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53

抑制剂 & 化合物

8

天然产物

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Cat. No. Product Name Target Signaling Pathways
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。
T3563 Lvguidingan

Others Others
Lvguidingan 是一种抗惊厥药。
T1052 Proglumide

二丙谷酰胺

cholecystokinin GPCR/G Protein
Proglumide (Binoside) 是一种非肽的、口服具有活性的胆囊收缩素(CCK)-A/B 受体拮抗剂。它能够选择性阻断 CCK 在中枢神经系统中的作用。它能够抑制胃分泌,具有保护胃十二指肠粘膜的能力,并表现出抗癫痫和抗氧化活性。
T8937 Soticlestat

TAK-935,OV935

P450 Metabolism
Soticlestat (OV935) 是一种首创的、口服有活性的胆固醇 24-羟化酶 (cholesterol 24-hydroxylase, CH24H) 选择性抑制剂。它可用于研究癫痫综合征。
T0939 Phenytoin

苯妥英,Diphenylhydantoin,5,5-Diphenylhydantoin

Virus Protease; Sodium Channel Membrane transporter/Ion channel; Microbiology/Virology
Phenytoin (5,5-Diphenylhydantoin) 是一种有效的电压门控钠离子通道阻滞剂,可减少小鼠乳腺肿瘤的生长和转移,具有抗癫痫活性。
T0192 Levetiracetam

左乙拉西坦,UCB L059,SIB-S1

DNA Methyltransferase; Others; Calcium Channel Chromatin/Epigenetic; Membrane transporter/Ion channel; Metabolism; Others
Levetiracetam (SIB-S1) 是一种化学增敏剂,增强 Temozolomide 对胶质母细胞瘤干细胞增殖和凋亡的影响。它调节 HDAC 水平,最终使 MGMT 沉默从而提高 Temozolomide 的有效性。它是一种抗癫痫药,可结合突触小泡蛋白 SV2A。
T0008 Phenytoin sodium

5,5-Diphenylhydantoin sodium salt,Diphantoine,苯妥英钠,Dilantin sodium,Diphenylhydantoin Sodium

Virus Protease; Sodium Channel Membrane transporter/Ion channel; Microbiology/Virology
Phenytoin sodium (Diphantoine) 是一种有效的电压门控钠离子通道阻滞剂,可减少小鼠乳腺肿瘤的生长和转移,具有抗癫痫活性。
T0128L Vigabatrin Hydrochloride

盐酸氨己烯酸,γ-Vinyl-GABA hydrochloride

GABA Receptor Membrane transporter/Ion channel; Neuroscience
Vigabatrin Hydrochloride (γ-Vinyl-GABA hydrochloride) 是抑制性神经递质 GABA 乙烯基衍生物,不可逆地抑制 GABA 转氨酶对 GABA 的分解代谢,增加脑中 GABA 的水平。
T16427 Padsevonil

UCB-0942

Others Others
Padsevonil is an effective antiepileptic compound.
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。
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。
T0628 Iminodibenzyl

Others Others
Iminodibenzyl 用作抗癫痫药carbamazepine 的中间体。
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。
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。
T28655 Sabeluzole

R 58735,R58735,R-58735

Microtubule Associated Cytoskeletal Signaling
Sabeluzole (R-58735) 具有抗癫痫和增强认知的作用,抑制神经毒素诱导的tau表达和细胞死亡。Sabeluzole 对氯氮卓诱导的习惯障碍有保护作用,可用于研究阿尔茨海默症。
T0028 Gamibetal

3-Hydroxy-GABA,4-氨基-3-羟基丁酸,4-Amino-3-hydroxybutyric Acid

HIV Protease Microbiology/Virology; Proteases/Proteasome
Gamibetal (4-Amino-3-hydroxybutyric Acid) 是 γ-氨基-β-羟基丁酸,对癫痫具有潜在的研究价值。
T16960 Sultiame

