83
65
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T4083 |
BAR501
BAR 501 |
GPCR19 | GPCR/G Protein |
BAR501是高效选择性的 GPBAR1激动剂(EC50:1 μM)。 | |||
TQ0252 |
BAR502
|
FXR; GPCR19; Autophagy | Autophagy; GPCR/G Protein; Metabolism |
BAR502 是一种 GPBAR1 和 FXR 双重激动剂,IC50分别为0.4 μM 和 2 μM。 | |||
T8599 |
Betazole dihydrochloride
盐酸倍他唑,Betazole hydrochloride |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Betazole dihydrochloride (Betazole hydrochloride) 是吡唑类组胺,是一种口服活性 H2受体激动剂,能诱导胃酸分泌,导致胆总管压力立即显著升高。它作为一种诊断剂,用于研究胃酸分泌能力。 | |||
T4352 |
SB756050
SB-756050,SB 756050 |
GPCR19 | GPCR/G Protein |
SB756050 是TGR5选择性激动剂。它用于二型糖尿病研究的潜力。 | |||
T11515 |
Gut restricted-7
GR-7 |
Potassium Channel | Membrane transporter/Ion channel |
Gut restricted-7 (GR-7) 是一种具有口服活性的共价泛胆盐水解酶 (BSH) 抑制剂,对肠道有组织选择性。它可减少小鼠粪便中肠道细菌的BSH 活性并降低去结合型胆汁酸水平。 | |||
T1824 |
TGR5 Receptor Agonist
|
GPCR19 | GPCR/G Protein |
TGR5 Receptor Agonist 是一种TGR5(GPCR19)激动剂。 | |||
T8818 |
TC-G 1005
(4-环丙基-3,4-二氢-1(2H)-喹喔啉基)[4-(2,5-二甲基苯氧基)-3-吡啶基]甲酮 |
GPCR19 | GPCR/G Protein |
TC-G 1005 是具有口服活性的TGR5选择性激动剂,能够激活 hTGR5 (EC50:0.72 nM)和 mTGR5 (EC50:6.2 nM)。它能够减少小鼠体内葡萄糖水平。 | |||
T74195 | 4′-Demethylnobiletin | ||
4′-Demethylnobiletin 是一种生物活性代谢物,可以激活PKA/ERK/CREB 信号通路,增强海马神经元中 CRE 介导的转录,并通过刺激ERK 信号逆转与 NMDA 受体拮抗相关的记忆障碍。 | |||
TP1740 |
GroES mobile loop
|
||
GroES mobile loop is a flexible region of unbound GroES that interacts with GroEL via the residues located at the tip of the loop. | |||
T124370 | 5'-Methoxynobiletin | ||
5'-Methoxynobiletin 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 T124370。 | |||
T32873 |
Maralixibat Chloride
SHP-625,SHP625,Livmarli,LUM001 chloride,Lopixibat chloride,Lopixibat,SHP625 chloride,SHP 625 |
Potassium Channel | Membrane transporter/Ion channel |
Maralixibat Chloride (LUM001 chloride) 是一种钠依赖性的胆汁酸转运抑制剂,可阻止胆汁酸在肠肝内的再循环 | |||
T35371 |
Colesevelam Hydrochloride
|
Others | Others |
Colesevelam Hydrochloride 是一种胆汁酸隔离剂,在体外对甘胆酸均具有更高的亲和力。 Colesevelam Hydrochloride 抑制胆汁酸重吸收,导致胆汁酸合成增加并降低胆汁淤积性瘙痒症和克罗恩病患者的胆固醇水平。 | |||
TP1198 |
Sincalide ammonium
SQ19844 ammonium,CCK-8 ammonium,Cholecystokinin octapeptide ammonium |
cholecystokinin | GPCR/G Protein |
Sincalide ammonium (CCK-8 ammonium) 是一种有效的氨基酸多肽激素胆囊收缩素 (CCK) 的类似物,是保留了 CCK 的大部分生物活性的活性片段。Sincalide ammonium 促进胆汁的分泌,使胆囊收缩并使 Oddi 的括约肌松弛,从而促进胆汁排入十二指肠。Sincalide ammonium 可通过注射促进胆囊收缩,常用于辅助诊断胆囊、胰腺疾病和胆囊造影术。 | |||
T15209 |
Elobixibat
AZD 7806,A 3309 |
Others | Others |
Elobixibat (A 3309) 是回肠胆汁酸转运蛋白的抑制剂(小鼠、人和犬 IBAT 的 IC50:0.13 nM、0.53 nM 和 5.8 nM)。 Elobixibat 可用于慢性特发性便秘的研究。 | |||
T20689 |
Temocaprilat
RNH-5139,RS-5139,RNH 5139,RNH5139,替莫普利,RS5139,RS 5139 |
Angiotensin-converting Enzyme (ACE) | Metabolism |
