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48

抑制剂 & 化合物

5

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T4007	Eticlopride hydrochloride	Dopamine Receptor	GPCR/G Protein; Neuroscience
	Eticlopride hydrochloride 是一种抗精神病药，是一种选择性多巴胺 D2/D3 受体拮抗剂（Ki：0.5/0.16 nM）。
T10603	BRD-6929	HIV Protease; HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome
	BRD-6929 是一种选择性的脑渗透性的HDAC1和HDAC2抑制剂，IC50值为 1 和 8 nM。它对 HDAC1 和 HDAC2 有高亲和力，Ki 值为 0.2 和 1.5 nM。它可研究情绪相关行为。
T21635	PD184161	MEK	MAPK
	PD 184161 是一种口服有效的，时间和浓度依赖的 MEK 抑制剂，IC50为10-100 nM。它诱导抑郁样行为，抑制细胞增殖并诱导细胞凋亡。
T26091	Riparin III
	Riparin III is an alcamide isolated from Aniba riparia that has exhibited effects of antidepressant and anxiolytic activities in acute stress behavioral models.
T27186	Divaplon RU-32698,RU32698,RU 32698	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Divaplon 是一种GABA 受体激动剂（IC50：0.056 µM），在大鼠模型中显示出非镇静性抗焦虑行为特征，可用于治疗焦虑症。
TP1578L	Neuropeptide EI, rat acetate Neuropeptide EI, rat acetate(125934-45-4 free base)	Melanocortin Receptor; Melanin-concentrating Hormone Receptor (MCHR)	GPCR/G Protein; Neuroscience
	Neuropeptide EI, rat acetate(125934-45-4 free base) 在不同的行为范例中显示功能性 MCH 拮抗剂和 MSH 激动剂活性。
T68080	Gevotroline	5-HT Receptor	GPCR/G Protein; Neuroscience
	Gevotroline 是棕榈酒中的一种可用来治疗精神病的化学物，是5-HT2 receptor 拮抗剂，可用于研究行为障碍。
T79909	AEF0117	Cannabinoid Receptor	GPCR/G Protein
	AEF0117为一种针对大麻素受体1 (CB1-SSi) 的信号传导特异性抑制剂，抑制大麻素自我给药和与四氢大麻酚相关的行为障碍，可用于研究大麻戒断。
T10142L	p-Ethynylphenylalanine hydrochloride 4-Ethynyl-L-phenylalanine HCL,p-Ethynylphenylalanine hydrochloride(278605-15-5 free base)	Hydroxylase	Metabolism
	p-Ethynylphenylalanine hydrochloride (4-Ethynyl-L-phenylalanine HCL) 是一种高效的、可逆的、选择性的、竞争性的色氨酸羟化酶 (TPH) 抑制剂，其Ki=32.6 μM。
T33816	Ordopidine ACR-325,ACR 325,ACR325	Dopamine Receptor	GPCR/G Protein; Neuroscience
	Ordopidine (ACR325) 是一种多巴胺能稳定剂，可抑制精神刺激剂引起的多动症，并在不活动时刺激行为。Ordopidine 在体外作为多巴胺 D2 受体拮抗剂起作用，尽管亲和力低，但其依赖于特定状态的行为效应特征是 D2 受体拮抗剂所不具备的。
T27806	Lecozotan HCl SRA-333,SRA333,SRA 333,Lecozotan hydrochloride	5-HT Receptor	GPCR/G Protein; Neuroscience
	Lecozotan HCl (SRA-333) 是一种强效且具有选择性的 5-HT 拮抗剂。Lecozotan HCl能明显增强氯化钾刺激海马齿状回谷氨酸和乙酰胆碱的释放并具有增强认知能力的特性。在表明 5-HT(1A) 受体功能的行为模型中，长期服用Lecozotan HCl不会诱发 5-HT(1A) 受体耐受或脱敏。
T68070	Fezolamine	Norepinephrine	Neuroscience
	Fezolamine 是一种新型可口服的非三环类化合物，具有抗抑郁活性。它在体外阻断[3H]去甲肾上腺素的突触体摄取方面的选择性是摄取[4H]3-羟色胺或[3H]多巴胺的3至2倍。在使用单胺耗尽动物的经典行为测试中，它阻止了利血平和四苯的抑制作用。
T22043	BCATc Inhibitor 2	Others	Others
	BCATc Inhibitor 2 是选择性分支链氨基转移酶抑制剂，可用于神经退行性疾病的研究。能够抑制 rBCATc (IC50:0.2 μM)，hBCATc (IC50:0.8 μM)、 rBCATm (IC50:3.0 μM)。其中BCATc 也称为 BCAT1，存在于细胞质基质中的亚型。
T28634	RY024
	RY024 is a behavioral alcohol antagonist.
T33696	NK-1145 NK-1145 hydrocholdoride,NK 1145,NK1145
	Nk-1145 is a parasympathetic drug of the autonomic nervous system, which can cause behavioral stimulation and excitement.
T33607	NBI-34041 NBI34041,SB 723620,SB-723620,SB723620
	NBI-34041 is an effective and high-affinity CRF1 receptor antagonist that effectively reduces endocrine responses to CRF(1) receptor-mediated pharmacological and behavioral challenges.
T27857	LSP4-2022 LSP42022,LSP4 2022