Others; Carbonic Anhydrase Metabolism; Others
Sultiame 是一种碳酸酐酶抑制剂。 Sultiame 可用于抗癫痫研究。
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。
TNU0187 2',5-Difluoro-2'-deoxy-1-arabinosyluracil

2'-Deoxy-2'-fluoro-5-fluoro-arabinouridine

Nucleoside Antimetabolite/Analog Cell Cycle/Checkpoint; DNA Damage/DNA Repair
2',5-Difluoro-2'-deoxy-1-arabinosyluracil (2'-Deoxy-2'-fluoro-5-fluoro-arabinouridine) 是一种尿嘧啶核苷类似物,具有潜在的抗癫痫活性和降压活性,可用于研究抗惊厥和焦虑症。
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。
T22171 WWL123

MAGL Metabolism
WWL123 是一种有效的选择性 ABHD6 抑制剂,IC50 为 430 nM。WWL123 可穿过血脑屏障并抑制脑实质中的 ABHD6。WWL123 阻断 ABHD6 在 Pentylenetetrazole (PTZ)诱导的 R6/2 小鼠癫痫样发作和自发性癫痫发作中发挥抗癫痫作用。
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。
T23651 AF-CX 921XX

AF-CX 921,AF-CX-921-XX

AF-CX 921XX is an antiepileptic agent.
T30848 CGP-47292

CGP 47,292,UNII-266244C47B,CGP 47292

CGP-47292 is a metabolite of the novel antiepileptic compound CGP 33,101.
T23567 Zonisamide sodium

Others Others
Zonisamide sodium is a 1,2 benzisoxazole derivative. It is the first agent of this chemical class to be developed as an antiepileptic drug.
T30748 Carisbamate

JNJ10234094,JNJ-10234094,RWJ 333369,RWJ-333369,RWJ333369

CarisbAMate (JNJ-10234094, RWJ 333369, YKP-509) is an antiepileptic drug candidate.
T24958 (R)-Licarbazepine Acetate

BIA2-059,Licarbazepine acetate, (R)-,BIA 2-059,BIA-2-059

(R)-Licarbazepine Acetate is a hopeful antiepileptic drug structurally related to Carbamazepine and Oxcarbazepine.
T12544 Proglumide hemicalcium

Others Others
Proglumide hemicalcium is a antagonist of nonpeptide and orally active cholecystokinin (CCK)-A/B receptors, has antiepileptic and antioxidant activities.
T26017 R 57720

R57720,R-57720

R 57720 is an antiepileptic agent.
T13185 Topiramate D12

RWJ 17021 D12,McN 4853 D12

Others Others
Topiramate D12 is a deuterium labeled Topiramate. Topiramate is an agent of broad-spectrum antiepileptic. Topiramate is an antagonist of GluR5 receptor.
T14281 Becampanel

AMP 397

Others Others
Becampanel (AMP397) is the first competitive AMPA antagonist. Becampanel (AMP397) also is an antiepileptic agent.
T23986 Dezinamide

ADD94057,ADD-94057,ADD 94057

Dezinamide is a potential antiepileptic drug. It shows preliminary evidence of efficacy and safety in an open-label study.
T61145 Topiramate lithium

Topiramate lithium (McN 4853) is a wide-ranging antiepileptic compound with GluR5 receptor antagonistic properties. Its mechanism of action involves enhancing GABAergic activity, inhibiting kainate/AMPA receptors, voltage-sensitive sodium and calcium channels, and increasing potassium conductance. Additionally, this compound inhibits carbonic anhydrase. [1][2][3]
T16869 Seletracetam

Ucb 44212

Others Others
Seletracetam is an analog of the antiepileptic agent Levetiracetam. Seletracetam is a small molecule SV2A modulator for the research of epilepsy.
T39708 Loreclezole hydrochloride

