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Search Results for " antidepressant-like "

49

抑制剂 & 化合物

16

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T18918	Azure B Azure B chloride,天青 B	MAO; Monoamine Oxidase	Metabolism; Neuroscience
	Azure B (Azure B chloride) 是一种 Methylene blue 的主要代谢物，是一种阳离子染料，用于 Azure 曙红染色剂以进行血液涂片染色。它是高选择性和可逆的抑制单胺氧化酶(MAO)-A 的抑制剂，对重组人的 MAO-A 和 MAO-B 的IC50分别为 11 和 968 nM。它具有显著的抗抑郁作用。
T39341	FCPR03	PDE	Metabolism
	FCPR03 是一种特异性磷酸二酯酶 4 (PDE4) 抑制剂，对 PDE4B1、PDE4D7 和 PDE4 催化结构域的 IC50 分别为 31 nM、47 nM 和 60 nM。 FCPR03 具有神经保护、抗炎和抗抑郁样作用。
T21995	XAP044	GluR	Neuroscience
	XAP044 是高效的选择性mGlu7拮抗剂。代谢型谷氨酸受体亚型 7 是哺乳动物 CNS 中神经传递的重要突触前调节剂。它在啮齿动物行为测试中表现出较好的大脑暴露、广谱抗应激、抗抑郁以及抗焦虑作用。
T16421	p-MPPI hydrochloride	5-HT Receptor	GPCR/G Protein; Neuroscience
	p-MPPI hydrochloride 是一种选择性的，具有高亲和力的5-HT1A 受体拮抗剂，能穿过血脑屏障，具有抗抑郁和抗焦虑样作用。
T15795	Luzindole N-乙酰-2-苄基色胺,N-0774	Melatonin Receptor; MT Receptor	GPCR/G Protein; Neuroscience
	Luzindole (N-0774) 是一种选择性褪黑素受体拮抗剂，可抑制实验性自身免疫性脑脊髓炎，有抗抑郁样活性。它优先靶向 MT2 (Mel1b)，对于人 MT2 和 MT1 的 Ki 值分别为 10.2 和 158 nM。
T19916	TRIM 1-(2-Trifluoromethylphenyl)imidazole,1-(2-三氟甲基苯基)咪唑	NOS	Immunology/Inflammation
	TRIM (1-(2-Trifluoromethylphenyl)imidazole) 是一氧化氮合酶抑制剂。它在体外能够抑制小鼠小脑 nNOS (IC50:28.2 µM)，以及大鼠肺 iNOS (IC50:27.0 µM)。它拥有抗焦虑以及抗抑郁的能力。
T6714	URB-597 KDS-4103,FAAH Inhibitor II	Mitophagy; FAAH; Autophagy	Autophagy; Metabolism; Neuroscience
	URB-597 (FAAH Inhibitor II) 是一种可口服的选择性FAAH 抑制剂。它抑制大鼠脑膜、体外大鼠神经元和人肝微粒体中的 FAAH 活性，IC50分别为 5、0.5和 3 nM。它具有抗抑郁样作用，可研究缓解疼痛。
T7601L	Carbetocin acetate 醋酸卡贝缩宫素,Carbetocin acetate(37025-55-1 free base),卡贝缩宫素醋酸盐	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	Carbetocin acetate 是催产素类似物，是催产素受体激动剂，Ki 是 7.1 nM。它对催产素受体的嵌合 N 末端具有高亲和力，Ki 为 1.17 μM。它能透过血脑屏障，可以通过激活 CNS 中的催产素受体而具有类抗抑郁活性，具有用于产后出血的研究潜力。
T7601	Carbetocin 卡贝缩宫素,醋酸卡贝缩宫素	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	Carbetocin 是催产素类似物，是催产素受体激动剂，Ki 是 7.1 nM。它对催产素受体的嵌合 N 末端具有高亲和力，Ki 为 1.17 μM。它能透过血脑屏障，可以通过激活 CNS 中的催产素受体而具有类抗抑郁活性，具有用于产后出血的研究潜力。
T61518	TAK-653	iGluR	Membrane transporter/Ion channel; Neuroscience
	TAK-653, a selective positive allosteric modulator (PAM) of AMPA receptors exhibiting minimal agonistic activity, elicits an antidepressant-like response while maintaining a favorable safety profile in rat models.
T22051	BU 224 hydrochloride	Imidazoline Receptor	Neuroscience
	BU 224 hydrochloride 是一种选择性的咪唑啉 I(2) 结合位点配体，具有镇痛和抗抑郁样活性。
T23349	SF 11	Others	Others
	SF 11是一种有效的脑渗透神经肽 Y Y2 受体拮抗剂 (IC50=199 nM)。具有抗抑郁药样活性。
T13164	Tipepidine hydrochloride	Potassium Channel; Dopamine Receptor	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Tipepidine hydrochloride 对多巴胺 D2受体介导的 GIRK 电流 (IDA(GIRK))具有可逆的抑制作用，从而激活 VTA 多巴胺神经元，对 IDA(GIRK)的IC50为 7.0 μM。它是镇咳药，具有抗抑郁样作用。
T60201	CX717	GluR	Neuroscience
	CX 717 是 AMPA 受体的正变构调节剂，具有抗抑郁样作用。CX 717 可用于成人注意力缺陷多动障碍（ADHD）的研究。
T34374	RO5203648 HCl RO5203648,RO-5203648,RO 5203648	Others	Others
	RO5203648 HCl 是一种微量胺相关受体 1 (TAAR1) 的部分激动剂，具有抗精神病和抗抑郁样活性。 RO5203648 HCl 可用于神经精神治疗的研究。
T62711	OPC-14523 hydrochloride
	OPC-14523 hydrochloride 是一种口服具有活力的 sigma 和 5-HT1A 受体激动剂，具有抗抑郁药样活性。。OPC-14523 对 sigma 受体 σ1/2 (IC50=47/56 nM)、5-HT1A 受体 (IC50=2.3 nM) 和 5-HT 转运体 (IC50=80 nM) 表现出高度亲和力。
