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77

抑制剂 & 化合物

12

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T11908	LY2365109 hydrochloride LY2365109盐酸盐	GlyT	Neuroscience
	LY2365109 hydrochloride 是高选择性GlyT1抑制剂，抑制过表达 hGlyT1 细胞摄取谷氨酸的IC50值为 15.8 nM.
T9833	Opiranserin hydrochloride	P2X Receptor; GlyT; 5-HT Receptor	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Opiranserin hydrochloride 是甘氨酸转运蛋白 2 型 (GlyT2) 和 5-羟色胺受体 2A (5HT2A) 的双重拮抗剂，IC50 分别为 0.86 和 1.3 μM。它显示对 rP2X3 的拮抗活性 (IC50=0.87 μM)。它正在开发为用于治疗术后疼痛的注射剂。
T6541	Ibutilide Fumarate Corvert Fumarate,U70226E,富马酸伊布利特	Calcium Channel; Sodium Channel	Membrane transporter/Ion channel; Metabolism
	Ibutilide Fumarate (U70226E) 是一种 III 类抗心律失常药物，可作用于急性心梗阻塞。
T6788	Bitopertin Paliflutine,比拓喷丁,RO4917838,RG1678,比托派汀	GlyT	Neuroscience
	Bitopertin (Paliflutine) 是一种有效的甘氨酸转运蛋白 1 (GlyT1) 抑制剂，对人 hGlyT1b 的 Ki 为 8.1 nM。
T6352	(-)-Dizocilpine maleate C13737,(-)-MK 801 (Maleate),(-)-MK 801马来酸,(-)-MK 801 Maleate	NMDAR; iGluR	Membrane transporter/Ion channel; Neuroscience
	(-)-Dizocilpine maleate ((-)-MK 801 (Maleate)) 是一种选择性且非竞争性的 N-甲基-D-天冬氨酸 (NMDA) 受体拮抗剂，Ki 为 211.7 nM。它是一种 Dizocilpine 的活性较低的 (-)-对映体，具有抗抑郁作用。
T1050	Prazosin hydrochloride Prazosin hydrochloride,哌唑嗪盐酸盐,Prazosin HCl,cp-12299-1,Peripress,Vasoflex,盐酸哌唑嗪,Minipress	Potassium Channel; MRP; Adrenergic Receptor; ABC; Autophagy	Autophagy; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience
	Prazosin hydrochloride (Vasoflex) 是一种选择性肾上腺素能 α-1 拮抗剂，可降低外周阻力并放松血管平滑肌。它可用于研究高血压和酒精使用障碍。它是一种合成哌嗪衍生物，具有降压抗肾上腺素能特性。它抑制有机阳离子转运蛋白 OCT-1 和 OCT-3，IC50分别为 1.8 和 13 μM 。
T16399	Opiranserin	P2X Receptor; GlyT; 5-HT Receptor	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Opiranserin 是一种非阿片类和非 NSAID 镇痛候选药物，是 2 型甘氨酸转运蛋白 (GlyT2) 和 5-羟色胺受体 2A (5HT2A) 的双重拮抗剂，IC50分别为 0.86 和 1.3 μM。它可用于术后疼痛的研究，对 rP2X3 有拮抗作用，IC50为0.87 μM。
T21102	L-4FPG L-4-氟苯甘氨酸,L4FPG,L 4FPG	Others	Others
	L-4FPG 是甘氨酸衍生物，抑制中性氨基酸转运蛋白 ASCT1 和 ASCT2。
T3215	JNJ-42165279 JNJ42165279	FAAH; Autophagy	Autophagy; Metabolism; Neuroscience
	JNJ-42165279 是一种 FAAH 抑制剂，抑制 hFAAH 和 rFAAH，IC50分别为70 ± 8 nM 和 313 ± 28 nM。它对其他酶、离子通道、转运蛋白和受体具有高度选择性。
T3526	Dasotraline hydrochloride SEP-225289 hydrochloride,达索曲林盐酸盐	Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Norepinephrine	GPCR/G Protein; Neuroscience
	Dasotraline hydrochloride (SEP-225289 hydrochloride) 是具有阻断多巴胺 (IC50=4 nM)，去甲肾上腺素 (IC50=6 nM) 和三羟色胺转运蛋白 (IC50=11 nM)的三重再摄取抑制剂。
T7941	Imipramine hydrochloride 盐酸丙咪嗪,Imipramine (hydrochloride),Tofranil,G 22355,Imipramine HCl,Melipramine	Serotonin Transporter	Neuroscience
	Imipramine hydrochloride (Imipramine HCl) 可抑制血清素转运蛋白，IC50=32 nM。它可阻止胰酶的易位，阻碍 MV 和外泌体的分泌。
T19649	PF-06273340 PF 6273340,PF 06273340,PF6273340,PF-6273340	Trk receptor	Tyrosine Kinase/Adaptors
	PF-06273340 是一种口服具有活力的、具有选择性的外周限制性Trk 泛抑制剂。
T4664	ML 297 ML297	Potassium Channel	Membrane transporter/Ion channel
	ML 297 是选择性的 GIRK1/2激活剂，EC50为 0.16 μM。ML 297 在癫痫病的研究中具有价值。
T9146	ms48107 Benzenemethanol, 2-[4-amino-6-[[(4-phenoxyphenyl)methyl]amino]-1,3,5-triazin-2-yl]-3-fluoro-	Others	Others
	MS48107 是 G 蛋白偶联受体 68 (GPR68) 的选择性正变构调节剂，对GPR68的选择性高于密切相关的神经递质转运蛋白，质子 GPCR 和 hERG 离子通道。它可以穿越过小鼠的血脑屏障。
T11689	ITI-214 ITI214	PDE	Metabolism