R 72063 hydrochloride,Loreclezole hydrochloride

Loreclezole hydrochloride, an antiepileptic compound, functions as a selective modulator of GABA A receptors. Specifically, it acts as a positive allosteric modulator on receptors containing β2 or β3-subunits.
T39428 Seletracetam lithium bromide

Ucb 44212 lithium bromide

Seletracetam (Ucb 44212) lithium bromide is a SV2A modulator, intended for epilepsy research. It is an analog of Levetiracetam, an antiepileptic agent.
TP1810 Somatostatin-25

Somatostatin is an endogenous neuropeptide hormone found in the brain and pancreas. Somatostatin binds several isoforms of the somatostatin receptor, exhibiting anxiolytic, antiepileptic/anticonvulsant, and anorexigenic activities.
T75079 5’(R)-C-Methyl-5-fluorouridine

5’(R)-C-Methyl-5-fluorouridine 是尿嘧啶核苷类似物,具有潜在抗癫痫能力。该类似物用于研究抗惊厥和抗焦虑活性,进而开发新型降压药物。
T75237 N3-[(Pyrid-4-yl)methyl]uridine

N3-[(Pyrid-4-yl)methyl]uridine 是尿嘧啶核苷类似物,潜在拥有抗癫痫作用。此类似物适用于探究抗惊厥和抗焦虑活性,进而用于开发新型降压药物。
T75080 2’-Deoxy-2’-fluoro-N3-[(pyrid-2-yl)methyl]uridine

2’-Deoxy-2’-fluoro-N3-[(pyrid-2-yl)methyl]uridine 为一种尿嘧啶核苷类似体,具备潜在抗癫痫效用。此类似物适用于探究抗惊厥与抗焦虑活性,并用于开发新型降压药物。
T15818 LY367385

FXR Metabolism
LY367385 is a highly effective and selective mGluR1a antagonist. LY367385 has neuroprotective, anticonvulsant, and antiepileptic effects. Compared with > 100 μM for mGlu5a, LY367385 has an IC50 of 8.8 μM for inhibits of quisqualate-induced phosphoinositide (PI) hydrolysis.
T60355 LY367385 hydrochloride

LY367385 hydrochloride 是一种高效且选择性的mGluR1a 拮抗剂,抑制喹喹啉诱导的磷酸肌醇水解的IC50值为 8.8 μM,而对 mGlu5a 的IC50值大于 100 μM。LY367385 hydrochloride 具有神经保护,抗惊厥和抗癫痫作用。
T75233 N3-(2S)-[2-(tert-Butoxycarbonyl)amino-3-(tert-butoxy carbonyl)]propyluridine

N3-(2S)-[2-(tert-Butoxycarbonyl)amino-3-(tert-butoxy carbonyl)]propyluridine是一种尿嘧啶核苷类似物,具有潜在的抗癫痫作用。这种类似物可用于抗惊厥和抗焦虑活性的研究,以及新型降压剂的开发。
T37149 Carbamazepine 10,11-epoxide

Others Others
Carbamazepine 10,11-epoxide 是抗惊厥药卡马西平 (carbamazepine) 的活性代谢物。它由卡马西平通过微粒体中的细胞色素 P450 (CYP) 同种型 CYP3A4 和 CYP2C8 形成,微粒体分别由表达 CYP3A4 或 CYP2C8 的 HepG2 细胞制备。它对小鼠电击诱发的癫痫发作具有抗惊厥活性。
T61086 HN37

HN37 是有效且稳定的抗癫痫活性的化合物,其对KCNQ2的EC50值为 37 nM。
T75232 2’-O-Acetyl-5’-O-benzoyl-3’-O-(2-methoxyethyl) uridine

2’-O-Acetyl-5’-O-benzoyl-3’-O-(2-methoxyethyl) uridine 是一种具有抗癫痫潜能的尿嘧啶核苷类似物。其不仅用于研究抗惊厥和抗焦虑活性,也用于开发新型降压药物。
T16948 Suclofenide