T8414	SNC 80 Snc-80,SNC80,NIH 10815	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	SNC 80 (NIH 10815) 是有效的，高度选择性的非肽类 δ 阿片 (δ-opioid) 受体激动剂，Ki 为1.78 nM，IC50 为 2.73 nM。SNC80 还以 EC50 为 52.8 nM 来选择性激活 HEK293 细胞中的 μ-δ 异聚体。SNC80 具有抗伤害性，抗痛觉过敏和抗抑郁样作用，并可用于多种头痛症的研究。
T26152	RU 43044 RU-43044,RU-044,RU044,RU43044
	RU 43044 is a selective glucocorticoid receptor antagonist that has exhibited an antidepressant-like effect.
T16408	Osanetant SR142801	Others	Others
	Osanetant produces anxiolytic- and antidepressant-like effects. Osanetant is a selective NK3 receptor antagonist. It is researched for schizophrenia.
T70880	TAK-137
	TAK-137 is a novel AMPA receptor potentiator with little agonistic effect, producing antidepressant-like effect without causing psychotomimetic effects.
T40778	Tyrosylleucine TFA Tyr-Leu TFA
	Tyrosylleucine (Tyr-Leu, YL) TFA is a dipeptide compound with potent antidepressant-like activity. This orally active compound demonstrates effective modulation of depressive symptoms.
T28034	MGS-0039 BCI 632,BCI-632,MGS0039,BCI632
	MGS-0039 is a group II metabotropic glutamate receptor (mgluR2/3) antagonist. Antidepressant-like action of group II mGlu receptor antagonists does not depend on serotonergic system activation. However, the AMPA receptor seems to play a key role in the an
T37622	F13714 fumarate F13714 fumarate
	F13714 fumarate, a selective biased agonist of the 5-HT1A receptor, exhibits antidepressant-like effects upon single administration in the mouse model of chronic mild stress[1].
T39120	Fluoroethylnormemantine
	Fluoroethylnormemantine, a derivative of Memantine, acts as an N-methyl-D-aspartate (NMDA) receptor antagonist. It can function as a positron emission tomography (PET) tracer, known as [18F]-fluoroethylnormemantine. This compound displays anti-amnesic, neuroprotective, antidepressant-like, and fear-attenuating properties.
T70292	DDPM-2571 HCl
	DDPM-2571 is a highly potent and in vivo active inhibitor of GABA transporter subtype 1 with anticonvulsant, anxiolytic, antidepressant and antinociceptive properties. DDPM-2571 was quickly distributed into the brain and was highly effective in the prevention of chemically-induced seizures (pentylenetetrazole and pilocarpine models) and 6-Hz convulsions. It demonstrated significant anxiolytic-like and antidepressant-like properties. DDPM-2571 had antinociceptive properties, both in the hot plate...
T11911	LY3020371 hydrochloride	GluR	Neuroscience
	LY3020371 hydrochloride exerts an antidepressant-like signature in vivo. LY3020371 hydrochloride is a potent, selective metabotropic glutamate 2/3 receptor (mGlu2/3) antagonist with Ki of 5.3 and 2.5 nM, potently blocks cAMP formation with IC50 of 16.2 nM.
T22194	BW 373U86
	BW373U86 (SNC86) 是一种δ-opioid 受体激动剂，IC50值为 1.49 nM。BW373U86 显示出抗抑郁样作用。
T39119	Fluoroethylnormemantine hydrochloride
	Fluoroethylnormemantine hydrochloride, a Memantine derivative, functions as an antagonist for the N-methyl-D-aspartate (NMDA) receptor. It can also serve as a positron emission tomography (PET) tracer, specifically as [18F]-Fluoroethylnormemantine hydrochloride. Notably, this compound displays a range of effects, including anti-amnesic, neuroprotective, antidepressant-like, and fear-attenuating properties.
