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Cat. No. | Product Name | ||
---|---|---|---|
L7810 | 高溶解性多官能团片段化合物库 | 1159 compounds | |
高溶解性多官能团片段库包含1159 种片段分子 |
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。 | |||
TP1250L |
Acetyl-PHF6 amide acetate
Acetyl-PHF6 amide acetate(878663-43-5 free base),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。 | |||
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。 | |||
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。 | |||
T3984 |
GLP-1(7-36), amide
MKC 253,胰高血糖素样肽-1,Human GLP-1-(7-36)-amide,Glucagon-like Peptide 1 (7-36) amide,Glucagon-Like Peptide (GLP) I (7-36), amide, human,GLP-1(7-36),GLP-1-(7-36)-amide |
Glucagon Receptor | GPCR/G Protein |
GLP-1(7-36), amide (MKC 253) 是一种生理性肠降血糖素,能够刺激胰岛素分泌。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T85009 |
Betulinic glycine amide
Betulinic glycine amide |
Others | Others |
Betulinic glycine amide, a pentacyclic triterpenoid derivative of betulinic acid, serves as a precursor for synthesizing derivatives with anticancer and antiviral activity. | |||
T35326 |
Labetalone hydrochloride
Labetalone hydrochloride,Benzoic amide |
Others; Adrenergic Receptor | GPCR/G Protein; Neuroscience; Others |
Labetalone hydrochloride 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。 | |||
T25474 |
GW-Amide
Glycyl-tryptophanamide,GW Amide |
Others | Others |
GW-Amide is a molluscan neuropeptide that exhibits potent modulatory effects on molluscan muscles. | |||
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 | |||
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 | |||
T35473 |
A 410099.1 amide-PEG5-amine
A 410099.1 amide-PEG5-amine |
Others | Others |
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. | |||
T35471 |
A 410099.1 amide-PEG3-amine
A 410099.1 amide-PEG3-amine |
Others | Others |
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. | |||
T35469 |
A 410099.1 amide-alkylC4-amine
A 410099.1 amide-alkylC4-amine |
Others | Others |
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 |
Others | Others |
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. | |||
T36278 |
VH 032 amide-alkylC3-acid
VH 032 amide-alkylC3-acid |
Others | Others |
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. | |||
T36277 |
VH 032 amide-alkylC2-acid
VH 032 amide-alkylC2-acid |
Others | Others |
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. | |||
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. | |||
T36282 |
VH 032 amide-alkylC7-amine
VH 032 amide-alkylC7-amine |
Others | Others |
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. | |||
T36283 |
VH 032 amide-alkylC8-acid
VH 032 amide-alkylC8-acid |
Others | Others |
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. | |||
T36266 |
VH 032 amide-PEG3-amine
VH 032 amide-PEG3-amine |
Others | Others |
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. | |||
T38756 |
Thiol-C10-amide-PEG8
Thiol-C10-amide-PEG8 |
Others | Others |
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. | |||
T38999 |
Biotin-C4-amide-C5-NH2
Biotin-C4-amide-C5-NH2 |
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Biotin-C4-amide-C5-NH2 is a cleavable linker employed for the synthesis of antibody-drug conjugates (ADCs). | |||
T84652 |
Prostaglandin F2α ethyl amide
Dinoprost ethyl amide |
Others | Others |
Prostaglandin F2αethyl amide (PGF2α-NEt), a PGF2α analog featuring an N-ethyl amide modification at the C-1 carboxyl group, possesses ocular hypotensive activity similar to PG esters. Introduced as alternative prostaglandin ocular hypotensive prodrugs, PGF2α-NEt and other PG N-ethyl amides, contrary to claims of not converting to free acids in vivo, have been demonstrated by our laboratory studies to undergo conversion by bovine and human corneal tissue into the respective free acids at a rate o... | |||
