160
37
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T65554 |
cholesterol-absorption inhibitor Intermediate 2
|
Others | Others |
cholesterol-absorption inhibitor Intermediate 2 是一种有效且具有口服活性的胆固醇吸收抑制剂,可降低血液中胆固醇含量。 | |||
T3279 |
Silver sulfadiazine
Silvadene,磺胺嘧啶银,Dermazin,Flamazine |
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Silver sulfadiazine (Dermazin) 是一种磺胺类抗生素,具有抗菌和抗真菌活性。它的通磺胺部分(SD-SDZ) 对细菌生长有双重抑制作用,可阻止细菌叶酸吸收以及 DNA 合成。它释放的银结合并破坏 DNA 结构,阻止细菌 DNA 复制。 | |||
T7587 |
Tenapanor
RDX-5791,RDX 5791,AZD 1722,Tenapanor free base,RDX5791,AZD-1722,AZD1722 |
Sodium Channel | Membrane transporter/Ion channel |
Tenapanor (RDX 5791) 是钠氢离子交换NHE3的有效抑制剂, 对人和大鼠NHE3的IC50分别是5和10 nM。 | |||
T20362 |
Glutamyl-glutamic acid
Glu-glu,Dipotassium glutamyl-glutamate,N-L-alpha-Glutamyl-L-glutamic acid |
Amino Acids and Derivatives | Metabolism |
Glutamyl-glutamic acid (Glu-glu) 是一些微球菌和节杆菌属菌的胞壁中的肽桥。 | |||
T8926 |
Salcaprozate sodium
8-(2-羟基苯甲酰胺基)辛酸钠,SNAC |
Others | Others |
Salcaprozate sodium (SNAC) 是口服吸收促进剂,有作为口服形式的肝素和胰岛素递送剂的潜力。它可提高非共价大分子络合引起的亲脂性,从而增加小肠上皮细胞的被动跨细胞渗透。 | |||
T1593 |
Ezetimibe
依泽替米贝,SCH 58235 |
Others; Nrf2; NPC1L1; Autophagy | Autophagy; Immunology/Inflammation; Membrane transporter/Ion channel; Others |
Ezetimibe (SCH 58235) 是一种膳食胆固醇吸收抑制剂。它是一种NPC1L1抑制剂,是有效的Nrf2激活剂。 | |||
T6675 |
Sodium Picosulfate
Evacuol,Picolax,匹克硫酸钠,Sodium Picosulphate,匹可硫酸钠,Laxoberal |
Others | Others |
Sodium Picosulfate (Laxoberal) 可以抑制水和电解质的吸收,促进它们的分泌。 | |||
T3286 |
Sodium picosulfate monohydrate
Sodium picosulfate hydrate,匹可硫酸钠一水合物,Laxoberal |
Others | Others |
Sodium picosulfate monohydrate (Sodium picosulfate hydrate) 增加水和电解质的分泌并抑制它们的吸收。 | |||
T11205 |
ent-Ezetimibe
ent-SCH 58235,ENT-依折麦布 |
Others | Others |
ent-Ezetimibe (ent-SCH 58235) 是 Ezetimibe 的 RRS 型对映体。其中Ezetimibe 是一种胆固醇吸收 (cholesterol-absorption) 抑制剂,是NPC1L1抑制剂,也是有效的Nrf2激活剂。 | |||
T31750 |
Faxeladol
EM906,GCR 9905,EM 906,GCR-9905,EM-906,GCR9905 |
5-HT Receptor; Opioid Receptor; Adrenergic Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Faxeladol 是一种有效的肾上腺素能吸收抑制剂和 5-羟色胺重摄取抑制剂,是一种小分子 Opioid receptors激动剂,可用于研究神经系统疾病。 | |||
T38851 |
SiR-COOH
|
||
SiR-COOH 可用于跟踪 GFP 细胞中治疗药物模型的细胞内位置(Abs,645 nm;Em,676 nm)。 | |||
T77556 |
2-(4-Hydroxyphenylazo)benzoicacid
|
||
2-(4-Hydroxyphenylazo)benzoicacid 是一种分光光度法探针,可显示与蛋白质结合时的吸收光谱变化,可与牛血清蛋白结合。 | |||
T39189 |
3,4,5-Trihydroxycinnamic acid decyl ester
|
||