	ITI-214 是一种中枢神经系统活性抑制剂，具有口服生物活性的PDE1抑制剂 (Kiof 58 pM)，对其他 PDE 家族成员和一系列酶、受体、转运体和离子通道具有良好的选择性，在各种运动和认知功能的动物模型中显示出有效性。
T17243	VU0463271 N-Cyclopropyl-N-(4-methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide	Potassium Channel	Membrane transporter/Ion channel
	VU0463271 (N-Cyclopropyl-N-(4-methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide) 是一种有效的、特异性的 KCC2 拮抗剂，其 IC50 为 61 nM，特异性是密切相关的 Na-K-2Cl 协同转运蛋白 1 (NKCC1) 的 100 倍以上，在更大的 GPCR、离子通道和转运蛋白面板中没有活性。
T4410	LM10	Others	Others
	LM10 是有效的色氨酸 2,3-双加氧酶的抑制剂。色氨酸 2,3-双加氧酶是一种无关的肝酶，它可通过犬尿氨酸途径降解色氨酸。它对研究癌症疾病具有潜在的研究价值。
T2194	Direct Blue 1 Pontamine sky blue,滂胺天蓝,Chicago Sky Blue 6B	GluR	Neuroscience
	Chicago Sky Blue 6B 是免疫荧光组织化学中背景自体荧光的一种复染料。Direct Blue 1 (Pontamine sky blue) 是第一个能够抑制 Aβ 结合的小分子 PrP 配体，在结构上与谷氨酸盐有关，是一种有效且具有竞争性的 VGLUT 抑制剂，不影响质膜转运体。
T3625	Bempedoic acid ETC1002,ESP-55016,ETC 1002,ETC-1002	ATP Citrate Lyase; AMPK	Chromatin/Epigenetic; Metabolism; PI3K/Akt/mTOR signaling
	Bempedoic acid (ETC1002) 是一种 ATP-柠檬酸裂解酶抑制剂，可激活AMPK。它是脂质和碳水化合物代谢的调节剂。
T15773	Lofepramine Gamanil,洛非帕明,Amplit,Leo 640,Lopramine	5-HT Receptor; Norepinephrine	GPCR/G Protein; Neuroscience
	Lofepramine (Leo 640) 是一种有效的三环抗抑郁药，广泛地代谢为 Desipramine。它能够抑制摄取促进去甲肾上腺素能神经传递，以及抑制神经元摄取 5-羟色胺和色氨酸吡咯酶，增强 5-羟色胺能神经传递，进而发挥其抗抑郁作用。它还具有显著的抗焦虑效果。
T8720	PRX-07034 hydrochloride PRX-07034	5-HT Receptor	GPCR/G Protein; Neuroscience
	PRX-07034 hydrochloride 是一种有效的高度选择性5-HT6受体拮抗剂，Ki 为 4-8 nM，IC50为 19 nM，可用于增强工作记忆和认知灵活性的研究。
T15411	GPNA hydrochloride	Apoptosis; Others	Apoptosis; Others
	GPNA hydrochloride 是一种 γ-谷氨酰转移酶的知名底物，可逆地诱导 A549 细胞凋亡。它是一种特定的谷氨酰胺转运蛋白ASCT2抑制剂，还抑制依赖 Na+的载体，如 SNAT 家族 (SNAT1/2/4/5) 和不依赖 Na+的亮氨酸转运蛋白 LAT1/2。
T41194	FFN 102 mesylate	Others	Others
	FFN 102 mesylate 是pH 响应型荧光假神经递质(FFN)，作为选择性多巴胺转运蛋白(DAT)和VMAT2底物。FFN 102 mesylate 与38个中枢神经系统受体(包括多巴胺和血清素受体)无明显结合。它的Ex-max在pH 值5时为340 nm，在pH 值7.5时为370 nm，在pH 值为5和7.5时，Em-max为435 nm。
T32873	Maralixibat Chloride SHP-625,SHP625,Livmarli,LUM001 chloride,Lopixibat chloride,Lopixibat,SHP625 chloride,SHP 625	Potassium Channel	Membrane transporter/Ion channel
	Maralixibat Chloride (LUM001 chloride) 是一种钠依赖性的胆汁酸转运抑制剂，可阻止胆汁酸在肠肝内的再循环
T23752	AR-C141990 ARC-141990,AR C141990,ARC141990,ARC 141990
	AR-C141990 is a lactate transporters inhibitor.
T22867	Indatraline hydrochloride	Others	Others
	Inhibits transporters for 5-HT (SERT), dopamine (DAT) and noradrenalin (NET)
T69767	NV-5440
	NV-5440 is a novel cell penetrant, potent and selective class I glucose transporters (GLUT1) inhibitor, selectively inhibiting mTORC1
T70341	D-473
	D-473 is a novel orally active triple reuptake inhibitor targeting dopamine, serotonin and norepinephrine transporters.
T39767	AR-C141990 hydrochloride AR-C141990 hydrochloride
	AR-C141990 hydrochloride is a potent inhibitor of lactate transporters known as monocarboxylate transporters (MCTs). It has pK i values of 7.6 and 6.6 for MCT-1 and MCT-2, respectively. Additionally, this compound exhibits immunosuppressive properties and effectively inhibits the graft versus host response.
T69889	JBP485
	JBP485 is an inhibitor of renal transporters OAT1 and OAT3. JBP485 is an antihepatitis agent as a substrate for intestinal PEPT1.
T70315	AGI-16903
