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70

抑制剂 & 化合物

15

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T38776	LP-922056	Wnt/beta-catenin	Cytoskeletal Signaling; Stem Cells
	LP-922056 是 Notum Pectinacetylesterase 的抑制剂，对人和小鼠的 EC50 值分别为 21 nM 和 55 nM。
T3198L	PRE-084 hydrochloride	Sigma receptor	GPCR/G Protein
	PRE-084 hydrochloride 是 σ1 的选择性激动剂在sigma 受体检测中，IC50值为44 nM。
T3217	PF-CBP1 hydrochloride PF-CBP1 HCl	Epigenetic Reader Domain; Histone Acetyltransferase	Chromatin/Epigenetic
	PF-CBP1 hydrochloride (PF-CBP1 HCl) 是 CREB 结合蛋白溴结构域的一种高选择性抑制剂，抑制 CREBBP 和 EP300溴结构域的 IC50分别为 125 和 363 nM。它降低 LPS 诱导的巨噬细胞中炎症因子的表达，也可下调皮质神经元 RGS4 的表达，可用于癫痫和帕金森病等神经疾病的研究。
T21460	Teriparatide acetate hPTH 1-34 (acetate salt),Parathar acetate,Forteo,醋酸立特帕肽	Others	Others
	Teriparatide acetate (Forteo) 是一种 PHT 激动剂，在 HEK293 细胞中的 IC50 为 2 nM。Teriparatide acetate 是一种重组形式的甲状旁腺激素。它是一种有效的合成代谢（即骨骼生长）剂，用于治疗某些形式的骨质疏松症。间歇使用特立帕肽比破骨细胞更能激活成骨细胞，从而导致骨骼整体增加。
T12472	Pifithrin-α, p-Nitro, Cyclic PFN-α	p53	Apoptosis
	Pifithrin-α, p-Nitro, Cyclic (PFN-α) 是 p53 的细胞渗透性和活性形式抑制剂。它对暴露于 Etoposide 的皮层神经元的保护作用比 Pifithrin-α 强一个数量级，ED50为30 nM。它也作为 p53 转录后的活性抑制剂。
T22517	5,7-Dichlorokynurenic acid 5,7-二氯犬尿喹啉酸,5,7-dichlorokynurenic acid sodium,5,7-DCKA	NMDAR	Neuroscience
	5,7-Dichlorokynurenic acid (5,7-dichlorokynurenic acid sodium) 是一种专门针对于NMDA 受体甘氨酸位点的竞争性拮抗剂(KB:65 nM)。它是犬尿酸的衍生物，可降低大鼠皮质细胞培养物中 NMDA 诱导的神经元损伤程度。
TP2045	CH 275
	Potent somatostatin receptor 1 (sst1) agonist; displays selectivity for sst1 (IC50 values are 30.9 nM, 345 nM, > 1 μM, > 10 μM and > 10μM for human sst1, sst3, sst4, sst2 and sst5 respectively). Attenuates somatostatin release in the rat nucleus accumbens
T21584	CP 465022	iGluR	Membrane transporter/Ion channel; Neuroscience
	CP 465022 hydrochloride 是强效的、选择性的AMPA 受体非竞争性拮抗剂，具有抗惊厥活性。CP 465022 hydrochloride 在大鼠皮层神经元中抑制Kainate 诱导的反应 (IC50= 25 nM)。
T11217	Eplivanserin 依利色林,SR-46349	5-HT Receptor	GPCR/G Protein; Neuroscience
	Eplivanserin (SR-46349) 是一种有效和特异性的 5-HT2A 受体拮抗剂，Kd 值为 1.14 nM，在大鼠皮质膜中 IC50 值为 5.8 nM。
T14490	Talipexole dihydrochloride Domnin,盐酸他利克索,B-HT 920 dihydrochloride	Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Talipexole dihydrochloride (Domnin) 是一种多巴胺 D2 受体激动剂、α2-肾上腺素受体激动剂和 5-HT3 受体拮抗剂，有抗帕金森病活性。
T69467	Azacosterol IMD760,Diazasterol	Others	Others
	Azacosterol (Diazasterol) 是一种DHCR24抑制剂。Azacosterol 口服或腹腔注射后会在皮质神经元中发生一系列反应。
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。
T11684	Isoguvacine hydrochloride 1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride,异四氢烟酸	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Isoguvacine hydrochloride (1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride) 是 GABA 受体激动剂。它与大鼠突触皮质膜结合并激活 α1β2γ2S、α2β2γ2S、α3β2γ2S、α5β2γ2S 和 ρ1 亚基 GABAA 受体。
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。
T10162	5-HT3 antagonist 3	5-HT Receptor	GPCR/G Protein; Neuroscience
	5-HT3 antagonist 3 是一种高亲和力的 5-HT3 受体拮抗剂。5-HT3 antagonist 3 结合到大鼠脑皮质膜中的 5-HT3 受体，Ki 为 0.25 nM。
