196
75
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T40707 |
Methyl-PEG4-acyl chloride
Methyl-PEG4-acyl chloride |
||
Methyl-PEG4-acyl chloride is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T35621 |
Febuxostat Acyl Glucuronide
|
||
Febuxostat acyl glucuronide is a metabolite of the xanthine oxidoreductase inhibitor febuxostat . Febuxostat acyl glucuronide is formed via glucuronidation of febuxostat by uridine diphosphate-glucuronosyltransferases (UGTs). | |||
T27167 |
Diclofenac Acyl Glucuronide
|
||
Diclofenac Acyl Glucuronide is a major biliary metabolite of Diclofenac (GLXC-07892), a nonsteroidal antiinflammatory drug and COX inhibitor. | |||
T37117 |
Etodolac Acyl Glucuronide
|
||
Etodolac acyl glucuronide is a phase II metabolite of the non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor etodolac .1It is formedviaglucuronidation of etodolac by the UDP-glucuronosyltransferase (UGT) isoforms UGT1A9, UGT1A10, and UGT2B7. 1.Kutsuno, Y., Itoh, T., Tukey, R.H., et al.Glucuronidation of drugs and drug-induced toxicity in humanized UDP-glucuronosyltransferase 1 miceDrug Metab. Dispos.42(7)1146-1152(2014) | |||
T83873 |
Dabigatran Acyl-β-D-Glucuronide TFA
Dabigatran β-1-O-Acyl Glucuronide |
||
Dabigatran acyl-β-D-glucuronide是凝血酶抑制剂dabigatran的一种活性代谢产物,主要通过UDP-葡萄糖醛酸转移酶(UGT)的UGT2B15亚型形成。在人体去除血小板的贫血浆中,Dabigatran acyl-β-D-glucuronide (0.46 µM) 能增加活化部分凝血活酶时间(aPTT)。 | |||
TP1837 |
Acyl Carrier Protein (ACP) (65-74)
Acyl Carrier Protein (ACP) 65-74 |
||
Acyl Carrier Protein (ACP) (65-74) is an active acyl carrier protein (ACP) fragment.Acyl Carrier Protein (ACP) is a component of plastid-located plant fatty acid synthetase. It binds acyl groups covalently via the prosthetic group, 4-phosphopantetheine, d | |||
T35939 |
Dabigatran Acyl-β-D-Glucuronide
|
||
Dabigatran acyl-β-D-glucuronide is a major active metabolite of the thrombin inhibitor dabigatran . The prodrug of dabigatran, dabigatran etexilate , is hydrolyzed by plasma esterases to form dabigatran, which is metabolized primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT2B15 to form dabigatran acyl-β-D-glucuronide. Dabigatran acyl-β-D-glucuronide increases activated partial thromboplastin time (aPTT) in isolated human platelet-poor plasma equipotently to dabigatran. | |||
T40557 |
Simvastatin Acyl-β-D-glucuronide
|
||
Simvastatin Acyl-β-D-glucuronide, a metabolite formed from Simvastatin, acts as a competitive inhibitor of HMG-CoA reductase, showcasing a potent Ki of 0.2 nM. | |||
T35865 |
Telmisartan Acyl-β-D-Glucuronide
|
||
Telmisartan acyl-β-D-glucuronide is a major metabolite of the angiotensin II receptor antagonist telmisartan . It does not bind human serum albumin and is cleared from rat plasma with a clearance rate of 180 ml/min/kg following intravenous administration. | |||