	AGI-16903 is a metabolite of enasidenib -- an isocitrate dehydrogenase-2 inhibitor that has been shown to inhibit human nucleoside transporters and uptake of azacitidine in oocytes.
T26363	Napitane Mesylate ABT-200,A-75200
	Napitane Mesylate is a potent alpha 2-adrenoceptor antagonist. Napitane Mesylate blocks norepinephrine uptake by inhibiting the norepinephrine transporter. Napitane Mesylate also binds to CA transporters in the central nervous system and blocks uptake.
T25292	DCCCyb
	DCCCyb is an orally bioavailable and selective GlyT1 Inhibitor. DCCCyb demonstrated excellent in vivo occupancy of GlyT1 transporters in rhesus monkeys as determined by the displacement of a PET tracer ligand.
T21451	Nefazodone Nefadar,Dutonin,Serzone
	Nefazodone is an antidepressant. It has low affinity for the serotonin (200 nM), dopamine (360 nM), and norepinephrine (360 nM) transporters, and therefore acts as a weak serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI).
T11688	ITI-214 free base ITI214 free base	Others	Others
	ITI-214 is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).
T70615	TAS-303
	TAS-303 is a selective norepinephrine reuptake inhibitor which displays significant norepinephrine transporter (NET) inhibitory activity toward serotonin or dopamine transporters. Radioligand-binding studies showed that TAS-303 selectively and potently inhibited [3H]norepinephrine binding to the human NET.
T70760	NVP018
	NVP018, also known as BC 556, is a potent inhibitor of hepatitis B virus, hepatitis C virus (HCV), and HIV-1 replication, shows minimal inhibition of major drug transporters, and has a high barrier to generation of both HCV and HIV-1 resistance..
T68326	Annamycin
	Annamycin is a semi-synthetic doxorubicin analogue annamycin with antineoplastic activity. Annamycin intercalates into DNA and inhibits topoisomerase II, resulting in the inhibition of DNA replication and repair and RNA and protein synthesis. This agent circumvents multidrug-resistance (MDR) transporters, including P-glycoprotein (P-gp).
T37453	Butyryl-L-carnitine (chloride)
	Butyryl-L-carnitine is a butyrate ester of carnitine. It is an inhibitor of intestinal transporters, blocking carnitine uptake by the carnitine transporter and glycine transport by the amino acid transporter in human retinal pigment epithelial (HRPE) cells (IC50s = 1.5 μM and 4.6 mM, respectively).
T39976	MS67
	MS67 is a potent and selective degrader of the WD40 repeat domain protein 5 (WDR5) with a dissociation constant (Kd) of 63 nM. It exhibits no activity against protein methyltransferases, kinases, G-protein-coupled receptors (GPCRs), ion channels, and transporters. Notably, MS67 demonstrates significant anticancer properties.
T70469	AK-42
	AK-42 is a novel potent and specific inhibitor of CLC-2, displaying unprecedented selectivity over CLC-1, the closest CLC-2 homolog, and exhibiting no off-target engagement against a panel of 61 common channels, receptors, and transporters expressed in brain tissue.
T39878	FFN270 hydrochloride FFN270 hydrochloride
	FFN270 hydrochloride, a fluorescent tracer for norepinephrine and vesicular monoamine transporters, features dual resolved absorption/excitation peaks that vary with solvent pH (FFN270 ex: 320 nm or 365 nm, em: 475 nm). It serves as a ratiometric fluorescent pH-sensor, highlighting its utility in monitoring norepinephrine.
