135
47
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10220 |
Abemaciclib metabolite M2
Abemaciclib Metabolites M2 |
CDK | Cell Cycle/Checkpoint |
Abemaciclib Metabolites M2 is a metabolite of abemaciclib, acts as a potent CDK4 and CDK6 inhibitor (IC50s: 1-3 nM) with anti-cancer activity. | |||
T7537 |
Norgestimate
炔诺肟酯,诺孕酯 |
Progesterone Receptor | Others |
Norgestimate 是一种具有口服活性、高度选择性的孕激素活性和较小雄激素作用的孕激素,是一种合成的孕激素类似物。它可用作口服的避孕药。 | |||
T12412L |
PDK4-IN-1 hydrochloride
|
Apoptosis; PDK | Apoptosis; PI3K/Akt/mTOR signaling |
PDK4-IN-1 hydrochloride 是一种蒽醌衍生物,对丙酮酸脱氢酶激酶 4有抑制作用,IC50为 84 nM,具有口服活性。它抑制细胞转化和细胞增殖并诱导细胞凋亡。它具有抗过敏,抗糖尿病和抗癌作用。 | |||
T3281 |
Delapril hydrochloride
indalapril,地拉普利盐酸盐,Alindapril Hydrochloride,Delapril Hydrochloride,盐酸地拉普利,CV 3317 |
RAAS | Endocrinology/Hormones |
Delapril hydrochloride (indalapril) 是一种血管紧张素转化酶抑制剂,能够用于心血管疾病的研究。 | |||
T40729 |
D-Threonine
H-D-Thr-OH,D-苏氨酸,D-Threonine |
Endogenous Metabolite | Metabolism |
D-Threonine (H-D-Thr-OH) 是酿酒酵母 Saccharomyces cerevisiae 的代谢产物之一。 | |||
T1690 |
BroMhexine IMpurity B
|
Others | Others |
BroMhexine IMpurity B 试剂用于制备 Ambroxol 和 Bromhexine (B678600) 代谢物 Ambroxol EP Impurity E。 | |||
T20026 |
WEB-1868
WEB 1868,WEB1868 |
Others | Others |
WEB-1868 是 nebracetam 的一种代谢产物,nebracetam 是人 M1-毒蕈碱受体的激动剂。 | |||
T37196 |
5-AAM-2-CP
|
AChR | Neuroscience |
5-AAM-2-CP 是 Acetamiprid 的主要代谢物之一。 Acetamiprid 是一种 nAChR 激动剂,是一种新烟碱类杀虫剂。 | |||
T19498 |
p-Cresyl sulfate potassium
p-Tolyl sulfate potassium salt,p-Cresol sulfate potassium,p-Methylphenyl potassium sulfate,对甲基硫酸钾,Potassium p-tolyl sulfate |
Endogenous Metabolite | Metabolism |
p-Cresyl sulfate potassium (p-Tolyl sulfate potassium salt) 是一种尿毒症毒素,能够与原型蛋白质结合。 | |||
T1414 |
Sodium 2-mercaptoethanesulfonate
Mitexan,美司那,美司钠,Uromitexan,Mesna,Mesnum,Mesnex |
Others | Others |
Sodium 2-mercaptoethanesulfonate (Uromitexan) 是一种抗氧化剂,具有细胞保护作用。它可用于减轻由环磷酰胺引起的出血性膀胱炎。它广泛用作抗化学疗法毒性的全身保护剂。 | |||
T22317 |
DRB18
|
transporter | Metabolism |
DRB18 is a highly effective pan-class inhibitor of glucose transporter proteins (GLUT). It significantly modulates energy-related metabolism in A549 cells by inducing alterations in the abundance of metabolites associated with glucose-related pathways. DRB18 exerts its effects by promoting G1/S phase arrest, increasing oxidative stress, and prompting necrotic cell death, ultimately displaying notable anti-tumor activity [1]. | |||
T8483 |
Cysteine thiol probe
Methyl (4-bromobenzoyl)-L-cysteinate |
Others | Others |
Cysteine thiol probe (Methyl (4-bromobenzoyl)-L-cysteinate) 是基于硫醇的探针,旨在标记亲电子的天然产物。它能够结合基于烯酮,β-内酰胺和 β-内酯的亲电子代谢物。它具有理想药效团探针的每个特征,并具有发色团。 | |||
T37359 |
Myristoyl-L-carnitine chloride
L-Myristoylcarnitine chloride |
Endogenous Metabolite | Metabolism |
Myristoyl-L-carnitine chloride (L-Myristoylcarnitine chloride) 是人体的代谢物之一,与遗传代谢疾病有关。Tetradecanoylcarnitine 是研究糖尿病和自身免疫性肝炎的潜在标记物。 | |||
TD0105 |
Sulfobromophthalein disodium salt
|
Others | Others |
Sulfobromophthalein disodium salt 是一种有机阴离子染料,能够参与药物和代谢物的运输,可用于研究动物组织中表达的多种膜载体。 | |||
T1229 |
Erdosteine
厄多司坦,RV 144,KW-9144 |