T37251 |
Celecoxib Carboxylic Acid Acyl-β-D-Glucuronide
|
||
Celecoxib carboxylic acid acyl-β-D-glucuronide is a phase II metabolite of celecoxib . Celecoxib is an anti-inflammatory compound from the diaryl heterocycle class that selectively inhibits cyclooxygenase-2 (COX-2; IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively). Celecoxib carboxylic acid acyl-β-D-glucuronide is a minor metabolite, accounting for 2% of the administered dose in human urine and rat bile. | |||
T76124 | Acyl coenzyme A synthetase | ||
Acyl coenzyme A synthetase (ACS),一种生化研究中常用的酶,主要通过两步硫酯化反应激活脂肪酸与辅酶A结合,形成酰基辅酶A。该过程为脂质代谢中的多种合成与分解代谢途径,以及参与TCA循环中的有氧呼吸提供了关键中间物。 | |||
T16129 |
MPI_5a
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
MPI_5a 是高效的 HDAC6选择性抑制剂,IC50=36 nM,对其他 HDAC 酶几乎无抑制作用。MPI_5a 抑制细胞内酰基微管蛋白积累, IC50为 210 nM。 | |||
T23521 |
VULM 1457
|
Acyltransferase | Metabolism |
VULM 1457 是有效的胆固醇酰基转移酶抑制剂,具有显著的降血脂活性,并改善了整体心肌缺血再灌注损伤结果。VULM 1457 显著降低肾上腺髓质素的产生和分泌,并下调人肝母细胞上的 AM 受体。VULM 1457 具有研究糖尿病和高胆固醇血症的潜力。 | |||
T78136 |
Perindopril acyl-β-D-glucuronide
|
Drug Metabolite | Metabolism |
Perindopril acyl-β-D-glucuronide为Perindopril的代谢产物,属于ACE抑制剂类药物。 | |||
T13373 |
YM17E
|
Acyltransferase; AChR | Metabolism; Neuroscience |
YM17E 是一种 ACAT 抑制剂,在体外兔肝微粒体中的 IC50 为 44 nM。 | |||
T9711 |
OGT-IN-2
|
Others | Others |
OGT-IN-2 是 OGT 抑制剂,抑制 sOGT 和 ncOGT 的 IC50分别为 30 μM 和 53 μM。它在关节疾病方面有研究的价值,如关节软骨疾病、骨关节炎。 | |||
T12767 |
RP 70676
|
Acyltransferase | Metabolism |
RP 70676 是ACAT 抑制剂,抑制大鼠和兔子中 ACAT 的IC50分别为 25 和 44 nM。 | |||
T8533 |
ML318
|
Others; Antibiotic | Microbiology/Virology; Others |
ML318 是 PvdQ 酰基转移酶的联芳基腈抑制剂,可以结合在酰基结合位点上,IC50为 20 nM。它抑制铜绿假单胞菌的 IC50为 19 μM。它可防止嘧啶的产生并限制了铜绿假单胞菌在铁限制条件下的生长。 | |||
T15109 |
DGAT1-IN-1
|
Transferase | Metabolism |
DGAT1-IN-1是 DGAT1的高效抑制剂,在 Hep3B 细胞过表达 DGAT1裂解物中,测得IC50低于10nM。 | |||
T8314 |
RP-64477
RP64477 |
Acyltransferase | Metabolism |
RP-64477 是有效的胆固醇酯化酶酰基辅酶 A:胆固醇 O-酰基转移酶 (ACAT) 抑制剂。 | |||
T12225L |
Nevanimibe hydrochloride
PD-132301 hydrochloride,ATR101 hydrochloride |
Apoptosis; Acyltransferase | Apoptosis; Metabolism |
Nevanimibe hydrochloride (PD-132301 hydrochloride) 是一种口服有效的,选择性酰基辅酶 A:胆固醇 O-酰基转移酶 1 抑制剂,EC50为 9 nM。它抑制 ACAT2,EC50为 368 nM。它诱导细胞凋亡,具有抗肾上腺皮质癌的潜力。 | |||
T12425 |
PF-06424439 methanesulfonate
|
Acyltransferase; Transferase | Metabolism |
PF-06424439 methanesulfonate 是一种口服有效咪唑并吡啶二酰基甘油酰基转移酶 2 (DGAT2)选择性抑制剂,IC50是14 nM。PF-06424439 methanesulfonate 具有缓慢可逆,时间依赖性的特点,其相对于酰基-CoA 底物以非竞争性模式抑制 DGAT2。 | |||
T16409 |
OSMI-1
|
Others; Acyltransferase | Metabolism; Others |
