98
17
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19399 |
L-Ornithine L-aspartate
Ornithine Aspartate,L-鸟氨酸 L-天冬氨酸 |
Others | Others |
L-Ornithine L-aspartate (Ornithine Aspartate) 由鸟氨酸和天冬氨酸组成。它能够减少血氨浓度,并消除与肝硬化相关的肝性脑病的症状。 | |||
T65796 |
β-Methyl L-aspartate hydrochloride
L-Aspartic acid β-methyl ester hydrochloride,H-Asp(OMe)-OH.HCl |
Amino Acids and Derivatives | Metabolism |
β-Methyl L-aspartate hydrochloride (L-Aspartic acid β-methyl ester hydrochloride)是一种天冬氨酸衍生物,常用于合成多种化合物且与机体免疫和代谢有关。 | |||
T31673 |
Erythromycin aspartate
Erythromycin L-aspartate |
||
Erythromycin aspartate is a enzyme. | |||
T12368 |
Pasireotide L-aspartate salt
帕瑞肽天门冬氨酸盐,SOM230 L-aspartate |
Others | Others |
Pasireotide L-aspartate salt is a stable cyclohexapeptide somatostatin mimic that exhibits unique high-affinity binding to human somatostatin receptors (subtypes sst1/2/3/4/5, pKi=8.2/9.0/9.1/<7.0/9.9 respectively). | |||
T21055 |
Lysine aspartate
|
||
Lysine aspartate is a bioactive chemical. | |||
T24818 |
Sparfosic Acid
NSC224131,NSC-224131,Acide sparfosique,N-Phosphonacetyl-L-aspartate,NSC 224131 |
Apoptosis | Apoptosis |
Sparfosic Acid (Acide sparfosique) 是一种天门冬氨酸氨甲酰转移酶抑制剂,具有抗肿瘤活性,可用于研究晚期肾细胞癌。 | |||
T24457 | Methotrexate-gamma-aspartate | ||
Methotrexate-gamma-aspartate has growth inhibitory effects. It is used in antibody-targeted liposomes. | |||
T28945 |
Tenofovir disoproxil aspartate
CKD-390,CKD390,CKD 390 |
||
Tenofovir disoproxil aspartate, a nucleotide reverse transcriptase inhibitor, is used potentially for the treatment of HBV infection. | |||
T23011 |
MNI-caged-D-aspartate
|
Others | Others |
Agonist at NMDA receptors and EAAT substrate | |||
T76178 |
Aspartate aminotransferase
|
||
Aspartate aminotransferase (AST) 是一种转氨酶,常用于生化研究。Aspartate aminotransferase 催化天冬氨酸和 α-酮戊二酸转化为草酰乙酸和谷氨酸。Aspartate aminotransferase 可存在于在脑脊液、渗出液和渗出物。 | |||
T63214 |
Lomefloxacin (aspartate)
|
||
Lomefloxacin (SC47111A) aspartate 是广谱的喹诺酮类抗菌剂,能够用于呼吸道感染、胃肠道感染、泌尿生殖系统感染、耳鼻喉感染等疾病的研究。 | |||
TP1234 |
Amlodipine aspartic acid impurity
Amlodipine aspartate |
||
Amlodipine aspartic acid is a calcium channel blocker compound that exhibits antihypertensive and antianginal properties. It is important to note that Amlodipine aspartic acid impurity is an impurity specific to this compound. | |||
T60613 |