NF-κB; Antibacterial; Adenosine deaminase | Metabolism; Microbiology/Virology; NF-κB |
Erdosteine (RV 144) 抑制脂多糖诱导的NF-κB 激活,具有粘液调节、抗菌、抗炎、抗氧化和自由基清除作用。 | |||
T2112 |
Fexinidazole
非昔硝唑,HOE 239 |
Others; Parasite | Microbiology/Virology; Others |
Fexinidazole (HOE 239) 是具有口服活性的硝基咪唑抗锥虫药物。它显示出对布鲁氏杆菌亚种和菌株的杀锥虫活性,IC50值为 0.7-3.3 μM (0.2-0.9 μg/ml)。它具有用于因感染布鲁氏菌引起的人类昏睡病的潜力。 | |||
T9831 |
MKC-1
Ro-31-7453 |
Apoptosis; Akt; Microtubule Associated; mTOR | Apoptosis; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
MKC-1 (Ro-31-7453) 是一种口服生物可利用的小分子双吲哚基马来酰亚胺细胞周期抑制剂,具有潜在的抗肿瘤活性。 | |||
T4630 |
NSC 404988
|
Others | Others |
NSC 404988 是一种苯甲酰胺类生物活性化合物,用于化合物的合成和药物的制备,还被用于药物代谢的研究和生物系统中代谢物的分析。 | |||
T16537 |
Pimonidazole
|
Others | Others |
Pimonidazole 是缺氧标记物,能够与大分子的共价结合或被还原形成还原性代谢物后在缺氧细胞中积累,可用于定性和定量评估肿瘤缺氧。它可用于瘤内缺氧和细胞增殖的补充性研究。 | |||
T0765 |
Fomepizole
Antizol-Vet,4-甲基吡唑,甲吡唑,4-Methylpyrazole,Antizol |
P450; CAT; AChR | Metabolism; Neuroscience; oxidation-reduction |
Fomepizole (4-Methylpyrazole) 是细胞色素 P450 (CYP2E1) 抑制剂。它是乙醇脱氢酶 (alcohol dehydrogenase) 竞争性抑制剂。它能够阻断甲醇和乙二醇进一步转化为有毒代谢产物。它具有成为乙二醇或甲醇中毒的解毒剂的潜力。 | |||
T36640 |
Xanomeline
LY-246708 |
AChR | Neuroscience |
Xanomeline (LY-246708) 是一种功能性选择性 M1/M4激活剂,用于精神分裂等神经疾病的研究,在临床前试验中显示出良好的治疗前景。Xanomeline 口服吸收良好,通过血脑屏障,并与至少六种代谢物进行广泛的肝脏代谢。 | |||
T16536 |
Pimonidazole hydrochloride
|
||
Pimonidazole hydrochloride 通过与大分子共价结合或在其硝基还原后形成还原性代谢物在缺氧细胞中积累。 可用于肿瘤缺氧的定性和定量评估。 它是一种新型的缺氧标志物,用于肿瘤缺氧和肿瘤细胞增殖的互补研究。 | |||
T6446 |
Clevudine
L-FMAU,克拉夫定,Levovir |
HBV; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Clevudine (Levovir) 是一种非自然 L-构型的核苷类似物,是一种与聚合酶结合的非竞争性抑制剂,具有较强的抗 HBV 活性,半衰期长,毒性低的特点。 | |||
T1408 |
Capecitabine
Xeloda,卡培他滨,Capecitibine,Capiibine,RO 09-1978 |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Capecitabine (Capecitibine) 是一种可口服的前药,可由胸苷磷酸化酶催化转变为其活性代谢物 Fluorouracil。 | |||
T36696 |
DMBA
|
||
7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.1,2It undergoes metabolic activation by numerous enzymes, including the cytochrome P450 (CYP450) isoform CYP1B1, as well as microsomal epoxide hydrolase (mEH), producing a variety of reactive metabolites that form DNA adductsin vivo, and it has been commonly used to induce tumor formation in various rodent models.2,3,1DMBA increase... | |||
T15498 |
HOKU-81
4-Hydroxytulobuterol |
Others | Others |
HOKU-81is a new bronchodilator and is one of the metabolites of tulobuterol. | |||
T31248 |
Deacetyl-N-monodemethyldiltiazem
|
||
Deacetyl-N-monodemethyldiltiazem is a major metabolites of diltiazem. | |||
T10956 |
Dansyl glutathione
DNS-glutathione |
Others | Others |
Dansyl glutathione is a capture agent used for quantitative assessment and identification of reactive metabolites. | |||
T21316 |
Apaziquone
EO-9,NSC382459,EO9,NSC 382459,EO 9,NSC-382459 |
||
Apaziquone has potential antineoplastic and radiosensitization activities. It is converted to active metabolites in hypoxic cells by intracellular reductases, which are present in greater amounts in hypoxic tumor cells. The active metabolites alkylate DNA | |||
T32783 |