3,4,5-Trihydroxycinnamic acid decyl ester, an effective inhibitor of lipid absorption and accumulation, exhibits anti-obesity properties. Additionally, this compound acts as a pancreatic lipase inhibitor, with an EC 50 of around 0.9 μM. | |||
T18987 |
Py-BODIPY-NHS ester
|
Autophagy | Autophagy |
Py-BODIPY-NHS ester 是一种具有强紫外吸收能力的小分子染料,可用于标记活细胞和固定细胞。 | |||
T6344 |
Sevelamer hydrochloride
Sevelamer HCl |
FXR; Autophagy | Autophagy; Metabolism |
Sevelamer hydrochloride (Sevelamer HCl) 是一种磷酸盐结合药物,用于通过与膳食磷酸盐结合并阻止其吸收来治疗高磷血症。 | |||
T19310 |
Ensulizole
2-PHENYLBENZIMIDAZOLE-5-SULFONIC ACID,苯基苯丙咪唑磺酸,2-Phenyl-1H-benzo[d]imidazole-5-sulfonic acid,Phenylbenzimidazole sulfonic acid |
Others | Others |
Ensulizole (2-PHENYLBENZIMIDAZOLE-5-SULFONIC ACID) 是磺化的紫外线吸收剂,可以强烈吸收 UVB 和部分 UVA。在紫外线或阳光照射下,它可以产生活性氧,进而破坏 DNA。 | |||
T7614 |
Eniluracil
GW776C85,5-Ethynyluracil |
Others | Others |
Eniluracil (GW776C85) 是不可逆的二氢嘧啶脱氢酶(DPD)抑制剂,是一种尿嘧啶类似物,能够使 5-FU 的口服生物利用度提高到 100%,促进均匀吸收和可预测的毒性。 | |||
T14057 |
6-CFDA
6-羧基荧光素二醋酸,6-Carboxyfluorescein diacetate |
Others | Others |
6-CFDA (6-Carboxyfluorescein diacetate) 是可用于流式细胞术和荧光显微镜的荧光探针,也可以用于活体多光子显微镜研究动物肝胆代谢。 | |||
T11063 |
DMT1 blocker 1
|
Others | Others |
DMT1 blocker 1 是二价金属转运蛋白1 (DMT1) 的阻断剂,IC50 为 0.64 μM,可以阻断体内肠细胞的铁摄取。 | |||
T4949 |
1,2-Didecanoyl-sn-glycero-3-phosphocholi
1,2-Didecanoyl Phosphatidylcholine,1,2-Didecanoyl PC,L-A-癸酰磷脂酰胆碱 |
Others | Others |
1,2-Didecanoyl-sn-glycero-3-phosphocholi (1,2-Didecanoyl PC) 是一种合成的、疏水性较低的磷脂,已被发现可用于增强肽类药物和激素(如胰岛素)的吸收。 | |||
T0790 |
Carbaryl
1-naphthyl methylcarbamate,甲萘威,Sevin |
AChR | Neuroscience |
Carbaryl (1-naphthyl methylcarbamate) 可作为一种杀虫剂。 | |||
T72054 |
SLC26A3-IN-1
|
transporter | Metabolism |
SLC26A3-IN-1 是一种阴离子交换蛋白 SLC26A3 的抑制剂 ,IC50值为340 nM。SLC26A3 属于溶质载体 (SLC) 蛋白,是 SLC26 家族成员之一。SLC26 家族对氯化物、碳酸氢盐、硫酸盐和草酸盐具有广泛的阴离子特异性。SLC26A3 在腺瘤 (DRA) 中下调,参与氯化物和草酸盐的肠道吸收且与氯离子丢失性腹泻有关。 | |||
T62893 |
SM-2470
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
SM-2470 是一种α1-adrenoceptor拮抗剂,具有降压活性,可减低前神经节肾上腺神经活性和主动脉降压神经活性。SM-2470 具有降胆固醇活性,可抑制胆固醇吸收。 | |||
T2400 |
Candesartan Cilexetil
TCV-116,坎地沙坦酯,坎地沙坦西酯 |
Apoptosis; RAAS | Apoptosis; Endocrinology/Hormones |
Candesartan Cilexetil (TCV-116) 是一种血管紧张素II 拮抗剂,可用于治疗高血压。 | |||
T35337L |
Teduglutide acetate
|
Glucagon Receptor | GPCR/G Protein |
Teduglutide acetate 是一种 GLP-2 类似物,可使小肠黏膜肥大。它通过改变 claudin-10 的分布部分恢复小肠上皮功能,促进钠再循环以进行钠耦合葡萄糖转运和水吸收。 | |||
T0923 |
Busulfan
Myleran,Sulphabutin,白消安,Busulphan |