Temocaprilat (RS5139) 是一种血管紧张素转换酶 (ACE) 抑制剂。 Temocaprilat 通过缺乏 EHBR 的 cMOAT 有效地从胆汁中排泄,而许多其他 ACE 抑制剂对 cMOAT 的亲和力较低。 | |||
T11426 |
Gly-β-MCA
|
FXR | Metabolism |
Gly-β-MCA 是一种具有口服生物活性、肠道选择性和有效的法尼酯X受体 (FXR) 抑制剂,是一种胆汁酸,可用于研究肥胖和糖尿病。 | |||
T64334 |
Glycolithocholic acid, sodium salt
|
Others | Others |
Glycolithocholic acid, sodium salt 是 Glycolithocholic acid 的钠盐。Glycolithocholic acid 是一种甘氨酸结合的次级胆汁酸。Glycolithocholic acid 可用于诊断溃疡性结肠炎 (UC),非酒精性脂肪性肝炎 (NASH0) 和原发性硬化性胆管炎 (PSC)。 | |||
T36522 |
Isoallolithocholic acid
Alloisolithocholic Acid,AILCA,3β-Hydroxy-5α-cholanic acid |
Others | Others |
Isoallolithocholic acid (3β-Hydroxy-5α-cholanic acid) 是一种 T 细胞调节剂,是一种胆汁酸代谢物,具有抗炎活性,与人类免疫稳态有关。 | |||
T9154 |
Sodium taurodeoxycholate hydrate
牛磺去氧胆酸钠,Taurodeoxycholic acid sodium salt monohydrate |
Others | Others |
Sodium taurodeoxycholate hydrate (Taurodeoxycholic acid sodium salt monohydrate) 已用于一项研究,以评估亚胶束浓度的胆汁盐对脂质双层膜的影响。 | |||
T14932 |
Ceruletide
Cerulein,Caerulein,雨蛙素,FI-6934 |
cholecystokinin | GPCR/G Protein |
Ceruletide (Caerulein) 是一种十肽,是一种安全有效的胆囊收缩剂,是一种胆囊收缩素受体激动剂,对胆囊肌肉和胆管有直接的痉挛性作用。 | |||
T8752 |
BAR 501 impurity
|
GPCR19 | GPCR/G Protein |
BAR 501 impurity 在 BAR501 制剂中发现的一种杂质,可作为 G 蛋白偶联胆汁酸激活受体 (GP-BAR1) 的激动剂。 BAR501 杂质 (10 µM) 在 GP-BAR1 报告基因检测中诱导荧光素酶活性增加 150%。 | |||
T10623 |
BSH-IN-1
|
Potassium Channel | Membrane transporter/Ion channel |
BSH-IN-1 是一种重组的肠道细菌胆汁盐水解酶 (BSHs) 的有效和共价抑制剂,对 B. longum BSH (革兰氏阳性) 和 B. theta BSH (革兰氏阴性菌) 的 IC50 分别为 108 和 427 nM。 | |||
T7294 |
Aramchol
C20-FABAC |
Others | Others |
Aramchol (C20-FABAC) 是一种胆酸和花生酸的结合物,能够降低硬脂酰辅酶 A 去饱和酶 1 (SCD1) 的活性。它具有用于非酒精性脂肪性肝病 (NAFLD) 和非酒精性脂肪性肝炎 (NASH) 的潜能。 | |||
T14932L1 |
Ceruletide Ammonium Salt
Caerulein Ammonium Salt,Ceruletide Ammonium Salt(17650-98-5 Free base),FI-6934 Ammonium Salt,Cerulein Ammonium Salt |
cholecystokinin | GPCR/G Protein |
Ceruletide Ammonium Salt 是一种十肽,起源于热带青蛙的皮肤,是一种有效的胆囊收缩素受体 (cholecystokinin receptor) 激动剂,也是一种安全有效的胆囊收缩剂,对胆囊肌肉和胆管有直接的痉挛性作用。Ceruletide Ammonium Salt 具有镇静活性,可用于研究慢性精神分裂症。 | |||
T34855 |
Thionalide
|
||
Thionalide can transport these cpds from liver to bile. | |||
T32420 |
Kryptogenin
Cryptogenine,Cryptogenin |
||
Kryptogenin, derived from carp bile, can be used to synthesize C27-intermediates in bile acid biosynthesis. | |||
T37845 |
Taurocholic Acid 3-sulfate (sodium salt)
|
||
Taurocholic acid 3-sulfate (TCA3S) is a metabolite of the conjugated bile acid taurocholic acid .1Plasma levels of TCA3S are elevated in wild-type andSortilin 1(Sort1) knockout mice at 6 hours following bile duct ligation (BDL) and are further elevated inSort1knockout mice at 24 hours post-BDL.2 1.Lefebvre, P., Cariou, B., Lien, F., et al.Role of bile acids and bile acid receptors in metabolic regulationPhysiol. Rev.89(1)147-191(2009) 2.Li, J., Woolbright, B.L., Zhao, W., et al.Sortilin 1 loss-o... | |||