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。 | |||
T36280 |
VH 032 amide-alkylC4-acid
VH 032 amide-alkylC4-acid |
Others | Others |
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 |
Others | Others |
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. | |||
T36267 |
VH 032 amide-PEG4-amine
VH 032 amide-PEG4-amine |
Others | Others |
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. | |||
T39900 |
Thalidomide-O-amide-C5-NH2
Thalidomide-O-amide-C5-NH2 |
Others | Others |
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. |
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。 | |||
T0934 |
Nicotinamide
Nicotinic acid amide,Vitamin B3,Niacinamide,烟酰胺,Vitamin PP |
Sirtuin; Endogenous Metabolite | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Nicotinamide 是维生素 B3 的吡啶核苷形式,可作为烟酰胺腺嘌呤二核苷酸或 NAD+ 的前体,可通过膳食摄入来补充,能预防或治疗黑舌病和糙皮病。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
TN6794 |
N-(3-methoxybenzyl)-octadecanamide
|
Others | Others |
N-(3-methoxybenzyl)-octadecanamide 从玛卡 (Lepidium meyenii Walp.) 转化而来。 | |||
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。 | |||
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 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。 | |||
T4721 |
β-Nicotinamide mononucleotide
NMN,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 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。 | |||
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。 | |||
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。 | |||
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。 | |||
TN1457 |
Bryonamide B
|
||
Bryonamide B 是一种可从 Bryonia aspera 中提取得到一种葫芦类三萜。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
TN7061 |
yuanamide
|
Others | Others |
yuanamide 是一种天然化合物,属于生物碱类。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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 是内源性代谢产物的一种,可改善内皮功能障碍。 | |||
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。 | |||
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。 | |||
TN7158 |
2-(4-methoxyphenyl)-N-methyl-2-oxoacetamide
N-Methyl-2-(4-methoxyphenyl)-2-oxoacetamide,2-(4-methoxy-phenyl)-N-methyl-2-oxo-acetamide |
Others | Others |
2-(4-methoxyphenyl)-N-methyl-2-oxoacetamide (2-(4-methoxy-phenyl)-N-methyl-2-oxo-acetamide) 是一种海洋来源的天然产物,存在于Polycarpa aurata。 | |||
TN2239 |
Strictosamide
异长春花苷内酰胺 |
ATPase; Potassium Channel; Sodium Channel; Parasite; Antifungal | Membrane transporter/Ion channel; Microbiology/Virology |
Strictosamide 具有抗炎、抗疟原虫和抗真菌活性。 | |||
T22644 |
C2 Ceramide
Ceramide |
Others | Others |
A potent modulator of cell proliferation and differentiation. | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01325 |
FAAH2 Protein, Human, Recombinant (His)
Amidase domain-containing protein,Anandamide amidoh... |
Human | E. coli |
Catalyzes the hydrolysis of endogenous amidated lipids like the sleep-inducing lipid oleamide ((9Z)-octadecenamide), the endocannabinoid anandamide (N-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-ethanolamine), as well as other fatty amides, to their corresponding fatty acids, thereby regulating the signaling functions of these molecules. Hydrolyzes monounsaturated substrate anandamide preferentially as compared to polyunsaturated substrates. FAAH2 Protein, Human, Recombinant (His) is expressed in E. coli e... | |||
TMPH-02561 |
CES1C Protein, Mouse, Recombinant (GST)
Liver carboxylesterase N,Es1,Lung surfactant convertase,Carb... |
Mouse | E. coli |
Involved in the detoxification of xenobiotics and in the activation of ester and amide prodrugs. Involved in the extracellular metabolism of lung surfactant. | |||
TMPH-02563 |
CES1C Protein, Mouse, Recombinant