T10998	Deriglidole SL 86-0715	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Deriglidole (SL 86-0715) 是一种外周肾上腺素能受体拮抗剂，是一种具有选择性的α2受体抑制剂。 Deriglidole 对可乐定和 Idazoxan 有抑制作用而对哌唑嗪与大鼠皮质和人血小板α2-肾上腺素能受体不显示活性。
T23394	SR 57227A SR57227盐酸盐,SR 57227 hydrochloride	5-HT Receptor	GPCR/G Protein; Neuroscience
	SR 57227A (SR 57227 hydrochloride) 是一种有效的、具有口服活性和选择性的 5-HT3 受体激动剂，具有穿越血脑屏障的能力和抗抑郁作用。它对大鼠皮质膜和整个 NG 108-15 细胞或其膜上的 5-HT3 受体结合位点的亲和力，IC50在 2.8 至 250 nM 之间。
TP1223L	Apamin acetate Apamine acetate,Apamin acetate(24345-16-2 Free base)	Potassium Channel	Membrane transporter/Ion channel
	Apamin acetate (Apamine acetate) 是一种具有选择性的 Ca2+ 激活的 K+ (SK) 通道的阻断剂，是在蜂毒素中发现的一种 18 个氨基酸的肽类神经毒素。Apamin acetate 可增强皮质神经元撕裂损伤后的神经突生长和再生。Apamin acetate 具有抗炎和抗纤维化的作用。
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。
T3486	3-MATIDA	GluR; NMDAR	Neuroscience
	3-MATIDA 是一种有效的 mGluR-1 拮抗剂（IC50：6.3 μM，大鼠 mGluR-1a）。显示出 ≥ 40 倍于其他受体的选择性：mGluR-5、mGluR-2、mGluR-4 (mGluR-4a) (IC50 > 300 μM)、NMDA 和 GluR (AMPA) (IC50 = 250 μM)。 3-MATIDA 在体外培养的鼠皮质细胞和大鼠海马切片培养物中充当神经保护剂。
T70540	Pinokalant LOE-908	SARS-CoV; TRP/TRPV Channel	Membrane transporter/Ion channel; Microbiology/Virology
	Pinokalant (LOE-908) 是一种新型非选性阳离子通道抑制剂。Pinokalant 在体内实验中可显著减少皮质梗死体积，可改善缺血半影区的代谢和电生理状态，可减少大鼠大脑中动脉闭塞后急性期磁共振图像上的病变大小。Pinokalant是一种潜在的SARS-CoV-2蛋白酶抑制剂，可用于研究脑卒中。
T36141	Boscalid	Mitochondrial Metabolism	Metabolism
	Boscalid 是一种广谱羧酰胺类杀菌剂，通过与线粒体复合物 II/琥珀酸脱氢酶的泛醌位点结合来抑制真菌呼吸。
T26482	A-57696
	A-57696 is a cholecystokinin antagonist with selective for cortical CCK-B receptors (IC50 = 25 nM).
T0068L	Fluphenazine Decanoate Dihydrochloride
	Fluphenazine Decanoate Dihydrochloride is an antipsychotic agent, it could block postsynaptic dopamine D2 receptors in the limbic, cortical system and basal ganglia.
T36446	Neuropeptide Y (human) (TFA)
	Neuropeptide Y (human) TFA, a compound implicated in Alzheimer's disease (AD), exhibits protective effects against β-Amyloid toxicity in rat cortical neurons.
TP1338	Neuropeptide Y (29-64), amide, human TFA
	Neuropeptide Y (29-64), amide, human (TFA) is involved in Alzheimer's disease (AD) and protects rat cortical neurons against β-Amyloid toxicity.It is showed that Neuropeptide Y (29-64), amide, human (TFA) is able to protect cortical neurons from Aβ25-35 t
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。
T71554	ARN 14494
	ARN 14494 is a potent serine palmitoyltransferase inhibitor (SPT; IC50 = 27.3 nM). ARN 14494 inhibits synthesis of long chain ceramides and dihydroceramides in an in vitro model of Alzheimer's diease. The compound prevents the synthesis of proinflammatory cytokines and the oxidative stress-related enzymes iNOS and COX-2 in mouse primary cortical astrocytes. ARN 14494 is neuroprotective against β-amyloid 1-42 induced neurotoxicity in primary cortical neurons co-cultured with astrocytes.
T38610	Pirepemat IRL752
	Pirepemat (IRL752) is a cortical-preferring catecholamine agent that enhances cognition. It is utilized in the investigation of Parkinson's disease.
