1257
135
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1254 |
[Met5]-Enkephalin, amide TFA
5-Methionine-enkephalin amide (TFA) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
[Met5]-Enkephalin, amide TFA (5-Methionine-enkephalin amide (TFA)) (60117-17-1 free base) 是一种 δ 阿片受体激动剂以及推定的 ζ (zeta) opioid 受体。 | |||
TP1113L |
[Leu5]-Enkephalin, amide acetate
[Leu5]-Enkephalin, amide acetate(60117-24-0 free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
[Leu5]-Enkephalin, amide acetate 是一种 δ 阿片受体激动剂。 | |||
T21983L |
PKI 14-22 amide, myristoylated Acetate
PKI 14-22 amide, myristoylated Acetate(201422-03-9 Free base) |
PKA | Tyrosine Kinase/Adaptors |
PKI 14-22 amide, myristoylated Acetate 抑制 cAMP 依赖性蛋白激酶 (PKA) 并阻断脊髓给药 8-溴-cAMP 产生的痛觉过敏。 | |||
TP1378 |
2-Furoyl-LIGRLO-amide TFA(729589-58-6 free base)
2-Furoyl-LIGRLO-amide |
Protease-activated Receptor | GPCR/G Protein |
2-Furoyl-LIGRLO-amide TFA(729589-58-6 free base) 是一种有效的选择性蛋白酶激活受体 2 (PAR2) 激动剂。 | |||
TP1002L |
γ-1-MSH, amide acetate (72629-65-3 free base)
γ-1-MSH, amide acetate |
Others | Others |
γ-1-MSH, amide acetate (72629-65-3 free base) 是 ACTH/β-内啡肽 (β-EP) 前体蛋白 N 末端区域的一种推定激素,RIA 使用抗 γ-3-MSH 抗血清对产生 ACTH 的小鼠进行了研究垂体肿瘤细胞,AtT-20/D16v。 | |||
TP2446L |
Angiotensin amide acetate
血管紧张素胺,Angiotensin amide acetate(53-73-6 Free base) |
Others | Others |
Angiotensin amide acetate 是Angiotensin amide 的衍生物。Angiotensin amide 是一种八肽酰胺,可以通过血管收缩来提高血压。 | |||
TP1858L |
Phe-Met-Arg-Phe, amide acetate
Phe-Met-Arg-Phe, amide acetate(64190-70-1 freebase) |
Potassium Channel | Membrane transporter/Ion channel |
Phe-Met-Arg-Phe, amide acetate(64190-70-1 freebase) 剂量依赖性 (ED50=23 nM) 激活肽能尾背神经元中的 K+ 电流。这种肽似乎在大脑的某些区域与神经肽 Y 一起定位。 | |||
T0643 |
Diclofenac Amide
|
Others | Others |
Diclofenac Amide 用作Diclofenac 的中间体。 | |||
T37891L |
GLP-1(32-36)amide acetate
GLP-1(32-36)amide 醋酸盐,GLP-1(32-36)amide acetate(1417302-71-6 Free base) |
Others | Others |
GLP-1(32-36)amide acetate 是一种五肽,衍生自糖调节激素 GLP-1 的 C 末端。GLP-1(32-36)amide acetate 可抑制糖尿病小鼠的体重增加并调节全身葡萄糖代谢。 | |||
T38852L |
TRAP-6 amide acetate
|
Protease-activated Receptor | GPCR/G Protein |
TRAP-6 amide acetate 是一种 PAR-1 凝血酶受体激动剂肽。 | |||
T37890L |
GLP-1(28-36)amide acetate
GLP-1(28-36)amide acetate(1225021-13-5 Free base) |
Antioxidant; Glucagon Receptor | GPCR/G Protein; oxidation-reduction |
GLP-1(28-36)amide acetate 抑制线粒体通透性转变,具有抗氧化、抗糖尿病和心脏保护活性。 | |||
T75888 |
PKA Inhibitor Fragment (6-22) amide TFA
PKI-(6-22)-amide TFA,PKA Inhibitor Fragment (6-22) amide TFA(121932-06-7 Free base) |
PKA | Tyrosine Kinase/Adaptors |
PKA Inhibitor Fragment (6-22) amide TFA (PKA Inhibitor Fragment (6-22) amide TFA) 是抑制高效 cAMP 依赖性蛋白激酶 A (PKA)抑制剂(Ki:2.8 nM)。PKA Inhibitor Fragment (6-22) amide TFA 可逆转小鼠低水平的吗啡缓解疼痛的作用。 | |||
TP1793L |
Nociceptin (1-13) amide TFA
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Nociceptin (1-13) amide TFA (178064-02-3 free base) 是一种有效的 Opioid receptor-like1 (ORL1) receptor 激动剂,对小鼠输精管的 pEC50 为 7.9,与大鼠前脑膜结合的 Ki 为 0.75 nM。 | |||
T21674L |
PKA inhibitor fragment (6-22) amide Acetate