Apoptosis; DNA Alkylator/Crosslinker; DNA Alkylation | Apoptosis; DNA Damage/DNA Repair |
Busulfan (Busulphan) 是二甲磺酸盐的合成衍生物,具有抗肿瘤和细胞毒特性。是一种烷化剂,对骨髓具有选择性免疫抑制作用。 | |||
T0195 |
Secnidazole
RP-14539,PM-185184,塞克硝唑 |
Antibiotic; Parasite | Microbiology/Virology |
Secnidazole (PM-185184) 是一种具有口服活性唑类抗生素,半衰期比甲硝唑更长。它有潜力研究细菌性阴道病。 | |||
T21302 |
UNC569
UNC 569 |
TAM Receptor | Tyrosine Kinase/Adaptors |
UNC569 (UNC 569) 是一种ATP 竞争性的、可逆、具有口服活性的Mer 激酶抑制剂,其IC50=2.9 nM,Ki=4.3 nM。它还抑制Axl 和Tyro3,IC50分别为 37 nM 和 48 nM。它可用于研究急性淋巴细胞白血病和非典型畸胎瘤/横纹肌瘤。 | |||
T20029 |
Buformin hydrochloride
NSC528218,NSC-528218,盐酸丁双胍,NSC 528218 |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Buformin hydrochloride (NSC-528218) 是一种有效的 AMPK 激活剂,是一种双胍类的口服抗糖尿病药物。Buformin 延缓胃肠道对葡萄糖的吸收,增加胰岛素敏感性和葡萄糖对细胞的吸收,并抑制肝脏对葡萄糖的合成。Buformin 也具有抗癌活性,可用于各种癌症研究。 | |||
T1101 |
Minocycline hydrochloride
Minocycline HCl,盐酸米诺环素,美满霉素 |
HIF/HIF Prolyl-Hydroxylase; Antibacterial; Antibiotic | Chromatin/Epigenetic; Metabolism; Microbiology/Virology |
Minocycline hydrochloride (Minocycline HCl) 是四环素抗生素,具有出色的吸收和组织渗透性,可用于多种细菌感染以及痤疮的治疗。米诺环素可导致在开始治疗后 1 至 3 个月内发生的急性肝炎样综合征或通常在长期治疗后具有自身免疫特征的更隐匿的慢性肝炎。 | |||
T71012 |
Nemazoline Free Base
|
||
Nemazoline Free Base is a nasal decongestant. It has alpha 1-agonist/alpha 2-antagonist activity and was more effective and long-acting than oxymetazoline on canine nasal mucosa, in-vitro and in-vivo. Upon intranasal administration to dogs, the compound was devoid of systemic effects up to a concentration 1000 times that needed for local decongestant effect (1.65 micrograms, atomized from a 1 microgram mL-1 solution) suggesting limited mucosal absorption. After nasal administration to rats for 1... | |||
T8947 |
dasiglucagon acetate
dasiglucagon acetate(1544300-84-6 free base) |
Others | Others |
dasiglucagon acetate 是一种用于糖尿病低血糖治疗的新型胰高血糖素类似物。 它已证明在水性制剂中的溶解度和稳定性。药代动力学研究表明,与传统的重组胰高血糖素相比,它的胰高血糖素具有更高的吸收率和更长的血浆消除半衰期。 | |||
T14835 |
BTRX-335140
CYM-53093 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
BTRX-335140 (CYM-53093) 是一种有效的选择性口服活性 κ 阿片受体 (KOR) 拮抗剂,对 κOR、μOR 和 δOR 具有拮抗活性,IC50 值分别为 0.8、110 和 6500 nM。它可以很好地分布到 CNS 中,在大鼠中具有良好的体外吸收、分布、代谢、排泄和毒性以及体内药代动力学特征。 | |||
T36126 |
TMP-153
|
||
