179
30
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T73586 |
Anticonvulsant agent 2
|
Others | Others |
Anticonvulsant agent 2 是一种有效的口服活性抗惊厥剂,在耐药性癫痫模型中显示出抗癫痫活性。 | |||
T10027 |
Anticonvulsant agent 1
4-(2,2-Difluoroethenyl)-α-ethyl-2-oxo-1-pyrrolidineacetamide |
Others | Others |
Anticonvulsant agent 1 is an anticonvulsant compound. | |||
T3563 |
Lvguidingan
|
Others | Others |
Lvguidingan 是一种抗惊厥药。 | |||
T8588 |
Buramate
|
Antibacterial | Microbiology/Virology |
Buramate 是抗精神病药和抗惊厥药。 | |||
T15545 |
ICA-27243
|
Potassium Channel | Membrane transporter/Ion channel |
ICA-27243 是选择性的,口服有效的 KCNQ2/Q3钾通道开放剂,EC50为 0.38 μM。对 KCNQ4 和 KCNQ3/Q5 的激活效果较差。它具有抗惊厥和抗癫痫作用。 | |||
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。 | |||
T0413 |
Cinromide
醒隆酰胺,trans-3-Bromo-N-ethylcinnamamide |
Others | Others |
Cinromide (trans-3-Bromo-N-ethylcinnamamide) 是抗惊厥药,能够抑制上皮中性氨基酸转运蛋白 B0AT1 (SLC6A19),其 IC50=0.5 μM。 | |||
T0600 |
10,11-Dihydrocarbamazepine
双氢卡马西平,10,11-二氢卡马西平,Dihydrocarbamazepine |
Others | Others |
10,11-Dihydrocarbamazepine (Dihydrocarbamazepine) 是一种 Oxcarbazepine 的活性代谢物,也是一种有机中间体。Oxcarbazepine 能够几乎完全的、迅速的转化为 10,11-Dihydrocarbamazepine,可能具有抗惊厥效果。 | |||
T7780 |
Blarcamesine
AE-37,AVex-73 |
AChR | Neuroscience |
Blarcamesine (AVex-73) 是一种毒蕈碱 M1 激动剂,具有抗惊厥、抗失忆、神经保护和抗抑郁的特性,可能用于治疗阿尔茨海默病。 | |||
T0440 |
Oxcarbazepine
GP 47680,奥卡西平 |
Apoptosis; Sodium Channel | Apoptosis; Membrane transporter/Ion channel |
Oxcarbazepine (GP 47680) 是一种钠通道阻滞剂,有效抑制胶质母细胞瘤细胞生长并诱导胶质母细胞瘤细胞凋亡或 G2/M 停滞,具有抗癌和抗惊厥作用。 | |||
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。 | |||
T22675 |
Co 102862
V 102862 |
Others; Sodium Channel | Membrane transporter/Ion channel; Others |
Co 102862 是一种电压门控钠通道阻滞剂。 Co 102862 可用于抗惊厥的研究。 | |||
T0283 |
Trimethadione
三甲双酮,3,5,5,-Trimethyloxazolidine-2,4-dione |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Trimethadione (3,5,5,-Trimethyloxazolidine-2,4-dione) 是恶唑烷二酮类抗惊厥剂,也是一种 T 型钙通道阻滞剂,具有抗痛觉过敏作用,可用于研究失神发作。 | |||
TP2036L |
DPDPE TFA (88373-73-3 free base)
DPDPE TFA |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
DPDPE TFA 是选择性 δ-阿片受体激动剂肽,在体内具有镇痛作用。 | |||
T0992 |
Carbenoxolone disodium
Biogastrone,Duogastrone,甘珀酸钠,Bioral |
Gap Junction Protein | Cytoskeletal Signaling |
Carbenoxolone disodium (Duogastrone) 是甘草酸的活性代谢物和人11β-HSD 和细菌3α, 20β-HSD 的抑制剂。它是一种缝隙连接的解耦剂,可抑制牛痘病毒生长,用于消化性、食道和口腔溃疡和炎症的相关研究。 | |||
T14983 |
Clomethiazole
Distraneurin,Chlormethiazole,氯美噻唑,5-(2-CHLOROETHYL)-4-METHYLTHIAZOLE |
P450; GABA Receptor | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Clomethiazole (Distraneurin) 是口服GABAA 激动剂,可抑制人肝微粒体中的细胞色素 P450 异构体,CYP2A6 和 CYP2E1。它有抗惊厥作用,具有治疗惊厥性癫痫持续状态的潜力。 | |||