PB385,Neosulfalepsine,琥氯非尼

Others Others
Suclofenide 是一种苯磺酰胺衍生物,可作为抗惊厥和抗癫痫剂。在临床前模型中,它对小鼠电击和戊四唑诱导的惊厥表现出强大的抗惊厥活性。亚致死毒性表现为嗜睡、肌阵挛抽搐和腹泻。
T25455L Glutaurine aceate

Thyroid hormone receptor(THR) Endocrinology/Hormones
含有谷氨酰胺和牛磺酸残基的 Glutaurine aceate 是甲状旁腺的一种口服活性激素。Glutaurine 作为一种激素,从甲状旁腺嗜氧细胞中分离出来。Glutaurine 可用于抗癫痫和抗遗忘的研究。
T77991 Glutaurine TFA

Litoralon TFA

Glutaurine (Litoralon) TFA,含谷氨酰胺与牛磺酸残基,为甲状旁腺源嗜氧细胞分离的口服活性激素。该化合物在抗癫痫与抗健忘症研究中有应用。
T60492 Lamotrigine hydrate

Lamotrigine hydrate 是口服有效的抗惊厥剂或抗癫痫剂 ,通过选择性地阻断电压门控Na+通道,稳定突触前神经元膜并抑制谷氨酸释放。Lamotrigine hydrate 可用于研究癫痫、局灶性癫痫等神经性疾病。