	LSP4-2022, a mGlu4 selective agonist, increases behavioral despair in mouse models of antidepressant action.
T24857	TBTC
	TBTC is a selective agonist of retinoid X receptor α that acts by improving behavioral deficit in Alzheimer's disease model mice.
T20821	EPPS
	EPPS is a rescuer of A aggregation and behavioral deficits. It binds to A aggregates and converts them into monomers.
TP1578	Neuropeptide EI, rat
	Displays functional MCH-antagonist and MSH-agonist activity in different behavioral paradigms.
T29206	ZCZ011 ZCZ 011,ZCZ-011
	ZCZ011 is a positive allosteric modulator of the cannabinoid CB1 receptor. ZCZ011 is brain penetrant, increased the potency of orthosteric agonists in mouse behavioral assays indicative of cannabimimetic activity, including antinociception, hypothermia, c
TP1504	Urocortin III, mouse TFA (357952-10-4 free base) Urocortin III, mouse TFA
	Urocortin III, mouse TFA is a corticotropin-releasing factor (CRF)-related peptide. Urocortin III preferentially binds and activates CRF-R2. Urocortin III (Ucn3) is a known component of the behavioral stress response system. Urocortin III and CRF-R2 in th
T28316	PD 118717 PD118717,PD-118717
	PD 118717 is a putative piperazinyl benzopyranone dopamine autoreceptor agonist. PD 118717 has the profile of a DA autoreceptor agonist and produces effects suggestive of antipsychotic efficacy without neurological side effect liability in preclinical beh
TP2052	CTOP
	Potent and selective μ opioid receptor antagonist (Ki values are 0.96 and >10,000 nM for μ and δ receptors respectively). Causes behavioral effects on central administration in vivo. Also increases K+ currents in rat locus ceruleus neurons in vitro via a
TP1732	Galanin (1-30), human
	Galanin (1-30), human is a 30-amino acid neuropeptide, and acts as an agonist of GalR1 and GalR2 receptors, with Kis of both 1 nM. Endogenous peptide with multiple endocrine, metabolic and behavioral effects. Has been shown to have an action on intestinal
T38005	P11149
	P11149 is a competitive, BBB-penetarated weakly, orally active and selective inhibitor of AChE. P11149 exhibits an IC50 of 1.3 μM for rat BChE/AChE. P11149, a Galanthamine derivative, demonstrates central cholinergic activity, behavioral efficacy and safety. P11149 is used in the study for Alzheimer’s disease[1]. P11149 is a GAL analog that is rapidly hydrolyzed in vivo to yield the potent AChE inhibitor, 6-DMG[1].P11149 exhibits greater s.c. bioavailability than p.o. [1].Oral P11149 in mice pr...
T60577	Cycrimine
	Cycrimine 是毒蕈碱胆碱能受体(mAChR)M1的口服活性拮抗剂，可降低帕金森模型中乙酰胆碱的水平。Cycrimine 具有解痉活性，可用于研究行为和精神障碍。
T79172	PF-06655075	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	PF-06655075为一新型非脑渗透性OT受体(oxytocin receptor)激动剂，具有显著提高对OT受体(oxytocin receptor)的选择性和药代动力学稳定性。PF-06655075可用作工具化合物，以研究外周OT在行为反应中的功能。
T70643	GT-0198 HCl