OSMI-1 是一种 O-GlcNAc 转移酶 (OGT) 抑制剂 (IC50=2.7 μM),具有口服活性和细胞渗透性。OSMI-1 可以抑制蛋白质 O-GlcNA 酰化,而不会定性地改变细胞表面 N- 或 O- 连接的聚糖。 | |||
T6937 |
PF-04620110
PF04620110,PF 04620110 |
Acyltransferase; Transferase | Metabolism |
PF-04620110 是一种口服有效的甘油二酯酰基转移酶 -1(DGAT1)选择性抑制剂,IC50为 19 nM。 | |||
T10035 |
10,12-Tricosadiynoic acid
TDA,TCDA |
Acyltransferase | Metabolism |
10,12-Tricosadiynoic acid 是一种口服有效的酰基辅酶 A 氧化酶-1 (ACOX1) 抑制剂,具有高特异性,选择性,高亲和力的特点。10,12-Tricosadiynoic acid 可改善线粒体脂质和 ROS 代谢,在高脂饮食或肥胖引起的代谢性疾病中有研究的价值。 | |||
T23550 |
YM-750
YM 750 |
Acyltransferase | Metabolism |
YM-750 是一种有效的酰基:胆固醇酰基转移酶(ACAT)抑制剂,IC50为0.18 μM。 | |||
T11733 |
K-604 dihydrochloride
|
Acyltransferase | Metabolism |
K-604 dihydrochloride 是酰基辅酶 A:胆固醇酰基转移酶 1 的选择性抑制剂,IC50为 0.45±0.06 μM。 | |||
T4681 |
T863
DGAT-3,DGAT-1 inhibitor |
Acyltransferase; Transferase | Metabolism |
T863 (DGAT-3) 是口服有效的二酰基甘油酰基转移酶1 选择性抑制剂。T863结合DGAT1的酰基辅酶A 结合位点,抑制三酰甘油在细胞内的合成。 | |||
T22665 |
PD 128042
CI 976 |
Acyltransferase | Metabolism |
PD 128042 (CI 976) 是口服有效的ACAT (酰基辅酶 A: 胆固醇酰基转移酶)选择性抑制剂。它也是LPAT(溶血磷脂酰基转移酶) 抑制剂。它抑制高尔基体相关 LPAT 活性 (IC50=15 μM)。它抑制多种膜运输步骤,包括在内吞和分泌途径中发现的步骤。 | |||
T70267 |
ADL 08-0011 HCl
|
||
ADL 08-0011 is an active metabolite of the μ-opioid receptor antagonist alvimopan. It is produced from alvimopan via amide hydrolysis by gut microbiota. ADL 08-0011 is a μ-opioid receptor antagonist (Ki = 0.25 nM). It is selective for μ-opioid receptors over κ- and δ-opioid receptors (Kis = 15.8 and 31.6 nM, respectively). ADL 08-0011 inhibits endomorphin 1-induced inhibition of electrically induced contraction of isolated guinea pig ileum (pA2 = 9.4). In vivo, ADL 08-0011 (0.03-1 mg/kg) reverse... | |||
T8236 |
RHC 80267
U-57908 |
Others; Phospholipase; COX; Acyltransferase; AChR | Immunology/Inflammation; Metabolism; Neuroscience; Others |
RHC 80267 (U-57908) 是一种选择性二酰基甘油脂酶(DAGL)抑制剂,对犬血小板的IC50为 4 μM。它抑制COX 活性和磷脂酰胆碱的水解,还抑制胆碱酯酶活性,IC50为 4 μM,增强乙酰胆碱引起的松弛。 | |||
T2753 |
Avasimibe
PD-148515,阿伐麦布,CI-1011 |
P450; Acyltransferase | Metabolism |
Avasimibe (PD-148515) 是一种口服有效的酰基辅酶 A: 胆固醇酰基转移酶 (ACAT) 抑制剂,对 ACAT1和 ACAT2的 IC50分别为 24 和 9.2 µM。Avasimibe 在前列腺癌中有研究的价值。 | |||
T15247 |
ESI-05
NSC 116966 |
cAMP | GPCR/G Protein |
ESI-05 (NSC-116966) 是特异性的 cAMP 直接激活交换蛋白 2 (EPAC2) 拮抗剂(IC50:0.4 µM),能够抑制 cAMP 诱导的 EPAC2 的活化,并 EAPC2 介导的 Rap1 的活化。 | |||
T6365 |
A 922500
A922500,(1R,2R)-2-[[4-[[(苯基氨基)羰基]氨基][1,1-联苯]-4-基]甲酰基]环戊烷羧酸,DGAT-1 Inhibitor 4a |
Acyltransferase; Transferase | Metabolism |
A 922500 (DGAT-1 Inhibitor 4a) 是一种口服有效的二酰甘油酰基转移酶 1(DGAT-1)选择性抑制剂,抑制小鼠和人 DGAT-1 的IC50s 分别为9 nM,22 nM。 | |||
T12426 |
PF-06424439
|
Acyltransferase; Transferase | Metabolism |
PF-06424439 是一种口服有效的咪唑并吡啶二酰基甘油酰基转移酶 2 (DGAT2)选择性抑制剂,IC50是 14 nM。PF-06424439 具有缓慢可逆的,时间依赖性的特点,其相对于酰基-CoA 底物以非竞争性模式抑制 DGAT2。 | |||