Lipoxin C4
15-OH-Ltc3 |
||
Lipoxin C4 is a bioactive autacoid metabolites of arachidonic acid made by various cell types. It is categorized as a nonclassic eicosanoid and member of the specialized pro-resolving mediator (SPMs) family of polyunsaturated fatty acid (PUFA) metabolites | |||
T37180 | Avanafil metabolite M16 | ||
Avanafil metabolite M16 is a major inactive metabolite of the phosphodiesterase 5 (PDE5) inhibitor avanafil . Avanafil is metabolized by the cytochrome P450 (CYP450) isoforms CYP3A4 and CYP2C to the major metabolites avanafil metabolite M16 and avanafil metabolite M4 , as well as minor metabolites. | |||
T33781 |
O-Demethyldeacetyldiltiazem
Deacetyl-O-demethyldiltiazem,Deacetyl-O-demethyl-D-diltiazem,Deacetyl o-desmethyl diltiazem |
||
O-Demethyldeacetyldiltiazem is one of the diltiazem metabolites in human plasma. | |||
T29407 |
3-Hydroxydecanedioic acid
|
||
3-hydroxydecanedioic acid can be found in ketoacidosis of urinary metabolites. | |||
T37195 |
5'-hydroxy Meloxicam
|
||
5'-hydroxy Meloxicam 是 meloxicam (MEL) 代谢物之一。 | |||
T37361 |
6β-hydroxy Dexamethasone
|
||
6β-hydroxy Dexamethasone is a metabolite of dexamethasone that is more hydrophilic than the parent compound. Dexamethasone is metabolized by CYP3A4; therefore, quantification of the dexamethasone metabolites, 6α- and 6β-hydroxy dexamethasone, can be used to determine CYP3A4 enzyme activity in humans., The formation of 6-hydroxy dexamethasone metabolites is species-specific, with hamsters producing the highest amount. In rats, dexamethasone hydroxylation is sex-specific, with male rats producing ... | |||
T38035 |
Phenol-13C6
Phenol-13C6 |
||
Phenol-13C6is a building block.1It has been used in the synthesis of13C6-labeled metabolites of (±)-asenapine . 1.Kuethe, J.T.Synthesis of stable isotope‐labeled metabolites of asenapineJ. Labelled Comp. Radiopharm.55(5)180-185(2012) | |||
T69406 | Sydnophene | ||
Sydnophene is an intermediate in the synthesis of metabolites of Mesocarb -- a CNS stimulant that acts as a dopamine reuptake inhibitor. | |||
T37181 |
Avanafil metabolite M4
Avanafil metabolite M4 |
||
Avanafil metabolite M4 is a major active metabolite of the phosphodiesterase 5 (PDE5) inhibitor avanafil . Avanafil is metabolized by the cytochrome P450 (CYP450) isoforms CYP3A4 and CYP2C to the major metabolites avanafil metabolite M4 and avanafil metabolite M16 , as well as minor metabolites. Avanafil metabolite M4 inhibits PDE5 with 18% of the potency of avanafil. | |||
T37708 |
17(R)-HETE
|
||
Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. 17-HETE is a cytochrome P450 (CYP450) metabolite of arachidonic acid that has stereospecific effects on sodium transport in the kidney. 17(R)-HETE is an inactive isomer of 17-HETE, whereas the (S) enantiomer can inhibit proximal tubule ATPase activity at a concentration of 2 μM. | |||
T37238 |
(±)19(20)-EpDPA
|
||