	GT-0198 is a novel glycine transporter 2 inhibitor showed activity in a mouse model of neuropathic pain. GT-0198 inhibited the function of glycine transporter 2 (GlyT2) in human GlyT2-expressing HEK293 cells and did not bind various major transporters or receptors of neurotransmitters in a competitive manner. GT-0198 is considered to be a comparatively selective GlyT2 inhibitor. GT-0198 is a structurally novel GlyT2 inhibitor bearing a phenoxymethylbenzamide moiety with in vivo efficacy in beha...
T81501	PF-06655075 TFA	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	PF-06655075(TFA)为PF-06655075的三氟乙酸（TFA）形态。该化合物是一种创新的非脑渗透性氧催产素（oxytocin receptor）受体激动剂，且对氧催产素受体具有较高的选择性，药代动力学稳定性得到显著增强。PF-06655075可用作工具化合物，以深入研究外围氧催产素受体在行为反应中的功能。
T76025	Urocortin III, mouse TFA
	Urocortin III, mouse TFA是CRF（促肾上腺皮质激素释放因子）相关的肽。该化合物主要通过结合并激活CRF-R2发挥作用。Urocortin III（Ucn3）是已知参与调节行为压力反应体系的组分之一。它和CRF-R2在大脑杏仁核中共同作用，从而参与调控复杂的社会动力学行为。
T80134	Pro8-Oxytocin TFA	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	Pro8-Oxytocin TFA 作为一种优化的OXT配体，在灵长类动物OXTR上展现出较Leu8-Oxytocin更强的功能反应和行为效应。相对于AVP，在人类AVPR1a上的活性较低，但在狨猴AVPR1a上则显示出更高的活性。
T80133	Pro8-Oxytocin	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	Pro8-Oxytocin是一种改良的OXT配体。在灵长类动物OXTR中，Pro8-Oxytocin比标准哺乳动物OXT配体Leu8-Oxytocin诱发更强效的反应和显著的行为影响。相较于Vasopressin (AVP)，Pro8-Oxytocin对人类AVPR1a的活性较低，但对狨猴AVPR1a的激活作用则高于AVP。
T63549	MRGPRX1 agonist 4
	MRGPRX1 agonist 4 是有效的、口服具有活力的 Mas 相关 G 蛋白偶联受体 X1 (MRGPRX1)正向变构调节剂 (EC50: 0.1 μM)。MRGPRX1 agonist 4 表现出良好的代谢稳定性以及口服生物利用度。MRGPRX1 agonist 4 能够改善人源性 MRGPRX1 神经疼痛模型小鼠行为性热过敏反应。
T76230	p-fin4
	p-fin4，作为一种针对STEP Phosphatase-GluA2 AMPA受体相互作用的肽抑制剂，具有0.4 μM的Ki值。在东莨菪碱处理的大鼠模型中，p-fin4能够恢复记忆功能，并展现出抗焦虑及抗抑郁效果。该化合物是开发新型认知增强剂和/或行为调节剂的有希望的先导物。
T71327	Paraxanthine-d6
	Paraxanthine-d6 is intended for use as an internal standard for the quantification of paraxanthine by GC- or LC-MS. Paraxanthine is an active metabolite of caffeine. It is formed via N3-demethylation of caffeine by the cytochrome P450 (CYP) isoform CYP1A2. Paraxanthine is an adenosine A1 and A2 receptor antagonist. In vivo, paraxanthine increases striatal cGMP and extracellular striatal dopamine levels and locomotor activity, as well as inhibits motor depression induced by the adenosine A1 agoni...
T76229	p3Ysh-3
	p3Ysh-3 是 STEP Phosphatase-GluA2 AMPA 受体相互作用的肽抑制剂，Ki 为 1.09 μM。p3Ysh-3 在东莨菪碱处理的大鼠模型中恢复记忆缺陷并表现出抗焦虑和抗抑郁作用。p3Ysh-3 是一种很有前途的先导化合物，可用于新型认知增强剂和/或行为调节剂。
T75832	Cyclotraxin B TFA
	Cyclotraxin B TFA 是一种环肽，是一种高效且选择性的 TrkB 抑制剂，且不会改变 BDNF 的结合。Cyclotraxin B TFA 非竞争性地抑制 BDNF 诱导的 TrkB 活性，IC50值为 0.30 nM。Cyclotraxin B TFA 可以穿越血脑屏障，并具有止痛和抗焦虑的行为作用。
T62303	PDE4B/7A-IN-1
	化合物22是一种1安/5-羟丁腈橡胶7受体拮抗剂（5-HT1a ki=8 nm, kb=0.04 nm；5-nitrile rubber 7K i=451 nm, kb=460 nm），同时具备PDE4B/PDE7A抑制活性（PDE4B IC50= 80.4 μM；PDE7A IC50= 151.3 μM）。该化合物在体外展现出了优秀的生物膜被动穿透能力和高代谢稳定性。进一步的药理学评估揭示，22在大鼠行为测试中展现了显著的认知改善和抗抑郁效果。
T36482	Lamotrigine isethionate
	Water-soluble salt of lamotrigine . Displays anticonvulsant effects and inhibits glutamate release, possibly through inhibition of Na+, K+ and Ca2+ currents. Leach et al (1991) Neurochemical and behavioral aspects of lamotr. Epilepsia 32 S4 PMID:1685439 \|Smith and Meldrum (1995) Cardioprotective effect of lamotr. after focal ischemia in rats. Stroke 26 117 PMID:7839380 \|Zona and Avoli (1997) Lamotrigine reduces voltage-gated sodium currents in rat central neurons in culture. Epilepsia 38 522 PMI...
