoietin-related protein 4(ANGPTL4)is a secreted protein and contains 1 fibrinogen C-terminal domain. The protein may act as a regulator of angiogenesis and modulate tumorigenesis. It inhibits proliferation, migration, and tubule formation of endothelial cells and reduces vascular leakage. ANGPTL4 may exert a protective function on endothelial cells through an endocrine action. It is directly involved in regulating glucose homeostasis, lipid metabolism, and insulin sensitivity (By similarity... | |||
TMPY-01442 |
DMBT1 Protein, Human, Recombinant (His)
GP340,deleted in malignant brain tumors 1,muclin |
Human | HEK293 Cells |
Deleted in malignant brain tumors 1 protein, also known as glycoprotein 34, surfactant pulmonary-associated D-binding protein, DMBT1 and GP34, is a secreted protein which belongs to theDMBT1 family. DMBT1 contains 2CUB domains, 14SRCR domains and 1ZP domain. It is highly expressed in alveolar and macrophage tissues. In some macrophages, expression is detected on the membrane, and in other macrophages, it is strongly expressed in the phagosome/phagolysosome compartments. Defects in DMBT1 are invo... | |||
TMPH-01578 |
KRT18 Protein, Human, Recombinant (His)
Keratin, type I cytoskeletal 18,KRT18,Cell proliferation-ind... |
Human | HEK293 Cells |
Involved in the uptake of thrombin-antithrombin complexes by hepatic cells. When phosphorylated, plays a role in filament reorganization. Involved in the delivery of mutated CFTR to the plasma membrane. Together with KRT8, is involved in interleukin-6 (IL-6)-mediated barrier protection. | |||
TMPY-02909 |
ASGR2 Protein, Human, Recombinant (His)
HBXBP,ASGPR2,HL-2,asialoglycoprotein receptor 2,ASGP-R2,CLEC... |
Human | HEK293 Cells |
ASGR2 is a subunit of the asialoglycoprotein receptor. Asialoglycoprotein receptor, also known as the Ashwell receptor, which is specific for desialylated (galactosyl-terminal) glycoproteins and is expressed exclusively in hepatic parenchymal cells. This receptor is a transmembrane protein that plays a critical role in serum glycoprotein homeostasis by mediating the endocytosis and lysosomal degradation of glycoproteins with exposed terminal galactose or N-acetylgalactosamine residues. ASGR2 is ... | |||
TMPY-00481 |
AKR1C4 Protein, Human, Recombinant (His)
aldo-keto reductase family 1, member C4,3-alpha-HSD,DD4,CHDR... |
Human | E. coli |
Aldo-keto reductases comprise of AKR1C1-AKR1C4, four enzymes that catalyze NADPH dependent reductions and have been implicated in biosynthesis, intermediary metabolism, and detoxification. there is a strong correlation between the expression levels of these family members and the malignant transformation as well as the resistance to cancer therapy. Type I human hepatic 3alpha-hydroxysteroid dehydrogenase (AKR1C4) plays a significant role in bile acid biosynthesis, steroid hormone metabolism, an... | |||
TMPH-01577 |
KRT18 Protein, Human, Recombinant (E. coli, His)
Keratin-18,KRT18,Cytokeratin-18,Cell proliferation-inducing ... |
Human | E. coli |
Involved in the uptake of thrombin-antithrombin complexes by hepatic cells. When phosphorylated, plays a role in filament reorganization. Involved in the delivery of mutated CFTR to the plasma membrane. Together with KRT8, is involved in interleukin-6 (IL-6)-mediated barrier protection. KRT18 Protein, Human, Recombinant (E. coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 52.0 kDa and the accession number is P05783. | |||
TMPH-01104 |
Claudin-9 Protein-VLP, Human, Recombinant (His)
CLDN9,Claudin-9 |
Human | HEK293 Cells |
Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity.; (Microbial infection) Acts as a receptor for hepatitis C virus (HCV) entry into hepatic cells. Claudin-9 Protein-VLP, Human, Recombinant (His) is expressed in HEK293 mammalian cells with C-10xHis tag. The predicted molecular weight is 24.2 kDa and the accession number is O95484. | |||