EDHF (endothelium-derived hyperpolarizing factor) is an unidentified mediator released from vascular endothelial cells in response to acetylcholine and bradykinin which is distinct from the NOS- (nitric oxide) and COX-derived (prostacyclin) vasodilators. Cytochrome P450 (CYP450) metabolism of polyunsaturated fatty acids produces epoxides such as (±)14(15)-EpETrE which are prime candidates for the actual active mediator. However, the CYP450 metabolites of eicosapentaenoic acid and docosahexaenoic... | |||
T35849 |
17(S)-HETE
|
||
Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites.17-HETE is a cytochrome P450 (CYP450) metabolite of arachidonic acid that has stereospecific effects on sodium transport in the kidney.17(S)-HETE inhibits proximal tubule ATPase activity by as much as 70% at a concentration of 2 μM. | |||
T37225 |
(±)7(8)-DiHDPA
|
||
(±)7(8)-DiHDPA is a major metabolite of docosahexaenoic acid that is produced via oxidation by cytochrome P450 epoxygenases. Epoxygenase metabolites of DHA, including (±)7(8)-DiHDPA, suppress aggregation and thromboxane synthesis in isolated platelets. | |||
T35495 |
(±)13(14)-DiHDPA
|
||
(±)13(14)-DiHDPA is a metabolite of docosahexaenoic acid that is produced via oxidation by cytochrome P450 epoxygenases. Epoxygenase metabolites of DHA, including (±)13(14)-DiHDPA, are reported to inhibit angiogenesis, tumor growth, and metastasis. | |||
T37149 |
Carbamazepine 10,11-epoxide
|
Others | Others |
Carbamazepine 10,11-epoxide 是抗惊厥药卡马西平 (carbamazepine) 的活性代谢物。它由卡马西平通过微粒体中的细胞色素 P450 (CYP) 同种型 CYP3A4 和 CYP2C8 形成,微粒体分别由表达 CYP3A4 或 CYP2C8 的 HepG2 细胞制备。它对小鼠电击诱发的癫痫发作具有抗惊厥活性。 | |||
T13658 |
DMEA-PNU-159682
|
Others | Others |
DMEA-PNU-159682 (molecule D12) is an ADC cytotoxin molecule, including neomycin (MMDX) metabolites from liver microsomes and effective ADC cytotoxin PNU-159682. | |||
T13291 |
VD3-D6
Vitamin D3-26,26,26,27,27,27-d6 |
Others | Others |
VD3-D6 is the deuterated form of Vitamin D3; tools for determination of Vitamin D3 metabolites in human serum. | |||
T35037 |
Vanilmandelic acid, L-(+)-
Vanilmandelic acid L-form,(+)-Vanilmandelic acid |
||
Vanilmandelic acid, L-(+)- is a chemical intermediate in the synthesis of artificial vanilla flavorings and is an end-stage metabolite of the catecholamines, epinephrine, and norepinephrine. It is produced via intermediary metabolites. | |||
T36237 |
5-hydroxy Propranolol
|
||
5-hydroxy Propranolol is a metabolite of propranolol , a β-adrenergic receptor antagonist. Propranolol is primarily metabolized in the liver, with cytochrome P450 isoform 2D6 directing ring hydroxylation and the generation of 5-hydroxy propranolol and related metabolites. | |||
T37235 |
(±)16(17)-EpDPA
(±)16,17-EpDPE,(±)16,17 EDP,(±)16,17-epoxy Docosapentaenoic Acid,(±)16,17-epoxy DPA,(±)16(17)-EpDPA |
||
EDHF (endothelium-derived hyperpolarizing factor) is an unidentified mediator released from vascular endothelial cells in response to acetylcholine and bradykinin which is distinct from the NOS- (nitric oxide) and COX-derived (prostacyclin) vasodilators.[1],[2]Cytochrome P450 (CYP450) metabolism of polyunsaturated fatty acids produces epoxides such as (±)14(15)-EET which are prime candidates for the actual active mediator.[3] However, the CYP450 metabolites of eicosapentaenoic acid and docosahex... | |||