T30270 |
Azidobenzamidotaurocholate
|
||
Azido Benzamido Taurocholate is a bile acid transporter. | |||
T37771 |
Taurolithocholic Acid 3-sulfate (sodium salt)
|
||
Taurolithocholic acid 3-sulfate (TLCA3S) is a metabolite of the conjugated bile acid taurolithocholic acid . TLCA3S has been used to study bile acid transport in cellular models and to induce pancreatitis in mouse models of bile acid infusion pancreatitis. | |||
T34077 |
Piprozoline
piprozolin |
||
Prazoline (or prazoline) is a drug used to treat bile. | |||
T70688 |
S 0960
|
||
S 0960 is a dimeric bile acid analogue that acts as a specific inhibitor of the apical sodium-dependent bile salt transporter (ASBT) in the ileum. | |||
T27015 |
Cicrotoic acid
|
||
Cicrotoic acid, a biochemical drug, acts on bile flow and liquid composition of human bile. | |||
T13622 |
Cholestyramine
Colestyramine,考来烯胺,Cholestyramine resin |
Others | Others |
Cholestyramine (Cholestyramine resin) 是一种胆汁酸结合树脂,能够抑制肠胆汁酸吸收导致增加粪便胆汁酸排泄,提高胆固醇胆汁酸合成。 | |||
T32797 |
Lithocholenic acid
|
||
Lithocholenic acid is a bile acid that acts as a detergent to solubilize fats for absorption. | |||
T20928 |
Febuprol
H33,K-10033,H 33,H-33,NSC 30151 |
||
Febuprol, a choleretic drug, stimulates bile secretion. In addition, it also has lipid-lowering (lowering blood lipid) and spasmolytic (anticonvulsant) properties. | |||
T69558 |
Barixibat
|
||
Barixibat is a bile acid transport inhibitor. | |||
T71790 |
WYE-176182
|
||
WYE-176182 is an apical sodium-dependent bile salt transporter (SLC10A2) inhibitor | |||
T21347 |
PYR-9588
PYR9588 |
||
PYR-9588 is an intermediate used for chemical synthesis of a number of biologically important molecules, including bile pigments, photosensitizers, porphyrins, anticancer drugs. | |||
T16818 | S-8921 | Others | Others |
S-8921 is an inhibitor of ileal Na+/bile acid cotransporter. | |||
T28700 |
SC-435 mesylate
SC-435,SC435,SC 435 |
||
SC-435 is an ileal apical sodium co-dependent bile acid transporter (ASBT). SC-435 inhibits plasma cholesterol. | |||
T21349 |
PYR-8750
PYR 8750 |
||
PYR-8750 is an intermediate used for chemical synthesis of a number of biologically important molecules, including bile pigments, photosensitizers, porphyrins, anticancer drugs. | |||
T34534 |
Sarpedobilin
|
||
Sarpedobilin is a doubly cyclized bile pigment. It is found in butterflies. | |||
T2968L |
Hyodeoxycholic acid sodium salt
Sodium hyodeoxycholate,HDCA sodium |
||