T21022 |
Deacylketoconazole
Deacyl ketoconazole,脱乙酰酮康唑 |
Antifungal | Microbiology/Virology |
Deacylketoconazole (Deacyl ketoconazole) 是一种酮康唑衍生物,也是一种抗真菌剂。 脱酰基酮康唑对恶性疟原虫的活性是酮康唑的 15 至 50 倍。 | |||
T75396 | Sphingolipid ceramide N-deacylase (SCDase) | ||
Sphingolipid ceramide N-deacylase (SCDase) 催化糖鞘脂中的脂肪酸与鞘氨醇碱基间的N-酰基键断裂,进而生成溶血糖鞘脂。 | |||
T65529 | Lipase, triacylglycerol | ||
Lipase, triacylglycerol 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 T65529,CAS号为 9001-62-1。 | |||
T31260 |
Deacylpolymyxin B
Deacylpolymyxin-B,DeacylpolymyxinB |
||
Deacylpolymyxin B increases outer membrane permeability. | |||
T125992 |
threo-Guaiacylglycerol β-dihydroconiferyl ether
|
||
threo-Guaiacylglycerol β-dihydroconiferyl ether 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 T125992。 | |||
T31259 |
Deacyljanerin
AC1L427K |
||
Deacyljanerin is a biochemical. | |||
T125621 |
erythro-Guaiacylglycerol β-coniferyl ether
|
||
erythro-Guaiacylglycerol β-coniferyl ether 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 T125621。 | |||
T32015 |
Guaiacyl acetate
NSC-3831,NSC 3831,NSC3831 |
||
Guaiacyl acetate is a biochemical. | |||
T131470 | N'-Phenacylpiperazineinnuchenenolide C | ||
N'-Phenacylpiperazineinnuchenenolide C 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 T131470。 | |||
T124473 | threo-Guaiacylglycerol-beta-coniferyl aldehyde ether | ||
threo-Guaiacylglycerol-beta-coniferyl aldehyde ether 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 T124473。 | |||
T11037 |
Diacylglycerol acyltransferase inhibitor-1
|
Others | Others |
Diacylglycerol Acyltransferase Inhibitor-1, a diacylglycerol acyltransferase (DGAT1) inhibitor, effectively suppresses the activity of DGAT1. | |||
T70266 |
Acyline
|
||
Acyline is a novel GnRH antagonist found in animal studies to be a potent suppressor of circulating gonadotropin and testosterone (T) levels. Acyline inhibits basal and GnRH-stimulated serum testosterone concentrations in male dogs. Acyline prevented ovulation, but did not affect ovarian follicular development or gestational corpora lutea in the domestic cat. A single dose of the potent gonadotropin-releasing hormone antagonist acyline suppresses gonadotropins and testosterone for 2 weeks in hea... | |||
T83845 |
8-(4-azidophenacylthio) NAD+ sodium
Click Tag™ 8-(4-azidophenacylthio) NAD+,8-(4-azidophenacylthio) Nicotinamide adenine dinucleotide |
||
8-(4-azidophenacylthio) NAD+ 是NAD+信号分子及酶辅因子的一种可点击形式。 | |||
T23975 |
Deacylcortivazol
UNII-3JO09QT49F,DAC,NSC 325316 |
||
Deacylcortivazol (DAC) is a potent glucocorticoid. When incubated with glucocorticoid-resistant mutants derived from the glucocorticoid-sensitive human leukemic cell line CEM-C7, DAC caused significant growth inhibition. The cytotoxicity of DAC at concent | |||