PKA inhibitor fragment (6-22) amide Acetate(121932-06-7 Free base) |
PKA | Tyrosine Kinase/Adaptors |
PKA inhibitor fragment (6-22) amide Acetate 是一种通过结合底物位点选择性抑制PKA 活性的合成肽(IC50 < 2 nM)。 | |||
T9417L |
gamma-preprotachykinin amide (72-92) acetate
gamma-preprotachykinin amide (72-92) acetate (114882-65-4 Free base) |
Others | Others |
gamma-preprotachykinin amide (72-92) acetate 是一种 21 个氨基酸的肽,属于速激肽 (TK) 家族,在其 C 末端序列中包括神经激肽 A (NKA)。它对中枢 NK-2 受体的亲和力高于 NKA;它对 NK-1 受体的亲和力较低,但是,它有效地刺激唾液分泌,这是由 NK-1 受体激活介导的。 | |||
T38063 |
N-Acetyl lysyltyrosylcysteine amide
|
Glutathione Peroxidase | Metabolism |
N-Acetyl lysyltyrosylcysteine amide 是一种无毒的髓过氧化物酶 (MPO) 三肽抑制剂,具有有效性,可逆性和特异性。N-Acetyl lysyltyrosylcysteine amide 在体内可有效抑制 MPO 产生。N-Acetyl lysyltyrosylcysteine amide 减轻中风后大脑的神经元损伤,并保留脑组织和神经功能。N-Acetyl lysyltyrosylcysteine amide 抑制MPO依赖性次氯酸 (HOCl) 的生成,蛋白质硝化和 LDL 氧化。N-Acetyl lysyltyrosylcysteine amide 可用于研究支气管发育不良。 | |||
T5518 |
N-acetylcysteine amide
|
Reactive Oxygen Species; ROS | Immunology/Inflammation; Metabolism; NF-κB |
N-Acetylcysteine amide 是一种硫醇抗氧化剂,也是一种神经保护剂,能够透过细胞膜和血脑屏障的,可降低ROS 的产生。 | |||
T37588L |
GIP (1-30) amide, porcine acetate
|
IGF-1R | Tyrosine Kinase/Adaptors |
GIP (1-30) amide, porcine acetate 是完全葡萄糖依赖性促胰岛素多肽 (GIP) 受体的激动剂。它可弱抑制胃酸分泌,强烈刺激胰岛素。 | |||
TP2252 |
GLP-1 (9-36) amide
|
Glucagon Receptor | GPCR/G Protein |
GLP-1(9-36)amide 是胰高血糖素样肽-1 (7-36) amide 的主要代谢产物,对人胰腺 GLP-1受体具有拮抗作用。 | |||
TP1140L |
Neuropeptide Y (29-64), amide, human acetate
|
Neuropeptide Y Receptor | GPCR/G Protein; Neuroscience |
Neuropeptide Y (29-64), amide, human acetate 参与阿尔茨海默病 (AD) 并保护大鼠皮质神经元免受 β-淀粉样蛋白毒性。 | |||
TP2212L |
a-MSH, amide Acetate(581-05-5 free base)
|
Melanocortin Receptor | GPCR/G Protein; Neuroscience |
a-MSH, amide Acetate(581-05-5 free base) 是一种内源性黑皮质素受体 4 (MC4R) 激动剂,具有抗炎和解热活性。 α-MSH 是阿片黑皮质素原 (POMC) 的翻译后衍生物。 | |||
TP1250L |
Acetyl-PHF6 amide acetate(878663-43-5 freebase)
AcPHF6 acetate,Ac-VQIVYK-NH2 acetate |
Others | Others |
Acetyl-PHF6 amide acetate(878663-43-5 freebase) (AcPHF6 acetate) 是一种 tau 衍生的六肽。 | |||
TP1065 |
PAR-4 Agonist Peptide, amide TFA
PAR-4-AP (TFA),AY-NH2 (TFA) |
Protease-activated Receptor | GPCR/G Protein |
PAR-4 Agonist Peptide, amide TFA (PAR-4-AP (TFA)) 是一种蛋白酶激活受体 4 (PAR-4) 激动剂,对 PAR-1 或 PAR-2 均无影响,其作用可被 PAR-4 拮抗剂阻断。 | |||
T17580 |
Biotin-PEG4-Amide-C6-Azide
生物素-四聚乙二醇-氨基-C6-叠氮 |
Others; PROTAC Linker | Others; PROTAC |
Biotin-PEG4-Amide-C6-Azide 是一种属于 PEG 类的 PROTAC linker,可用于 PROTAC 分子的合成。 | |||
T7513 |
Protease-Activated Receptor-2, amide
蛋白酶活化的受体-2,酰胺,SLIGKV-NH2,H-丝氨酰亮氨酰异亮氨酰甘氨酰赖氨酰缬氨酰NH2 |
Protease-activated Receptor | GPCR/G Protein |
Protease-Activated Receptor-2, amide (SLIGKV-NH2) 是 PAR2 的激动剂,IC50为 10.4 M。 | |||
T35326 |
Labetalone hydrochloride
Labetalone hydrochloride,Benzoic amide |
Others | Others |
Labetalone hydrochloride (Benzoic amide) 是 Labetalol 的一种杂质。Labetalol 是一种口服有效的肾上腺素能受体阻断药物,对 α 和 β 受体部位都有竞争性拮抗作用。 | |||
TP1183 |
Amylin, amide, human
DAP amide, human |
||