TP1127	Nemifitide diTFA INN 00835 diTFA	5-HT Receptor	GPCR/G Protein; Neuroscience
	Nemifitide diTFA (INN 00835 diTFA) 是一种合成的五肽，是一种可透过血脑屏障的黑色素细胞抑制因子 (MIF) 的肽类似物，具有有效的抗抑郁活性。
T61506	NBI-31772 hydrate
	NBI-31772 hydrate is a powerful inhibitor of the interaction between insulin-like growth factor (IGF) and IGF-binding proteins (IGFBPs). It acts as a nonpeptide ligand, effectively releasing bioactive IGF-I from the IGF-I/IGFBP-3 complex (Ki values for all six human subtypes range from 1-24 nM). This compound demonstrates significant anxiolytic and antidepressant-like effects [1] [2] [3].
T79229	ETAP	Monoamine Oxidase	Neuroscience
	ETAP为一种既抑制MAO-A也抑制MAO-B的化合物，展现出抗抑郁样活性，可应用于重度抑郁症的研究领域。
T70487	Tofenacin (free base)
	Tofenacin (free base) is an antidepressant drug with a tricyclic-like structure. It acts as a serotonin-norepinephrine reuptake inhibitor, and based on its close relation to orphenadrine, may also possess anticholinergic and antihistamine properties. Tofenacin is also the major active metabolite of orphenadrine and likely plays a role in its beneficial effects against depressive symptoms seen in Parkinson's disease patients.
T74413	(S)-Osanetant
	(S)-Osanetant 是 Osanetant 的S 对映体。Osanetant (SR142801) 是一种选择性的NK3受体拮抗剂。Osanetant 有抗焦虑和抗抑郁的作用，并被研究用于精神分裂症。
T71537	Tofenacin hydrochloride
	Tofenacin hydrochloride is an antidepressant drug with a tricyclic-like structure. It acts as a serotonin-norepinephrine reuptake inhibitor, and based on its close relation to orphenadrine, may also possess anticholinergic and antihistamine properties. Tofenacin is also the major active metabolite of orphenadrine and likely plays a role in its beneficial effects against depressive symptoms seen in Parkinson's disease patients.
T73568	MTEP
	MTEP，一种非竞争性且高选择性的mGluR5拮抗剂，具有显著的抗抑郁和抗焦虑效果，亦被用于帕金森疾病的研究。
T35560	SAR502250
	SAR502250 is a potent, selective, ATP competitive, orally active and brain-penetrant inhibitor of GSK3, with an IC50 of 12 nM for human GSK-3β. SAR502250 displays antidepressant-like activity. SAR502250 can be used for the research of Alzheimer’s disease (AD)[1][2]. SAR502250 (0.01-1 μM; 36 h) attenuates the Aβ25-35-induced cell death in rat embryonic hippocampal neurons[2]. SAR502250 (1-100 mg/kg; a single p.o,) attenuates tau hyperphosphorylation in the cortex and spinal cord of transgenic mic...
T37823	M 084 hydrochloride
	TRPC4/5 channel blocker (IC50 values are 3.7-10.3 and 8.2 μM, respectively). Also weakly blocks TRPC3 channels. Exhibits rapid antidepressant and anxiolytic effects in vivo. Zhu et al (2015) Identification and optimization of 2-aminobenzimidazole derivatives as novel inhibitors of TRPC4 and TRPC5 channels. Br.J.Pharmacol. 172 3495 PMID:25816897 \|Yang et al (2015) Acute treatment with a novel TRPC4/C5 channel inhibitor produces antidepressant and anxiolytic-like effects in mice. PLoS One 10 e0136...
T60501	Tipepidine
	Tipepidine 是一种非麻醉性镇咳药，具有抗抑郁样作用。 Tipepidine 可逆地抑制多巴胺 (DA) D2 受体介导的 GIRK 电流 (IDA(GIRK) )，IC50值为 7.0 μM，随后激活 VTA 多巴胺神经元。
T79325	5-HT6 agonist 1	5-HT Receptor	GPCR/G Protein; Neuroscience
	5-HT6 agonist 1 (Compound 19)为一种5-HT6激动剂 (Ki: 5 nM)，展现出抗抑郁样特性并能改善认知缺陷，同时能抑制血小板聚集，具备高代谢稳定性。
T61617	Hcyb1