TMPH-01948 |
PPP1R3G Protein, Human, Recombinant (His & Myc)
PPP1R3G,Protein phosphatase 1 regulatory subunit 3G |
Human | E. coli |
Glycogen-targeting subunit for protein phosphatase 1 (PP1). Involved in the regulation of hepatic glycogenesis in a manner coupled to the fasting-feeding cycle and distinct from other glycogen-targeting subunits. PPP1R3G Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 45.5 kDa and the accession number is B7ZBB8. | |||
TMPJ-00805 |
Apolipoprotein E/APOE Protein, Mouse, Recombinant (His)
Apo-E,APOE,Apolipoprotein E |
Mouse | HEK293 Cells |
Apolipoprotein E (Apo-E), is a member of the apolipoprotein A1/A4/E family. ApoE is a major protein component of serum LDL, VLDL, HDL, and chylomicrons. APOE may function in mediating the binding, internalization, and catabolism of lipoprotein particles. It can serve as a ligand for the LDL (apo B/E) receptor and for the specific apo-E receptor (chylomicron remnant) of hepatic tissues. APOE is usually secreted in plasma. Phosphorylation sites are present in the extracellular medium. | |||
TMPY-02686 |
PON3 Protein, Human, Recombinant (S50N, His)
paraoxonase 3 |
Human | Baculovirus Insect Cells |
PON3 was enriched in the mitochondria-associated membrane fraction of hepatocytes. PON3 deficiency resulted in impaired mitochondrial respiration, increased mitochondrial superoxide levels, and increased hepatic expression of inflammatory genes. PON3 deficiency did not influence atherosclerosis development on an apolipoprotein E null hyperlipidemic background, but it did lead to a significant 60% increase in atherosclerotic lesion size in Pon3KO mice on the C57BL/6J background when fed a cholate... | |||
TMPJ-00876 |
FAH Protein, Human, Recombinant (His)
Fumarylacetoacetate Hydrolase,β-Diketonase,FAH,FAA,Fumarylac... |
Human | HEK293 Cells |
Fumarylacetoacetase belongs to the FAH family. Fumarylacetoacetase is primary expressed in liver and kidney. It exists as a homodimer and catalyzes the hydrolysis of 4-fumarylacetoacetate into fumarate and acetoacetate. Defects in Fumarylacetoacetase cause tyrosinemia type 1, which is congenital metabolism defect characterized by elevated levels of tyrosine in the blood and urine, and hepatorenal manifestations. Typical features include renal tubular injury, self-mutilation, hepatic necrosis, ep... | |||
TMPH-02675 |
GCGR Protein, Mouse, Recombinant (GST)
Glucagon receptor,Gcgr |
Mouse | E. coli |
G-protein coupled receptor for glucagon that plays a central role in the regulation of blood glucose levels and glucose homeostasis. Regulates the rate of hepatic glucose production by promoting glycogen hydrolysis and gluconeogenesis. Plays an important role in mediating the responses to fasting. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. ... | |||
TMPJ-01142 |
CDO1 Protein, Human, Recombinant (His)
CDO-I,CDO,Cysteine Dioxygenase Type I,CDO1,Cysteine Dioxygen... |
Human | E. coli |
Cysteine Dioxygenase Type 1 (CDO1) is a mammalian non-heme iron enzyme that belongs to the cysteine dioxygenase family. CDO1 is highly expressed in the liver and placenta, and has a low expression in heart, brain and pancreas. CDO1 can also be detected in hepatoblastoma HepG2 cells. CDO1 catalyzes the conversion of L-cysteine to cysteine sulfinic acid by incorporation of dioxygen. CDO1 is a vital regulator of cellular cysteine concentrations and has an essential role in maintaining the hepatic c... | |||
TMPJ-00365 |
GAS6 Protein, Human, Recombinant (Avi & His), Biotinylated
AXLLG,Growth arrest-specific protein 6,AXL receptor tyrosine... |
Human | HEK293 Cells |
Human Growth arrest-specific protein 6 (GAS6) is ligand for tyrosine-protein kinase receptors AXL, TYRO3 and MER whose signaling is implicated in cell growth and survival, cell adhesion and cell migration. GAS6/AXL signaling plays a role in various processes such as endothelial cell survival during acidification by preventing apoptosis, optimal cytokine signaling during human natural killer cell development, hepatic regeneration, gonadotropin-releasing hormone neuron survival and migration, plat... | |||