T76014	IGF-I (24-41) (TFA)
	IGF-I (24-41) TFA（Insulin-like Growth Factor I (24-41) TFA）是类胰岛素生长因子I的一个氨基酸片段，覆盖24至41位点。作为一种70个氨基酸组成的多肽激素，IGF-I TFA对神经元和神经胶质细胞具有营养作用，而且在调节全身生长激素（GH）活性中扮演关键角色。它还具备合成代谢、抗氧化、抗炎及细胞保护功能，对躯体生长及行为发育调节作用显著。
T38228	R 121919 hydrochloride
	High affinity corticotropin releasing factor receptor1 (CRF1) antagonist (Ki = 3.5 nM). Reduces stress-induced elevations of plasma ACTH. Anxiolytic and antidepressant in vivo. Orally bioavailable. Chen and Grigoriadis (2005) NBI 30775 (R121919), an orally active antagonist of the corticotropin-releasing factor (CRF) type-1 receptor for the treatment of anxiety and depression. Drug Dev.Res. 65 216 \|Jutkiewicz et al (2005) The effects of CRF antagonists, antalarmin, CP154,526, LWH234, and R121919...
T65396	Piperazine 2HCl
	Piperazine (2HCl) is gamma-aminobutyric acid (GABA) agonists and its major effects appear to be on the central nervous system. Piperazine was the anthelmintic with the greatest number of reports of toxicoses and suspected toxicoses in cats. Piperazine neurotoxicity in cats and dogs usually was manifested by muscle tremors, ataxia, and/or behavioral disturbances within 24 hours after estimated daily dose(s) between 20 and 110 mg/kg[1]. For di-substituted derivatives, ciprofloxacin was selected an...
T37837	2-Methylhexacosane
	2-Methylhexacosane is a saturated hydrocarbon and an insect pheromone.1,2It has been found in the cuticle ofM. dasystomusfemales, but not males, where it contributes to the mating behavior of males, as well as inD. melanogasterfemales where it modulates aggression of males towards females. 2-methylhexacosane has also been found in yellow jacket (V. vulgaris) trail extracts.3 1.Spikes, A.E., Pashen, M.A., Millar, J.G., et al.First contact pheromone identified for a longhorned beetle (Coleoptera: ...
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)....
T35836	PMX-205 (trifluoroacetate salt)
	PMX-205 is a cyclic hexapeptide that acts as a potent antagonist of C5a receptor (C5aR; IC50= 31 nM).1It is orally active and blocks inflammatory signaling and symptoms in animal models of colitis and allergic asthma.2,3PMX-205 is also brain penetrant and reduces neuroinflammation and neurodegeneration in an animal model of Alzheimer's disease.4 1.March, D.R., Proctor, L.M., Stoermer, M.J., et al.Potent cyclic antagonists of the complement C5a receptor on human polymorphonuclear leukocytes. Rela...
T35892	Q134R Q134R
	Q134R, a neuroprotective hydroxyquinoline derivative that suppresses nuclear factor of activated T cell (NFAT) signaling. Q134R can across blood-brain barrier. Q134R has the potential for Alzheimer’s disease (AD) and aging-related disorders research[1]. Q134R (1-10 μM) suppresses NFAT signaling, without inhibiting calcineurin activity. Q134R partially inhibits NFAT activity in primary rat astrocytes, but does not prevent calcineurin-mediated dephosphorylation of a non-NFAT target, either in vivo...
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...