T36769 |
10-hydroxy Warfarin
|
||
10-hydroxy Warfarin is a metabolite of (R)-warfarin .1It is formed from (R)-warfarin by the cytochrome P450 (CYP) isoform CYP3A4. 10-hydroxy Warfarin is an inhibitor of CYP2C9 (IC50= 1.6 μM), the enzyme that converts (S)-warfarin to its 6-hydroxy warfarin and 7-hydroxy warfarin metabolites.2 1.Kaminsky, L.S., and Zhang, Z.-Y.Human P450 metabolism of warfarinPharmacol. Ther.73(1)67-74(1997) 2.Jones, D.R., Kim, S.-Y., Guderyon, M., et al.Hydroxywarfarin metabolites potently inhibit CYP2C9 metaboli... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2S2173 |
(E)-Naringenin chalcone
Isosalipurpol,柚皮苷查尔酮,Chalconaringenin,trans-2'4'6'4-tetrahydroxychalcone,柚皮素查耳酮 |
Others | Others |
Naringenin chalcone (Isosalipurpol) 是一种黄酮醇生物合成的中间体,在查耳酮异构酶的作用下,自发代谢成柚皮素。它具有抗炎和抗过敏活性。 | |||
TN7068 |
Sinomenine N-oxide
|
Others | Others |
Sinomenine N-oxide 是青藤碱循环代谢机制的主要代谢产物之一。 | |||
T8120 |
N-Benzyloctadecanamide
N-苄基硬脂酰胺,N-Benzylstearamide |
Others | Others |
N-Benzyloctadecanamide 是一种 Macamide,Macamides 是Lepidium meyeniiWalp (玛咖)中的一类独特的次级代谢产物。 | |||
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。 | |||
TQ0024 |
3-Hydroxyglutaric acid
|
Endogenous Metabolite | Metabolism |
3-Hydroxyglutaric acid 是一种戊二酸的衍生物。 | |||
TN6088 |
tricoumaroyl spermidine
N1,N5,N10-(Z)-tri-p-coumaroylspermidine,N1,N5,N10-(E)-Tri-p-coumaroylspermidine,N1,N5,N10-Tri-p-coumaroylspermidine |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Tricoumaroyl spermidine(N1,N5,N10-(Z)-tri-p-coumaroylspermidine) 被发现是一种独特的茶(Camellia sinensis) 花代谢物。 | |||
T7437 |
3-(3-Hydroxyphenyl)propionic Acid
m-Hydroxyphenylpropionic acid,3-Hydroxyhydrocinnamic acid,3-(3-羟基苯基)丙酸 |
Others; Endogenous Metabolite | Metabolism; Others |
3-(3-Hydroxyphenyl)propionic Acid (m-Hydroxyphenylpropionic acid) 是一种黄酮类代谢产物,由人体微生物区系形成,具有舒张血管的特性。 | |||
T13542 |
α-Zearalenol
|
Estrogen Receptor/ERR | Endocrinology/Hormones |
α-Zearalenol 是一种霉菌毒素,对雌激素受体具有高亲和力。它是 zearalenone (ZEN) 的一种衍生物,由于其异种雌激素效应可引起动物的生殖障碍。 | |||
T4940 |
3-Methylhistamine dihydrochloride
|
Others; Endogenous Metabolite | Metabolism; Others |
3-Methylhistamine dihydrochloride 是一种组胺的降解产物,与免疫反应有关,并在接种过疫苗的小鼠中表现出上调作用。 | |||
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。 | |||
T5256 |
All-trans-retinal
视黄醛,All trans-Retinal,Retinaldehyde,Vitamin A aldehyde |
Others; Endogenous Metabolite | Metabolism; Others |
All-trans-retinal (Vitamin A aldehyde) 是视网膜中维生素A 代谢物之一。 生理条件下,它再生为视觉发色团,11-顺式-视黄醛。 | |||
T21977 |
p-Cresyl sulfate
|
Others | Others |
p-Cresyl Sulfate 是主要的尿毒症毒素,存在于慢性肾病患者的血液,来源于肝脏中酪氨酸和苯丙氨酸的代谢物。 | |||
TN1714 |
Grosvenorine
罗汉果黄素,Grosvenorin |
Antibacterial | Microbiology/Virology |
Grosvenorine (Grosvenorin) 具有良好的抗菌和抗氧化活性,是罗汉果中主要的黄酮类物质。 | |||
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。 | |||
T16338 |
Norgestimate metabolite Norelgestromin
17-Deacetyl norgestimate,17-Deacylnorgestimate,甲基孕酮 |
Drug Metabolite | Metabolism |