T124284 | Erythro-Guaiacylglycerol-beta-coniferyl aldehyde ether | ||
Erythro-Guaiacylglycerol-beta-coniferyl aldehyde ether 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 T124284。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11843 |
Levothyroxine acyl glucuronide
Thyroxine acyl-β-D-glucuronide |
Others | Others |
Levothyroxine acyl glucuronide (Thyroxine Acyl-β-D-glucuronide), the acyl glucuronide formation of thyroxine (T4), an endogenous metabolite. | |||
T40832 |
Ferulic acid acyl-β-D-glucoside
Ferulic acid glucoside,Ferulic acid acyl-β-D-glucoside |
||
Ferulic acid acyl-β-D-glucoside, a metabolite of Ferulic Acid, is a novel inhibitor of fibroblast growth factor receptor 1 (FGFR1). It exhibits IC50 values of 3.78 µM and 12.5 µM for FGFR1 and FGFR2, respectively. | |||
T13060 |
T3 Acyl glucuronide
|
Others | Others |
T3 Acyl glucuronide is the acyl glucuronide formation of triiodothyronine (T3). T3 Acyl glucuronide is an endogenous metabolite | |||
T80020 |
UDP-3-O-acyl-GlcNAc diammonium
UDP-3-O-(3-hydroxytetradecanoyl)-N-acetylglucosamine diammonium |
Endogenous Metabolite | Metabolism |
UDP-3-O-acyl-GlcNAc diammonium 是一种E. coli代谢产物,涉及3-deoxy-D-manno-octulosonate (KDO) 生物合成途径。 | |||
T75685 | UDP-3-O-acyl-GlcNAc | ||
UDP-3-O-acyl-GlcNAc (UDP-3-O-(3-hydroxytetradecanoyl)-N-acetylglucosamine) 是一种E. coli 代谢产物,参与 3-deoxy-D-manno-octulosonate (KDO) 生物合成途径。 | |||
T10857 |
Coenzyme A
|
Endogenous Metabolite | Metabolism |
Coenzyme A 是所有活细胞中必需的辅助因子,由泛酸,三磷酸腺苷和半胱氨酸合成的。Coenzyme A 与过氧化物酶 5 共价结合导致其过氧化物酶活性完全抑制,通过 DTT 还原能够逆转。Coenzyme A 及其硫酯衍生物是主要分解代谢,合成代谢途径和基因表达调控的关键参与者。 | |||
T3342 |
Xanthohumol
|
Apoptosis; Others; Influenza Virus; COX; Acyltransferase; HSV | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; Others |
Xanthohumol 是从啤酒花中分离到的黄酮类化合物,可抑制 COX-1 和 COX-2 活性,具有抗肿瘤,抗血管生成的作用,还具有抗多种病毒的活性。 | |||
TN1691 |
Glabrol
光甘草酚,光甘草醇 |
P450; NF-κB; NO Synthase; Acyltransferase | Immunology/Inflammation; Metabolism; NF-κB |
Glabrol 是分离自甘草根的乙醇提取物中的一种异戊二烯类黄酮,是一种有效且非竞争性的酰基辅酶 A:胆固醇酰基转移酶(ACAT)抑制剂,抑制大鼠肝脏微粒体 ACAT 的 IC50为 24.6 μM。 | |||
T5544 |
2-Furoic acid
Furan-2-carboxylic acid,糠酸 |
Anti-infection; ATP Citrate Lyase; Endogenous Metabolite; Acyltransferase | Metabolism; Microbiology/Virology |
2-Furoic acid (Furan-2-carboxylic acid) 2-Furoic acid 能够降低血清中胆固醇和甘油三酯的水平,具有抗血脂作用。 | |||
T13638 |
Deacylmetaplexigenin
|
Others | Others |
Deacylmetaplexigenin is a pregnane glycoside isolated from Asclepias incarnate. | |||
TN4004 |
Erythro-Guaiacylglycerol β-dihydroconiferyl ether
|
||
Erythro-Guaiacylglycerol β-dihydroconiferyl ether 是从加拿大枫糖浆中提取的,具有潜在的抗氧化活性,可用于研究营养保健品。 | |||