Es1,PES-N,Liver carboxylesterase N,Carboxylesterase 1C,Lung ... |
Mouse | E. coli |
Involved in the detoxification of xenobiotics and in the activation of ester and amide prodrugs. Involved in the extracellular metabolism of lung surfactant. CES1C Protein, Mouse, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 58.6 kDa and the accession number is P23953. | |||
TMPH-02562 |
CES1C Protein, Mouse, Recombinant (His & Myc)
Ces1c,Liver carboxylesterase N,Es1,Lung surfactant convertas... |
Mouse | HEK293 Cells |
Involved in the detoxification of xenobiotics and in the activation of ester and amide prodrugs. Involved in the extracellular metabolism of lung surfactant. | |||
TMPY-01189 |
GFPT1 Protein, Human, Recombinant
GFAT1,CMSTA1,GFAT,glutamine--fructose-6-phosphate transamina... |
Human | E. coli |
Glutamine:fructose-6-phosphate amidotransferase 1 (GFAT), also known as GFPT1, is a member of the N-terminal nucleophile aminotransferases and the first rate-limiting enzyme for the entry of glucose into the hexosamine biosynthesis pathway (HBP) in mammals. GFAT transfers the amino group from the L-glutamine amide to the D-fructose 6-phosphate, producing glutamic acid and glucosamine 6-phosphate. GFAT exists as a homotetramer in cytoplasm, and is proposed to be most likely involved in re... | |||
TMPH-03260 |
Carboxypeptidase A1 Protein, Rat, Recombinant (His & Myc)
Cpa1,Carboxypeptidase A1,Cpa |
Rat | E. coli |
Carboxypeptidase that catalyzes the release of a C-terminal amino acid, but has little or no action with -Asp, -Glu, -Arg, -Lys or -Pro. Catalyzes the conversion of leukotriene C4 to leukotriene F4 via the hydrolysis of an amide bond. Carboxypeptidase A1 Protein, Rat, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 39.6 kDa and the accession number is P00731. | |||
TMPH-02778 |
Mcpt4 Protein, Mouse, Recombinant (E. coli, His)
MSMCP,Mast cell protease 4,Myonase,Serosal mast cell proteas... |
Mouse | E. coli |
Has chymotrypsin-like activity. Hydrolyzes the amide bonds of synthetic substrates having Tyr and Phe residues at the P1 position. Preferentially hydrolyzes the 'Tyr-4-|-Ile-5' bond of angiotensin I and the 'Phe-20-|-Ala-21' bond of amyloid beta-protein, and is less active towards the 'Phe-8-|-His-9' bond of angiotensin I and the 'Phe-4-|-Ala-5' and 'Tyr-10-|-Glu-11' bonds of amyloid beta-protein. Involved in thrombin regulation and fibronectin processing. Mcpt4 Protein, Mouse, Recombinant (E. c... | |||
TMPJ-00474 |
CPA1 Protein, Human, Recombinant (His)
CPA,Carboxypeptidase A1,CPA1 |
Human | HEK293 Cells |
Carboxypeptidase A1 (CPA1) is secreted as a pancreatic peptidase that comes from the precursor form of inactive procarboxypeptidase. CPA1 comprises a signal peptide, a pro region and a mature chain, and can be activated after cleavage of the pro peptide. It has a free C-terminal carboxyl group, with the preference of residues with aromatic or branched aliphatic side chains. CPA1 cleaves the C-terminal amide or ester bond of peptides and involves in zymogen inhibition. Three different forms of hu... | |||
TMPJ-00602 |
CPA2 Protein, Human, Recombinant (His)
CPA2,Carboxypeptidase A2 |
Human | HEK293 Cells |
Carboxypeptidase A2 (CPA) is a secreted pancreatic procarboxy-peptidase that cleaves the C-terminal amide or ester bond of peptides that have a free C-terminal carboxyl group. The hydrolytic action of CPA2 was identified with a preference towards long substrates with aromatic amino acids in their C-terminal end, particularly tryptophan. CPA2 comprises a signal peptide, a pro region and a mature chain, and can be activated after cleavage of the pro peptide. Three different forms of human pancreat... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T69395 |
Nicotinamide-d4
|
||