	Hcyb1 is a potent and specific inhibitor of phosphodiesterase 2 (PDE2). It exhibits a high degree of selectivity for inhibiting PDE2A with an IC50 value of 0.57 μM. In addition, Hcyb1 displays over 250-fold selectivity against other recombinant members of the PDE family. Moreover, its pharmacological actions include neuroprotective and antidepressant-like effects, which are believed to be mediated through the cAMP/cGMP-CREB-BDNF signaling pathway [1].
T28851	SRA880 free base SRA 880,NVPSRA880,NVP SRA880,NVP-SRA880,SRA-880,SRA880
	SRA880 is a non-peptide antagonist of somatostatin sst1-receptor. SRA880 displayed significantly lower affinity for the other human recombinant somatostatin receptors ( pK(d) < or = 6.0). SRA880 shows a certain binding affinity to the human dopamine D4 re
T75895	UFP-101 TFA
	UFP-101 TFA 是一种强效、选择性和竞争性的 NOP 受体拮抗剂，pKi 为 10.24。UFP-101 TFA 对 δ、μ 和 κ 类阿片受体的选择性大于 3000 倍。UFP-101 TFA 具有抗抑郁药样作用。
T62064	PDE4B/7A-IN-2
	5-HT1A/5-HT7受体拮抗剂（5-HT1A Ki=8 nM，Kb=0.04 nM；5-HT7 Ki=451 nM，Kb=460 nM）具有 PDE4B/PDE7A 抑制活性（PDE4BIC50=80.4μM；PDE7AIC50=151.3μM），其抗抑郁样作用强于作为参考活性分子的依西酞普兰。
T26225	SRA880 malonate SRA880,NVPSRA880,NVP-SRA880,NVP-SRA-880,NVP-SRA 880,NVP SRA880
	SRA880 is a non-peptide somatostatin sst(1) receptor antagonist which displays a significantly lower affinity for the other human recombinant somatostatin receptors ( pK(d)= 6.0) or a wide range of neurotransmitter receptors, except for the human dopamine
T73631	(Rac)-SNC80
	(Rac)-SNC80 是SNC80 的外消旋体。SNC80 (NIH 10815) 是一种有效的，高度选择性的非肽类 δ 阿片 (δ-opioid) 受体激动剂，Ki 为1.78 nM，IC50为 2.73 nM。SNC80 具有抗伤害性，抗痛觉过敏和抗抑郁样作用，并可用于多种头痛症的研究。
T78868	TWIK-1/TREK-1-IN-1	Potassium Channel	Membrane transporter/Ion channel
	TWIK-1/TREK-1-IN-1 (compound 2a) 是一种针对 TWIK 相关钾通道 (Potassium Channel) TREK-1 的抑制剂，有效抑制 TREK-1 的双孔域钾 (K2p) 通道，阻止其二聚化形成 TREK-1 同二聚体和 TWIK-1/TREK-1 异二聚体。作为抗抑郁治疗的潜在靶点，TWIK-1/TREK-1-IN-3 对 TREK-1 同二聚体和 TWIK-1/TREK-1 异二聚体表现出相当的选择性，IC50s 分别是 9.36 μM 和 14.6 μM，显示出抗抑郁样活性。
T83676	Tianeptine Metabolite MC5 sodium
	Tianeptine metabolite MC5是一种来自非典型抗抑郁化合物tianeptine的活性代谢物，通过β-氧化形成。此代谢物在使用表达人类μ-阿片受体（MOR）而非人类δ-阿片受体（DOR；EC50s = 0.454和 >100 µM, 分别）的HEK293T细胞进行的生物发光共振能量转移(BRET)试验中，特异性诱导G蛋白激活。在野生型小鼠上，30 mg/kg剂量的Tianeptine metabolite MC5可减少强迫游泳测试中的静止时间，但在MOR敲除小鼠中则不会，表明其具有MOR依赖的抗抑郁样活性。
T35814	Urocortin III (human) (trifluoroacetate salt)
	Urocortin III is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF , urocortin , urocortin II , frog sauvagine, and piscine urotensin I.1 Human urocortin III shares 90, 40, 37, and 21% identity to mouse urocortin III , mouse urocortin II , human urocortin , and mouse urocortin, respectively. Urocortin III selectively binds to type 2 CRF receptors (Kis = 21.7, 13.5, and >100 nM for rat CRF2α, rat CRF2β, and human CRF1, respectively)....
T36521	Alaproclate (hydrochloride)
	Alaproclate is a selective serotonin reuptake inhibitor (SSRI).1,2 It inhibits depletion of serotonin (5-HT) induced by 4-methyl-α-ethyl-m-tyramine in rat cerebral cortex, hippocampus, hypothalamus, and striatum (EC50s = 18, 4, 8, and 12 mg/kg, respectively).1 Alaproclate inhibits NMDA-evoked currents and depolarization-induced voltage-dependent potassium currents in rat hippocampal neurons (IC50s = 1.1 and 6.9 μM, respectively) and does not inhibit GABA-evoked currents when used at concentratio...