TP2036 |
DPDPE
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
DPDPE 是选择性 δ-阿片受体激动剂肽,在体内具有镇痛作用。 | |||
T2535 |
Ivabradine hydrochloride
盐酸伊伐布雷定,S 16257-2,Ivabradine HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Ivabradine hydrochloride (S 16257-2) 是一种可口服的,超极化激活的环核苷酸门控离子通道通道阻滞剂。 | |||
T21029 |
Norfluoxetine Hydrochloride
Norfluoxetine HCl,去甲氟西汀 |
Others | Others |
Norfluoxetine Hydrochloride (Norfluoxetine HCl) 是氟西汀的活性代谢物。氟西汀是一种抗抑郁药。 | |||
T7806 |
Licarbazepine
10,11-hydroxy-10,11 Dihydrocarbamezer,10,11-二氢-10-羟基卡马西平 |
Others | Others |
Licarbazepine (10,11-hydroxy-10,11 Dihydrocarbamezer) 是一种有效的电压门控钠通道阻滞剂,具有抗惊厥和稳定情绪的功效。 | |||
T1602 |
Valproic acid sodium salt
丙戊酸钠,Sodium Valproate |
Mitophagy; Gamma-secretase; HIV Protease; GABA Receptor; HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Proteases/Proteasome; Stem Cells |
Valproic acid sodium salt (Sodium Valproate) 是一种HDAC 抑制剂,可抑制HDAC1的活性,诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、偏头痛和双相情感障碍等。 | |||
T8456 |
GALNON
|
Neuropeptide Y Receptor | GPCR/G Protein; Neuroscience |
Galnon 是一种甘丙肽受体激动剂,可改善内在的皮质骨组织特性。 | |||
T6474 |
Divalproex Sodium
Valproate semisodium,Epival,双丙戊酸钠 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Divalproex Sodium (Valproate semisodium) 结合并抑制 γ-氨基丁酸 (GABA) 转氨酶,其抗惊厥活性可通过增加 GABA 脑浓度和抑制分解 GABA 或阻止 GABA 再摄取到神经胶质和神经末梢的酶来发挥。它也是一种 HDAC 抑制剂。由丙戊酸钠和丙戊酸组成,具有抗惊厥和抗癫痫活性。 Divalproex 还可以通过抑制电压敏感的钠通道来抑制重复的神经元放电。 | |||
T8435 |
YM90K
YM90K hydrochloride,6-(1H-imidazol-1-yl)-7-nitro-2,3(1H,4H)-,1,4-二氢-6-(1H-咪唑-1-基)-7-硝基-2,3-喹喔啉二酮单盐酸盐 |
GluR; iGluR | Membrane transporter/Ion channel; Neuroscience |
YM90K (6-(1H-imidazol-1-yl)-7-nitro-2,3(1H,4H)-) hydrochloride 是一种选择性的、有效的AMPA 受体拮抗剂,Ki=84 nM。YM90K 抑制海藻酸酯 (Ki 为 2.2 μM) 和 NMDA (Ki 为 37 μM) 受体的效力较低,并具有神经保护活性。 | |||
T6651 |
Safinamide mesylate
PNU-151774E,FCE28073,PNU-151774E,NW-1015,EMD 1195686 mesylate,沙芬酰胺甲磺酸盐 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Safinamide mesylate (EMD 1195686 mesylate) 是选择性的、有效的、可逆的单胺氧化酶 B 的抑制剂,对 MAO-A 选择性较低。它能够阻断钠通道和调节谷氨酸释放。它具有神经保护作用,可用于研究帕金森病、缺血脑卒中等疾病。 | |||
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。 | |||
T1249 |
Beclamide
N-Benzyl-3-chloropropionamide,Chloracon,Chlorakon,贝克拉胺(INN) |
Others | Others |
Beclamide (Chlorakon) 是一种抗惊厥药,具有抗惊厥作用。 | |||
T28503 |
Ralitoline
GOE-4942,PD-117818,Ralitolina,CI-946,Ralitolinum |
||
Ralitoline (Ralitolinum) 是一种抗惊厥剂,具有抗癌活性和钠通道阻断活性。 | |||
T14863 |
Carabersat
SB 204269 |
Others | Others |
Carabersat (SB 204269)是一种新型有效的抗惊厥和抗癫痫试剂。 | |||
T40709 |
3-Diethylamino-1-propanol