Mab Aspartate Decarboxylase-IN-1
|
||
Mab Aspartate Decarboxylase-IN-1 是天冬氨酸脱羧酶 (PanD)的有效抑制剂(IC50 = 56.3 μM),具有抗菌活性。 | |||
T8765 |
iGOT1-01
|
Others | Others |
iGOT1-01 是一种天冬氨酸转氨酶 1 (谷氨酸草酰乙酸转氨酶 1;GOT1) 抑制剂,在 GOT1/GLOX/HRP 测定中IC50为 11.3 μM,在 MDH 偶联 GOT1 酶法测定中IC50为 85 μM。它显示出抗癌活性。 | |||
T3470 |
Cis-ACBD
cis-1-aminocyclobutane-1,3-dicarboxylic acid,氨基二羧酸 |
Amino Acids and Derivatives | Metabolism |
Cis-ACBD (cis-1-aminocyclobutane-1,3-dicarboxylic acid) 是一种有效的选择性 N-甲基-D-天冬氨酸受体激动剂。 | |||
T8766 |
GOT1 inhibitor-1
GOT1 inhibitor 2c |
Others | Others |
GOT1 inhibitor-1 (GOT1 inhibitor 2c) 是一种新型的、非共价的谷氨酸草酰乙酸转氨酶 1 (GOT1) 抑制剂(IC50:8.2 uM),是一种戊酸衍生物。 它可用于以及胰腺导管腺癌 (PDAC) 。 | |||
T75248 | Pasireotide (diaspartate) | ||
Pasireotide (SOM230) diaspartate 是一种长效的环己肽生长激素抑制素类似物,可以提高生长抑素受体的激动剂活性,对sst1/2/3/4/5的pKi 分别为 8.2/9.0/9.1/<7.0/9.9。Pasireotide diaspartate 具有抗分泌、抗增殖和促凋亡活性。 | |||
T28298 |
Pasireotide diaspartate
SOM-230,SOM230,trade name: Signifor,SOM 230,Signifor LAR |
||
Pasireotide is a somatostatin analog with a 40-fold increased affinity to somatostatin receptor 5 compared to other somatostatin analogs. | |||
T29295 |
1-Adamantylaspartate
beta-1-Adamantylaspartic acid |
||
1-Adamantylaspartate can be used as a protecting group for protein synthesis. | |||
T16286 |
Nelonemdaz
Neu2000 |
Topoisomerase | DNA Damage/DNA Repair |
Neu2000 is an uncompetitive antagonist of N-methyl-D-aspartate (NMDA) receptor. | |||
T12733 |
Rislenemdaz
CERC-301,MK-0657 |
iGluR | Membrane transporter/Ion channel; Neuroscience |
Rislenemdaz (CERC-301) (CERC-301)是 N-methyl-D-aspartate (NMDA) receptor subunit 2B (GluN2B) 的拮抗剂。 | |||
T7626 |
Budipine
|
Others | Others |
Budipine 是抗帕金森病剂的一种。 | |||
T3407L |
Rapastinel acetate
Rapastinel acetate (117928-94-6 Free base) |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Rapastinel acetate 是 N-甲基-D-天冬氨酸 (NMDA) 受体的调节剂和甘氨酸位点的部分激动剂,具有长效抗抑郁作用。 | |||
T36333 |
Z-IETD-AFC
|
||
Z-IETD-AFC 是 caspase-8 和颗粒酶 B 的荧光底物,可用于定量半胱天冬酶-8 或颗粒酶 B 的活性。 | |||
T6259 |
Dizocilpine
地佐环平,MK-801 |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Dizocilpine (MK-801) 是一种选择性非竞争性NMDA 受体拮抗剂,Kd=37.2 nM,是一种抗惊厥剂。它通过与 NMDA 相关离子通道内的一个位点结合而起作用,从而阻止 Ca2+的流动。 | |||
T8920 |
Sepimostat
|
iGluR | Membrane transporter/Ion channel; Neuroscience |
Sepimostat 通过 NR2B 亚基的 Ifenprodil 结合位点的 NR2B N-甲基-D-天冬氨酸受体拮抗作用表现出神经保护活性。它抑制 Ifenprodil 结合的 Ki 值为27.7 µM。 | |||