TMPJ-00924 |
Decorin Protein, Mouse, Recombinant (His)
PG40,Bone proteoglycan II,Decorin,Dcn,PG-S2 |
Mouse | HEK293 Cells |
Decorin, also known as PG40 and DCN, is a member of the class I family of small leucine-rich proteoglycans (SLRPs) that is expressed in the stroma of various forms of cancer and has been recently proposed to act as a guardian from the matrix. Mature human Decorin contains 12 tandem LRR and shares 80% and 78% aa sequence identity with mouse and rat Decorin, respectively. Decorin embraces numerous functions including: regulation of collagen fibrillogenesis, hepatic carcinogenesis, fetal membrane a... | |||
TMPJ-00834 |
ACADM Protein, Human, Recombinant (His)
ACADM,Medium-Chain Specific Acyl-CoA Dehydrogenase Mitochond... |
Human | E. coli |
Medium-Chain Specific Acyl-CoA Dehydrogenase (ACADM) is a mitochondrial fatty acid beta-oxidation that belongs to the acyl-CoA dehydrogenase family. ACADM is a homotetramer enzyme that catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. ACADM is specific for acyl chain lengths of 4 to 16. It is essential for converting these particular fatty acids to energy, especially during fasting periods. Defects in ACADM cause medium-chain acyl-CoA dehydrogenase deficiency, a ... | |||
TMPY-01587 |
SULT2A1 Protein, Human, Recombinant (His)
hSTa,HST,ST2,ST2A1,STD,DHEAS,ST2A3,sulfotransferase family, ... |
Human | E. coli |
Hydroxysteroid sulfotransferase ( SULT2A1 ) is a key enzyme in the testicular and hepatic metabolism of 5alpha-androstenone, which is a major component of the off-odor and off-flavor in pork known as boar taint. Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar amon... | |||
TMPY-05029 |
INHBE Protein, Human, Recombinant (hFc)
inhibin beta E,inhibin β E |
Human | HEK293 Cells |
INHBE (Inhibin Subunit Beta E) is a Protein Coding gene. This gene encodes a member of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate an inhibin beta subunit. INHBE was identified as a novel putative hepatokine with hepatic gene expression that positively correlated with insulin resistance and body mass index in humans. The quantitative real time-PCR analysis also showed an increase in INHBE gene expressi... | |||
TMPY-01140 |
ACOT13/THEM2 Protein, Human, Recombinant (His)
THEM2,HT012,ACOT13,PNAS-27,acyl-CoA thioesterase 13 |
Human | E. coli |
The metabolites of fatty acyl-Coenzyme A (CoA) and metabolic enzymes contribute to lipid biosynthesis, signal transduction, and gene transcription. Members of the acyl-CoA thioesterase (Acot) gene family hydrolyze fatty acyl-CoAs, but their biological functions remain incompletely understood. Thioesterase superfamily member 2 (Them2; synonym Acot13) is enriched in oxidative tissues, associated with mitochondria, and relatively specific for long chain fatty acyl-CoA substrates. Using Them2(-/-) m... | |||
TMPJ-00366 |
GAS6 Protein, Human, Recombinant (hFc)
AXLLG,Gas6,GAS-6,AXLLGAXL stimulatory factor,growth arrest-s... |
Human | HEK293 Cells |
GAS6 (Growth arrest-specific protein 6) is also known as AXL receptor tyrosine kinase ligand, AXLLG, is a multimodular protein that is up-regulated by a wide variety of cell types in response to growth arrest. Gas6 binds and induces signaling through the receptor tyrosine kinases Axl, Dtk, and Mer whose signaling is implicated in cell growth and survival, cell adhesion and cell migration. GAS6/AXL signaling plays a role in various processes such as endothelial cell survival during acidification ... | |||
TMPY-04999 |
GAS6 Protein, Human, Recombinant (His)
|
Human | HEK293 cells |