|
Others | Others |
3-Diethylamino-1-propanol 具有抗惊厥作用。 | |||
T10774 |
CFM-2
|
iGluR | Membrane transporter/Ion channel; Neuroscience |
CFM-2, a potent and selective non-competitive antagonist of AMPAR (AMPAR), exhibits anticonvulsant activity across various seizure models. | |||
T31614 |
Elpetrigine
GW-273293,JZP 4,JZP4,GW273293,JZP-4,GW 273293 |
||
Elpetrigine( GW 273293, JZP-4) is effective calcium and sodium channel blocker and is currently being evaluated in patients as an anticonvulsant and mood stabilizer. | |||
T3562 |
Valrocemide
TV1901,N-丙戊酰基甘氨酰胺,N-Valproylglycinamide,丙戊塞胺 |
Others | Others |
Valrocemide (TV1901) 是有前景的抗癫痫候选药物,具有广泛的抗惊厥特性。 | |||
T5517 |
(R)-Carisbamate
|
Others | Others |
(R)-Carisbamate 是 Carisbamate 的 R-异构体。 Carisbamate 是一种实验性抗惊厥药。 | |||
T15302 |
Fluzinamide
AHR-8559 |
Others | Others |
Fluzinamide(AHR-8559)对点燃性杏仁核癫痫发作有抗惊厥作用。 | |||
T8604 |
Fenaclon
Fenaclonum |
Others | Others |
Fenaclon (Fenaclonum) 是一种抗惊厥药。它适用于治疗癫痫。 | |||
T6744 |
Methylbenactyzium Bromide
Noinarin,Paragone,Methylbenactyzine Bromide,溴甲贝那替秦,Semulgin,Gastrimade |
AChR | Neuroscience |
Methylbenactyzium Bromide (Semulgin) 是毒蕈碱性乙酰胆碱受体抑制剂,是一种抗惊厥药。 | |||
T36839 |
(R)-Mephenytoin
R-Mephenytoin,(R)-Mephenytoin,(–)-Mephenytoin |
Others | Others |
(R)-Mephenytoin ((–)-Mephenytoin) 是 Mephenytoin 的 R-对映体,Mephenytoin 是一种抗惊厥药。 | |||
T10796 |
Chlormethiazole hydrochloride
氯美噻唑盐酸盐,Clomethiazole hydrochloride |
Others | Others |
Chlormethiazole hydrochloride 是抗惊厥药。它具有神经保护作用,能够阻碍 MDMA 诱导的血清素能神经末梢退化。 | |||
T11349 |
GABAA receptor agent 1
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
GABAA receptor agent 1 是GABAA 受体的高亲和力配体,有抗惊厥活性。 | |||
T27047 |
Clovoxamine fumarate
DU23811 fumarate,DU 23811 fumarate,DU-23811 fumarate |
5-HT Receptor; Serotonin Transporter; Norepinephrine | GPCR/G Protein; Neuroscience |
Clovoxamine fumarate (DU 23811 fumarate) 是一种 5-羟色胺再摄取、血清素和去甲肾上腺素抑制剂,具有抗抑郁和抗惊厥活性。 | |||
T21425 |
Mephenytoin
Mesantoin,Methoin,Insulton,Phenantoin,美芬妥因,Methylphenetoin |
P450 | Metabolism |
Mephenytoin (Phenantoin) 是 CYP2C19 及 CYP2B6 的底物,是一种抗惊厥剂。 | |||
T4688 |
Pipequaline hydrochloride
PK-8165 hydrochloride,盐酸哌夸林 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Pipequaline hydrochloride (PK-8165 hydrochloride) 是一种苯二氮卓受体部分激动剂,有抗焦虑作用。 | |||
T11278 |
FG8119
NNC13-8119 |
Others | Others |
FG8119 是一种新型苯二氮卓 (benzodiazepine) 激动剂,具有潜在的抗惊厥和抗癫痫活性,可用于研究神经系统疾病。 | |||
T14974 |
Citenamide
Cytenamide,AY-15613 |
Others | Others |
Citenamide (AY-15613) 具有抗癌和抗惊厥活性,具有促进睡眠的作用,可用于研究神经系统疾病。 | |||
T7843 |
4-phenoxypiperidine
|
Others | Others |