TN4005 |
erythro-Guaiacylglycerol-beta-O-4'-dehydrodisinapyl ether
|
Serine Protease | Proteases/Proteasome |
erythro-Guaiacylglycerol-beta-O-4'-dehydrodisinapyl ether 是一种从巴西橡胶种子壳中提取的化合物,对人白细胞弹性蛋白酶具有抑制活性(IC50 :171 umol/L)。 | |||
TN5406 |
threo-Guaiacylglycerol β-coniferyl ether
|
||
Threo-Guaiacylglycerol beta-coniferyl ether displays significant inhibitory effects on NO production. | |||
TN4007 | erythro-Guaiacylglycerol beta-sinapyl ether | Others | Others |
erythro-Guaiacylglycerol beta-sinapyl ether是一种天然产物,属于忍冬科接骨木属,其产品编号为 TN4007,CAS号为 877875-96-2。erythro-Guaiacylglycerol beta-sinapyl ether可用作对照参考。 | |||
TN5421 | threo-Guaiacylglycerol-β-O-4'-dehydrodisinapyl ether | ||
threo-Guaiacylglycerol-β-O-4'-dehydrodisinapyl ether 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 TN5421,CAS号为 844637-85-0。 | |||
TN5814 |
Digalactosyldiacylglycerol
DGDG,双半乳糖二酰甘油 |
||
Digalactosyldiacylglycerol 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 TN5814,CAS号为 145033-48-3。 | |||
TN4006 | erythro-Guaiacylglycerol beta-sinapyl ether 7-O-glucoside | Others | Others |
erythro-Guaiacylglycerol beta-sinapyl ether 7-O-glucoside 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 TN4006,CAS号为 412029-03-9。 | |||
TN4003 |
Erythro-Guaiacylglycerol beta-coniferyl ether
|
Glucosidase | Metabolism |
Erythro-Guaiacylglycerol beta-coniferyl ether 可以从绿豆的茎和叶中提取出来的化合物,对 α-糖苷酶有抑制作用,EC50 值为 18.71 μM。 | |||
TN5145 |
threo-Guaiacylglycerol
|
Others | Others |
threo-Guaiacylglycerol 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 TN5145,CAS号为 27391-16-8。 | |||
T82441 | Erythro-guaiacylglycerol-β-ferulic acid ether | ||
Erythro-guaiacylglycerol-β-ferulic acid ether为Gueldenstaedtia verna中分离得到的天然产物。 | |||
TN4008 | erythro-Guaiacylglycerol | Others | Others |
erythro-Guaiacylglycerol是一种天然产物,属于杜仲科杜仲属,其产品编号为 TN4008,CAS号为 38916-91-5。erythro-Guaiacylglycerol可用作对照参考。 | |||
TN5416 | threo-7-O-Methylguaiacylglycerol β-coniferyl ether | ||
threo-7-O-Methylguaiacylglycerol β-coniferyl ether 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 TN5416,CAS号为 150333-85-0。 | |||
T5215 |
N-(3-Phenylpropionyl)glycine
N-(3-苯基丙酰基)甘氨酸,Phenylpropionylglycine |
Others | Others |
N-(3-Phenylpropionyl)glycine (Phenylpropionylglycine) 是一种酰基甘氨酸。酰基甘氨酸通常是脂肪酸的次要代谢物。 | |||
TN1474 |
Caulilexin C
板蓝根,1-甲氧基-3-吲哚乙腈 |
Others; Antifungal | Microbiology/Virology; Others |
Caulilexin C 是一种来自十字花科植物的植物抗毒素,具有抗真菌活性。 | |||
T5245 |
N-Isovaleroylglycine
N-异戊酰氨基乙酸,Isovaleroylglycine,N-Isovalerylglycine |
Others; Endogenous Metabolite | Metabolism; Others |
N-Isovaleroylglycine (Isovaleroylglycine) 是酰基甘氨酸,能够作为体重提高和肥胖的生物标记物。 | |||
T5228 |
Nicotinuric acid
|