T67946 |
EP2 receptor antagonist-2
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
EP2 receptor antagonist-2 (CID891729)为EP2受体拮抗剂,能够抑制PGE2诱导的EP2受体激活,并阻断由N-甲基-D-天冬氨酸(NMDA)引起的乳酸脱氢酶(LDH)释放。 | |||
T3471 |
Trans-ACBD
Trans-1-aminocyclobutane-1,3-dicarboxylic acid,氨基二羧酸 |
Amino Acids and Derivatives | Metabolism |
Trans-ACBD (Trans-1-aminocyclobutane-1,3-dicarboxylic acid) 是一种有效且特异性的 N-甲基-D-天冬氨酸受体激动剂。 | |||
T5880 |
Aminooxyacetic acid hemihydrochloride
氨氧基乙酸半盐酸盐,羧甲基羟胺半盐酸盐,Carboxymethoxylamine Hemihydrochloride |
Others; GABA Receptor | Membrane transporter/Ion channel; Neuroscience; Others |
Aminooxyacetic acid hemihydrochloride (Carboxymethoxylamine Hemihydrochloride) 是一种苹果酸-天冬氨酸穿梭 (MAS) 抑制剂,也能抑制 GABA 降解酶GABA-T。 | |||
T9558 |
KL-11743
|
transporter | Metabolism |
KL-11743 是葡萄糖竞争性 I 类葡萄糖转运蛋白抑制剂,口服有活性,能够抑制GLUT1 (IC50:115 nM) 、GLUT2 (IC50:137 nM) 、GLUT3 (IC50:90 nM) 及GLUT4 (IC50:68 nM) 。它能够特异性阻断葡萄糖代谢,也可与电子传递抑制剂协同作用诱导细胞死亡。 | |||
T27947L |
LY339434 HCl
LY339434 HCl(219566-62-8 Free base) |
GluR; NMDAR | Neuroscience |
LY339434 HCl是一种亲和力很低的GluR5红氨酸受体激动剂。LY339434 HCl 主要通过影响 N-甲基-D-天冬氨酸(NMDA)受体来快速的神经元死亡。 | |||
T27397 |
Gacyclidine
GK 11,OTO311,OTO-311,OTO 311,GK-11 |
NMDAR | Neuroscience |
Gacyclidine (OTO311) 是一种小分子 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂。在耳蜗局部注射加西环定可抑制水杨酸盐引起的耳鸣,可用于治疗脑损伤、脊髓损伤和耳鸣。 | |||
T7720 |
CGP 37849
CGP-37849,CGP37849 |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
CGP 37849 是一种竞争性口服活性 N-甲基-D-天冬氨酸 (NMDA) 受体拮抗剂((Ki = 35 nM)),具有有效性。CGP 37849 是啮齿动物的抗惊厥药,也具有抗抑郁和抗焦虑的特性。 | |||
T16801 |
(RS)-(Tetrazol-5-yl)glycine
LY 285265,D,L-(tetrazol-5-yl)glycine |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
(RS)-(Tetrazol-5-yl)glycine (LY 285265) 是一种高效且选择性的 N-甲基-D-天冬氨酸 (NMDA) 受体激动剂。它能够诱导小鼠癫痫发作反应和 Fos。它对 GluN1/GluN2D 和 GluN1/GluN2A 的EC50分别为 99 nM,1.7 μM。 | |||
T73447 |
NP10679
|
||
NP10679 是一种选择性、pH 依赖性的GluN2B 亚基特异的 N-methyl-D-aspartate (NMDA) 受体抑制剂,具有较高的口服生物利用度和良好的脑穿透性。NP10679 在 pH 6.9 和 7.6 下,抑制 GluN2B 的IC50分别为 23 和 142 nM。NP10679 是histamine H1的拮抗剂和hERG 通道抑制剂,IC50分别为 73 和 620 nM。NP10679 是一种可逆的人肝脏CYP 酶抑制剂。 | |||
T3320 |
Dizocilpine Maleate
(+)-Mk-801 Hydrogen Maleate,MK 801,地卓亚平马来酸盐,Dizocilpine hydrogen maleate,地佐环平马来酸盐,(+)-MK 801 maleate,(+)-MK 801 (Maleate) |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Dizocilpine Maleate (MK 801) 是一种选择性和非竞争性的 NMDA 受体拮抗剂,Kd 值为 37.2 nM。它用于治疗 NMDA 受体可能发挥重要作用的多种神经退行性疾病或疾病。 | |||