Acyl-CoA:cholesterol acyltransferase (ACAT) catalyses the esterification of excess cellular cholesterol with fatty acids and is important for intestinal cholesterol absorption, hepatic lipoprotein secretion, and cholesterol accumulation in vascular tissues. ACAT inhibitors improve plasma lipid profile and ameliorate proteinuria in nephrotic animals. TMP-153 is a quinolyl derivative that inhibits ACAT with IC50 values of 5-10 nM in various animals. At 0.5-1.5 mg/kg, TMP-153 dose-dependently reduc... | |||
T30297 |
Bay-02752
|
||
BAY-02752 is a lipid lowering agent that has been shown in rats to inhibit the absorption of intestinal cholesterol. | |||
TNU0598 |
Dodecyl 2-(N,N-dimethylamino)propionate Hydrochloride
|
||
Formulation product; absorption enhancer | |||
T33443 |
MK-8970
|
||
MK-8970 is an acetal carbonate prodrug of raltegravir with enhanced colonic absorption. | |||
T17174 |
Troriluzole
BHV-4157 |
Others | Others |
Troriluzole is an orally active glutamate modulator. Troriluzole reduces the synaptic glutamate level and increases synaptic glutamate absorption. | |||
T70849 | AZD-4121 | ||
AZD-4121 is an oral cholesterol absorption inhibitor targeting NPC1L1 for the treatment of dyslipidaemia. | |||
T70848 |
AZD-4121 tert-butylammonium
|
||
AZD-4121 tert-butylammonium is an oral cholesterol absorption inhibitor targeting NPC1L1 for the treatment of dyslipidaemia. | |||
T68724 |
Canosimibe
|
||
Canosimibe is a cholesterol absorption inhibitor | |||
T31522 |
Dipropyl sulfone
|
||
Dipropyl sulfone may function as an enhancer of heparin absorption in the intestine. | |||
T21417 |
Dihydrotachysterol
Hytakerol,HSDB-3314,双氢速甾醇,HSDB3314,Parterol,HSDB 3314 |
||
Dihydrotachysterol (DHT) is a biologically active synthetic analog of vitamin D. It promotes intestinal absorption of active calcium and phosphate . It is also beneficial in the treatment of hypoparathyroidism. | |||
T71222 |
Metformin glycinate
|
||
Metformin glycinate is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T70806 |
Metformin icosapent
|
||
Metformin icosapent is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T32797 |
Lithocholenic acid
|
||
Lithocholenic acid is a bile acid that acts as a detergent to solubilize fats for absorption. | |||
T71562 | Boxidine | ||
Boxidine inhibits the transformation of 7-dehydrocholesterol to cholesterol & also inhibits sterol absorption. | |||
T71738 |
DRAinh-A250
|
||
DRAinh-A250 is a SLC26A3 inhibitor which blocks colonic fluid absorption and reduces constipation. | |||
T27565 |
Hyzetimibe
HS25,HS 25,HS-25 |
||
Hyzetimibe, a cholesterol absorption blocker, is used potentially for the treatment of hypercholesterolemia. | |||