化合物

Cat.No: T18918

Synonym: Azure B chloride,天青 B

Target: MAO, Monoamine Oxidase

Cat.No: T39341

Target: PDE

Cat.No: T21995

Target: GluR

p-MPPI hydrochloride

Cat.No: T16421

Target: 5-HT Receptor

Cat.No: T15795

Synonym: N-乙酰-2-苄基色胺,N-0774

Target: Melatonin Receptor, MT Receptor

Cat.No: T19916

Synonym: 1-(2-Trifluoromethylphenyl)imidazole,1-(2-三氟甲基苯基)咪唑

Target: NOS

Cat.No: T6714

Synonym: KDS-4103,FAAH Inhibitor II

Target: Mitophagy, FAAH, Autophagy

Carbetocin acetate

Cat.No: T7601L

Synonym: 醋酸卡贝缩宫素,Carbetocin acetate(37025-55-1 free base),卡贝缩宫素醋酸盐

Target: Oxytocin Receptor

Cat.No: T7601

Synonym: 卡贝缩宫素,醋酸卡贝缩宫素

Target: Oxytocin Receptor

Cat.No: T61518

Target: iGluR

BU 224 hydrochloride

Cat.No: T22051

Target: Imidazoline Receptor

Cat.No: T23349

Target: Others

Tipepidine hydrochloride

Cat.No: T13164

Target: Potassium Channel, Dopamine Receptor

Cat.No: T60201

Target: GluR

Cat.No: T34374

Synonym: RO5203648,RO-5203648,RO 5203648

Target: Others

OPC-14523 hydrochloride

Cat.No: T62711

Cat.No: T8414

Synonym: Snc-80,SNC80,NIH 10815

Target: Opioid Receptor

Cat.No: T26152

Synonym: RU-43044,RU-044,RU044,RU43044

Cat.No: T16408

Synonym: SR142801

Target: Others

Cat.No: T70880

Tyrosylleucine TFA

Cat.No: T40778

Synonym: Tyr-Leu TFA

Cat.No: T28034

Synonym: BCI 632,BCI-632,MGS0039,BCI632

F13714 fumarate

Cat.No: T37622

Synonym: F13714 fumarate

Fluoroethylnormemantine

Cat.No: T39120

Cat.No: T70292

LY3020371 hydrochloride

Cat.No: T11911

Target: GluR

Cat.No: T22194

Fluoroethylnormemantine hydrochloride

Cat.No: T39119

Nemifitide diTFA

Cat.No: TP1127

Synonym: INN 00835 diTFA

Target: 5-HT Receptor

NBI-31772 hydrate

Cat.No: T61506

Cat.No: T79229

Target: Monoamine Oxidase

Tofenacin (free base)