T74582	Trimipramine N-oxide
	Trimipramine N-oxide 为三环抗抑郁药trimipramine的活性代谢物，其对人去甲肾上腺素单胺转运体(hNAT)、血清素(hSERT)、多巴胺(hDAT)以及人体有机阳离子转运蛋白(hOCT1与hOCT2)的IC50值分别为11.7、3.59、9.4、9.35及27.4 nM。因此，Trimipramine N-oxide在忧郁和焦虑研究中有应用价值。
T28183	NNC052090 NNC-052090,NNC-05-2090,NNC05-2090,NNC 052090,NNC 05-2090
	NNC052090 is a GABA uptake inhibitor that displays moderate selectivity for BGT-1 transporters with Ki values are 1.4, 15, 19 and 41 μM for hBGT-1, hGAT-3, hGAT-1 and hGAT-2 respectively. NNC052090 also displays affinity at α1- and D2-receptors with IC50
T37699	Org 24598
	Potent and selective inhibitor of the glial glycine transporter GlyT1b (IC50 = 6.9 nM). Displays negligible activity at GlyT-2, adrenoreceptors, dopamine, 5HT receptors and noradrenaline, dopamine, 5HT and GABA transporters (pIC50 in vivo. Chue et al (2013) Glycine reuptake inhibition as a new therapeutic approach in schizophrenia: focus on the glycine transporter 1 (GlyT1). Curr.Pharm.Des. 19 1311 PMID:23194655 \|Brown et al (2001) Discovery and SAR of org 24598-a selective glycine uptake inhibi...
T71764	YM 298198 Hydrochloride
	YM 298198 Hydrochloride is a non-competitive antagonist with high affinity and selectivity for mGlu1 receptors (Ki = 19 nM). YM 298198 Hydrochloride is inactive at other mGlu receptor subtypes (mGlu2-7), ionotropic receptors and glutamate transporters (IC50 > 10 μM). It inhibits glutamate-induced IP production more potently than CPCCOEt (IC50 values are 16 nM and 6.3 μM respectively).
T39397	S-MGB-234
	S-MGB-234 is a minor groove binder utilized for the treatment of Animal African Trypanosomiasis (AAT). It exhibits exceptional in vitro efficacy against the primary causative agents of AAT, namely Trypanosoma congolense and Trypanosoma vivax. Moreover, S-MGB-234 does not demonstrate cross-resistance with existing diamidine drugs and is not internalized through the transporters employed by diamidines.
T16393	ONO-2952	Others	Others
	ONO-2952 is more selective for TSPO than other receptors, transporters, ion channels, and enzymes. ONO-2952 is a potent and selective translocator protein 18 kDa (TSPO) antagonist (Ki: 0.33-9.30 nM for rat and human TSPO). ONO-2952 has the potential for i
T28648	S39625 S-39625,S 39625
	S39625, an E-ring camptothecin keto analogue, is a stable, potent, and selective topoisomerase I inhibitor without being substrates of drug efflux transporters. Nanomolar concentrations of S39625 induces intense and persistent histone gamma-H2AX. The chem
T16547	PK14105	Others	Others
	PK14105 has been evaluated biologically as a potential radioligand for positron emission tomography (PET) studies targeting peripheral benzodiazepine binding sites (PBBS) receptors. When administered to rats with unilaterally lesioned striata, PK14105 was observed to quickly cross the blood-brain barrier, displaying significant radioactivity retention in the lesioned striatum, in contrast to the unlesioned striatum or cerebellar vermis. Additionally, PK14105 has the capability to inhibit recepto...