Nicotinamide-d4 is intended for use as an internal standard for the quantification of nicotinamide by GC- or LC-MS. Nicotinamide is an amide form of niacin, which is also known as vitamin B3, that can be biosynthesized in vivo or obtained through the diet. It is a precursor in the synthesis of the metabolic cofactor NAD+ and an inhibitor of sirtuin 1 (SIRT1; IC50 = <50 µM). Nicotinamide (10 µM) increases the activity of serine palmitoyltransferase (SPT) and the biosynthesis of ceramide, glucosyl... | |||
TMIJ-0310 |
Pyrazinamide-d3
|
||
Pyrazinamide-d3 是 Pyrazinamide 的氘代化合物。Pyrazinamide 的 CAS 号为 98-96-4。Pyrazinamide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。 | |||
T11208 |
Enzalutamide-d3
MDV3100 D3 |
Others | Others |
Enzalutamide D3 is a deuterium labeled Enzalutamide . Enzalutamide is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells. | |||
T70186 |
Methazolamide-d6
|
||
Methazolamide-d6 is intended for use as an internal standard for the quantification of methazolamide by GC- or LC-MS. Methazolamide is a carbonic anhydrase inhibitor. It reduces intraocular pressure and cerebrospinal fluid flow in a rat model of glaucoma. Methazolamide reduces electroshock-induced seizures in rats with an ED50 value of 19.2 mg/kg. It also inhibits production of reactive oxygen species (ROS) in a primary cortical neuron (PCN) cellular model of subarachnoid hemorrhage (SAH) and re... | |||
TMIJ-0240 |
Lacosamide-d3 (Acetyl-d3)
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Lacosamide-d3 (Acetyl-d3) 是 Lacosamide 的氘代化合物。Lacosamide 的 CAS 号为 175481-36-4。Lacosamide是一种功能化氨基酸。Lacosamide以一种新的方式调节钠通道:它选择性地增强钠通道缓慢失活,而对快速失活没有影响Lacosamine在不同的啮齿类动物癫痫发作模型中显示出抗癫痫作用,在反映神经性疼痛和慢性炎性疼痛的不同类型和症状的实验动物模型中显示了抗伤害潜力。 | |||
TMID-0204 |
Cyclophosphamide-d4
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Cyclophosphamide-d4 是 Cyclophosphamide 的氘代化合物。Cyclophosphamide 的 CAS 号为 50-18-0。Cyclophosphamide 是一种烷化剂,具有抗肿瘤及免疫抑制活性,用于治疗多种癌症。 | |||
TMIJ-0278 |
4,6-Dichloro-N-(methyl-d3)-3-pyridazinecarboxamide
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4,6-Dichloro-N-(methyl-d3)-3-pyridazinecarboxamide 是 4,6-Dichloro-N-(methyl)-3-pyridazinecarboxamide 的氘代化合物。4,6-Dichloro-N-(methyl)-3-pyridazinecarboxamide 的 CAS 号为 1609394-78-6。 | |||
TMIJ-0391 |
Acrylamide-2,3,3-d3
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Acrylamide-2,3,3-d3 是 Acrylamide 的氘代化合物。Acrylamide 的 CAS 号为 79-06-1。Acrylamide monomer 是丙烯酰胺类的成员。它具有致癌剂、神经毒素、诱变剂、烷化剂和美拉德反应产物的作用。 | |||
T69758 |
Flutamide-d7
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Flutamide-d7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 µM, respectively. Flutamide (50 mg/kg per day) reduces tumor growth in a PC-82 mouse xenograft mo... | |||
T36059 |
Dichlorphenamide-13C6
Dichlorphenamide-13C6 |
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Dichlorphenamide-13C6is intended for use as an internal standard for the quantification of dichlorphenamide by GC- or LC-MS. Dichlorphenamide is a sulfonamide and an orally bioavailable carbonic anhydrase (CA) inhibitor (Kis = 1.20, 38, 50, and 50 nM for the human CA isoforms CAI, CAII, CAIX, and CAXII, respectively).1It lowers intraocular pressure in rabbits when 50 μl of a 10% solution is applied topically to the eye.2Dichlorphenamide rescues the potassium deficiency and prevents insulin-induc... | |||
T10231 |
Acetazolamide-d3
醋氮酰胺 D3 |
Others | Others |
Acetazolamide D3 is a deuterium-labeled Acetazolamide. Acetazolamide is a potent carbonic anhydrase inhibitor. | |||
TMIH-0307 |
Loperamide-d6
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Loperamide-d6 是 Loperamide 的氘代化合物。Loperamide 的 CAS 号为 53179-11-6。 | |||
T19449 |
N-desmethyl Enzalutamide D6
N-desmethyl MDV 3100 D6 |
Androgen Receptor | Endocrinology/Hormones |