Others; Endogenous Metabolite | Metabolism; Others |
Nicotinuric acid 是一种酰基甘氨酸,通常是脂肪酸的次要代谢物。 酰基甘氨酸是通过甘氨酸 N-酰基转移酶的作用产生的。 | |||
T0912L |
Tetracycline
Deschlorobiomycin,Tetracyclinum,Tetracyclin,四环素 |
Others; ribosome; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Tetracycline (Tetracyclin) 是一种对多种革兰氏阳性和革兰氏阴性细菌有抑制活性的广谱抗生素。 | |||
T5226 |
2-(2-Methylbenzamido)acetic acid
2-Methylhippuric acid,2-甲基马尿酸,O-Toluric acid,N-(O-Toluoyl)glycine |
Others; Endogenous Metabolite | Metabolism; Others |
2-(2-Methylbenzamido)acetic acid (O-Toluric acid) 是一种能够在尿液中检测到的代谢物。 | |||
T5217 |
2-(2-Phenylacetamido)acetic acid
Phenaceturic acid,Phenyl-ac-Gly-OH,苯乙酰甘氨酸,Phenylacetyl glycine |
Others; Endogenous Metabolite | Metabolism; Others |
2-(2-Phenylacetamido)acetic acid (Phenyl-ac-Gly-OH) 是内源性代谢产物的一种。 | |||
T4753 |
Imidazoleacetic acid hydrochloride
I4AA,(4-Imidazolyl)acetic acid hydrochloride,4-咪唑乙酸盐酸盐,4-Imidazoleacetic acid hydrochloride |
Endogenous Metabolite; Antibiotic | Metabolism; Microbiology/Virology |
Imidazoleacetic acid hydrochloride (I4AA) 是咪唑衍生物,具有潜在的抗结核性能。它还用于制备β-分泌酶的酰基胍抑制剂。 | |||
TN7218 |
Diformylphloroglucinol
2,4,6-Trihydroxyisophthalaldehyde |
Antioxidant | oxidation-reduction |
Diformylphloroglucinol (2,4,6-Trihydroxyisophthalaldehyde) 是从蓝桉树的叶子中分离出的酰基间苯三酚,是合成具有抗氧化和抗溃疡活性间苯三酚化合物的原料。 | |||
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。 | |||
T4734 |
Suberic acid
Octanedioic acid,1,8-Octanedioic acid,辛二酸 |
Others; Endogenous Metabolite | Metabolism; Others |
Suberic acid (1,8-Octanedioic acid) 被发现和肉毒碱-甲酰基-丙氨酸转位酶缺乏(丙二醇-羧基酶缺乏症)有关。 | |||
T4815 |
Hippuric acid
马尿酸,2-Benzamidoacetic acid,Benzoylglycine |
Others; Endogenous Metabolite | Metabolism; Others |
Hippuric acid (2-Benzamidoacetic acid) 是一种正常的尿液成分,是苯酸和甘氨酸结合作用下产生的一种酰基甘氨酸,来自食物的芳香化合物的代谢。 | |||
T5279 |
Ethylmalonic acid
alpha-Carboxybutyrate,2-Ethylmalonic acid,乙基丙二酸 |
Others; Endogenous Metabolite | Metabolism; Others |
Ethylmalonic acid (alpha-Carboxybutyrate) 是潜在有毒物质,非致癌性,与神经性厌食和甲氧基脱羧酶缺乏症有关。 | |||
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。 | |||
T4867 |
Erucic acid
Prifac 2990,芥酸,13(Z)-Docosenoic Acid,cis-13-docosenoic acid |
PI3K; Endogenous Metabolite | Metabolism; PI3K/Akt/mTOR signaling |
Erucic acid (13(Z)-Docosenoic Acid) 是单不饱和脂肪酸,分离自萝卜的种子。Erucic acid 可以容易地穿过血脑屏障,使大脑中长链脂肪酸的积累正常化。Erucic acid 能够改善认知障碍并有效预防痴呆。 | |||
T3339 |
Sophoridine
5-Epidihydrosophocarpine,槐定碱,Dihydro-5-episophocarpine |
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
Sophoridine (Dihydro-5-episophocarpine) 是一种从豆科植物槐豆斜生植物的叶子中分离出来的喹喔啉生物碱。它是胰腺癌的候选药物,诱导细胞凋亡。 | |||
T38141 |
Glycerophospholipids, cephalins
Phosphatidylethanolamines (egg) |
||