Amylin, a 37-amino acid polypeptide that is structurally related to calcitonin, is secreted from the B cells of the pancreas. Amylin has anoretic effects in rats. Amylin may be responsible for the etiology of insulin resistance of type II diabetes mellitu | |||
T25474 |
GW-Amide
Glycyl-tryptophanamide,GW Amide |
||
GW-Amide is a molluscan neuropeptide that exhibits potent modulatory effects on molluscan muscles. | |||
T35471 |
A 410099.1 amide-PEG3-amine
A 410099.1 amide-PEG3-amine |
||
Functionalized IAP ligand for PROTAC research and development; incorporates an IAP ligand plus a short amide-PEG linker with terminal amine ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
T35473 |
A 410099.1 amide-PEG5-amine
A 410099.1 amide-PEG5-amine |
||
Functionalized IAP ligand for PROTAC research and development; incorporates an IAP ligand plus an amide-PEG5 linker with terminal amine ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
T9691L |
(D-Trp12,Tyr34)-pTH (7-34) amide (bovine) acetate
|
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
(D-Trp12,Tyr34)-pTH (7-34) amide (bovine) acetate 是一种高效的甲状旁腺激素 (PTH) 拮抗剂,在牛肾皮质膜中的 Ki 值为 69 nM。 | |||
TP1255 |
[Met5]-Enkephalin, amide
5-Methionine-enkephalin amide |
||
[Met5]-Enkephalin, amide is an agonist for δ opioid receptors as well as putative ζ (zeta) opioid receptors.Met-enkephalin circulates in several forms, some of which may be derived from proteins other than proenkephalin A, and plasma levels of both free n | |||
T36277 |
VH 032 amide-alkylC2-acid
VH 032 amide-alkylC2-acid |
||
Functionalized von-Hippel-Lindau protein ligand (VHL) for PROTAC research and development; incorporates an E3 ligase ligand plus alkylC2 linker with terminal carboxylic acid ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
T36278 |
VH 032 amide-alkylC3-acid
VH 032 amide-alkylC3-acid |
||
Functionalized von-Hippel-Lindau protein ligand (VHL) for research and development; incorporates an E3 ligase ligand plus alkylC3 linker with terminal carboxylic acid ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules. | |||
T35469 |
A 410099.1 amide-alkylC4-amine
A 410099.1 amide-alkylC4-amine |
||
Functionalized IAP ligand for PROTAC research and development; incorporates an IAP ligand plus an amide-alkylC4 linker with terminal amine ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
T37618 |
Leukotriene B4 dimethyl amide
Leukotriene B4 dimethyl amide |
||
LTB4 dimethyl amide is a moderate inhibitor of LTB4-induced degranulation of human neutrophils (Ki = 130 nM) and lysozyme release from rat PMNL. LTB4 dimethyl amide appears to be an antagonist of the LTB4 receptor on guinea pig lung membranes. | |||
T38784 |
Histone H3 (1-25), amide
Histone H3 (1-25), amide |
||
Histone H3 (1-25), amide is a N-terminal peptide fragment of histone H3 that serves as a substrate for histone methyltransferases (HMTs). It can be utilized to identify the substrate for HMTs. Compared to histone H3 (15-39) and full-length histone H3, Histone H3 (1-25), amide proves to be more efficient as a substrate for HMT G9a. | |||