T70916	AGN-190851
	AGN-190851 is an alpha-2 adrenoceptor agonist which acts as a water diuretic by inhibiting vasopressin-stimulated cyclic AMP accumulation in cortical collecting tubules in mouse models.
T71733	VU0606170
	VU0606170 is a slack channels inhibitor and was shown to successfully decrease the malfunctioning spontaneous firing rate of cortical neurons, providing a potential avenue for achieving an anti-epileptic effect not previously attainable.
T28850	SR57227A SR 57227A,SR-57227A
	SR 57227A is a highly selective of peripheral and central 5-HT3 receptors and an inhibitor of NMDA receptor-mediated responses in rat cortical pyramidal cells. It exhibits anti-depressant like effects in rats and decreased isolation-induced aggressive beh
T60950	Pirepemat fumarate
	Pirepemat (IRL752) fumarate 可用于研究帕金森病。Pireemat fumarate 是一种偏向皮质的儿茶酚胺传递剂和认知促进剂。
T16155	MSN-125	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	MSN-125 effectively inhibits Bax/Bak-mediated apoptosis in HCT-116, BMK Cells, and primary cortical neurons protect primary neurons against glutamate excitotoxicity. MSN-125 is an effective Bax and Bak oligomerization inhibitor. MSN-125 prevents mitochond
T29809	AL-1 AL 1,AL1
	AL-1 is a GLYCOINOSITOL PHOSPHOLIPID MEMBRANE ANCHOR containing ephrin found in developing tectum. It can mediate the bundling of cortical axons and repel the axonal growth of retinal ganglia axons. It exists in a variety of adult tissues of BRAIN; HEART;
T0068L2	Fluphenazine free base Siqualine,Fluphenazine,Fluorophenazine,Fluorphenazine,Triflumethazine,Fluorfenazine
	Flufenazine is an antipsychotic drug. It is used to treat chronic mental illnesses such as schizophrenia. Flufenazine works by blocking postsynaptic dopamine D2 receptors in the limbic system, cortical system, and basal ganglia. This prevents the effects
T40510	Ac-RYYRWK-NH2 TFA Ac-RYYRWK-NH2 TFA
	Ac-RYYRWK-NH2 is a highly effective and specific partial agonist for the nociceptin receptor (NOP). It demonstrates a remarkable affinity for rat cortical membranes ORL1, with [3H]Ac-RYYRWK-NH2 exhibiting a Kd value of 0.071 nM. However, it shows negligible affinity towards μ-, κ-, or δ-opioid receptors.
T3648	Hypidone hydrochloride YL0919	5-HT Receptor	GPCR/G Protein; Neuroscience
	Hypidone hydrochloride (YL0919) 是一种新型抗抑郁候选药物，具有作为 5-HT1A 受体激动剂和选择性 5-羟色胺再摄取抑制剂的双重活性。
T73408	Immepip
	Immepip 是一种 H3激动剂。Immepip 可以减少皮质组胺的释放。Immepip 可用于神经系统疾病的研究。
T37203	CCK (26-30) (sulfated)
	CCK (26-30) is an N-terminal fragment of CCK , a peptide hormone found in the intestine and brain that stimulates digestion, mediates satiety, and is involved in anxiety. The sulfated form of CCK (26-30) inhibits binding of [125I]CCK-33 to guinea pig cortical membranes by 10% when used at a concentration of 0.1 mM.
T29002	Trazium Esilate EGYT3615,EGYT-3615,EGYT 3615