4-phenoxypiperidine 具有肌肉松弛和抗惊厥活性。 | |||
T8594 |
Pheneturide
2-PHENYLBUTYRYLUREA,S-46,Benuride,苯丁酰脲 |
Others | Others |
Pheneturide (Benuride) 是Phenobarbita l 脱羧后的产物,可阻止精神运动性癫痫发作。 | |||
T27288 |
Esuprone
LU-43839,LU 43839,LU43839 |
MAO | Metabolism; Neuroscience |
Esuprone (LU-43839) 是一种新型可逆且具有高选择性的MAO-A 抑制剂,具有抗惊厥活性,可用于治疗抑郁症。 | |||
T31354 |
Decimemide
V 285,V-285,V285 |
Others | Others |
Decimemide (V-285)是一种烷氧基苯甲酸衍生物,具有抗癫痫活性和潜在的抗惊厥活性,可用研究神经系统疾病。 | |||
T1860 |
Imepitoin
AWD 131-138,ELB-138,伊匹妥英 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Imepitoin (AWD 131-138) 是一种新型的低亲和力部分苯二氮卓受体激动剂,有抗惊厥和抗焦虑作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5563 |
Cyclohexanecarboxylic Acid
环己甲酸,环己烷羧酸 |
Others; Endogenous Metabolite | Metabolism; Others |
Cyclohexanecarboxylic acid 是 Valproate 结构类似物,具有抗惊厥的作用。 | |||
T8014 |
Epoxylinalool
氧化芳樟醇,2-(2-Hydroxy-2-Propyl)-5-Methyl-5-Vinyltetrahydrofuran |
Others | Others |
Epoxylinalool (2-(2-Hydroxy-2-Propyl)-5-Methyl-5-Vinyltetrahydrofuran) 是一种天然存在的单萜醇,广泛用于香水和调味品的生产。 | |||
T3248 |
alpha-Boswellic acid
α-Boswellic acid,α-乳香酸 |
Others | Others |
alpha-Boswellic acid (α-Boswellic acid) 是一种从乳香中提取得到的五环三萜类天然产物,具有抗惊厥和抗癌作用。在动物体内,它是预防和减少阿尔茨海默病标志物,可用于阿尔茨海默病的研究。 | |||
T7064 |
Valproic Acid
Sodium valproate,2-Propylpentanoic Acid,丙戊酸,VPA,Depakine,2-Propylvaleric Acid |
Mitophagy; Gamma-secretase; HIV Protease; GABA Receptor; Sodium Channel; HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Proteases/Proteasome; Stem Cells |
Valproic Acid (2-Propylpentanoic Acid) 是一种 HDAC 抑制剂,可抑制 HDAC1 活性,诱导 HDAC2 降解,具有口服活性。Valproic Acid 可以用于癫痫和躁郁症的研究。 | |||
TN2865 |
(E)-3,4,5-Trimethoxycinnamic acid
O-Methylsinapic acid,3,4,5-三甲氧基肉桂酸,3,4,5-Trimethoxy-trans-cinnamic acid,3,4,5-Trimethoxyphenylacrylic acid |
Others | Others |
(E)-3,4,5-Trimethoxycinnamic acid (O-Methylsinapic acid) 是一种来自羌活根和根茎的天然产物。 | |||
T65135 |
Kynurenic acid
Fibrostop 2,Quinurenic acid |
GPR; GluR; NMDAR | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Kynurenic acid (Quinurenic acid) 是一种内源性色氨酸活性代谢物,是一种 NMDA, glutamate, α7 nicotinic acetylcholine receptor 三重拮抗剂,也是 GPR35/CXCR8 激动剂,具有神经保护和抗惊厥特性,可用于研究神经分裂和与代谢相关的疾病。 | |||
TN4114 |
Gardenin A
|
ERK; LDL; MAPK; PKA; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK; Metabolism; Tyrosine Kinase/Adaptors |
Gardenin A 通过激活 MAPK/ERK、PKC 和 PKA 表现出神经营养作用。 Gardenin A 具有抗抑郁、抗惊厥和抗焦虑作用。 | |||
T20587 |
2-Acetonaphthone
2-萘乙酮,beta-Acetylnaphthalene,beta-Acetonaphthalene,2Acetylnaphthalene,2-Acetylnaphthalene,2 Acetylnaphthalene,beta-Naphthyl methyl ketone |
Endogenous Metabolite | Metabolism |