化合物

Eticlopride hydrochloride

Cat.No: T4007

Target: Dopamine Receptor

Cat.No: T10603

Target: HIV Protease, HDAC

Cat.No: T21635

Target: MEK

Cat.No: T26091

Cat.No: T27186

Synonym: RU-32698,RU32698,RU 32698

Target: GABA Receptor

Neuropeptide EI, rat acetate

Cat.No: TP1578L

Synonym: Neuropeptide EI, rat acetate(125934-45-4 free base)

Target: Melanocortin Receptor, Melanin-concentrating Hormone Receptor (MCHR)

Cat.No: T68080

Target: 5-HT Receptor

Cat.No: T79909

Target: Cannabinoid Receptor

p-Ethynylphenylalanine hydrochloride

Cat.No: T10142L

Synonym: 4-Ethynyl-L-phenylalanine HCL,p-Ethynylphenylalanine hydrochloride(278605-15-5 free base)

Target: Hydroxylase

Cat.No: T33816

Synonym: ACR-325,ACR 325,ACR325

Target: Dopamine Receptor

Cat.No: T27806

Synonym: SRA-333,SRA333,SRA 333,Lecozotan hydrochloride

Target: 5-HT Receptor

Cat.No: T68070

Target: Norepinephrine

BCATc Inhibitor 2

Cat.No: T22043

Target: Others

Cat.No: T28634

Cat.No: T33696

Synonym: NK-1145 hydrocholdoride,NK 1145,NK1145

Cat.No: T33607

Synonym: NBI34041,SB 723620,SB-723620,SB723620

Cat.No: T27857

Synonym: LSP42022,LSP4 2022

Cat.No: T24857

Cat.No: T20821

Neuropeptide EI, rat

Cat.No: TP1578

Cat.No: T29206

Synonym: ZCZ 011,ZCZ-011

Urocortin III, mouse TFA (357952-10-4 free base)