T4118 |
SB 271046 hydrochloride
SB 271046A |
5-HT Receptor | GPCR/G Protein; Neuroscience |
SB 271046 hydrochloride (SB 271046A) 是高效、选择性和具有口服活性的5-HT6受体拮抗剂,对大鼠、猪和人的pKi 分别为 9.02、8.55 和 8.81。它增加额叶皮层中的细胞外天冬氨酸和谷氨酸并表现出抗惊厥活性,EC50为 0.16 μM。它对 5-HT6 受体、结合位点和离子通道的选择性超过 200 倍。 | |||
T40376 |
L-Phenylalanine-15N
L-苯丙氨酸 15N,(S)-2-Amino-3-phenylpropionic acid-15N,L-Phenylalanine-15N |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
L-Phenylalanine-15N ((S)-2-Amino-3-phenylpropionic acid-15N) 是 15N 标记的 L-Phenylalanine。L-Phenylalanine 是从大肠杆菌中分离出来的一种必需氨基酸。 L-Phenylalanine 广泛用于食品香精和药物的生产。 | |||
T68599 |
Orphenadrine
Orphenadrine (free base) |
Sodium Channel; NMDAR; AChR | Membrane transporter/Ion channel; Neuroscience |
Orphenadrine 是一种非竞争性的 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,以浓度依赖性方式抑制克隆的 HERG 通道,在 HEK 细胞中产生0.85μM 的 IC。Orphenadrine 是中枢和外周毒蕈碱受体的拮抗剂,通过孔残基 Y652或 F656突变阻断衰减。 Orphenadrine 具有抗痉挛、镇痛和抗胆碱能活性,对在体外和体内对谷氨酸神经毒性具有保护作用。Orphenadrine 对钠离子通道具有抑制作用,可用来治疗帕金森。 | |||
T31029 |
CP 69799
CP-69,799,CP69799,CP-69799 |
||
CP 69799 is an inhibitor of aspartate proteinases. | |||
T29036 |
UBP141
UBP 141,UBP-141 |
||
UBP141 is a antagonist of N-methyl-D-aspartate (NMDA) receptor. | |||
T22913 |
L-CCG-lll
|
Others | Others |
inhibitor of both glial and neuronal uptake of glutamate, aspartate and cysteate. | |||
T40433 |
D-Cystine
|
||
D-Cystine, the D-enantiomer of L-Cystine, functions as an inhibitor of L-aspartate-β-semialdehyde dehydrogenase (ASADH) derived from Escherichia coli. | |||
T12983 | Sparfosic acid trisodium | Others | Others |
Sparfosic acid trisodium is a potent aspartate transcarbamoyl transferase inhibitor, with anti-tumor and antimetabolite activity. | |||
T27309 |
Fenazinel Dihydrochloride
SIPI5052,SIPI 5052,SIPI-5052 |
||
Fenazinel Dihydrochloride, a N-methyl-D-aspartate (NMDA) receptor antagonist, is used potentially for the treatment of ischemic stroke. | |||
T22722 |
Dihydrokainic acid
|
Others | Others |
EAAT2(GLT1)-selective non-transportable inhibitor of L-glutamate and L-aspartate uptake | |||
T19727 |
G-Glu-Glu
G Glu Glu,gamma-Glutamyl-glutamic acid,H-gGlu-Glu-OH |
||