N-desmethyl Enzalutamide D6 is a deuterium labeled N-desmethyl Enzalutamide. | |||
TMIH-0093 |
Apalutamide-d4
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Apalutamide-d4 是 Apalutamide 的氘代化合物。 | |||
TMIH-0134 |
C24:1 Ceramide-d7
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C24:1 Ceramide-d7 是 C24:1 Ceramide 的氘代化合物。 | |||
TMIH-0176 |
Darolutamide-d4
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Darolutamide-d4 是 Darolutamide 的氘代化合物。 | |||
TMIH-0131 |
C16 Ceramide-d7
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C16 Ceramide-d7 是 C16 Ceramide 的氘代化合物。 | |||
TMID-0299 |
Zonisamide-d4
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Zonisamide-d4 是 Zonisamide 的氘代化合物。Zonisamide 的 CAS 号为 68291-97-4。Zonisamide 是锌酶碳酸酐酶 (carbonic anhydrase) 的有效抑制剂,对人类线粒体同工酶 hCA II 和 hCA V 作用的Ki值分别为 35.2 nM 和 20.6 nM。Zonisamide 具有抗癫痫活性,在癫痫、癫痫发作和帕金森病的研究中具有价值。 | |||
TMID-0192 |
Procainamide-d10
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Procainamide-d10 是 Procainamide 的氘代化合物。Procainamide 的 CAS 号为 51-06-9。Procainamide 是一种特异性强效的 DNA 甲基转移酶 1 (DNMT1) 抑制剂。普鲁卡因胺是一种 1A 类抗心律失常药物。Procainamide 具有研究癌症和心律失常的潜力。 | |||
T11867 |
Loperamide-d6 hydrochloride
R-18553 D6 hydrochloride |
Others | Others |
Loperamide D6 hydrochloride, a deuterium-labeled variant of Loperamide hydrochloride, acts as an opioid receptor agonist utilized for diarrhea treatment. | |||
T13204 |
Trimethobenzamide D6
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Others | Others |
Trimethobenzamide D6 is deuterium labeled Trimethobenzamide. Trimethobenzamide is a the D2 receptor blocker. Trimethobenzamide is an antiemetic. | |||
TMID-0247 |
LacosaMide-d3
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LacosaMide-d3 是 LacosaMide 的氘代化合物。LacosaMide 的 CAS 号为 175481-36-4。Lacosamide是一种功能化氨基酸。Lacosamide以一种新的方式调节钠通道:它选择性地增强钠通道缓慢失活,而对快速失活没有影响Lacosamine在不同的啮齿类动物癫痫发作模型中显示出抗癫痫作用,在反映神经性疼痛和慢性炎性疼痛的不同类型和症状的实验动物模型中显示了抗伤害潜力。 | |||
TMID-0066 |
rac-Lacosamide-d6
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rac-Lacosamide-d6 是 rac-Lacosamide 的氘代化合物。rac-Lacosamide 的 CAS 号为 175481-36-4。 | |||
TMIJ-0390 |
N,N-Dimethylformamide-d7
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N,N-Dimethylformamide-d7 是 N,N-Dimethylformamide 的氘代化合物。N,N-Dimethylformamide 的 CAS 号为 68-12-2。 | |||
TMIH-0034 |
2-Ethyl-2-phenylmalonamide-d5
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2-Ethyl-2-phenylmalonamide-d5 是 2-Ethyl-2-phenylmalonamide 的氘代化合物。 | |||
TMIH-0132 |
C18 Ceramide-d7
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C18 Ceramide-d7 是 C18 Ceramide 的氘代化合物。 | |||
TMIH-0092 |
Apalutamide-13C-d3
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Apalutamide-13C-d3 是 Apalutamide 的 13C 和氘代化合物。Apalutamide 的 CAS 号为 956104-40-8。Apalutamide 是一种有效、竞争性的雄激素受体 (AR) 拮抗剂(IC50:16 nM)。 | |||
TMIH-0133 |
C24 Ceramide-d7
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C24 Ceramide-d7 是 C24 Ceramide 的氘代化合物。 | |||
TMIJ-0264 |
Cyclophosphamide-d8
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Cyclophosphamide-d8 是 Cyclophosphamide 的氘代化合物。Cyclophosphamide 的 CAS 号为 50-18-0。Cyclophosphamide 是一种烷化剂,具有抗肿瘤及免疫抑制活性,用于治疗多种癌症。 | |||
T19311 |
Enzalutamide carboxylic acid D6
MDV3100 carboxylic acid D6 |
Others | Others |
Enzalutamide carboxylic acid is an inactive metabolite of Enzalutamide. Enzalutamide carboxylic acid D6 is the deuterium labeled Enzalutamide carboxylic acid (MDV3100 carboxylic acid). | |||
T37847 |
Zonisamide-13C2,15N
Zonisamide-13C2,15N |
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Zonisamide-13C2,15N is intended for use as an internal standard for the quantification of zonisamide by GC- or LC-MS. Zonisamide is an antiepileptic agent.1 It selectively inhibits the repeated firing of sodium channels (IC50 = 2 μg/ml) in mouse embryo spinal cord neurons and inhibits spontaneous channel firing when used at concentrations greater than 10 μg/ml.2 In rat cerebral cortex neurons, zonisamide (1-1,000 μM) inhibits T-type calcium channels with a maximum reduction of 60% of the calcium... | |||