Cat.No: TP1504

Synonym: Urocortin III, mouse TFA

Cat.No: T28316

Synonym: PD118717,PD-118717

Cat.No: TP2052

Galanin (1-30), human

Cat.No: TP1732

Cat.No: T38005

Cat.No: T60577

Cat.No: T79172

Target: Oxytocin Receptor

Cat.No: T70643

PF-06655075 TFA

Cat.No: T81501

Target: Oxytocin Receptor

Urocortin III, mouse TFA

Cat.No: T76025

Pro8-Oxytocin TFA

Cat.No: T80134

Target: Oxytocin Receptor

Cat.No: T80133

Target: Oxytocin Receptor

MRGPRX1 agonist 4

Cat.No: T63549

Cat.No: T76230

Paraxanthine-d6

Cat.No: T71327

Cat.No: T76229

Cyclotraxin B TFA

Cat.No: T75832

Cat.No: T62303

Lamotrigine isethionate

Cat.No: T36482

IGF-I (24-41) (TFA)

Cat.No: T76014

R 121919 hydrochloride

Cat.No: T38228

Piperazine 2HCl

Cat.No: T65396

2-Methylhexacosane

Cat.No: T37837

Urocortin III (human) (trifluoroacetate salt)

Cat.No: T35814

PMX-205 (trifluoroacetate salt)

Cat.No: T35836

Cat.No: T35892

Synonym: Q134R

Cat.No: T35560

Cat. No.	Product Name	Target	Signaling Pathways
T0632	3,4,5-Trimethoxybenzoic acid Gallic acid trimethyl ether,Eudesmic acid,3,4,5-三甲氧基苯甲酸,Trimethylgallic Acid,Benzoic acid,Tri-O-methylgallic acid,没食子酸三甲醚	Antioxidant	oxidation-reduction
	3,4,5-Trimethoxybenzoic acid (Gallic acid trimethyl ether) 是一种苯甲酸衍生物，可用作医药和有机合成中的砌块。
T4S1999	Valepotriate 戊曲酯/缬草素,Valtrate	Apoptosis; HIV Protease	Apoptosis; Microbiology/Virology; Proteases/Proteasome
	Valepotriate (Valtrate) 是从蜘蛛香分离而来的一种天然产物，是一类新的细胞毒剂和抗肿瘤剂，对 HTC 肝癌细胞是非常有效的细胞毒剂。它可能对焦虑的精神症状具有潜在的抗焦虑作用。
T5S0661	Koumine	Others	Others
	Koumine 是一种从钩吻中得到的生物碱，具有高效抗肿瘤活性，在肿瘤细胞中能够提高 Bax/Bcl-2 的蛋白比例和 caspase-3 的表达。在类风湿性关节炎动物模型中，它能够预防关节炎的发展。它具有抗焦虑、抗应激、抗银屑病作用，也可用于缓解疼痛的研究。
T4S0969	Obtusifolin 决明蒽醌,决明蒽醌；美决明子素	Antioxidant; NF-κB	NF-κB; oxidation-reduction
	Obtusifolin 是分离自决明子的种子中，能够抑制NF-kB 通路，调节气道上皮细胞中 MUC5AC 粘蛋白的基因表达和产生。它通过靶向甲状旁腺激素相关蛋白来抑制邻苯二甲酸酯诱导的乳腺癌骨转移。
TN1766	(-)-Integerrimine Integerrimine,全緣千里光鹼,全缘千里光碱	Others	Others
	Prenatal exposure to Integerrimine N-oxide induces maternal toxicity, impairment of maternal care and delayed in physical and behavioral development of the offspring. Doses of Integerrimine N-oxide here employed did not produce marked immunotoxic effects.

天然产物

3,4,5-Trimethoxybenzoic acid

Cat.No: T0632

Synonym: Gallic acid trimethyl ether,Eudesmic acid,3,4,5-三甲氧基苯甲酸,Trimethylgallic Acid,Benzoic acid,Tri-O-methylgallic acid,没食子酸三甲醚

Target: Antioxidant

Cat.No: T4S1999

Synonym: 戊曲酯/缬草素,Valtrate

Target: Apoptosis, HIV Protease

Cat.No: T5S0661

Target: Others

Cat.No: T4S0969

Synonym: 决明蒽醌,决明蒽醌；美决明子素

Target: Antioxidant, NF-κB

(-)-Integerrimine

Cat.No: TN1766

Synonym: Integerrimine,全緣千里光鹼,全缘千里光碱

Target: Others

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