	Trazium esilate is an adrenergic receptor antagonist. Trazium esilate is a weak displacer on a1-, a2- and D2-receptors, however, it induced a2-receptor desenzitization after repeated treatment. It had no influence on rat brain cortical noradrenaline and s
T37661	LY 2886721 Hydrochloride
	Potent and selective β-secretase (BACE) inhibitor (IC50 values are 10.2 and 20.3 nM for human BACE2 and BACE1, respectively). Displays >5,000-fold selectivity for BACE over other proteases including cathepsin D, pepsin and renin. Inhibits Aβ1-40 and Aβ1-42 production in cells expressing mutated APP. Reduces hippocampal and cortical Aβ and sAPPβ levels in an Alzheimer's disease mouse model.
T79784	VU6004909
	VU6004909为mGlu5受体正构效应调节剂，pEC50值为7.59。其具有抗精神病样效应，并能逆转MK801引起的皮质活动增强和认知功能障碍。
TP2060	Conantokin G
	GluN2B (formally NR2B) selective, competitive antagonist of the NMDA receptor. Blocks NMDA-evoked current in mouse cortical neurons (IC50 = 480 nM); also inhibits NMDA-evoked responses in oocytes expressing GluN2B (formally NR2B), but not GluN2A (formally
T81899	LY836	iGluR	Membrane transporter/Ion channel; Neuroscience
	LY836是口服活性神经保护剂，有效阻断皮层神经元中PSD95-nNOS的关联，适用于缺血性脑卒中研究。
T37205	CCK (26-31) (sulfated)
	CCK (26-31) is an N-terminal fragment of CCK , a peptide hormone found in the intestine and brain that stimulates digestion, mediates satiety, and is involved in anxiety. The sulfated form of CCK (26-31) inhibits binding of [125I]CCK-33 to guinea pig cortical membranes by 21% when used at a concentration of 0.1 mM.
T21875	CP-465022 (maleate)
	CP-465022 Maleate is a potent, selective, noncompetitive AMPA receptor antagonist with anticonvulsant activity. It effectively counters the Kainate-induced response in rat cortical neurons, exhibiting an IC 50 of 25 nM. As such, CP-465022 Maleate presents a valuable instrument for studying the involvement of AMPA receptors in various physiological and pathophysiological processes [1] [2].
T35920	N-methyl Paroxetine
	N-methyl Paroxetine is a derivative of the selective serotonin reuptake inhibitor (SSRI) antidepressant paroxetine that inhibits [3H]paroxetine binding to rat cortical membranes (Ki = 4.3 nM). It inhibits serotonin uptake in rat brain synaptosomes with an IC50 value of 22 nM. N-methyl Paroxetine has been used as a precursor in the synthesis of paroxetine and is a potential impurity in commercial preparations of paroxetine.
T36811	uPSEM 817 tartrate
	Selective ultrapotent PSEM (uPSEM) agonist for α7L131G,Q139L,Y217F-GlyR (PSAM4-GlyR) and PSAM4-5-HT3 chimeric ion channel agonist (EC50 values are 0.3 and 0.5 nM, respectively). Suppresses firing of layer 2/3 cortical neurons expressing PSAM4-GlyR in brain slices. Increases contralateral rotation in mice expressing PSAM4-GlyR unilaterally in the substantia nigra reticulata (LED 0.1 mg/kg). Magnus et al (2019) Ultrapotent chemogenetics for research and potential clinical applications. Science 3...
T76061	Parathyroid hormone (1-34) (rat) acetate
	Parathyroid hormone (1-34) (rat) (acetate) 是一种甲状旁腺激素，主要用于骨质疏松症的研究，具有改善皮质和松质骨结构的功能。