化合物

ICA-27243
Cat.No: T15545
Synonym:
Target: Potassium Channel
Lvguidingan
Cat.No: T3563
Synonym:
Target: Others
Proglumide
Cat.No: T1052
Synonym: 二丙谷酰胺
Target: cholecystokinin
Soticlestat
Cat.No: T8937
Synonym: TAK-935,OV935
Target: P450
Phenytoin
Cat.No: T0939
Synonym: 苯妥英,Diphenylhydantoin,5,5-Diphenylhydantoin
Target: Virus Protease, Sodium Channel
Levetiracetam
Cat.No: T0192
Synonym: 左乙拉西坦,UCB L059,SIB-S1
Target: DNA Methyltransferase, Others, Calcium Channel
Phenytoin sodium
Cat.No: T0008
Synonym: 5,5-Diphenylhydantoin sodium salt,Diphantoine,苯妥英钠,Dilantin sodium,Diphenylhydantoin Sodium
Target: Virus Protease, Sodium Channel
Vigabatrin Hydrochloride
Cat.No: T0128L
Synonym: 盐酸氨己烯酸,γ-Vinyl-GABA hydrochloride
Target: GABA Receptor
Padsevonil
Cat.No: T16427
Synonym: UCB-0942
Target: Others
FG8119
Cat.No: T11278
Synonym: NNC13-8119
Target: Others
Carabersat
Cat.No: T14863
Synonym: SB 204269
Target: Others
Iminodibenzyl
Cat.No: T0628
Synonym:
Target: Others
Trimethadione
Cat.No: T0283
Synonym: 三甲双酮,3,5,5,-Trimethyloxazolidine-2,4-dione
Target: Calcium Channel
Decimemide
Cat.No: T31354
Synonym: V 285,V-285,V285
Target: Others
Sabeluzole
Cat.No: T28655
Synonym: R 58735,R58735,R-58735
Target: Microtubule Associated
Gamibetal
Cat.No: T0028
Synonym: 3-Hydroxy-GABA,4-氨基-3-羟基丁酸,4-Amino-3-hydroxybutyric Acid
Target: HIV Protease
Sultiame
Cat.No: T16960
Synonym:
Target: Others, Carbonic Anhydrase
Anticonvulsant agent 2
Cat.No: T73586
Synonym:
Target: Others
2',5-Difluoro-2'-deoxy-1-arabinosyluracil
Cat.No: TNU0187
Synonym: 2'-Deoxy-2'-fluoro-5-fluoro-arabinouridine
Target: Nucleoside Antimetabolite/Analog
Valrocemide
Cat.No: T3562
Synonym: TV1901,N-丙戊酰基甘氨酰胺,N-Valproylglycinamide,丙戊塞胺
Target: Others
WWL123
Cat.No: T22171
Synonym:
Target: MAGL
Divalproex Sodium
Cat.No: T6474
Synonym: Valproate semisodium,Epival,双丙戊酸钠
Target: HDAC
AF-CX 921XX
Cat.No: T23651
Synonym: AF-CX 921,AF-CX-921-XX
Target:
CGP-47292
Cat.No: T30848
Synonym: CGP 47,292,UNII-266244C47B,CGP 47292
Target:
Zonisamide sodium
Cat.No: T23567
Synonym:
Target: Others
Carisbamate
Cat.No: T30748
Synonym: JNJ10234094,JNJ-10234094,RWJ 333369,RWJ-333369,RWJ333369
Target:
(R)-Licarbazepine Acetate
Cat.No: T24958
Synonym: BIA2-059,Licarbazepine acetate, (R)-,BIA 2-059,BIA-2-059
Target:
Proglumide hemicalcium
Cat.No: T12544
Synonym:
Target: Others
R 57720
Cat.No: T26017
Synonym: R57720,R-57720
Target:
Topiramate D12
Cat.No: T13185
Synonym: RWJ 17021 D12,McN 4853 D12
Target: Others
Becampanel
Cat.No: T14281
Synonym: AMP 397
Target: Others
Dezinamide
Cat.No: T23986
Synonym: ADD94057,ADD-94057,ADD 94057
Target:
Topiramate lithium
Cat.No: T61145
Synonym:
Target:
Seletracetam
Cat.No: T16869
Synonym: Ucb 44212
Target: Others
Loreclezole hydrochloride
Cat.No: T39708
Synonym: R 72063 hydrochloride,Loreclezole hydrochloride
Target:
Seletracetam lithium bromide
Cat.No: T39428
Synonym: Ucb 44212 lithium bromide
Target:
Somatostatin-25
Cat.No: TP1810
Synonym:
Target:
5’(R)-C-Methyl-5-fluorouridine
Cat.No: T75079
Synonym:
Target:
N3-[(Pyrid-4-yl)methyl]uridine
Cat.No: T75237
Synonym:
Target:
2’-Deoxy-2’-fluoro-N3-[(pyrid-2-yl)methyl]uridine
Cat.No: T75080
Synonym:
Target:
LY367385
Cat.No: T15818
Synonym:
Target: FXR
LY367385 hydrochloride
Cat.No: T60355
Synonym:
Target:
N3-(2S)-[2-(tert-Butoxycarbonyl)amino-3-(tert-butoxy carbonyl)]propyluridine
Cat.No: T75233
Synonym:
Target:
Carbamazepine 10,11-epoxide
Cat.No: T37149
Synonym:
Target: Others
HN37
Cat.No: T61086
Synonym:
Target:
2’-O-Acetyl-5’-O-benzoyl-3’-O-(2-methoxyethyl) uridine
Cat.No: T75232
Synonym:
Target:
Suclofenide
Cat.No: T16948
Synonym: PB385,Neosulfalepsine,琥氯非尼
Target: Others
Glutaurine aceate
Cat.No: T25455L
Synonym:
Target: Thyroid hormone receptor(THR)
Glutaurine TFA
Cat.No: T77991
Synonym: Litoralon TFA
Target:
Lamotrigine hydrate
Cat.No: T60492
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T10147 4-Hydroxymephenytoin

(+/-)-4'-Hydroxymephenytoin

Others; Drug Metabolite Metabolism; Others
4-Hydroxymephenytoin ((+/-)-4'-Hydroxymephenytoin) 是抗癫痫药 mephenytoin 的代谢产物。Mephenytoin 是 CYP2C19的配体。
T7024 Qingyangshengenin