T7813 |
α-MSH
MSH, amide,CZEN-002,美拉诺坦,α-Melanocyte-Stimulating Hormone (MSH), amide |
Melanocortin Receptor; Adenylyl cyclase | GPCR/G Protein; Neuroscience |
α-MSH (MSH, amide) 是一种内源性神经肽,是一种内源性黑皮质素受体 4 (MC4R) 激动剂,具有抗炎和解热活性。 | |||
T38999 |
Biotin-C4-amide-C5-NH2
Biotin-C4-amide-C5-NH2 |
||
Biotin-C4-amide-C5-NH2 is a cleavable linker employed for the synthesis of antibody-drug conjugates (ADCs). | |||
T36282 |
VH 032 amide-alkylC7-amine
VH 032 amide-alkylC7-amine |
||
Functionalized von-Hippel-Lindau protein ligand (VHL) for PROTAC research and development; incorporates an E3 ligase ligand plus an alkyl linker ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
T36266 |
VH 032 amide-PEG3-amine
VH 032 amide-PEG3-amine |
||
Functionalized von-Hippel-Lindau protein ligand (VHL) for PROTAC research and development; incorporates an E3 ligase ligand plus a PEG linker ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. This product has been recently renamed. The previous name for this product was VH 032 - linker 1 PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
T36283 |
VH 032 amide-alkylC8-acid
VH 032 amide-alkylC8-acid |
||
Functionalized von-Hippel-Lindau protein ligand (VHL) for PROTAC research and development; incorporates an E3 ligase ligand plus alkylC8 linker with terminal carboxylic acid ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
TP1024 |
Rusalatide acetate (497221-38-2 free base)
Rusalatide acetate,TP508 amide acetate |
Others | Others |
Rusalatide acetate (TP508 amide acetate) 是一种再生肽,可诱导干细胞再生修复,保护隐窝完整性,减缓辐照引起的胃肠道损伤。 | |||
T38756 |
Thiol-C10-amide-PEG8
Thiol-C10-amide-PEG8 |
||
Thiol-C10-amide-PEG8 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. | |||
T36267 |
VH 032 amide-PEG4-amine
VH 032 amide-PEG4-amine |
||
Functionalized von-Hippel-Lindau protein ligand (VHL) for PROTAC research and development; incorporates an E3 ligase ligand plus a PEG linker ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. This product has been recently renamed. The previous name for this product was VH 032 - linker 2 PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
T36280 |
VH 032 amide-alkylC4-acid
VH 032 amide-alkylC4-acid |
||
Functionalized von-Hippel-Lindau protein ligand (VHL) for PROTAC research and development; incorporates an E3 ligase ligand plus alkylC4 linker with terminal carboxylic acid ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. This product has been recently renamed. The previous name for this product was VH 032 - linker 5 PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
T36285 |
VH 032 amide-PEG1-acid
VH 032 amide-PEG1-acid |
||
Functionalized von-Hippel-Lindau (VHL) protein ligand for PROTAC research and development; incorporates an E3 ligase ligand plus a PEG1 linker with terminal carboxylic acid ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. | |||
T0823 |
Thioctamide
Lipoamide,Thioctic acid amide,硫辛酰胺 |
Others | Others |