化合物

Cat.No: T38776

Target: Wnt/beta-catenin

PRE-084 hydrochloride

Cat.No: T3198L

Target: Sigma receptor

PF-CBP1 hydrochloride

Cat.No: T3217

Synonym: PF-CBP1 HCl

Target: Epigenetic Reader Domain, Histone Acetyltransferase

Teriparatide acetate

Cat.No: T21460

Synonym: hPTH 1-34 (acetate salt),Parathar acetate,Forteo,醋酸立特帕肽

Target: Others

Pifithrin-α, p-Nitro, Cyclic

Cat.No: T12472

Synonym: PFN-α

Target: p53

5,7-Dichlorokynurenic acid

Cat.No: T22517

Synonym: 5,7-二氯犬尿喹啉酸,5,7-dichlorokynurenic acid sodium,5,7-DCKA

Target: NMDAR

Cat.No: TP2045

Cat.No: T21584

Target: iGluR

Cat.No: T11217

Synonym: 依利色林,SR-46349

Target: 5-HT Receptor

Talipexole dihydrochloride

Cat.No: T14490

Synonym: Domnin,盐酸他利克索,B-HT 920 dihydrochloride

Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor

Cat.No: T69467

Synonym: IMD760,Diazasterol

Target: Others

Neuropeptide Y (29-64), amide, human acetate

Cat.No: TP1140L

Target: Neuropeptide Y Receptor

Isoguvacine hydrochloride

Cat.No: T11684

Synonym: 1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride,异四氢烟酸

Target: GABA Receptor

(D-Trp12,Tyr34)-pTH (7-34) amide (bovine) acetate

Cat.No: T9691L

Target: Thyroid hormone receptor(THR)

5-HT3 antagonist 3

Cat.No: T10162

Target: 5-HT Receptor

Cat.No: T10998

Synonym: SL 86-0715

Target: Adrenergic Receptor

Cat.No: T23394

Synonym: SR57227盐酸盐,SR 57227 hydrochloride

Target: 5-HT Receptor

Cat.No: TP1223L

Synonym: Apamine acetate,Apamin acetate(24345-16-2 Free base)

Target: Potassium Channel

Cat.No: T0939

Synonym: 苯妥英,Diphenylhydantoin,5,5-Diphenylhydantoin

Target: Virus Protease, Sodium Channel

Cat.No: T3486

Target: GluR, NMDAR

Cat.No: T70540

Synonym: LOE-908

Target: SARS-CoV, TRP/TRPV Channel

Cat.No: T36141

Target: Mitochondrial Metabolism

Cat.No: T26482

Fluphenazine Decanoate Dihydrochloride

Cat.No: T0068L

Neuropeptide Y (human) (TFA)