Hyodeoxycholic acid sodium salt is a natural secondary bile acid. It improves high-density lipoprotein function, reduces farnesoid X receptor antagonist bile acids, and induces strong cytotoxicity, apoptosis, and IL-8 synthesis. | |||
T69622 | Ritivixibat | ||
Ritivixibat为回肠胆汁酸转运蛋白(IBAT)抑制剂,同时也是胆汁酸调节剂,主要适用于心血管疾病、脂肪酸代谢及葡萄糖利用障碍、胃肠道和肝脏疾病的研究。 | |||
T10090 |
264W94
|
Others | Others |
264W94 is a robust inhibitor of the ileal bile acid transporter (IBAT) and a novel agent for reducing cholesterol levels. It exhibits CYP7A1 induction and demonstrates significant antilipemic activity. | |||
T34895 |
Tocamphyl
Tocanfil,Biliphorin,Gallogen |
||
Tocamphyl is a cholagogic agent that stimulates pancreatic exocrine and bile flow when administered in the duodenum. | |||
T31820 |
Fluorescein lisicol
NRL972,NRL-972,NRL 972 |
||
Fluorescein lisicol, as an investigational marker of hepatic biliary transporter function, is a fluorescent-labeled bile salt. | |||
T37178 |
Norhyodeoxycholic Acid
|
||
Norhyodeoxycholic acid (NHDCA) is a synthetic bile acid and a derivative of hyodeoxycholic acid .1,2 NHDCA is an intermediate in the synthesis of 3β-sulfooxy-7β-hydroxy-24-nor-5-cholen-23-oic acid, which has been used as an internal standard for the quantification of δ5-bile acid conjugates that have been identified in patients with Niemann-Pick disease type C1.3 |1. Schteingart, C.D., and Hofmann, A.F. Synthesis of 24-nor-5β-cholan-23-oic acid derivatives: A convenient and efficient one-carbon ... | |||
T63616 | AAA-10 formic | ||
AAA-10 formic 是口服具有活力的肠道细菌胆盐水解酶 (BSH) 抑制剂,对B. thetarBSH (IC50: 10 nM) 和B. longumrBSH (IC50: 80 nM)。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2934 |
Bilirubin
胆红素,Bilibubin,Principal bile pigment,Hematoidin,Hemetoidin |
Endogenous Metabolite | Metabolism |
Bilirubin (Principal bile pigment) 是血红素分解代谢产生的黄色产物,是肝功能的重要指标。Bilirubin 具有抗诱变和抗氧化作用。 | |||
T5077 |
Deoxycholic acid sodium salt
脱氧胆酸钠,Sodium deoxycholate,Sodium Desoxycholate |
Endogenous Metabolite; GPCR19 | GPCR/G Protein; Metabolism |
Deoxycholic acid sodium salt (Sodium deoxycholate) 是 G 蛋白偶联胆汁酸受体TGR5的激活剂。 | |||
T2965 |
Deoxycholic acid
Cholorebic,去氧胆酸,脱氧胆酸,Deoxycholate,Desoxycholic acid,Cholanoic Acid,Cholerebic |
Endogenous Metabolite; GPCR19 | GPCR/G Protein; Metabolism |
Deoxycholic acid (Cholanoic Acid) 是 G 蛋白偶联胆汁酸受体 TGR5的激活剂。 | |||
T19189 |
Allocholic acid
|
Others | Others |
Allocholic acid 是一种胆汁酸,在脊椎动物中发现,在肝脏再生和致癌过程中会重新出现,也是成熟嗅觉系统的特定性刺激物。 | |||
T8153 |
glycohyodeoxycholic acid
|
Others; Endogenous Metabolite | Metabolism; Others |
Glycohyodeoxycholic acid 是一种人体次级胆汁酸猪去氧胆酸的主要代谢物,能够预防胆结石的形成。 | |||
T0022 |
Taurine
牛磺酸,2-Aminoethanesulfonic acid |