Thioctamide (Thioctic acid amide) 是 6, 8-dithiooctanoic amide 的俗称。它是 6, 8-dithiooctanoic amide 的功能形式,其中羧基通过酰胺键(包含 -NH2)与蛋白质(或任何其他胺)连接。 | |||
T39900 |
Thalidomide-O-amide-C5-NH2
Thalidomide-O-amide-C5-NH2 |
||
Thalidomide-O-amide-C5-NH2 is a chemically synthesized conjugate, serving as an E3 ligase ligand-linker, which combines a cereblon ligand derived from Thalidomide with a linker that is commonly employed in PROTAC technology. | |||
T35470 |
A 410099.1 amide-PEG2-amine
A 410099.1 amide-PEG2-amine |
||
Functionalized IAP ligand for PROTAC research and development; incorporates an IAP ligand plus a short amide-PEG linker with terminal amine ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1232L |
Amylin, amide, rat acetate(124447-81-0,free base)
|
Amylin Receptor | GPCR/G Protein |
Amylin, amide, rat acetate(124447-81-0,free base) 是 AMY1 和 AMY3 受体以及 AMY2 受体的强效和高亲和力配体。 | |||
T13802 |
Oleamide
Oleic acid amide |
Others; Endogenous Metabolite | Metabolism; Others |
Oleamide (Oleic acid amide) 是一种内源性脂肪酸酰胺,可用于哺乳动物神经系统的从头合成。 | |||
T7445 |
Acetamide
ethanamide,乙酰胺,Acetic acid amide |
Endogenous Metabolite | Metabolism |
Acetamide (ethanamide) 是一种合成甲胺,是硫代乙酰胺和杀虫剂中间体。它可用作皮革、布料、涂料中的增塑剂。它具有致癌作用。 | |||
T22455 |
Vindesine sulfate
DVA,Desacetylvinblastine amide,硫酸长春地辛,DAVA,Desacetyl Vinblastine amide,VDS |
Others | Others |
Vindesine sulfate (Desacetyl Vinblastine amide) 是一种长春花生物碱,它是长春碱的合成衍生物,与有丝分裂纺锤体的微管蛋白结合,导致微管结晶和有丝分裂停滞或细胞死亡。 | |||
T1426 |
Pyrazinamide
Pyrazinoic acid amide,Pyrazinecarboxamide,吡嗪酰胺 |
Antibacterial; Antibiotic; Autophagy; Fatty Acid Synthase | Autophagy; Metabolism; Microbiology/Virology |
Pyrazinamide (Pyrazinecarboxamide) 是一种口服抗结核类抗生素。它是一种前药,通过结核分枝杆菌pncA 基因编码的 PZase/烟酰胺酶转化为活性吡嗪酸形式。 | |||
T20091 |
Stearamide
Stearic acid amide,NSC 66462,NSC66462,NSC-66462 |
||
Stearamide(Stearic acid amide)是一种初级脂肪酸酰胺,具有细胞毒性和鱼类毒性,可用于增加纳米颗粒的性能。 | |||
T0326L |
L-Glutamine
L-Glutamic acid 5-amide,L-谷氨酰胺 |
Ferroptosis; Endogenous Metabolite; GluR | Apoptosis; Metabolism; Neuroscience |
L-Glutamine (L-Glutamic acid 5-amide) 是在人体中大量存在的一种非必需氨基酸,由谷氨酸和氨合成。它为某些细胞中的氧化提供了碳源。 | |||
T39007 |
3,4-Dimethoxybenzamide
|
Others | Others |
3,4-Dimethoxybenzamide 是分离自Streptoverticillium morookaense 固体培养物的酰胺。它是制备盐酸伊托必利的起始原料。 | |||
TN2085 |
Piperlonguminine
|
Anti-infection; Antibacterial; Antifungal | Microbiology/Virology |
Piperlonguminine 是一种从 Piper 中分离出的生物碱酰胺。它具有多种生物活性,如神经保护、抗炎、抗肿瘤、抗血小板、抗黑素生成、抗真菌和抗菌活性。 | |||
TN1965 |
N-Benzyllinolenamide
N-苄基-(9Z,12Z,15Z)-十八碳三烯酰胺,N-Benzyllinolenamide |
FAAH; Autophagy | Autophagy; Metabolism; Neuroscience |
N-Benzyllinolenamide 是从玛卡中得到的一种生物碱,是脂肪酰胺水解酶抑制剂,IC50 为 41.8 μM。 | |||
T2859 |
Biochanin A
4-Methylgenistein,鹰嘴豆芽素A,Olmelin |
EGFR; FAAH; Autophagy | Angiogenesis; Autophagy; JAK/STAT signaling; Metabolism; Neuroscience; Tyrosine Kinase/Adaptors |
Biochanin A (4-Methylgenistein) 是一种从红三叶车轴草中分离出来的异黄酮衍生物,具有抗癌特性。它是脂肪酸酰胺水解酶抑制剂,作用于小鼠、大鼠和人 FAAH,IC50分别为 1.8、1.4 和 2.4 μM。 | |||
T12139 |
N-(3-Methoxybenzyl)Palmitamide
N-(3-甲氧基苄基)十六碳酰胺,玛卡酰胺杂质5 |
FAAH | Metabolism; Neuroscience |