Norgestimate metabolite Norelgestromin (17-Deacylnorgestimate) 是norgestimate 的一种活性代谢物。它是用于避孕贴片的甾体孕激素,与雌激素乙炔雌二醇结合使用。 | |||
T4840 |
3-Hydroxybenzoic acid
|
Others; Endogenous Metabolite | Metabolism; Others |
3-Hydroxybenzoic acid 是内源性代谢产物的一种。 | |||
T74862 |
N-Lactoyl-Phenylalanine
N-Lactoylphenylalanine |
Endogenous Metabolite | Metabolism |
N-Lactoyl-Phenylalanine (Lac-Phe) 是一种乳酸和苯丙氨酸的肽偶联物,是急性运动中代谢物之一,可用于研究肥胖和代谢相关疾病。 | |||
T6520 |
Grape Seed Extract
Grape Seed P.E.,葡萄籽提取物 |
Apoptosis; Others | Apoptosis; Others |
Grape Seed Extract (Grape Seed P.E.) 是葡萄植物 Vitis vinifera 的种子分泌物,能诱导人类结肠直肠癌细胞凋亡,具有抗炎和抗增殖作用。它对脂肪代谢酶、胰脂肪酶和脂蛋白脂肪酶有抑制作用。 | |||
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。 | |||
T5285 |
3-(Methylthio)propionic acid
3-Methylthiopropionate,3-甲基硫代丙酸,4-Thiapentanoic acid,3-Methylsulfanylpropionic acid |
Others; Endogenous Metabolite; Antifungal | Metabolism; Microbiology/Virology; Others |
3-(Methylthio)propionic acid (4-Thiapentanoic acid) 是methionine 的代谢物,是中间体。 | |||
T3665 |
Tectoridin
射干苷,Shekanin |
Estrogen Receptor/ERR; Reductase | Endocrinology/Hormones; Metabolism |
Tectoridin (Shekanin) 是分离自 Maackia amurensis 中的异黄酮,是一种植物雌激素,能够激活雌激素和甲状腺激素受体。它通过 ER 依赖性基因组途径和 GPR30 依赖性非基因组途径发挥雌激素作用。 | |||
T3S1227 |
Aristolactam I
Aristolactam,Aristololactam I,马兜铃内酰胺I,Aristololactum |
Apoptosis; Caspase | Apoptosis; Proteases/Proteasome |
Aristolactam I (Aristololactum) 是马兜铃酸 I (AA-I) 的主要代谢产物,参与导致肾损伤的过程。它具有细胞毒性,通过诱导半胱天冬酶 3 依赖性途径中的细胞凋亡介导。 | |||
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。 | |||
T5294 |
(S)-Leucic acid
L-alpha-羟基异己酸,L-LEUCIC ACID,Hydroxyisocaproic acid,(S)-2-羟基-4-甲基戊酸,(S)-(−)-2-Hydroxyisocaproic acid |
Others; Endogenous Metabolite | Metabolism; Others |
(S)-Leucic acid (Hydroxyisocaproic acid) 是氨基酸代谢物。 | |||
T13265 |
Urolithin B
尿石素B,3-羟基-6H-苯并[C]苯并吡喃-6-酮 |
ERK; NF-κB; Akt; Endogenous Metabolite; JNK; AMPK | Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK; Metabolism; NF-κB; PI3K/Akt/mTOR signaling |
Urolithin B 是一种 ellagitannins 的肠道微生物代谢产物,具有抗炎和抗氧化作用。它也是骨骼肌质量的调节因子,通过减少 IκBα 的磷酸化和降解来抑制 NF-κB 活性,并抑制 JNK、ERK 和 Akt 的磷酸化,并增强 AMPK 的磷酸化。 | |||
T3578 |
Pyridoxal phosphate
PLP,PAL-P,磷酸吡哆醛,pyridoxal 5'-phosphate,Pyridoxyl phosphate,Pyridoxal 5′-phosphate,Vitamin B6 phosphate |
Reverse Transcriptase; Endogenous Metabolite | Metabolism; Microbiology/Virology |
Pyridoxal phosphate (Vitamin B6 phosphate) 是维生素 B6 的活性形式,可抑制逆转录酶活性,用于研究迟发性运动障碍症。 | |||
T38373 |
2-heptyl-3-hydroxy-4(1H)-Quinolone
2-heptyl-3-hydroxy-4(1H)-Quinolone,PQS,Pseudomonas Quinolone Signal |
Others | Others |
2-heptyl-3-hydroxy-4(1H)-Quinolone (Pseudomonas Quinolone Signal) 是一种铜绿假单胞菌为应对细胞密度增加而产生的一种法定人数感应信号分子。 它增加了铜绿假单胞菌中lasB 基因的表达,增加代谢物焦蓝蛋白和凝集素PA-IL 的分泌,以及增加铜绿假单胞菌种群的生物膜生产。当使用浓度为40 μM 时,它还会降低铜绿假单胞菌生长介质中的铁含量,并在硫酸铁溶液中充当一种铁螯合剂。 | |||
T4838 |
(S)-Malic acid
L-(-)-Malic acid,(S)-(-)-HYDROXYSUCCINIC ACID,(S)-2-Hydroxysuccinic acid,L-苹果酸 |
Others; Endogenous Metabolite | Metabolism; Others |
(S)-Malic acid ((S)-2-Hydroxysuccinic acid) 是天然存在的二羧酸,是水果酸甜味的来源,常用作食品添加剂。 | |||
T14031 |
3-Hydroxyhippuric acid