G-Glu-Glu is an endogenous constituent of the brain. G-Glu-Glu activates N-methyl-D-aspartate receptors in rats. | |||
T22778 | Felbamate hydrate | Others | Others |
Felbamate hydrate is an effective nonsedative anticonvulsant. It is a clinical effect that may be related to the inhibition of N-methyl-D-aspartate. | |||
T81927 |
Lithium citrate
Litarex |
||
锂柠檬酸用于降低卡纳万病患者脑内过量的N-乙酰天冬氨酸含量。 | |||
T30127 | Argininosuccinic acid | ||
Argininosuccinic acid can be obtained during the urea cycle from citrulline, aspartate, and ATP by argininosuccinic acid synthetase. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T65269 |
L-Aspartic acid potasium salt
Aspartic acid potasium salt,Potassium L-aspartate |
Others | Others |
L-aspartic acid potasium salt(VX-548) 是一种广泛存在于动植物体内的氨基酸。L-aspartic acid potasium salt驱动氮氧化物的产生,从而促进吞噬作用,有助于提高鱼类的成活率。L-aspartic acid potasium salt 可对抗生素产生刺激,刺激作用可能与参与天冬氨酸-4-半醛生物合成的前体有关。 | |||
T19554 |
L-Aspartic aicd sodium
L-Aspartic acid sodium,Sodium L-aspartate |
Others; Sodium Channel; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Others |
L-Aspartic aicd sodium (Sodium L-aspartate) 是一种氨基酸,是一种结肠特异性活性分子输送的前体活性分子,可促进大鼠前脑膜囊泡的 Na+外排。 | |||
T8267 |
Aspartic acid calcium
天冬氨酸钙,Calcium L-aspartate,Aspartic acid (calcium) |
Others | Others |
Aspartic acid calcium (Calcium L-aspartate) 是一种钙和 L-Aspartic acid (L-天冬氨酸) 连接的螯合物。其中L-Aspartic acid 是一种氨基酸,是体内蛋白质的结构单元。 | |||
T5083 |
L-Cysteic acid monohydrate
L-磺基丙氨酸 一水合物,3-Sulfo-L-alanine Monohydrate |
Endogenous Metabolite; GluR | Metabolism; Neuroscience |
L-Cysteic acid monohydrate (3-Sulfo-L-alanine Monohydrate) 是内源性代谢产物的一种。 | |||
T60237 |
L-Cysteine S-sulfate
S-Sulfo-L-cysteine |
NMDAR | Neuroscience |
L-Cysteine S-sulfate (S-Sulfo-L-cysteine) 是有效的 N-methyl-d-aspartate (NMDA) 谷氨酸受体激动剂。L-Cysteine S-sulfate 是胱氨酸裂解酶的底物。 | |||
T5080 |
Spermidine trihydrochloride
Spermidine hydrochloride,4-Azaoctamethylenediamine trihydrochloride,三盐酸亚精胺,亚精胺盐酸盐 |
NMDAR; Autophagy | Autophagy; Neuroscience |
Spermidine trihydrochloride (4-Azaoctamethylenediamine trihydrochloride) 能够维持细胞膜稳定性,提高抗氧化酶特性,改善光系统 II (PSII) 以及相关基因表达,也能够显著抑制 H2O2和 O2.-含量。 | |||
T4096 |
Quinolinic acid
喹啉酸,pyridine-2,3-dicarboxylic acid,QUIN |
Endogenous Metabolite; NMDAR; iGluR | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Quinolinic acid (QUIN) 是一种内源性 N-甲基-D-天冬氨酸 (NMDA) 受体激动剂,由 L-色氨酸通过犬尿氨酸途径合成,具有调节 NMDA 神经元损伤和功能障碍的潜力。 | |||