Cat.No: T36446

Neuropeptide Y (29-64), amide, human TFA

Cat.No: TP1338

Cat.No: T8456

Target: Neuropeptide Y Receptor

Cat.No: T71554

Cat.No: T38610

Synonym: IRL752

Cat.No: T70916

Cat.No: T71733

Cat.No: T28850

Synonym: SR 57227A,SR-57227A

Pirepemat fumarate

Cat.No: T60950

Cat.No: T16155

Target: Akt

Cat.No: T29809

Synonym: AL 1,AL1

Fluphenazine free base

Cat.No: T0068L2

Synonym: Siqualine,Fluphenazine,Fluorophenazine,Fluorphenazine,Triflumethazine,Fluorfenazine

Ac-RYYRWK-NH2 TFA

Cat.No: T40510

Synonym: Ac-RYYRWK-NH2 TFA

Hypidone hydrochloride

Cat.No: T3648

Synonym: YL0919

Target: 5-HT Receptor

Cat.No: T73408

CCK (26-30) (sulfated)

Cat.No: T37203

Trazium Esilate

Cat.No: T29002

Synonym: EGYT3615,EGYT-3615,EGYT 3615

LY 2886721 Hydrochloride

Cat.No: T37661

Cat.No: T79784

Cat.No: TP2060

Cat.No: T81899

Target: iGluR

CCK (26-31) (sulfated)

Cat.No: T37205

CP-465022 (maleate)

Cat.No: T21875

N-methyl Paroxetine

Cat.No: T35920

uPSEM 817 tartrate

Cat.No: T36811

Parathyroid hormone (1-34) (rat) acetate

Cat.No: T76061

Cat. No.	Product Name	Target	Signaling Pathways
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。
T6S1418	Praeruptorin C	Antioxidant; Calcium Channel	Membrane transporter/Ion channel; Metabolism; oxidation-reduction
	Praeruptorin C 是白花前胡中的一种主要成分，是钙拮抗剂，pD2′值为 5.7。
T5S2129	Sciadopitysin	TNF; NF-κB	Apoptosis; NF-κB
	Sciadopitysin 是一种双黄酮类化合物，来自银杏叶片中。它通过抑制NF-κB 活化并降低c-Fos 和NFATc1的表达来抑制 RANKL 诱导的破骨细胞生成和骨丢失。
TN2037	Paeonilactone C (3S,3AR,6S,7AR)-3-[(苯甲酰基氧基)甲基]四氢-6-羟基-6-甲基-2,5(3H,4H)-苯并呋喃二酮,芍药内苷 C	Others	Others
	Paeonilactone C significantly protects primary cultures of rat cortical cells against H2O2-induced neurotoxicity.
TN5169	Traxillaside 香榧	Others	Others
	Traxillaside has significant neuroprotective activities against glutamate-induced toxicity in primary cultures of rat cortical cells .
TN2257	Tanshinone IIB 丹参酮ⅡB	BCL; Caspase; P-gp	Apoptosis; Membrane transporter/Ion channel; Neuroscience; Proteases/Proteasome
	Co-treatment with Tanshinone IIB (TSB) significantly inhibits the DNA laddering, cytotoxicity and apoptosis of rat cortical neurons induced by staurosporine in a concentration-dependent manner; TSB also suppresses the elevated Bax protein and decreased bc
TN3771	Dasycarpol	Others	Others
	Dasycarpol(9beta-Hydroxyfraxinellone) shows significant neuroprotective activity against glutamate-induced neurotoxicity in primary cultures of rat cortical cells at a concentration of 0.1 microM. Dasycarpol also shows moderate inhibitory activity on lung
TCA2511	11Beta-hydroxyprogesterone	Sodium Channel	Membrane transporter/Ion channel
	The progesterone derivatives 11 alpha- and 11 beta-hydroxyprogesterone are potent inhibitors of 11 beta-hydroxysteroid dehydrogenase (isoforms 1 and 2) in vitro and can confer mineralocorticoid activity on corticosterone in the rat in vivo. 11beta-Hydroxyprogesterone acts as a mineralocorticoid agonist in stimulating Na+ absorption in mammalian principal cortical collecting duct cells.
TN2036	Paeonilactone B (+)-Paeonilactone B	NADPH-oxidase	Immunology/Inflammation
	Paeonilactone B ((+)-Paeonilactone B) 是一种来自白芍的单萜类化合物，具有神经保护活性，抑制氧化应激，在大鼠皮质细胞在抑制 H2O2 诱导的神经毒性。
T16846	Sauristolactam Saurolactam	Others	Others
	Sauristolactam inhibits the receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclastogenesis and has the potential to inhibit osteoclast differentiation. Sauristolactam, a natural aristolactam isolated from aerial portions of Saururus Chi
T83288	5-Hydroxy-2-[2-(2-hydroxyphenyl)ethyl]chromone
	Hydroxy-2-[2-(2-hydroxyphenyl)ethyl]chromone 是一种神经保护剂，对谷氨酸诱导的大鼠皮质细胞原代培养显示显著的神经保护效果。
TN4286	Isodunnianol	NOS; NF-κB; ROS; AChR	Immunology/Inflammation; Neuroscience; NF-κB
	Isodunnianol exhibits anti-AChE activity with an IC50 value of 13.0 uM; it also exhibits neurite outgrowth-promoting activity at the concentration ranging from 0.1 to 10 uM in the primary cultured rat cortical neurons. Isodunnianol, dunnianol, and Macrant
TN3444	Aristolactam BII	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Aristolactam BII exhibits antimicrobial and antiinflammatory activity, it shows significant activity towards DPPH radical scavenging and potent inhibitory effects against tyrosinase mushroom. Aristolactam BII also exerts its significant neuroprotective ef
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。
TN5164	trans-Hinokiresinol	IL Receptor; TNF; NOS; LTR	Apoptosis; Immunology/Inflammation
	Hinokiresinol is a novel inhibitor of LTB4 binding to the human neutrophils, it has antiallergic effect, it inhibits IgE-induced mouse passive cutaneous anaphylaxis reaction. Hinokiresinol (trans-hinokiresinol) and nyasol (cis-hinokiresinol) are estrogen