T29359 |
2-n-Nonyl-1,3-dioxolane
AI3-22560,Decanal ethylene acetal,2-Nonyldioxolane |
||
2-n-Nonyl-1,3-dioxolane is a biochemical. It is used as an absorption and penetration enhanceron transdermal. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5S1172 |
Tiliroside
银椴甙,Tribuloside,银椴苷;椴树苷 |
Antioxidant | oxidation-reduction |
Tiliroside (Tribuloside) 是糖苷类黄酮,是 α-淀粉酶的非竞争性抑制剂(Ki:84.2 μM)。它抑制胃肠道中碳水化合物的消化和葡萄糖的吸收,具有抗糖尿病作用。 | |||
T13082 |
Tarasaponin VI
|
Others | Others |
Tarasaponin VI 是从 Aralia elata 中分离出来的,对乙醇吸收具有有效的抑制活性。 | |||
T2A2509 |
Laurocapram
月桂氮酮,Tranzone,Azone,N-Lauryl caprolactam,N-0252,月桂氮卓酮,N-Dodecylcaprolactam |
Others | Others |
Laurocapram (N-Lauryl caprolactam) 是吸收促进剂,对于亲脂性和亲水性物质都是一种最有效的吸收剂。 | |||
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. | |||
T5812 |
Zinc Phytate
|
Others | Others |
Zinc Phytate 存在于食物中,对人类吸收营养有重要意义。 | |||
T39312 |
2-Hexylthiophene
|
Others | Others |
2-Hexylthiophene 是一种碱性极弱的杂芳香族化合物。2-己基噻吩可用于改变和提高钌敏化剂的摩尔吸收系数。 | |||
T8071 |
L-Lysine hydrochloride
赖氨酸盐酸盐,Lysine hydrochloride,L-赖氨酸盐酸盐 |
Virus Protease | Microbiology/Virology |
L-Lysine hydrochloride 是一种人类必需氨基酸,能增加钙吸收,减少糖尿病相关疾病和改善肠道健康,可用于疱疹的研究。 | |||
T4957 |
Carnosic acid
|
Apoptosis; ROS; Antibacterial | Apoptosis; Immunology/Inflammation; Microbiology/Virology |
Carnosic acid 抑制细胞增殖,有抗菌、抗炎和抗氧化应激作用。 | |||
T4763 |
trans-Cyclohexane-1,2-diol
trans-1,2-Cyclohexanediol,反式-1,2-环己二醇 |
Others; Endogenous Metabolite | Metabolism; Others |
trans-Cyclohexane-1,2-diol (trans-1,2-Cyclohexanediol) 是内源性代谢产物的一种。 | |||
T4946 |
(+)-Columbianetin acetate
二氢欧山芹醇醋酸酯,COLUMBIANETIN ACETATE |
Others | Others |
(+)-Columbianetin acetate (COLUMBIANETIN ACETATE) 是一种 Columbianetin 异构体。其中Columbianetin 是植物抗毒素,与芹菜贮藏过程中对病原体的抗性有关,表现出良好的抗炎及抗真菌活性。 | |||
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。 | |||
T6316 |
Calcitriol
Topitriol,Rocaltrol,Calcijex,RO215535,骨化三醇,1,25-Dihydroxyvitamin D3 |
Endogenous Metabolite | Metabolism |
Calcitriol (1,25-Dihydroxyvitamin D3) 是一种维他命 D 的代谢物,一种维他命 D 受体 (VDR) 的激动剂 (IC50=0.4 nM)。Calcitriol 增加肠道对钙和磷的吸收,并与甲状旁腺激素一起增加了骨吸收。 | |||
T6S0653 |
Linarin
Buddleoflavonoloside,Buddleoside,Acacetin-7-O-rutinoside,Acaciin,Linarine,蒙花苷 |
TNF; AChE | Apoptosis; Neuroscience |
Linarin (Acacetin-7-O-rutinoside) 是一种选择性的乙酰胆碱酯酶 (AChE) 抑制剂,从薄荷花提取物中分离得到。 | |||
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。 | |||
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。 | |||