2-Acetonaphthone (beta-Naphthyl methyl ketone) 是内源性代谢产物的一种。 | |||
T0728 |
Ethosuximide
Zarontin,乙琥胺 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Ethosuximide (Zarontin) 是一种抗癫痫药物,可改善多种神经退行性疾病模型的表型,且阻断低电压激活的 T 型钙通道。 | |||
T0361 |
Isovaleramide
异戊酰胺,3-Methylbutanamide |
Dehydrogenase | Metabolism |
Isovaleramide (3-Methylbutanamide) 是抗惊厥剂,能够调节中枢神经系统的活性。 | |||
T2S1814 |
p-Hydroxybenzaldehyde
4-Formylphenol,4-羟基苯甲醛;对羟基苯甲醛,4-hydroxybenzaldehyde,对羟基苯甲醛,p-Oxybenzaldehyde |
Transaminase; GABA Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
p-Hydroxybenzaldehyde (p-Oxybenzaldehyde) 是从天麻中提取的一种天然产物,对 GABA 转氨酶有抑制作用,有助于抗癫痫和抗惊厥活性。 | |||
T4842 |
1H-pyrazole
1,2-Diazole,Pyrazole,吡唑 |
Others; Endogenous Metabolite | Metabolism; Others |
1H-pyrazole (1,2-Diazole) 是内源性代谢产物的一种。 | |||
T5266 |
Tricaprilin
Glycerol Tri-n-octanoate,三辛酸甘油酯,trioctanoin,tricaprylic glyceride,Glyceryl trioctanoate |
Others; Endogenous Metabolite | Metabolism; Others |
Tricaprilin (Glycerol Tri-n-octanoate) 能够用于研究轻度到中度阿尔茨海默病患者,具有抗惊厥和植物代谢产物的活性。 | |||
TN7252 |
Olivetolic acid
2,4-Dihydroxy-6-pentylbenzoic acid |
Antibiotic | Microbiology/Virology |
Olivetolic acid (OLA) 是一种来自大麻中大麻素的前体,在Dravet综合征的小鼠模型中显示抗惊厥活性。Olivetolic acid 具有潜在的抗菌活性。 | |||
TN5131 |
Tetrahydrocannabivarin
THCV,delta9-Tetrahydrocannabivarin,CRM,Tetrahydrocannavarin |
Cannabinoid Receptor | GPCR/G Protein |
Tetrahydrocannabivarin (CRM) 是 cannabinoid type 1 receptor 的中性拮抗剂,对 2 型糖尿病有潜在治疗价值。 | |||
T3836 |
Eudesmin
|
MAPK; S6 Kinase | MAPK; PI3K/Akt/mTOR signaling |
Eudesmin 通过抑制S6K1信号通路来干扰成脂分化,具有抗肿瘤、抗炎和抗菌活性。 | |||
Fr14115 |
α-Terpineol
Terpineol,α-松油醇 |
IL Receptor; Anti-infection; Antibacterial | Immunology/Inflammation; Microbiology/Virology |
α-Terpineol (Terpineol) 是从蓝桉中分离出来的,对须癣毛癣菌有抗真菌活性,对牙周病和致龋菌有抗菌活性。它还具有抗惊厥和抗炎活性。 | |||
TMO2713 |
4(3H)-Quinazolinone
Quinazolin-4-ol,4-Hydroxyquinazoline,4-羟基喹唑啉,4-Quinazolinol,4-Quinazolone,4-Quinazolinone |
Antibacterial; Platelet aggregation | Microbiology/Virology; Others |
4(3H)-Quinazolinone (4-Hydroxyquinazoline) 是化学合成中的砌块,是一种生物活性氮杂环化合物。它具有多种生物学特性,如抗菌,抗真菌,抗惊厥,抗炎,抗 HIV,抗癌和缓解疼痛活性。 | |||
T5758 |
sphondin
6-甲氧基当归素,牛防风素,牛防风素 |
COX; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Sphondin 具有抗惊厥、抗炎和抗增殖活性,对 IL-1beta 诱导的 A549 细胞中 COX-2 蛋白水平和 PGE(2) 释放的增加具有抑制作用。 | |||
T0883 |
Tramiprosate
Homotaurine,3-Amino-1-propanesulfonic acid,Alzhemed,高牛黄酸 |
Beta Amyloid; GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Tramiprosate (Alzhemed) 是一种具有口服活性的、可透过血脑屏障的天然氨基酸,存在于各种红色海藻中,能够可溶性 Aβ 结合并以非原纤维形式维持 Aβ。它是一种 GABA 类似物,具有神经保护,抗惊厥和抗高血压的活性。 | |||
T5566 |
Ethyl maltol