化合物

LY2365109 hydrochloride

Cat.No: T11908

Synonym: LY2365109盐酸盐

Target: GlyT

Opiranserin hydrochloride

Cat.No: T9833

Target: P2X Receptor, GlyT, 5-HT Receptor

Ibutilide Fumarate

Cat.No: T6541

Synonym: Corvert Fumarate,U70226E,富马酸伊布利特

Target: Calcium Channel, Sodium Channel

Cat.No: T6788

Synonym: Paliflutine,比拓喷丁,RO4917838,RG1678,比托派汀

Target: GlyT

(-)-Dizocilpine maleate

Cat.No: T6352

Synonym: C13737,(-)-MK 801 (Maleate),(-)-MK 801马来酸,(-)-MK 801 Maleate

Target: NMDAR, iGluR

Prazosin hydrochloride

Cat.No: T1050

Synonym: Prazosin hydrochloride,哌唑嗪盐酸盐,Prazosin HCl,cp-12299-1,Peripress,Vasoflex,盐酸哌唑嗪,Minipress

Target: Potassium Channel, MRP, Adrenergic Receptor, ABC, Autophagy

Cat.No: T16399

Target: P2X Receptor, GlyT, 5-HT Receptor

Cat.No: T21102

Synonym: L-4-氟苯甘氨酸,L4FPG,L 4FPG

Target: Others

Cat.No: T3215

Synonym: JNJ42165279

Target: FAAH, Autophagy

Dasotraline hydrochloride

Cat.No: T3526

Synonym: SEP-225289 hydrochloride,达索曲林盐酸盐

Target: Dopamine Receptor, 5-HT Receptor, Serotonin Transporter, Norepinephrine

Imipramine hydrochloride

Cat.No: T7941

Synonym: 盐酸丙咪嗪,Imipramine (hydrochloride),Tofranil,G 22355,Imipramine HCl,Melipramine

Target: Serotonin Transporter

Cat.No: T19649

Synonym: PF 6273340,PF 06273340,PF6273340,PF-6273340

Target: Trk receptor

Cat.No: T4664

Synonym: ML297

Target: Potassium Channel

Cat.No: T9146

Synonym: Benzenemethanol, 2-[4-amino-6-[[(4-phenoxyphenyl)methyl]amino]-1,3,5-triazin-2-yl]-3-fluoro-

Target: Others

Cat.No: T11689

Synonym: ITI214

Target: PDE

Cat.No: T17243

Synonym: N-Cyclopropyl-N-(4-methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide

Target: Potassium Channel

Cat.No: T4410

Target: Others

Cat.No: T2194

Synonym: Pontamine sky blue,滂胺天蓝,Chicago Sky Blue 6B

Target: GluR

Cat.No: T3625

Synonym: ETC1002,ESP-55016,ETC 1002,ETC-1002

Target: ATP Citrate Lyase, AMPK

Cat.No: T15773

Synonym: Gamanil,洛非帕明,Amplit,Leo 640,Lopramine

Target: 5-HT Receptor, Norepinephrine

PRX-07034 hydrochloride

Cat.No: T8720

Synonym: PRX-07034

Target: 5-HT Receptor

GPNA hydrochloride

Cat.No: T15411

Target: Apoptosis, Others

FFN 102 mesylate

Cat.No: T41194

Target: Others

Maralixibat Chloride

Cat.No: T32873

Synonym: SHP-625,SHP625,Livmarli,LUM001 chloride,Lopixibat chloride,Lopixibat,SHP625 chloride,SHP 625