LDL; Endogenous Metabolite; Autophagy | Autophagy; Metabolism |
Taurine (2-Aminoethanesulfonic acid) 是一种含硫氨基酸的有机渗透剂,为胆汁盐的形成提供底物,并在调节细胞内游离钙浓度方面发挥作用,有激活脂肪细胞自噬的能力。 | |||
T1285 |
Anethole trithione
茴三硫,Anetholtrithion |
Others; AChR | Neuroscience; Others |
Anethole trithione (Anetholtrithion) 是硫杂环胆碱,是一种胆汁分泌刺激剂,可增强唾液分泌并增加 mAChR 受体,用于口干症的研究。 | |||
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。 | |||
TN2215 |
Taurochenodeoxycholic acid sodium
牛磺鹅去氧胆酸钠盐,Sodium taurochenodeoxycholate,牛磺鹅去氧胆酸钠 |
Apoptosis; Endogenous Metabolite | Apoptosis; Metabolism |
Taurochenodeoxycholic acid sodium (Sodium taurochenodeoxycholate) 是动物胆汁酸的主要生物活性物质之一。它可诱导细胞凋亡,具有抗炎和免疫调节作用。 | |||
T31964 |
Glycolithocholic acid
Lithocholic acid glycine conjugate,甘氨石胆酸,Lithocholylglycine |
Others | Others |
Glycolithocholic acid (Lithocholic acid glycine conjugate) 属于内源性代谢产物,是甘氨酸结合的次级胆汁酸。它可用于诊断非酒精性脂肪性肝炎,溃疡性结肠炎和原发性硬化性胆管炎。 | |||
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)。 | |||
T2968 |
Hyodeoxycholic acid
NSC 60672,猪去氧胆酸,α-Hyodeoxycholic Acid,HDCA |
FXR; Endogenous Metabolite; GPCR19 | GPCR/G Protein; Metabolism |
Hyodeoxycholic acid (NSC 60672) 是由肠道菌群在小肠中形成的次级胆汁酸,是TGR5(GPCR19)的激动剂, CHO 细胞中的EC50=31.6 µM。它已用于研究高胆固醇血症的治疗。 | |||
T2A2481 |
Taurochenodeoxycholic Acid
Chenodeoxycholyltaurine,TCDCA,Chenyltaurine,Taurochenodeoxycholate,12-Deoxycholyltaurine,牛磺鹅去氧胆酸 |
Apoptosis; TNF; Caspase; Endogenous Metabolite | Apoptosis; Metabolism; Proteases/Proteasome |
Taurochenodeoxycholic Acid (12-Deoxycholyltaurine) 是动物胆汁酸的主要生物活性物质之一,可诱导细胞凋亡,具有明显的抗炎和免疫调节作用。 | |||
T13502 |
3-Oxo-5β-cholanoic acid
3-氧代-5β-胆烷酸,Dehydrolithocholic acid |
ROR | Metabolism |
3-Oxo-5β-cholanoic acid (Dehydrolithocholic acid) 是胆汁酸的一种代谢产物。3-Oxo-5β-cholanoic acid 直接与关键转录因子RORγt(Kd=1.13 μM) 结合抑制TH17细胞分化。 | |||
T13522 |
7-Ketolithocholic acid
3α-Hydroxy-7-oxo-5β-cholanic acid |
Endogenous Metabolite | Metabolism |
7-Ketolithocholic acid (3α-Hydroxy-7-oxo-5β-cholanic acid) (3α-Hydroxy-7-oxo-5β-cholanic acid) is capable of absorption and serves to suppress the production of endogenous bile acid and the secretion of biliary cholesterol. | |||
T2834 |
Nobiletin
Hexamethoxyflavone,川陈皮素,川皮苷 |
Apoptosis; MMP; Reactive Oxygen Species; ROR; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Metabolism; NF-κB; Proteases/Proteasome |
Nobiletin (Hexamethoxyflavone) 是一种来自柑橘皮的聚甲氧基黄酮,是RORs 激动剂,可改善记忆力丧失。它可降低分化的 C2C12 肌管中的ROS 水平,并具有抗炎,抗癌,抗血管生成,抗增殖,抗转移和诱导细胞凋亡作用。 | |||
T5714 |
5-O-Demethylnobiletin
5-DEMETHYLNOBILETIN,去甲基川陈皮素 |
Leukotriene Receptor; Lipoxygenase | GPCR/G Protein; Metabolism |
5-O-Demethylnobiletin (5-DEMETHYLNOBILETIN) 是从黄芪中分离出的多甲氧基黄酮,具有抗炎活性,可通过直接抑制 5-LOX 发挥作用,IC50为 0.1 μM。 | |||
TN1244 |
3'-Demethylnobiletin