青阳参甙元,Qingyangshengenin A,Cynanchagenin

Others Others
Qingyangshengenin (Cynanchagenin) 是一种孕烷糖苷,是一种分离自Cychuchumot ophyllum(Asclepiadaceae) 的根中的 C21 类固醇糖苷配基。它具有抗癌作用。
T3003 5-hydroxytryptophan

5-羟基色氨酸,NSC-92523

Others; Endogenous Metabolite Metabolism; Others
5-hydroxytryptophan (NSC-92523) 是色氨酸的代谢物,是5-羟色胺直接的前体,是芳香氨基酸脱羧酶底物。
T1379 L-5-Hydroxytryptophan

5-羟基色氨酸,L-oxitriptan,Oxitriptan,L-5-HTP

Amino Acids and Derivatives; Endogenous Metabolite Metabolism
L-5-Hydroxytryptophan (L-5-HTP) 是一种天然氨基酸和膳食补充剂,可以用作抗抑郁剂、食欲抑制剂和睡眠辅助剂,是神经递质血清素的前体,是利血平(reserpine) 的拮抗剂。它能够用于肌阵挛、纤维肌痛症、偏头痛和小脑共济失调的研究。
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。
TMS1461 Qingyangshengenin B

青阳参甙元B,青阳参苷元B,Otophylloside B

Beta Amyloid Neuroscience
Qingyangshengenin B (Otophylloside B) 是一种分离自 Qingyangshen 的 C-21 甾体苷。它能够在 mRNA 水平上抑制 Aβ 的表达来减少 Aβ 的沉积,对 Aβ 的毒性有保护作用。它具有抗癫痫作用。
T2768 Saikosaponin A

柴胡皂苷A,柴胡皂苷 A

NF-κB; Antibacterial; Liver X Receptor Metabolism; Microbiology/Virology; NF-κB
Saikosaponin A 是银柴胡中的主要活性成分,有抗炎活性,可上调 LXRα的表达。
T3S1416 Decursin

Decursinol angelate,前胡素,(+)-Decursin,紫花前胡素

Apoptosis; PKC Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling
Decursin (Decursinol angelate) 是一种细胞毒性剂,是一种来自朝鲜当归根的有效蛋白激酶 C 激活剂。它通过 Hippo/YAP 信号通路抑制 HepG2 细胞的生长。它通过下调 CXCR7 表达来抑制胃癌中的肿瘤生长,迁移和侵袭。

天然产物

4-Hydroxymephenytoin
Cat.No: T10147
Synonym: (+/-)-4'-Hydroxymephenytoin
Target: Others, Drug Metabolite
Qingyangshengenin
Cat.No: T7024
Synonym: 青阳参甙元,Qingyangshengenin A,Cynanchagenin
Target: Others
5-hydroxytryptophan
Cat.No: T3003
Synonym: 5-羟基色氨酸,NSC-92523
Target: Others, Endogenous Metabolite
L-5-Hydroxytryptophan
Cat.No: T1379
Synonym: 5-羟基色氨酸,L-oxitriptan,Oxitriptan,L-5-HTP
Target: Amino Acids and Derivatives, Endogenous Metabolite
p-Hydroxybenzaldehyde
Cat.No: T2S1814
Synonym: 4-Formylphenol,4-羟基苯甲醛;对羟基苯甲醛,4-hydroxybenzaldehyde,对羟基苯甲醛,p-Oxybenzaldehyde
Target: Transaminase, GABA Receptor, Endogenous Metabolite
Qingyangshengenin B
Cat.No: TMS1461
Synonym: 青阳参甙元B,青阳参苷元B,Otophylloside B
Target: Beta Amyloid
Saikosaponin A
Cat.No: T2768
Synonym: 柴胡皂苷A,柴胡皂苷 A
Target: NF-κB, Antibacterial, Liver X Receptor
Decursin
Cat.No: T3S1416
Synonym: Decursinol angelate,前胡素,(+)-Decursin,紫花前胡素
Target: Apoptosis, PKC
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