N-(3-Methoxybenzyl)Palmitamide 是FAAH 抑制剂,可用于研究疼痛,炎症和中枢神经系统退行性疾病。 | |||
T3S2105 |
N-Benzylpalmitamide
Macamide 1,玛卡酰胺 B,N-苄基十六烷酰胺,N-Benzylhexadecanamide |
Others; FAAH; Autophagy | Autophagy; Metabolism; Neuroscience; Others |
N-Benzylpalmitamide (Macamide 1) 是从玛卡中得到的一种生物碱,可以时间依赖性方式抑制脂肪酸酰胺水解酶,有治疗疼痛、炎症和中枢神经系统退行性疾病的研究潜力。 | |||
T4859 |
1-Monomyristin
rac-Glycerol 1-myristate,Glyceryl myristate,1-肉豆蔻酸单甘油酯,肉豆寇酸单甘油酯,Monomyristin,2,3-Dihydroxypropyl tetradecanoate |
Others; FAAH; Endogenous Metabolite; Antibacterial; Autophagy; Antifungal | Autophagy; Metabolism; Microbiology/Virology; Neuroscience; Others |
1-Monomyristin (2,3-Dihydroxypropyl tetradecanoate) 是从 Serenoa repens 中提取的,抑制脂肪酸酰胺水解酶活性(IC50=18 μM) 和 2-油酰甘油的水解 (IC50=32 μM)。它对白色念珠菌有抗真菌活性,对金黄色葡萄球菌和聚集性放线菌有抗菌活性。 | |||
T1321 |
Nonivamide
Nonanoic acid vanillylamide,Pelargonic acid vanillylamide,辣椒素,Vanillyl-N-nonylamide,Pseudocapsaicin |
TRP/TRPV Channel | Membrane transporter/Ion channel |
Nonivamide (Nonanoic acid vanillylamide) 具有激动活性,在静态毒性检测中,4d-EC50为 5.1 mg/L。 | |||
T6926 |
Palmitoylethanolamide
Mackpeart DR 14V,帕米醇,N-palmitoylethanolamine,Loramine P 256,Impulsin,AM 3112,Palmidrol |
Influenza Virus; Endogenous Metabolite; PPAR | DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Palmitoylethanolamide (Impulsin) 是一种内源性脂肪酸酰胺。它有消炎药、降压药、神经保护剂和抗惊厥药的作用。在给药后,Palmitoylethanolamide 可抑制促炎介质从活化肥大细胞的释放。 | |||
TN4171 |
Grossamide
|
NO Synthase | Immunology/Inflammation |
Grossamide (GSE) 是一种来自虎杖的木脂酰胺。Grossamide 具有抗炎症活性,可通过上调精氨酸酶和下调诱导型一氧化氮合酶来抑制精氨酸产生一氧化氮(NO),抑制NO对OXPHOS的抑制作用。 | |||
T4834 |
Indole-3-acetamide
3-Indoleacetamide,3-Indolylacetamide,3-吲哚乙酰胺 |
Others; Endogenous Metabolite | Metabolism; Others |
Indole-3-acetamide (3-Indolylacetamide) 是一种 indole-3-acetic acid 的生物合成中间体。其中 Indole-3-acetic acid 是植物生长素类中最常见的天然植物生长激素。 | |||
T8150 |
Nudifloramide
1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxamide,1-甲基-6-氧代吡啶-3-甲酰胺 |
PARP; Endogenous Metabolite | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Nudifloramide (1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxamide) 是烟酰胺-腺嘌呤二核苷酸(NAD) 降解的一种最终产物,可显著抑制PARP-1活性。 | |||
T5222 |
N-(5-Aminopentyl)acetamide
Monoacetylcadaverine,N-(5-氨基戊基)乙酰胺,N-Acetylcadaverine,N-Acetyl-1,5-pentanediamine |
Others; Endogenous Metabolite | Metabolism; Others |
N-(5-Aminopentyl)acetamide (N-Acetylcadaverine) 是用作多胺尸胺的乙酰化形式。尸胺是有机体中的氨基酸分解产生的,大剂量时有毒。 | |||
T13903 |
Stearoylethanolamide
N-(2-Hydroxyethyl)octadecanamide |
Apoptosis | Apoptosis |
Stearoylethanolamide(N-(2-Hydroxyethyl)octadecanamide) 是一种存在于人、大鼠和小鼠大脑中的大麻素类化合物,具有促细胞凋亡活性。 | |||
T4721 |
β-Nicotinamide mononucleotide
β-NM,β烟酰胺单核苷酸,烟酰胺单核苷酸 |
Others; Endogenous Metabolite | Metabolism; Others |
β-Nicotinamide mononucleotide (β-NM) 是烟酰胺磷酸核糖转移酶 (NAMPT) 反应的产物。β-nicotinamide mononucleotide 的作用包括其在细胞生化功能、心脏保护、糖尿病、肥胖相关并发症和阿尔茨海默病中的作用。 | |||
T32614 |
L-Clausenamide
(-)-Clausenamide |
Microtubule Associated | Cytoskeletal Signaling |
L-Clausenamide 是从黄皮 (Clausena lansium (Lour) skeels) 的树叶中提取出来的生物碱,可用于提高认知功能。L-Clausenamide 对β-淀粉样蛋白 (Aβ) 毒性有抑制作用,通过抑制 tau 蛋白磷酸化阻止神经纤维缠结的形成。L-Clausenamide 具有神经保护活性,可用于调节 Aβ25-35 引发的刺激。L-Clausenamide 可用于研究阿尔兹海默症类的神经系统疾病。 | |||