|
LDL; NF-κB; Integrin; Lipoxygenase; DNA/RNA Synthesis | Cell Cycle/Checkpoint; Cytoskeletal Signaling; DNA Damage/DNA Repair; Metabolism; NF-κB |
3'-Demethylnobiletin 是样一种存在于柑橘类水果中的多甲氧基黄酮类化合物,是一种 Nobiletin 的衍生物。N 其中 obiletin 能够调节 Src,FAK 和 STAT3 信号传导来抗肿瘤,并能够抑制肿瘤血管生成。 | |||
T19124 |
3-Oxocholic acid
3-Ketocholic acid |
Endogenous Metabolite | Metabolism |
3-Oxocholic acid(3-Ketocholic acid) 是胆汁酸的代谢产物,也是产气荚膜梭菌在肠道中由胆汁降解的主要产物。33-Oxocholic acid 是一种主要存在于哺乳动物的胆汁中类固醇酸。 | |||
T5259 |
Glycochenodeoxycholic acid sodium salt
GCDCA,甘氨鹅脱氧胆酸钠,Sodium glycochenodeoxycholate |
Apoptosis; Others; Endogenous Metabolite | Apoptosis; Metabolism; Others |
Glycochenodeoxycholic acid sodium salt (GCDCA) 是一种从脱氧鹅胆酸和甘氨酸在肝脏中形成的胆汁盐,可诱导肝细胞凋亡。它起到洗涤剂的作用,可溶解脂肪吸收,并本身被吸收。 | |||
T5234 |
Glycoursodeoxycholic acid
Ursodeoxycholylglycine,甘氨熊胆酸,GUDCA |
Others; Endogenous Metabolite | Metabolism; Others |
Glycoursodeoxycholic acid (Ursodeoxycholylglycine) 是一种酰基甘氨酸和胆汁酸-甘氨酸缀合物,是熊去氧胆酸的代谢物。 | |||
TJA2398 |
Taurodeoxycholic acid sodium hydrate
Sodium taurodeoxycholate monohydrate,Taurodeoxychloic Acid sodium hydrate,Taurohyodeoxycholic acid sodium salt,牛磺猪去氧胆酸 |
Apoptosis; Caspase | Apoptosis; Proteases/Proteasome |
Taurodeoxycholic acid sodium hydrate (Sodium taurodeoxycholate monohydrate) 通过阻断钙介导的凋亡通路和 Caspase-12的活化来阻止细胞凋亡。它可用于原发性胆汁性肝硬化、胰岛素抵抗、淀粉样变性、囊性纤维化、胆汁淤积和肌萎缩侧索硬化症。 | |||
T7331 |
Ursocholic acid
|
Endogenous Metabolite | Metabolism |
Ursocholic acid 是存在于哺乳动物胆汁中的胆酸,通过小鼠肠道菌群转化为脱氧胆酸。脱氧胆酸是7α-羟化类固醇脱氢酶和肝细胞核因子1α的抑制剂。 | |||
T0516 |
Dehydrocholate sodium
去氢胆酸钠,Sodium dehydrocholate |
Endogenous Metabolite; Lipid | Metabolism |
Dehydrocholate sodium 是胆液排泄增多剂,能够提高胆汁输出,清除提高的胆汁酸负载。 | |||
T5352 |
GLYCODEOXYCHOLIC ACID
|
Others; Endogenous Metabolite | Metabolism; Others |
Glycodeoxycholic Acid 是内源性代谢产物的一种。 | |||
T5072 |
Glycocholic acid hydrate
|
Others; Endogenous Metabolite | Metabolism; Others |
Glycocholic acid hydrate 是内源性代谢产物的一种。 | |||
T7628 |
3b-Hydroxy-5-cholenoic acid
|
Endogenous Metabolite | Metabolism |
3b-Hydroxy-5-cholenoic acid 是内源性的单羟基胆酸的一种,大量崔乃在于患有肝胆管状发育不全的儿童体内。 | |||
T14002 |
12-Ketodeoxycholic acid
|
Endogenous Metabolite | Metabolism |
12-Ketodeoxycholic acid 是一种胆汁酸,由肾脏代谢产生。它是肾脏损伤的标志物。 | |||
T4727 |
Taurolithocholic acid sodium salt
牛磺石胆酸钠,Sodium taurolithocholate |
Others; Calcium Channel | Membrane transporter/Ion channel; Metabolism; Others |
Taurolithocholic acid sodium salt (Sodium taurolithocholate) 是抑胆剂和 Ca2+激动剂,可抑制放射性配体与毒蕈碱 M1 结合。 | |||
T2744 |
Methyl Cholate
胆酸甲酯,Cholic acid methyl ester |
Others | Others |
Methyl Cholate (Cholic acid methyl ester) 是胆酸的甲酯形式。其中胆酸是一种由肝脏产生的主要胆汁酸,由胆固醇合成。 | |||
T2963 |
Cholic Acid