2-Ethyl-3-hydroxy-4H-pyran-4-one,乙基麦芽酚,2-Ethyl pyromeconic acid |
Others | Others |
Ethyl maltol (2-Ethyl-3-hydroxy-4H-pyran-4-one) 是一种化合物,在食品添加剂中占有重要地位,主要作用于增强食品的香气,具备显著的气味活性。 | |||
TN1712 |
Gossypin
|
NF-κB; S6 Kinase | MAPK; NF-κB; PI3K/Akt/mTOR signaling |
Gossypin 是一种从Hibiscus vitifolius 中分离得到的黄酮,能够抑制NF-κB 和 NF-κB 的调节基因表达。在小鼠原代骨髓细胞和 RAW264.7 细胞中,它也可抑制 RANKL 诱导的破骨细胞形成。它具有抗氧化、抗炎、抗癌、抗衰老、抗糖尿病和保护肝脏的活性。 | |||
T5739 |
Paederosidic acid
鸡屎藤苷酸,异戊二酸 紫草酸 |
Apoptosis; BCL | Apoptosis |
Paederosidic acid 是从鸡矢藤分离出的一种天然产物,通过诱导线粒体介导的凋亡抑制肺癌细胞,具有显着的抗肿瘤、抗惊厥和镇静作用。 | |||
T6S1653 |
Albiflorin
Alibiflorin,芍药内酯苷 |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Albiflorin (Alibiflorin) 是一种牡丹根中的主要成分,是一种单萜糖苷。它具有神经保护、抗炎、抗氧化和缓解疼痛作用。 | |||
T37491 |
11-Oxo etiocholanolone
|
||
11-Ketoetiocholanolone is a metabolite of testosterone's excreted metabolite, etiocholanolone, and exhibits anticonvulsant activity[1][2]. | |||
T12373 |
Paxilline
|
Others | Others |
Paxilline is an indole alkaloid mycotoxin from Penicillium paxilli, acts as a potent BK channels inhibitor by an almost exclusively closed-channel block mechanism. Paxilline possesses significant anticonvulsant activity. | |||
T11534 |
Haemanthamine
|
Others | Others |
Haemanthamine is an alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. It inhibits protein biosynthesis during the elongation stage of translation. It has antimalarial, pro-apoptotic, antiviral, antioxidant, and anticonvulsa | |||
TN4322 |
Isopulegol
|
ATPase; Potassium Channel; GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Isopulegol presents depressant- and anxiolytic-like effects, it also has anticonvulsant and bioprotective effects against PTZ-induced convulsions are possibly related to positive modulation of benzodiazepine-sensitive GABAA receptors and to antioxidant properties.Isopulegol presents significant gastroprotective effects in both ethanol- and indomethacin-induced ulcer models, which appear to be mediated, at least in part, by endogenous prostaglandins, K(ATP) channel opening, and antioxidant proper... | |||
TN4624 | Nantenine | Others | Others |
Nantenine is an acetylcholinesterase inhibitor, it functions as an effective antagonist against a wide range of MDMA-induced effects in mice. Nantenine has anticonvulsant effect, which seems attributable to its stimulation and the resultant decrease of Ca | |||
T73813 | Haemanthamine hydrochloride | ||
Haemanthamine hydrochloride 是从Amaryllidaceae 植物中分离出来的一种蛇毒碱样生物碱,具有强大的抗癌活性。Haemanthamine hydrochloride 靶向核糖体以在翻译的延长阶段抑制蛋白质的生物合成。Haemanthamine hydrochloride 具有促凋亡,抗氧化剂,抗病毒,抗疟疾和抗惊厥活性。 |