GAS6 (Growth arrest-specific protein 6) is also known as AXL receptor tyrosine kinase ligand, AXLLG, is a multimodular protein that is up-regulated by a wide variety of cell types in response to growth arrest. Gas6 binds and induces signaling through the receptor tyrosine kinases Axl, Dtk, and Mer whose signaling is implicated in cell growth and survival, cell adhesion and cell migration. GAS6/AXL signaling plays a role in various processes such as endothelial cell survival during acidification ... | |||
TMPJ-00361 |
Endoglin Protein, Human, Recombinant (Trx & His)
CD105,END,Endoglin,ENG |
Human | E. coli |
Endoglin is a single-pass type I membrane protein which restricted to endothelial cells in all tissues except bone marrow. Endoglin as major glycoprotein of vascular endothelium, it has been found on endothelial cells, activated macrophages, fibroblasts, and smooth muscle cells. Furthermore, Homodimer forms a heteromeric complex with the signaling receptors for transforming growth factor-beta: TGFBR1 and/or TGFBR2. It may have an important role in the binding of endothelial cells to integrins an... | |||
TMPY-01595 |
PCBP1 Protein, Human, Recombinant (His)
HNRPE1,hnRNP-E1,HEL-S-85,HNRPX,poly(rC) binding protein 1,hn... |
Human | E. coli |
Poly(rC)-binding protein 1, also known as Heterogeneous nuclear ribonucleoprotein E1, Alpha-CP1, Nucleic acid-binding protein SUB2.3 and PCBP1, is a family member of heterogeneous nuclear ribonucleoproteins (hnRNPs) that belong to RNA-binding proteins and bear three KH domains. PCBP1 is loosely bound in the nucleus. It may shuttle between the nucleus and the cytoplasm. It is abundantly expressed in skeletal muscle, thymus and peripheral blood leukocytes while a lower expression is observed in pr... | |||
TMPY-01100 |
GPT2 Protein, Rat, Recombinant (His)
glutamic pyruvate transaminase (alanine aminotransferase) 2 |
Rat | Baculovirus Insect Cells |
Alanine aminotransferase (ALT), also known as glutamate pyruvate transaminase (Gpt), is a pyridoxal enzyme that catalyzes the reversible interconversion of L-alanine and 2-oxoglutalate to pyruvate and L-glutamate and plays a key role in the intermediary metabolism of glucose and amino acids. As a key enzyme for gluconeogenesis, Gpt is a widely-used serum marker for liver injury. Two ALT isoenzymes have been identified, ALT1 and ALT2 (GPT1 and GPT2), which are encoded by separate genes and share ... | |||
TMPJ-00817 |
HO-1 Protein, Human, Recombinant
HO,HMOX1,HO-1,Heme Oxygenase 1,HO1 |
Human | E. coli |
Heme Oxygenase 1 (HO-1) is an enzyme in endoplasmic reticulum that belongs to the heme oxygenase family. HO-1 cleaves the heme ring at the alpha methene bridge to form Biliverdin. Biliverdin is subsequently converted to Bilirubin by Biliverdin reductase. In physiological state, the highest activity of HO-1 is found in the spleen, where senescent erythrocytes are sequestrated and destroyed. HO-1 activity is highly inducible by its substrate heme and by various non-heme substances such as heavy me... | |||
TMPJ-00785 |
FABP3 Protein, Human, Recombinant (His)
H-FABP,FABP11,Fatty Acid-Binding Protein Heart,MDGIMuscle Fa... |
Human | E. coli |
Fatty Acid Binding Protein 3 (FABP3) is a small cytoplasmic protein (15 kDa) that is released from cardiac myocytes following an ischemic episode. Like the nine other distinct FABPs that have been identified, FABP3 is involved in active fatty acid metabolism where it transports fatty acids from the cell membrane to mitochondria for oxidation. FABPs are divided into at least three distinct types, namely the hepatic-, intestinal- and cardiac-types. They form 14-15 kDa proteins and are thought to p... | |||
TMPY-04394 |
Glucokinase Protein, Human, Recombinant
glucokinase (hexokinase 4),HXKP,MODY2,FGQTL3,LGLK,HKIV,GLK,H... |
Human | E. coli |