T2840 |
Phloracetophenone
2,4,6-三羟基苯乙酮,2,4,6-trihydroxyacetophenone,1-(2,4,6-Trihydroxyphenyl)ethanone |
Others; P450; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology; Others |
Phloracetophenone (1-(2,4,6-Trihydroxyphenyl)ethanone) 是多叶姜黄中苯乙酮糖苷的糖苷配基部分,具有抗肥胖,降血脂和降低胆固醇作用,能够增强胆固醇 7α-羟化酶的活性。 | |||
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。 | |||
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。 | |||
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。 | |||
T6194 |
Fidaxomicin
非达米星,Tiacumicin B,OPT-80,Clostomicin B1,PAR-101 |
Apoptosis; DNA/RNA Synthesis; Antibacterial; Antibiotic | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Fidaxomicin (Tiacumicin B) 是一种大环RNA 聚合酶抑制剂,具有窄谱活性。它选择性地根除致病性艰难梭菌,对构成正常健康肠道菌群的多种细菌影响很小。 | |||
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。 | |||
T1040 |
Vitamin B12
Cyanocobalamin,Cobalamin,维生素B12 |
Endogenous Metabolite | Metabolism |
Vitamin B12 (Cobalamin) 是一种维生素,在维持血流形成和脑、神经系统正常功能等方面发挥关键作用。 | |||
T3051 |
Theaflavin-3-gallate
茶黄素-3-没食子酸酯,茶黄素 3-没食子酸酯,茶黄素 -3-没食子酸,Theaflavine-3-Gallate |
Others | Others |
Theaflavin-3-gallate (Theaflavine-3-Gallate) 是红茶茶黄素单体,是红茶生物学上重要的活性成分,对健康有益。它以时间和浓度依赖性方式与还原型谷胱甘肽直接反应。它充当促氧化剂并在癌细胞中诱导氧化应激。 | |||
T2A2498 |
L-Lysine
Aminutrin,Lysine Acid,lysine,L-赖氨酸,赖氨酸 |
Virus Protease; Endogenous Metabolite; Antifection | Metabolism; Microbiology/Virology |
L-Lysine (Aminutrin) 是一种人类必需氨基酸,能增加钙吸收,减少糖尿病相关疾病和改善肠道健康,可用于疱疹的研究。 | |||
T1311 |
4-aminobenzoic acid
PABA,Vitamin H1,Vitamin Bx,para-Aminobenzoic acid,对氨基苯甲酸 |
Endogenous Metabolite | Metabolism |
4-aminobenzoic acid (para-Aminobenzoic acid) 是一种具有紫外线吸收和抗纤维化特性的有机酸。当暴露在光线下时,4-aminobenzoic acid 吸收紫外线并通过光化学反应释放多余的能量,这可能会对DNA造成损害。4-aminobenzoic acid 还可以增加组织水平的摄氧量,并可能增强单胺氧化酶(MAO)活性以促进血清素的降解,过量可能导致纤维化变化。 | |||
T35749 |
Thymohydroquinone
Thymoquinol |
Antioxidant; Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction |
Thymohydroquinone (Thymoquinol) 是中药材百里香、牛至和其他唇形科植物中含有的单萜酚类化合物。 Thymohydroquinone 抑制癌细胞生长、减少氧化应激和调节炎症反应,在无细胞实验中清除2,2-二苯基-1-picrylhydrazyl 自由基(IC50 = 2.4 μg/ml),在浓度为1.6至6.4 μg/ml 的氧自由基吸收能力(ORAC)实验中,它的Trolox 当量值为2.6胸腺对苯二酚对A2780、OVCAR-8和CIS-A2780卵巢癌细胞(IC50分别为3.1、8.9和9.8 μM)和人卵巢永生化上皮细胞(IC50 = 14 μM)的生长有抑制作用,体外对恶性疟原虫也有抑制作用(IC50 = 15.9 μM)。 | |||
TN1387 |
Angelol B
|
Others | Others |
The absorption and transport of angelol A and Angelol B are passive diffusion as the dominating process in Caco-2 cell monolayer model. | |||