天然产物

Tetrahydrocannabivarin

Cat.No: TN5131

Synonym: THCV,delta9-Tetrahydrocannabivarin,CRM,Tetrahydrocannavarin

Target: Cannabinoid Receptor

Cat.No: T6S1418

Target: Antioxidant, Calcium Channel

Cat.No: T5S2129

Target: TNF, NF-κB

Paeonilactone C

Cat.No: TN2037

Synonym: (3S,3AR,6S,7AR)-3-[(苯甲酰基氧基)甲基]四氢-6-羟基-6-甲基-2,5(3H,4H)-苯并呋喃二酮,芍药内苷 C

Target: Others

Cat.No: TN5169

Synonym: 香榧

Target: Others

Cat.No: TN2257

Synonym: 丹参酮ⅡB

Target: BCL, Caspase, P-gp

Cat.No: TN3771

Target: Others

11Beta-hydroxyprogesterone

Cat.No: TCA2511

Target: Sodium Channel

Paeonilactone B

Cat.No: TN2036

Synonym: (+)-Paeonilactone B

Target: NADPH-oxidase

Cat.No: T16846

Synonym: Saurolactam

Target: Others

5-Hydroxy-2-[2-(2-hydroxyphenyl)ethyl]chromone

Cat.No: T83288

Cat.No: TN4286

Target: NOS, NF-κB, ROS, AChR

Aristolactam BII

Cat.No: TN3444

Target: HIV Protease

Conantokin G TFA

Cat.No: T75890

trans-Hinokiresinol

Cat.No: TN5164

Target: IL Receptor, TNF, NOS, LTR

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