Glycerophospholipids, cephalins (Phosphatidylethanolamines (egg)) 是一种从鸡蛋中分离出来的磷脂酰乙醇胺的混合物,在 sn-1和 sn-2位置有各种脂肪酰基。Glycerophospholipids, cephalins 完全水解可得到1mol 的甘油、磷酸、乙醇胺和2mol 的脂肪酸。Phosphatidylethanolamines 在膜融合和细胞分裂过程中收缩环的拆卸中起作用,可调节膜的弯曲度。Phosphatidylethanolamines 能够在没有任何蛋白质或核酸的帮助下传播传染性朊病毒。Phosphatidylethanolamines 在细菌膜中的主要作用之一是分散由阴离子膜磷脂引起的负电荷。 | |||
T5267 |
N-Acetyl-L-glutamic acid
Ac-L-Glu-OH,N-乙酰-L-谷氨酰胺,N-Acetylglutamic acid |
Others; Endogenous Metabolite | Metabolism; Others |
N-Acetyl-L-glutamic acid (Ac-L-Glu-OH) 是一种 N-Acyl-L-氨基酸,是动物细胞培养基的组成成分,是一种酿酒酵母和人类的代谢物。 | |||
T8053 |
N-Acetyl-L-arginine
N-Α-乙酰-L-精氨酸,Ac-Arg-OH |
Endogenous Metabolite | Metabolism |
N-Acetyl-L-arginine (Ac-Arg-OH) 是一种胍基诺化合物,被发现存在于血液渗析性肾不足儿童患者血清中的。 | |||
T4947 |
3-Hydroxybutyric acid
Butanoic acid,3-羟基丁酸 |
Endogenous Metabolite | Metabolism |
3-Hydroxybutyric acid (Butanoic acid) 是一种人内源性代谢物,在 I 型糖尿病中升高。它能够调节膜脂的性质。 | |||
T24117 |
Guineesine
Pipyahyine |
||
Guineesine is an Acyl-CoA. It acts by inhibiting cholesterol acyltransferase. | |||
T13199 |
Triacsin C
WS 1228A,FR 900190 |
Others | Others |
Triacsin C, from Streptomyces aureofaciens, is a natural intracellular long-chain inhibitor of acyl-CoA synthetases (ACSL). | |||
T75696 | Ilexoside XLVIII | ||
Ilexoside XLVIII为一种三萜皂苷,自苦冬青叶片水提物分离而得,功能为抑制酰基辅酶A胆固醇酰基转移酶(ACAT)。 | |||
T12592 |
Pyripyropene A
|
Others | Others |
Pyripyropene A is a potent and selective inhibitor of sterol O-acyltransferase 2 (SOAT2)/acyl-coenzyme A:cholesterol acyltransferase 2 (ACAT2)(IC50 of 0.07 µM). | |||
T13678 |
Enniatin A
|
||
Enniatin A is a Fusarium mycotoxin. Enniatin A inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity with an IC50 of 22 μM in an enzyme assay using rat liver microsomes. | |||
T11202 |
Enniatin complex
|
Others | Others |
Enniatin complex, a mixture of cyclohexadepsipeptides predominantly derived from various Fusarium species of fungi, exhibits inhibitory effects on enzymes such as acyl-CoA: cholesterol acyl transferase. Furthermore, it has demonstrated the ability to induce apoptosis in multiple cancer cell lines. In addition to these activities, the Enniatin complex possesses ionophoric, antibiotic, and in vitro hypolipidemic properties. | |||
T38299 |
Tunicamycin V
|
||
Tunicamycin 15:1 is a mixture of tunicamycin structural isomers that contains a 15-carbon N-acyl chain with variable branching patterns.References Tunicamycin 15:1 is a mixture of tunicamycin structural isomers that contains a 15-carbon N-acyl chain with variable branching patterns. References | |||
T13498 |
3-Methylcrotonylglycine
|
Others | Others |
3-Methylcrotonylglycine is an acyl glycine, a normal amino acid metabolite found in urine. | |||
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