Cat.No: T70487

Cat.No: T74413

Tofenacin hydrochloride

Cat.No: T71537

Cat.No: T73568

Cat.No: T35560

M 084 hydrochloride

Cat.No: T37823

Cat.No: T60501

5-HT6 agonist 1

Cat.No: T79325

Target: 5-HT Receptor

Cat.No: T61617

SRA880 free base

Cat.No: T28851

Synonym: SRA 880,NVPSRA880,NVP SRA880,NVP-SRA880,SRA-880,SRA880

Cat.No: T75895

Cat.No: T62064

SRA880 malonate

Cat.No: T26225

Synonym: SRA880,NVPSRA880,NVP-SRA880,NVP-SRA-880,NVP-SRA 880,NVP SRA880

Cat.No: T73631

TWIK-1/TREK-1-IN-1

Cat.No: T78868

Target: Potassium Channel

Tianeptine Metabolite MC5 sodium

Cat.No: T83676

Urocortin III (human) (trifluoroacetate salt)

Cat.No: T35814

Alaproclate (hydrochloride)

Cat.No: T36521

Cat. No.	Product Name	Target	Signaling Pathways
T3886	Rosavin Rosavidin,络塞维	P450	Metabolism
	Rosavin (Rosavidin) 是从R. rosea 中获得的，在小鼠模型中表现出抗抑郁、适应原性和抗焦虑样作用。
T3856	Tenuifoliside A	ERK; Others	MAPK; Others
	Tenuifoliside A 是从远志分离得到的一种天然产物，具有抗凋亡、抗抑郁、抗炎和神经保护活性。
T5648	Purpurin 吡啉,1,2,4-Trihydroxyanthraquinone,Hydroxylizaric acid,Verantin	MAO; Antibacterial; Antibiotic; Antifungal	Metabolism; Microbiology/Virology; Neuroscience
	Purpurin (Verantin) 是来自Rubia tinctorumL. 的天然蒽醌，具有抗抑郁样作用。
T3933	Jatrorrhizine Yatrorizine,neprotin,药根碱	MAO; 5-HT Receptor; Antibacterial; AChE	GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience
	Jatrorrhizine (neprotin) 是一种从黄连中分离得到的生物碱，具有抗菌、抗氧化、抗疟原虫和神经保护活性。它通过抑制 uptake-2 transporter 的活性减少血清素和去甲肾上腺素的摄取。它是一种有口服活性的乙酰胆碱酯酶制剂。
T4912	Jatrorrhizine chloride 盐酸药根碱,Yatrorhizine chloride,Neprotine chloride	Others; 5-HT Receptor; OCT; Antibacterial; AChE	GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Others
	Jatrorrhizine chloride (Neprotine chloride) 是从黄连中分离得到的生物碱，具有神经保护、抗菌、抗氧化和抗疟原虫活性。它通过抑制摄取2转运蛋白的活性减少血清素和去甲肾上腺素的摄取。它是具有口服活性的乙酰胆碱酯酶抑制剂。
T9112	(-)-Perillaldehyde	AhR; ROS; Nrf2	Immunology/Inflammation; Metabolism
	L-Perillaldehyde 是紫苏草精油的主要成分，吸入后经由嗅觉神经功能表现出抗抑郁功能。
T3698	alpha-Asarone α-Asarone,trans-Asarone,α-细辛脑	P450; GABA Receptor; HMG-CoA Reductase	Membrane transporter/Ion channel; Metabolism; Neuroscience
	alpha-Asarone (trans-Asarone) 是来自胡萝卜的一种天然产物，具有抗抑郁等功效。
T5S2195	Sibiricose A5 西伯利亚远志糖A5	Dehydrogenase	Metabolism
	Sibiricose A5 是一种寡糖酯，分离自Polygalae Radix，具有抗氧化作用。
T7448	4-Hydroxyisoleucine 4-羟基-L-异亮氨酸,4-Hydroxy-L-isoleucine	Others	Others
	4-Hydroxyisoleucine (4-Hydroxy-L-isoleucine) 是从胡芦巴种子中提取和纯化的一种氨基酸，具有促胰岛素作用。
T5S2204	Sibiricose A6 西伯利亚远志糖A6	Antioxidant	oxidation-reduction
	Sibiricose A6 是一种寡糖酯，分离自Polygalae Radix，具有抗氧化作用。
T5S0331	Isoliquiritin 异甘草苷,Neoisoliquritin	p53; Antifungal	Apoptosis; Microbiology/Virology
	Isoliquiritin (Neoisoliquritin) 是从甘草根中分离得到的，具有镇咳、抗抑郁作用和抗真菌活性。它还能抑制血管生成和导管形成。
TN1420	Bacopaside I	Others	Others
	Bacopaside I 是一种皂苷，分离自 Bacopa monniera 中，具有抗氧化活性和清除自由基的功能，有抗抑郁作用。
T3386	Kaempferitrin Lespedin,Kaempferol,Lespenephryl,Lespenefril,Kaempferol 3,7-dirhamnoside,山奈苷	cell cycle arrest; Glucokinase; IGF-1R	Cell Cycle/Checkpoint; Metabolism; Tyrosine Kinase/Adaptors
	Kaempferitrin (Lespenephryl) 是天然黄酮苷类化合物，具有缓解疼痛、抗糖尿病、消炎、抗肿瘤和化疗作用，可激活胰岛素信号传导。
T3S1553	trans-Cinnamaldehyde Cinnamaldehyde,Cinnamic aldehyde,桂皮醛,反式肉桂醛,Cinnamal,Phenylacrolein	COX; Endogenous Metabolite	Immunology/Inflammation; Metabolism; Neuroscience
	trans-Cinnamaldehyde (Phenylacrolein) 是一种能够用于合成反式肉桂醛-β-环糊精复合物，一种能够食用的抗菌涂层，能够延长鲜切水果的保质期。它是一种能够通过烷基异氰化物与乙炔二羧酸二烷基酯的反应来合成高度多官能的呋喃环。
T6S0721	Orientin 荭草苷,Lutexin,Luteolin-8-glucoside	Others	Others
	Orientin (Luteolin-8-glucoside) 是天然存在的生物活性类黄酮，是一种有前景的神经保护剂，具有多种生物特性，如抗炎、抗肿瘤、抗氧化、保护心脏等。它有用于神经性疼痛研究潜力。
TN1415	Auraptenol 酸橙素烯醇	5-HT Receptor	GPCR/G Protein; Neuroscience
	Auraptenol possesses robust antidepressant-like efficacy in mice.