TN6794 |
N-(3-methoxybenzyl)-octadecanamide
|
Others | Others |
N-(3-methoxybenzyl)-octadecanamide 从玛卡 (Lepidium meyenii Walp.) 转化而来。 | |||
T14046 |
Anandamide
花生四烯酸乙醇胺,(5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide |
Cannabinoid Receptor; Endogenous Metabolite | GPCR/G Protein; Metabolism |
Anandamide ((5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide) 是一种免疫调节剂,通过大麻素受体 CB1 和 CB2 起作用,还通过中枢神经系统中的其他靶点起作用,如 GPR18/GPR55。 | |||
T0769 |
Aceglutamide
N-乙酰-L-谷氨酰胺,N2-Acetylglutamine,α-N-Acetyl-L-glutamine,乙酰谷酰胺 |
Amino Acids and Derivatives; Endogenous Metabolite; Autophagy | Autophagy; Metabolism |
Aceglutamide (N2-Acetylglutamine) 是一种精神激活剂和促智剂,是氨基酸 L-谷氨酰胺的乙酰衍生物,用于改善记忆和集中注意力。 | |||
T14193 |
α-Galactosylceramide
KRN7000,α-GalCer |
Others | Others |
α-Galactosylceramide (KRN7000) 是一种具有抗肿瘤和免疫刺激作用的合成糖脂。它是一种高效的 NKT 细胞激动剂,可与 CD1d 有效结合。它与 CD1d 的复合物可与 NKT 细胞的 T 细胞抗原受体结合。 | |||
TN7061 |
yuanamide
|
Others | Others |
yuanamide 是一种天然化合物,属于生物碱类。 | |||
TN7157 |
(+/-)-Longamide
Pyrrolo[1,2-a]pyrazin-1(2H)-one, 6,7-dibromo-3,4-dihydro-4-hydroxy-,6,7-dibromo-4-hydroxy-3,4-dihydro-2H-pyrrolo[1,2-a]pyrazin-1-one,6,7-dibromo-4-hydroxy-1H,2H,3H,4H-pyrrolo[1,2-a]pyrazin-1-one |
Others | Others |
(+/-)-Longamide (6,7-dibromo-4-hydroxy-1H,2H,3H,4H-pyrrolo[1,2-a]pyrazin-1-one) 是一种海洋来源的天然产物,存在于Agelas flabelliformis。 | |||
T13669 |
(E)-Cinnamamide
trans-Cinnamamide,肉桂酰胺 |
Others | Others |
(E)-Cinnamamide (trans-Cinnamamide) 是 Cinnamamide 的活性较低的异构体,Cinnamamide 是一种有效的非致命化学驱虫剂,适用于减少鸟类害虫的损害。 | |||
T66582 |
6-Methylnicotinamide
|
Endogenous Metabolite | Metabolism |
6-Methylnicotinamide 是烟酰胺的衍生物,是一种内源性代谢物。在脑出血 (ICH) 急性期, 6-Methylnicotinamide 突然增加会加剧神经损伤。6-Methylnicotinamide 可用于制作共晶体/盐。 | |||
TN7036 |
N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamide
(9Z,12Z,15Z)-N-[(3-Methoxyphenyl)methyl]-9,12,15-octadecatrienamide,间-甲氧基苄基-亚麻酰胺,Macamide Impurity 14 |
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamide (Macamide Impurity 14) 是一种从玛卡中分离得到的玛卡酰胺。它能够激活典型的Wnt/β‐catenin 信号通路,诱导间充质干细胞成骨分化和随后的骨形成,可用于研究骨质疏松症。 | |||
TN1457 |
Bryonamide B
|
||
Bryonamide B 是一种可从 Bryonia aspera 中提取得到一种葫芦类三萜。 | |||
TQ0131 |
Rocaglamide
Rocaglamide A,楝酰胺,Roc-A |
HSP; NF-κB; PERK | Apoptosis; Cytoskeletal Signaling; Metabolism; NF-κB |
Rocaglamide (Roc-A) 是从米仔兰中分离出来的一种天然产物,具有抗癌特性,可用于咳嗽,受伤,哮喘和炎症性皮肤病。它是一种有效的选择性热休克因子 1 活化抑制剂,IC50约为 50 nM。它是 T 细胞中 NF-κB 活化的有效抑制剂,还抑制翻译起始因子eIF4A 的功能。 | |||
T26288 |
Clovamide
trans-Clovamide,N-trans-Caffeoy-L-dopa |
Apoptosis; Influenza Virus; ROS; Antibacterial | Apoptosis; Immunology/Inflammation; Microbiology/Virology |
Clovamide (trans-Clovamide) 是一种天然存在的咖啡酰结合物,具有抗菌、抗炎、抗氧化和神经保护作用。它是一种极好的活性氧和氧自由基清除剂。 | |||
TN7034 |
N-benzyl-heptadecanamide
N-Benzylheptadecanamide,N-苄基十七烷酰胺 |
Others | Others |
N-benzyl-heptadecanamide (N-Benzylheptadecanamide) 是玛咖中的一种玛卡酰胺。 | |||
TN1558 |
N-Vanillyldecanamide
癸酸香草酰胺,Decylic acid vanillylamide |
Others | Others |