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Others | Others |
3-Hydroxyhippuric acid is an acyl glycine, which are normally minor metabolites of fatty acids. | |||
TN5376 |
Axinysone B
(-)-Axinysone B |
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Axinysone B is a natiral product from the metabolites of the mushroom Anthracophyllum sp. BCC18695. | |||
TN5600 |
Paniculoside III
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Paniculoside III is a natural product from the metabolites of the algicolous fungus Stevia paniculata. | |||
TN5788 |
Phyllostine
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Phyllostine appears to be their more immediate precursor, since PCMB-treated extracts of J2 converted Phyllostine but not isoepoxydon to these new metabolites. | |||
TN2801 |
20-Hydroxyaflavinine
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Others | Others |
20-Hydroxyaflavinine is a natural product from the metabolites of the ascomycete fungus Tricladium sp. | |||
TN2679 |
2,2-Dimethyl-6-phenylpyrano[3,4-b]pyran-8-one
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Others | Others |
2,2-Dimethyl-6-phenylpyrano[3,4-b]pyran-8-one is a natural product from the metabolites of Hypericum revolutum ssp. | |||
T9456 |
4-Methoxy 17β-Estradiol
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Others | Others |
4-Methoxy 17β-Estradiol 是雌激素代谢物之一,也是 4-羟基雌二醇的甲基化代谢物。 | |||
TN5278 | Zederone | NADPH-oxidase; P450; TNF; Nrf2; Antifection | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology |
Zederone has anti-bacterial activity,it inhibits gram-positive bacteria activity. Zederone induces hepatotoxicity implicated the induction of Cyps, which leads to the formation of biological reactive metabolites and that cause the oxidative stress and liver cell injuries. | |||
TN3878 |
dl-Aloesol
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Others | Others |
dl-Aloesol is a natural product from the secondary metabolites of endophytic fungus HCCB06030. | |||
TN3890 |
Drechslerine A
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Others | Others |
Drechslerine A is a natural product from the metabolites of the algicolous fungus Drechslera dematioidea. | |||
T83138 |
Aloinoside A
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Aloinoside A,一种可自黄芪分离的芦荟素,为Aloinoside B的对映异构体,应用于代谢研究的生物标志物。其通过大鼠肠道细菌代谢生成物包括芦荟苷、异芦荟苷及羟基代谢物。 | |||
T73607 | UDP-xylose | ||
UDP-xylose是一种从Cryptococcus laurentii(NRRL Y-1401)提取的天然产物。它作为糖供体,在植物、脊椎动物和真菌中参与糖蛋白、多糖及多种代谢物和寡糖的合成。 | |||
T75621 | Secalonic acid D | ||
Secalonic acid D 是一种抗肿瘤细胞的有毒化合物。Secalonic acid D 可以从Aspergillus aculeatus 的代谢产物中分离得到。Secalonic acid D 激活GSK3-β,并降解β-catenin。因此,Secalonic acid D 下调c-Myc 表达,使细胞周期停滞在 G1 期,诱导细胞凋亡 (apoptosis)。 | |||
T36438 |
Sporogen-AO 1
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Sporogen-AO 1 is a fungal metabolite originally isolated fromA. oryzaethat has diverse biological activities.1,2,3,4,5It inhibits HIV-1 Tat transactivation in a cell-based assay with an IC50value of 15.8 μM.4Sporogen-AO 1 is cytotoxic to HeLa, KB, and NCI H187 cancer cells (IC50s = 8.3, 9, and 5.1 μM, respectively).2,5It is active againstC. albicans(MIC = 4 mM).3 1.Tanaka, S., Wada, K., Marumo, S., et al.Structure of sporogen-ao 1, a sporogenic substance of Aspergillus oryzaeTetrahedron Lett.25(... | |||