Glucokinase belongs to the bacterial glucokinase family. Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. Alternative splicing of this gene results in three tissue-specific forms of glucokinase, one found in pancreatic islet beta cells and two found in liver. The protein localizes to the outer membrane of mitochondria. In contrast to other forms of hexokinase, this enzyme is not inhibited by its product glucose-6-phosphate but ... | |||
TMPJ-00353 |
ILDR2 Protein, Human, Recombinant (His)
Angulin-3,immunoglobulin-like domain containing receptor 2,D... |
Human | HEK293 Cells |
ILDR2 is a member of the B7-like family of proteins that regulate T cell activity, is also a known endoplasmic reticulum molecule that regulates lipid homeostasis. The human ILDR2 lumenal domain shares a 99% and 98% homology with the mouse and rat respectively. The human gene encoding ILDR2 is located in a region on Chr1q23–25 that has been associated with type 2 diabetes. ILDR2 plays critical roles in hepatic clearance of lipoproteins and in lipid homeostasis. ILDR2 regulates human dendritic ce... | |||
TMPY-02803 |
IDO2 Protein, Human, Recombinant (His)
indoleamine 2,3-dioxygenase 2,INDOL1 |
Human | E. coli |
IDO2 belongs to the indoleamine 2,3-dioxygenase family. Indoleamine 2,3-dioxgyenase (IDO), is a cytosolic haem protein which, together with the hepatic enzyme tryptophan 2,3-dioxygenase, catalyzes the conversion of tryptophan and other indole derivatives to kynurenines. In addition to classic IDO (IDO1), a new variant, IDO2, has recently been described. IDO2 is expressed in the liver, small intestine, spleen, placenta, thymus, lung, brain, kidney, and colon. IDO is widely distributed in human ti... | |||
TMPH-02613 |
ATF-5 Protein, Mouse, Recombinant (His & Myc)
Transcription factor ATFx,Transcription factor-like protein ... |
Mouse | E. coli |
Transcription factor that either stimulates or represses gene transcription through binding of different DNA regulatory elements such as cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3'), ATF5-specific response element (ARE) (consensus: 5'-C[CT]TCT[CT]CCTT[AT]-3') but also the amino acid response element (AARE), present in many viral and cellular promoters. Critically involved, often in a cell type-dependent manner, in cell survival, proliferation, and differentiation. Its transcrip... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T35519 |
Aflatoxin B2-13C17
Aflatoxin B2-13C17 |
||
Aflatoxin B2-13C17(AFB2-13C17) is intended for use as an internal standard for the quantification of AFB2by GC- or LC-MS. AFB2is a mycotoxin that has been found inA. terricola.1It induces hepatic autophagy and apoptosis in broiler chickens when administered at doses of 0.2, 0.4, and 0.8 mg/kg.2AFB2(0.5 and 1 mg/animal) also induces parenchymal cell hyperplasia in rats.3 1.Moubasher, A.H., el-Kady, I.A., and Shoriet, A.Toxigenic Aspergilli isolated from different sources in EgyptAnn. Nutr. Alimen... | |||
TMIJ-0039 |
Norethindrone Acetate-2,2,4,6,6,10-d6
|
||
Norethindrone Acetate-2,2,4,6,6,10-d6 是 Norethindrone Acetate 的氘代化合物。Norethindrone Acetate 的 CAS 号为 51-98-9。Norethindrone acetate 是一种雌性激素,对青少年月经和肝腺瘤有抑制作用,常与孕激素联合使用,可用于研究子宫内膜异位症。 | |||
TMIH-0504 |
Rosuvastatin-d6 Calcium Salt
|
||
Rosuvastatin-d6 Calcium Salt 是 Rosuvastatin Calcium Salt 的氘代化合物。Rosuvastatin Calcium Salt 的 CAS 号为 147098-20-2。Rosuvastatin calcium 是肝羟甲基戊二酰辅酶 A 还原酶的选择性和竞争性抑制剂,具有抗血脂活性。它降低成熟 hERG 的表达以及热休克蛋白 70 与 hERG 蛋白的相互作用,还降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go相关基因电流,延迟心脏复极化,来延长动作电位持续时间和校正 QT 间期间隔。 | |||
T36055 |
Nitisinone-13C6
Nitisinone-13C6 |
||
Nitisinone-13C6is intended for use as an internal standard for the quantification of nitisinone by GC- or LC-MS. Nitisinone is an inhibitor of 4-hydroxyphenylpyruvate dioxygenase (HPPD), which converts 4-hydroxyphenylpyruvate (HPPA) to homogentisate in the tyrosine catabolic pathway.1Nitisinone increases urinary levels of HPPA and 4-hydroxyphenyllactate (HPLA) in rats when administered at a dose of 10 mg/kg. Nitisinone (3 mg/kg) prevents the neonatal lethality of fumarylacetoacetate hydrolase (F... |