Target: Potassium Channel

Cat.No: T23752

Synonym: ARC-141990,AR C141990,ARC141990,ARC 141990

Indatraline hydrochloride

Cat.No: T22867

Target: Others

Cat.No: T69767

Cat.No: T70341

AR-C141990 hydrochloride

Cat.No: T39767

Synonym: AR-C141990 hydrochloride

Cat.No: T69889

Cat.No: T70315

Napitane Mesylate

Cat.No: T26363

Synonym: ABT-200,A-75200

Cat.No: T25292

Cat.No: T21451

Synonym: Nefadar,Dutonin,Serzone

ITI-214 free base

Cat.No: T11688

Synonym: ITI214 free base

Target: Others

Cat.No: T70615

Cat.No: T70760

Cat.No: T68326

Butyryl-L-carnitine (chloride)

Cat.No: T37453

Cat.No: T39976

Cat.No: T70469

FFN270 hydrochloride

Cat.No: T39878

Synonym: FFN270 hydrochloride

Trimipramine N-oxide

Cat.No: T74582

Cat.No: T28183

Synonym: NNC-052090,NNC-05-2090,NNC05-2090,NNC 052090,NNC 05-2090

Cat.No: T37699

YM 298198 Hydrochloride

Cat.No: T71764

Cat.No: T39397

Cat.No: T16393

Target: Others

Cat.No: T28648

Synonym: S-39625,S 39625

Cat.No: T16547

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
T0760	Cholesterol Cholesterin,Cholesteryl alcohol,胆固醇	Estrogen Receptor/ERR; MRP; Endogenous Metabolite; ROR	Endocrinology/Hormones; Immunology/Inflammation; Metabolism
	Cholesterol (Cholesteryl alcohol) 属于天然产物，是哺乳动物中的主要固醇，是一种雌激素相关受体 α (ERRα) 的激动剂。Cholesterol 广泛存在于动物的细胞膜，也是合成几种重要荷尔蒙及胆酸的材料。
T6975	Sarcosine Sarcosinic acid,Methylaminoacetic acid,Sarcosin,肌氨酸,Methylglycine,N-Methylaminoacetic acid,N-methylglycine	Others; GlyT; Endogenous Metabolite	Metabolism; Neuroscience; Others
	Sarcosine (Methylglycine) 是 I 型甘氨酸转运蛋白 (GlyT1) 的竞争性抑制剂和 N-甲基-D-天冬氨酸受体 (NMDAR) 共激动剂，通过增加甘氨酸的浓度增强 NMDA 受体的功能，可用于精神分裂症的研究。
T1045	Trimipramine maleate Surmontil maleate,马来酸三甲丙咪嗪,三甲丙咪嗪马来酸盐	Dopamine Receptor; 5-HT Receptor; Antibacterial; Adrenergic Receptor; Norepinephrine; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience
	Trimipramine maleate (Surmontil maleate) 是一种 5-HT 受体拮抗剂，对 5-HT1C、5-HT2和 5-HT1A 受体的 pKi 值分别为 6.39、8.10和 4.66。
T4921	Oxoadipic acid 2-氧代己二酸,2-Oxoadipic acid	Endogenous Metabolite	Metabolism
	Oxoadipic acid (2-Oxoadipic acid) 是必需氨基酸色氨酸和赖氨酸的一种代谢物。
T4927	4-Guanidinobutanoic acid 4-GBA,4-胍基丁酸,4-Guanidinobutyric acid	Endogenous Metabolite	Metabolism
	4-Guanidinobutanoic acid (4-GBA) 是一种 L-精氨酸代谢物，已用于肠道转运研究。它已专门用于人质子偶联氨基酸转运蛋白 hPAT1。
T5242	Triarachidin Triarachin,1,2,3-Trieicosanoyl Glycerol,Glycerol Trieicosanoate,三花生精	Others; Endogenous Metabolite	Metabolism; Others
	Triarachidin (1,2,3-Trieicosanoyl Glycerol) 是内源性代谢产物的一种。
T5061	Lumichrome 7,8-Dimethylalloxazine,光色素	Others	Others
	Lumichrome (7,8-Dimethylalloxazine) 是人类体内的内源性化合物，由核黄素光降解产生。它利用 p53 依赖机制抑制人肺癌细胞生长并诱导凋亡。
T6S2246	Alisol B 23-acetate Alisol B Acetate,Alisol B monoacetate,23-O-Acetylalisol B,23-Acetylalismol B,泽泻醇B乙酸酯	Others	Others
	Alisol B 23-acetate (Alisol B Acetate) 是三萜类化合物，能够激活法尼醇受体，诱导受损的肝脏再生。
T16223	N-Dodecyl-β-D-maltoside 十二烷基-β-D-麦芽糖苷,Lauryl Maltoside	Others	Others
	N-Dodecyl-β-D-maltoside (Lauryl Maltoside) 是一种芘 (Py) 的衍生物。它可用作烷基吡喃麦芽糖苷清洁剂，尤其是在转运蛋白和呼吸复合物中。它已用于诸如 RNA 聚合酶的纯化和稳定化，以及蛋白质-脂质相互作用的检测的应用中。
T2924	Phloretin 根皮素,Dihydronaringenin,NSC 407292,RJC 02792	SGLT; transporter; Endogenous Metabolite	GPCR/G Protein; Metabolism
	Phloretin (NSC-407292) 是从苹果树叶中提取的一种查耳酮，具有抗炎、抗氧化和抗癌活性。它是真核尿素转运蛋白抑制剂，可阻断 VacA 介导的尿素和离子转运，有潜力用于类风湿性关节炎和过敏性气道炎症的相关研究。
T15097	Deoxynivalenol Vomitoxin,4-Deoxynivalenol
	Deoxynivalenol (Vomitoxin) 是一种单端孢菌素家族镰刀菌属产生的霉菌毒素，常见于受到污染的食物和饲料中。Deoxynivalenol 通过紧密连接处的细胞旁路来穿过肠粘膜。Deoxynivalenol 转运不受P-糖蛋白 (PgP) 或多药耐药相关蛋白 (MRP) 抑制剂的影响。Deoxynivalenol 通常会导致人类和动物腹泻、呕吐和胃肠道炎症。
T75436	Jatrorrhizine hydroxide
	Jatrorrhizine hydroxide, 一种从黄连中提取的生物碱，展现了神经保护、抗菌、抗疟原虫及抗氧化的活性。作为一种高效的乙酰胆碱酯酶(AChE)抑制剂(IC50=872 nM)，其对BuChE的选择性高达115倍。此外，Jatrorrhizine hydroxide还能通过抑制uptake-2 transporter活性来减少血清素(5-HT)和去甲肾上腺素(NE)的摄取，表现出口服活性。