Cholanic acid,胆汁酸,Cholate,Colalin |
Endogenous Metabolite | Metabolism |
Cholic Acid (Cholate) 是肝脏产生的主要胆汁酸,与牛磺酸或甘氨酸缀合,有助于脂肪吸收和胆固醇排泄。 | |||
T0408 |
Dehydrocholic acid
Dehystolin,Felacrinos,去氢胆酸,Sanocholen,Decholin |
Others | Others |
Dehydrocholic acid (Dehystolin) 是一种由胆酸氧化生成的胆汁酸,用作胆液排泄增多剂,能够增加胆汁产量,清除增加的胆汁酸负荷。 | |||
T2831 |
Glycocholic acid
Glycocholate,甘氨胆酸,cholylglycine |
Others; Endogenous Metabolite | Metabolism; Others |
Glycocholic acid (Glycocholate) 是一种胆汁酸,具有抗肿瘤活性,能够靶向作用于耐药泵和非耐药泵通路。 | |||
TN2349 |
Taurodeoxycholate sodium salt
Sodium taurodeoxylate,牛磺脱氧胆酸钠 |
Endogenous Metabolite | Metabolism |
Taurodeoxycholate sodium salt (Sodium taurodeoxylate) 是胆盐相关的阴离子洗涤剂,用于分离膜蛋白,包括线粒体内膜蛋白。它还可以抑制各种炎症反应。 | |||
T4070 |
Glycocholic Acid Sodium Salt
Glycocholate Sodium,Sodium Glycocholate,甘氨胆酸钠盐 |
Others | Others |
Glycocholic Acid Sodium Salt (Sodium Glycocholate) 是一种结合胆汁盐和离子生物去污剂。它参与脂肪的乳化。 | |||
T4588 |
Glycochenodeoxycholic Acid
甘氨鹅脱氧胆酸,Glycine chenodeoxycholate,Chenodeoxycholylglycine,GCDCA,Glycochenodeoxycholate,Lithocholylglycine |
Apoptosis; Endogenous Metabolite | Apoptosis; Metabolism |
Glycochenodeoxycholic Acid (Lithocholylglycine) 是一种从脱氧鹅胆酸和甘氨酸在肝脏中形成的胆汁盐,可诱导肝细胞凋亡。它有洗涤剂的作用,可溶解脂肪吸收,并本身被吸收。 | |||
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。 | |||
T2532 |
Tauroursodeoxycholate
Taurolite,牛磺熊去氧胆酸,Tauroursodeoxycholic Acid,UR 906,Ursodeoxycholyltaurine,TUDCA |
Apoptosis; ERK; P450; Caspase; Endogenous Metabolite | Apoptosis; MAPK; Metabolism; Proteases/Proteasome |
Tauroursodeoxycholate (UR 906),又称 ursodoxicoltaurine,是一种高度亲水性的三级胆汁酸,在人体内以低浓度产生。Tauroursodeoxycholate 是 ursodeoxycholic acid 更亲水的形式,而 ursodeoxycholic acid 是人类体内自然产生的更丰富的胆汁酸。Tauroursodeoxycholate 正在研究用于几种疾病,如原发性胆汁性肝硬化(PBC)、胰岛素抵抗、淀粉样变性、囊性纤维化、胆汁淤滞和肌萎缩性侧索硬化症。 | |||
T35792 |
Isolithocholic Acid
3-Epilithocholic acid,3β-Hydroxy-5β-cholanic acid,β-Lithocholic acid,isoLCA |
Endogenous Metabolite | Metabolism |
Isolithocholic Acid (3-Epilithocholic acid) (β-Lithocholic acid) 是石胆酸的一种同分异构体。Isolithocholic Acid 是一种胆酸,由 Lithocholic acid 或 Lithocholic acid 3α-sulfate 经微生物代谢形成。 | |||
T15245 |
Erythromycin estolate
Phtalic anhydride,ilosone |
Antibacterial | Microbiology/Virology |
Erythromycin estolate 是红霉素的衍生物,属于大环内酯类抗生素,常用于研究多种细菌感染。酯酸红霉素对胆汁酸转运有抑制作用,可引起肝损伤,主要是胆汁淤积性肝炎。 | |||
TN2259 |
Taurocholic acid
N-Choloyltaurine |
TNF; PI3K | Apoptosis; PI3K/Akt/mTOR signaling |
Taurocholic acid (N-Choloyltaurine) 是一种胆汁酸,参与脂肪的乳化。Taurocholic acid 具有细胞保护作用,可通过 PI3K 介导的途径防止肿瘤坏死因子-α 诱导的胆管细胞损伤。 | |||
T5254 |
Glycodeoxycholate Sodium
Sodium glycyldeoxycholate,Sodium glycodeoxycholate,Glycodeoxycholic acid sodium salt,脱氧甘胆酸钠 |
Others; Endogenous Metabolite | Metabolism; Others |