T35761 |
Carviolin
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Carviolin is an anthraquinone fungal metabolite that has been found inZ. longicaudatawith immunosuppressive and antitrypanosomal activities.1,2It inhibits LPS- or concanavalin A-induced proliferation of mouse splenocytes (IC50s = 4 and 4.5 μg/ml, respectively).1Carviolin is active againstT. b. brucei(MIC = 41.66 μM).2 1.Fujimoto, H., Nakamura, E., Okuyama, E., et al.Six immunosuppressive features from an ascomycete, Zopfiella longicaudata, found in a screening study monitored by immunomodulatory... | |||
T37609 |
(rel)-Asperparaline A
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Aspergillimide is a fungal metabolite originally isolated from A. japonicus.1 It reduces nicotinic acetylcholine receptor (nAChR) peak and slowly-desensitizing amplitudes induced by acetylcholine in silkworm (B. mori) larval neurons (IC50s = 20.2 and 39.6 nM, respectively) but has no effect on chicken α3β4-, α4β2-, and α7-containing nAChRs.2 Dietary administration of aspergillimide A (10 μg/g of diet) induces paralysis in silkworm fourth instar larvae.1 Aspergillimide A (10 and 20 mg/kg) reduces... | |||
T35750 |
Trypacidin
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Trypacidin is a fungal metabolite originally isolated fromA. fumigatus.1It is active againstB. subtilisandM. bovis(MICs = 12.5 and 1.25 μg/ml, respectively), as well asT. cruziandT. gondii(MICs = 5-10 and 10-20 μg/ml, respectively).1,2It reduces viability and induces lysis of A549 human lung cancer cells (IC50s = 7.4 μM for both).3Trypacidin increases survival in a mouse model ofT. gondiiinfection when administered in six doses of 12.5 mg/kg each.1 1.Balan, J., Ebringer, L., Nemec, P., et al.Ant... | |||
T36000 |
3-Hydroxyterphenyllin
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3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,3,4 It has a 96% scavenging effect on 2,2-diphenyl-1-picrylhydrazyl radicals when used at a concentration of 100 μg/ml.2 3-Hydroxyterphenyllin inhibits the growth of HeLa cervical, A549 lung, and HepG2 liver cancer cells (IC50s = 23, 36, and 32 μM, respectively), as well as methi... | |||
T35779 |
Oosporein
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Oosporein is a mycotoxin that has been found inBeauveriaand has diverse biological activities.1,2It is cytotoxic to Sf9 and Sf21 insect cells with 50% cytotoxic concentration (CC50) values of 4.23 and 10.43 μM, respectively.3Oosporin induces lethality in day-old cockerels (LD50= 6.12 mg/kg).4It inhibits Na+/K+-, Ca2+-, and Mg2+-ATPase activities by 27, 52, and 100%, respectively, in equine erythrocyte ghosts when used at a concentration of 200 μg/ml.2Oosporein inhibits herpes simplex 1 (HSV-1), ... |