T6975 |
Sarcosine
Sarcosinic acid,Methylaminoacetic acid,Sarcosin,肌氨酸,Methylglycine,N-Methylaminoacetic acid,N-methylglycine |
Others; GlyT; Endogenous Metabolite | Metabolism; Neuroscience; Others |
Sarcosine (Methylglycine) 是 I 型甘氨酸转运蛋白 (GlyT1) 的竞争性抑制剂和 N-甲基-D-天冬氨酸受体 (NMDAR) 共激动剂,通过增加甘氨酸的浓度增强 NMDA 受体的功能,可用于精神分裂症的研究。 | |||
T10086 |
24-Hydroxycholesterol
Cholest-5-ene-3beta,24-diol |
Liver X Receptor; NMDAR | Metabolism; Neuroscience |
24-Hydroxycholesterol (Cholest-5-ene-3beta,24-diol) 是一种氧甾醇化合物,是一种 n-甲基-d-天门冬氨酸受体 (NMDA) 和转录因子 LXR 的激活剂,可用于研究心血管生成和胰腺癌。 | |||
T4705 |
Aminoadipic acid
DL-2-Aminoadipic acid,DL-2-氨基己二酸 |
Others; Endogenous Metabolite | Metabolism; Others |
Aminoadipic acid (DL-2-Aminoadipic acid) 是赖氨酸主要生化途径中的代谢物。 它是赖氨酸和糖碱代谢的中间体。 它拮抗由谷氨酸受体 N-甲基-D-天冬氨酸调节的神经兴奋特性。 | |||
T2S1008 |
Oxysophoridine
Sophoridine N-oxide,氧化槐定碱 |
Apoptosis; Antioxidant | Apoptosis; oxidation-reduction |
Oxysophoridine (Sophoridine N-oxide) 是从苦豆子中提取的一种生物碱,具有抗发炎,抗氧化应激和抗凋亡的作用。 | |||
T5287 |
N-Acetyl-L-aspartic acid
AC-ASP-OH,N-Acetylaspartic acid,N-乙酰-L-天门冬氨酸 |
Others; Endogenous Metabolite | Metabolism; Others |
N-Acetyl-L-aspartic acid (AC-ASP-OH) 是天冬氨酸的衍生物, 是由氨基酸天冬氨酸和乙酰辅酶 A 在神经元中合成的。 | |||
T22583 |
Arcaine sulfate
|
NMDAR | Neuroscience |
Arcaine sulfate 是一种多胺,是 N-甲基-d-天冬氨酸 (NMDA) 受体多胺结合位点的拮抗剂。 Arcaine 是一种胍丁胺类似物,与 ifenprodil 一起,可能有可能用于治疗癫痫疾病。 | |||
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。 | |||
T75571 | Withaphysalin D | ||
Withaphysalin D 是一种选择性抑制含GluN2B的N-甲基-D-天冬氨酸受体(NMDAR)的化合物。该物质可从睡莲中提取,对神经保护有益,能穿过血脑屏障。 | |||
T75890 |
Conantokin G TFA
|
||
Conantokin G TFA 是一种 17 个氨基酸的肽,是一种有效,选择性和竞争性的 N-甲基-D-天冬氨酸 (NMDA) 受体拮抗剂。Conantokin G TFA 抑制鼠皮质神经元中NMDA 诱发的电流,IC50为 480 nM,具有神经保护作用。 | |||
T36179 |
Aspulvinone O
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Aspulvinone O is a fungal metabolite that has been found in P. variotti and has antioxidant and anticancer activities.1,2 It scavenges 2,2-diphenyl-1-picrylhydrazyl radicals in a cell-free assay (IC50 = 11.6 μM).1 Aspulvinone O inhibits aspartate transaminase 1 (GOT1; Kd = 3.32 μM) and is cytotoxic to PANC-1, AsPC-1, and SW1990 pancreatic cancer cells (IC50s = 20.54-26.8 μM).2 It reduces the oxygen consumption rate (OCR) and induces apoptosis in SW1990 cells. Aspulvinone O (2.5 and 5 mg/kg) redu... |