TN4474 |
Macrocarpal B
|
c-Met/HGFR | Tyrosine Kinase/Adaptors |
The intestinal absorption of M-A, Macrocarpal B, and Cy-C was passive diffusion as the dominating process and Cy-C was partly ATP-dependent. | |||
T40814 |
Colominic acid sodium salt
Polysialic acid sodium salt,Colominic acid sodium salt |
||
Colominic acid sodium salt, also known as polysialic acid sodium salt, is naturally isolated from the cell wall of Escherichia coli and animals. It exhibits a red color with an absorption maximum of 530 nm and possesses anti-bacterial activity. | |||
T73338 | Obtusalin | ||
Obtusalin 是首次在R. dauricum 中发现的一种三萜类化合物,在 210 nm 处有紫外吸收。Obtusalin 具有一定的抗菌活性。 | |||
T81741 |
Multiflorin A
|
||
Multiflorin A,源于Pruni semen的活性成分,具泻药效果,能够抑制肠道葡萄糖吸收并促进细菌代谢。 | |||
T33492 |
Methyl pyropheophorbide-a
MPPa (Methyl pyropheophorbide-a),NSC267052,Pyropheophorbidea,MPPa,NSC-267052,NSC 267052 |
||
Pyropheophorbide-a methyl ester (MPPa) is a PDT photosensitizer, and is also a semisynthetic natural product derived from chlorophyll a. The absorption peak of MPPa in organic solvent and in cells was at 667 and 674 nm, respectively. 3-(4,5-Dimethylthiazo | |||
TCA2511 |
11Beta-hydroxyprogesterone
|
Sodium Channel | Membrane transporter/Ion channel |
The progesterone derivatives 11 alpha- and 11 beta-hydroxyprogesterone are potent inhibitors of 11 beta-hydroxysteroid dehydrogenase (isoforms 1 and 2) in vitro and can confer mineralocorticoid activity on corticosterone in the rat in vivo. 11beta-Hydroxyprogesterone acts as a mineralocorticoid agonist in stimulating Na+ absorption in mammalian principal cortical collecting duct cells. | |||
T74293 |
Allolithocholic acid
|
||
Allolithocholic acid 是一种类固醇酸,在正常血清和粪便中可发现。该化合物促进脂肪与甾醇在肠道及肝脏的排泄、吸收与运输。 | |||
T75427 | Cholic acid sodium hydrate | ||
Cholic acid sodium hydrate, 为肝脏主要产生的胆汁酸,常与甘氨酸或牛磺酸结合,促进脂肪吸收及胆固醇排出,具备口服活性。 | |||
TN5129 | Tetrahydro tanshinone I | Others | Others |
Tetrahydro tanshinone I is one compound of Fufang Danshen Prescription (FDP) , liposome equilibrium dialysis system could simply and effectively esti-mate the absorption of multiple components in FDP in vivo, and predicts the potential bioactivity of thes | |||
T74199 |
Beauverolide Ka
|
||
Beauverolide Ka 是一种环四缩酚肽,是 Beauveria bassiana 真菌的代谢产物。Beauverolide Ka 浓度为 50 μM 时可刺激培养的大鼠 L6 成肌细胞的葡萄糖摄取。Beauverolide Ka 在 10 μM 时表现出对 HEI-OC1 细胞的保护作用,并且在 L6 成肌细胞和肌管中表现出剂量依赖性活性。 |