天然产物

Cat.No: T0760

Synonym: Cholesterin,Cholesteryl alcohol,胆固醇

Target: Estrogen Receptor/ERR, MRP, Endogenous Metabolite, ROR

Cat.No: T6975

Synonym: Sarcosinic acid,Methylaminoacetic acid,Sarcosin,肌氨酸,Methylglycine,N-Methylaminoacetic acid,N-methylglycine

Target: Others, GlyT, Endogenous Metabolite

Trimipramine maleate

Cat.No: T1045

Synonym: Surmontil maleate,马来酸三甲丙咪嗪,三甲丙咪嗪马来酸盐

Target: Dopamine Receptor, 5-HT Receptor, Antibacterial, Adrenergic Receptor, Norepinephrine, Histamine Receptor

Cat.No: T4921

Synonym: 2-氧代己二酸,2-Oxoadipic acid

Target: Endogenous Metabolite

4-Guanidinobutanoic acid

Cat.No: T4927

Synonym: 4-GBA,4-胍基丁酸,4-Guanidinobutyric acid

Target: Endogenous Metabolite

Cat.No: T5242

Synonym: Triarachin,1,2,3-Trieicosanoyl Glycerol,Glycerol Trieicosanoate,三花生精

Target: Others, Endogenous Metabolite

Cat.No: T5061

Synonym: 7,8-Dimethylalloxazine,光色素

Target: Others

Alisol B 23-acetate

Cat.No: T6S2246

Synonym: Alisol B Acetate,Alisol B monoacetate,23-O-Acetylalisol B,23-Acetylalismol B,泽泻醇B乙酸酯

Target: Others

N-Dodecyl-β-D-maltoside

Cat.No: T16223

Synonym: 十二烷基-β-D-麦芽糖苷,Lauryl Maltoside

Target: Others

Cat.No: T2924

Synonym: 根皮素,Dihydronaringenin,NSC 407292,RJC 02792

Target: SGLT, transporter, Endogenous Metabolite

Cat.No: T15097

Synonym: Vomitoxin,4-Deoxynivalenol

Jatrorrhizine hydroxide

Cat.No: T75436

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