天然产物

Cat.No: T3886

Synonym: Rosavidin,络塞维

Target: P450

Tenuifoliside A

Cat.No: T3856

Target: ERK, Others

Cat.No: T5648

Synonym: 吡啉,1,2,4-Trihydroxyanthraquinone,Hydroxylizaric acid,Verantin

Target: MAO, Antibacterial, Antibiotic, Antifungal

Cat.No: T3933

Synonym: Yatrorizine,neprotin,药根碱

Target: MAO, 5-HT Receptor, Antibacterial, AChE

Jatrorrhizine chloride

Cat.No: T4912

Synonym: 盐酸药根碱,Yatrorhizine chloride,Neprotine chloride

Target: Others, 5-HT Receptor, OCT, Antibacterial, AChE

(-)-Perillaldehyde

Cat.No: T9112

Target: AhR, ROS, Nrf2

Cat.No: T3698

Synonym: α-Asarone,trans-Asarone,α-细辛脑

Target: P450, GABA Receptor, HMG-CoA Reductase

Cat.No: T5S2195

Synonym: 西伯利亚远志糖A5

Target: Dehydrogenase

4-Hydroxyisoleucine

Cat.No: T7448

Synonym: 4-羟基-L-异亮氨酸,4-Hydroxy-L-isoleucine

Target: Others

Cat.No: T5S2204

Synonym: 西伯利亚远志糖A6

Target: Antioxidant

Cat.No: T5S0331

Synonym: 异甘草苷,Neoisoliquritin

Target: p53, Antifungal

Cat.No: TN1420

Target: Others

Cat.No: T3386

Synonym: Lespedin,Kaempferol,Lespenephryl,Lespenefril,Kaempferol 3,7-dirhamnoside,山奈苷

Target: cell cycle arrest, Glucokinase, IGF-1R

trans-Cinnamaldehyde

Cat.No: T3S1553

Synonym: Cinnamaldehyde,Cinnamic aldehyde,桂皮醛,反式肉桂醛,Cinnamal,Phenylacrolein

Target: COX, Endogenous Metabolite

Cat.No: T6S0721

Synonym: 荭草苷,Lutexin,Luteolin-8-glucoside

Target: Others

Cat.No: TN1415

Synonym: 酸橙素烯醇

Target: 5-HT Receptor

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