Glycodeoxycholate Sodium (Glycodeoxycholic acid sodium salt) 诱导肝细胞凋亡的机制与内切酶的DNA裂解有关。它是一种次级胆汁酸,由结肠环境中微生物菌群中存在的酶的作用产生。 | |||
T13506 |
3β-Ursodeoxycholic acid
Isoursodeoxycholic acid |
||
3β-Ursodeoxycholic acid (Isoursodeoxycholic acid) 是一种胆汁酸。3β-Ursodeoxycholic acid 经口服给药表现出良好的耐受性和良好的肠道吸收能力。3β-Ursodeoxycholic acid 可以在肠道和肝脏经历酶异构化,并生成UDCA。 | |||
T0760 |
Cholesterol
Cholesterin,Cholesteryl alcohol,胆固醇 |
Estrogen Receptor/ERR; MRP; Endogenous Metabolite; ROR | Endocrinology/Hormones; Immunology/Inflammation; Metabolism |
Cholesterol (Cholesteryl alcohol) 属于天然产物,是哺乳动物中的主要固醇,是一种雌激素相关受体 α (ERRα) 的激动剂。Cholesterol 广泛存在于动物的细胞膜,也是合成几种重要荷尔蒙及胆酸的材料。 | |||
T1138 |
Taurocholic acid sodium salt hydrate
牛胆酸钠,牛磺胆酸钠水合物,Sodium taurocholate hydrate,Taurocholic Acid sodium hydrate |
Others; Potassium Channel; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Others |
Taurocholic acid sodium salt hydrate (Sodium taurocholate hydrate) 是一种胆汁酸钠盐水合物,作用是参与脂肪的乳化。 | |||
TN6909 |
Polyporusterone B
猪苓酮B,(1R,2R,4S,5R,7R,11R,14S,15R)-14-[(2R,3R)-2,3-dihydroxy-6-methyl-5-methylideneheptan-2-yl]-4,5,11-trihydroxy-2,15-dimethyltetracyclo[8.7.0.02,?.011,1?]heptadec-9-en-8-one |
Others | Others |
Polyporusterone B ((1R,2R,4S,5R,7R,11R,14S,15R)-14-[(2R,3R)-2,3-dihydroxy-6-methyl-5-methylideneheptan-2-yl]-4,5,11-trihydroxy-2,15-dimethyltetracyclo[8.7.0.02,?.011,1?]heptadec-9-en-8-one) 是一种三萜羧酸,从Polyporus umbellatusFries 中分离得到。它对自由基诱导的红细胞裂解 (溶血) 具有抑制作用。 | |||
T0847 |
Chenodeoxycholic acid
CDCA,鹅去氧胆酸,Chenodiol |
Potassium Channel; FXR; Endogenous Metabolite; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Chenodeoxycholic acid (CDCA) 是一种胆汁酸,通常与甘氨酸或牛磺酸结合。它作为清洁剂溶解脂肪以供肠道吸收,并被小肠重新吸收。它被用作利胆剂、利胆泻药,以及预防或溶解胆结石。 | |||
T2202 |
Lithocholic acid
3α-Hydroxy-5β-cholanic acid,石胆酸 |
Apoptosis; Others; FXR; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Metabolism; Others |
Lithocholic acid (3α-Hydroxy-5β-cholanic acid) 是由鹅去氧胆酸盐通过细菌作用形成的胆汁酸,通常与甘氨酸或牛磺酸结合,被用作利胆剂。 它作为清洁剂溶解脂肪以供吸收,并且本身被吸收。 | |||
TJO2758 |
D-Glucuronic acid
D-葡萄糖醛酸,Aldehydo-D-Glucuronic Acid |
Others; Endogenous Metabolite | Metabolism; Others |
D-Glucuronic acid (Aldehydo-D-Glucuronic Acid) 是一种从许多树胶中分离出的重要中间体。它对皮肤具有抗炎作用。它及其衍生物葡萄糖醛酸内酯作为预防人类健康的肝脏解毒剂。 | |||
T75319 |
Taurodeoxycholic acid
Taurodeoxychloic acid |
Apoptosis; Calcium Channel; Caspase | Apoptosis; Membrane transporter/Ion channel; Metabolism; Proteases/Proteasome |
Taurodeoxycholic acid (Taurodeoxychloic acid) 是脱氧胆酸的胆汁酸牛磺酸共轭物,是一种人体代谢物,可稳定线粒体膜,减少自由基形成。Taurodeoxycholic acid 通过阻断钙介导的凋亡通路以及 Caspase-12 激活来抑制凋亡 (apoptosis)。Taurodeoxycholic acid具有神经保护活性,可用于研究 3-硝基丙酸诱导或稳定遗传的亨廷顿舞蹈病 (HD) 。 | |||
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