N-Vanillyldecanamide (Decylic acid vanillylamide) 分离自辣椒果实,以剂量依赖的方式显著减小紫花苜蓿幼苗的自由基长度。 | |||
T0004 |
Salicylamide
水杨酰胺,Salamide,2-Hydroxybenzamide |
COX | Immunology/Inflammation; Neuroscience |
Salicylamide(2-Hydroxybenzamide) 是一种止痛剂和抗热解药剂,是一种微粒体 UDP-葡糖醛酸基转移酶抑制剂。 | |||
TN1643 |
Ferulamide
4-Hydroxy-3-methoxycinnamide,阿魏酸酰胺 |
PAFR; AChR | GPCR/G Protein; Neuroscience |
Ferulamide (4-Hydroxy-3-methoxycinnamide) 是从巴豆中分离的阿魏酸衍生物,具有抗胆碱酯酶活性。 | |||
TN7126 |
N-Vanillyloctanamide
|
Others | Others |
N-Vanillyloctanamide 是一种来自 Capsicum annuum L. var. 果实的辣椒素。年鉴。 N-Vanillyloctanamide 减少 Lactuca sativa 幼苗的自由基长度,这种抑制是剂量依赖性的。 | |||
T5233 |
N-Methylnicotinamide
N'-Methylnicotinamide,Nicotinic Acid Methylamide,N-Methylpyridine-3-carboxamide,N-甲基烟酰胺 |
Others; Endogenous Metabolite | Metabolism; Others |
N-Methylnicotinamide (Nicotinic Acid Methylamide) 是内源性代谢产物的一种。 | |||
TJS2216 |
Aurantiamide acetate
金色酰胺醇酯,Asperglaucide |
Cysteine Protease | Proteases/Proteasome |
Aurantiamide acetate (Asperglaucide) 是抑制口服有活性的 cathepsin 选择性抑制剂,分离自 Portulaca oleracea L。它具有抗炎作用,可用于研究炎性相关疾病。 | |||
T6780 |
Benzamide
Amid kyseliny benzoove,苯甲酰胺,Phenylcarboxyamide,Benzoylamide |
PARP; Endogenous Metabolite | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Benzamide (Amid kyseliny benzoove) 是聚(ADP-核糖)聚合酶的抑制剂,是苯甲酸的衍生物。 | |||
T13795 |
Nicotinamide riboside
|
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Nicotinamide riboside 是维生素 B3 的来源,可以增强氧化代谢并防止高脂肪饮食诱导的代谢异常。它是具有口服活性的 NAD+的前体,增加 NAD+水平并激活SIRT1和SIRT3,可用于研究阿尔茨海默氏病的认知退化。 | |||
T5704 |
Entadamide-A-β-D-glucopyranoside
(E)-N-[2-(β-D-Glucopyranosyloxy)ethyl]-,榼藤子酰胺A-Β-D-吡喃葡萄糖苷,榼藤子酰胺A-β-D-吡喃葡萄糖 |
Others | Others |
Entadamide-A-β-D-glucopyranoside ((E)-N-[2-(β-D-Glucopyranosyloxy)ethyl]-) 是一种菜豆虫种子的主要成分,具有抗补体作用。 | |||
T1165 |
Ethionamide
Bayer 5312,乙硫异烟胺,2-ethylthioisonicotinamide,Ethinamide |
Dehydrogenase; CAT; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology; oxidation-reduction |
Ethionamide (2-ethylthioisonicotinamide) 是一种抗结核抗生素。 | |||
T6220 |
Nicotinamide riboside chloride
烟酰胺核糖氯酸盐,烟酰胺核苷 |
Sirtuin; Endogenous Metabolite | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Nicotinamide riboside Chloride 是维生素 B3 的来源,可以增强氧化代谢并防止高脂肪饮食诱导的代谢异常。它是具有口服活性的 NAD+的前体,增加 NAD+水平并激活SIRT1和SIRT3,可用于研究阿尔茨海默氏病的认知退化。 | |||
TN1352 |
N-(3-Methoxybenzyl-(9z,12z)-octadecadienamide
12顺-亚油酸酰胺,(9Z,12Z)-N-(3-Methoxybenzyl)octadeca-9,12-dienamide,n-3-methoxybenzyl-9z-12z-octadecadienamide,玛卡酰胺杂质10 |
Drug Metabolite | Metabolism |
N-(3-Methoxybenzyl-(9z,12z)-octadecadienamide ((9Z,12Z)-N-(3-Methoxybenzyl)octadeca-9,12-dienamide) 是一种 Macamide 杂质,可能用于代谢疾病的研究。 | |||
T1705 |
5-Amino-3H-imidazole-4-Carboxamide
4-Amino-5-imidazolecarboxamide,AICA,4-氨基-5-咪唑甲酰胺,5-Aminoimidazole-4-carboxamide |
Endogenous Metabolite | Metabolism |
5-Amino-3H-imidazole-4-Carboxamide (AICA) 是一种合成嘌呤(尤其是核碱基腺嘌呤和鸟嘌呤)的重要前体。 | |||
TN2298 |
Vincosamide
喜果苷 |
AChE | Neuroscience |
Vincosamide 是一种来自Psychotria leiocarpa 提取物的生物碱,具有抑制乙酰胆碱酯酶 (AChE) 作用,具有抗炎活性。 | |||
------------------------ 更多 ------------------------ |