T40394 |
Benzamide-15N
Phenylamide-15N,Benzenecarboxamide-15N,NSC-3114-15N,Benzamide-15N |
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Benzamide-15N (NSC-3114-15N) is a 15N-labeled Benzamide. Benzamide inhibits poly(ADP-ribose) polymerase (PARP). | |||
TMIH-0620 |
Arachidonoyl Ethanolamide-d4
AEA-d4 |
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Deuterated anandamide, a synthetically modified version of anandamide where hydrogen atoms are replaced with deuterium (D), exhibits enhanced stability against oxidative degradation. This modification conserves the compound's pharmacological properties while prolonging its shelf life and efficacy in research applications, particularly in analytical and biochemical studies to elucidate the complex mechanisms of the endocannabinoid system. | |||
TMIH-0372 |
N-desmethyl Apalutamide-d4
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N-desmethyl Apalutamide-d4 是 N-desmethyl Apalutamide 的氘代化合物。N-desmethyl Apalutamide 的 CAS 号为 1332391-11-3。N-Desmethyl Apalutamide 是一种 Apalutamide 的活性代谢产物,主要由 CYP2C8 和 CYP3A4 介导形成。它是一种低活性的雄激素受体拮抗剂,其作用力是 Apalutamide 活性的三分之一。它是中等至强的CYP3A4和CYP2B6诱导剂,并具有优异的血浆蛋白结合浓度。 | |||
TMIH-0094 |
Apalutamide-d7
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Apalutamide-d7 是 Apalutamide 的氘代化合物。Apalutamide 的 CAS 号为 956104-40-8。Apalutamide 是一种有效、竞争性的雄激素受体 (AR) 拮抗剂(IC50:16 nM)。 | |||
TMIH-0053 |
4-amino-N-(4-nitrophenyl)benzenesulfonamide-d4
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4-amino-N-(4-nitrophenyl)benzenesulfonamide-d4 是 4-amino-N-(4-nitrophenyl)benzenesulfonamide 的氘代化合物。 | |||
TMIH-0035 |
2-Furamide-3,4,5-d3
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2-Furamide-3,4,5-d3 是 2-Furamide-3,4,5 的氘代化合物。 | |||
TMIH-0218 |
Enzalutamide-d6 Carboxylic Acid
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Enzalutamide-d6 Carboxylic Acid 是 Enzalutamide Carboxylic Acid 的氘代化合物。Enzalutamide Carboxylic Acid 的 CAS 号为 1242137-15-0。Enzalutamide carboxylic acid 是 Enzalutamide 非活性代谢物。Enzalutamide 是雄激素受体 (AR) 拮抗剂。 | |||
TMID-0185 |
(±)-Ropivacaine-d7
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(±)-Ropivacaine-d7 是 (±)-Ropivacaine 的氘代化合物。(±)-Ropivacaine 的 CAS 号为 84057-95-4。Ropivacaine 是有效的钠通道阻断剂,通过可逆地抑制钠离子内流从而引起神经纤维脉冲传导阻滞。Ropivacaine 也是一种 K2P(双孔钾通道)TREK-1的抑制剂,在 COS-7 细胞膜上的 IC50值为 402.7 μM。Ropivacaine 可以用于神经性疼痛的缓解的相关研究。 | |||
TMIJ-0102 |
Ropivacaine-d7
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Ropivacaine-d7 是 Ropivacaine 的氘代化合物。Ropivacaine 的 CAS 号为 84057-95-4。Ropivacaine 是有效的钠通道阻断剂,通过可逆地抑制钠离子内流从而引起神经纤维脉冲传导阻滞。Ropivacaine 也是一种 K2P(双孔钾通道)TREK-1的抑制剂,在 COS-7 细胞膜上的 IC50值为 402.7 μM。Ropivacaine 可以用于神经性疼痛的缓解的相关研究。 | |||
TMID-0262 |
Lidocaine-d10 (N,N-diethyl-d10)
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Lidocaine-d10 (N,N-diethyl-d10) 是 Lidocaine 的氘代化合物。Lidocaine 的 CAS 号为 137-58-6。Lidocaine是一种酰胺衍生物,抑制涉及复杂电压和依赖性的钠通道,可用于研究室性心律失常。它通过调节 miR-145 表达和进一步抑制MEK/ERK和NF-κB信号通路来减少胃癌细胞的生长,迁移和侵袭。 | |||
T70882 |
Orlistat-d3
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Orlistat-d3 is intended for use as an internal standard for the quantification of orlistat by GC- or LC-MS. Orlistat is a digestive lipase inhibitor. It inhibits diacylglycerol lipase α (DAGLα), DAGLβ, α/β-hydrolase domain-containing protein 12 (ABHD12), ABHD16A, and platelet-activating factor acetylhydrolase (PAF-AH; IC50s = 0.06, 0.1, 0.08, 0.03, and 0.05 µM, respectively), as well as pancreatic lipase and hormone-sensitive lipase (IC50s = 0.65 and 2.1 µg/ml, respectively) but does not inhibit... |