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28

抑制剂 & 化合物

17

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T7127	DC260126	Apoptosis; GPR	Apoptosis; Endocrinology/Hormones; GPCR/G Protein
	DC260126 是一种 GPR40 (FFAR1)拮抗剂，对棕榈酸酯诱导的内质网应激和凋亡有保护作用。它剂量依赖性地抑制亚油酸、油酸、棕榈油酸和月桂酸刺激的 GPR40 介导的 Ca2+升高，IC50分别 6.28、5.96、7.07和4.58 μM。
T69795	Crobenetine BIII 890 CL,Crobenetine Free Base	Calcium Channel; Sodium Channel	Membrane transporter/Ion channel; Metabolism
	Crobenetine (BIII 890 CL) Free Base 是一种选择性 NaV 通道阻断剂，能消除VTD诱导的[Ca2+]升高。
T3543	NS-638 NS 638	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	NS-638 是一种 Ca2+ 通道阻滞剂，可阻断 K+ 刺激的细胞内 Ca2+ 升高，IC50值为3.4 μM。
T15648	KDM5-C70	Histone Demethylase	Chromatin/Epigenetic
	KDM5-C70 是 KDM5-C49 的乙酯衍生物，是一种有效的细胞渗透性泛 KDM5 组蛋白去甲基化酶抑制剂。它在骨髓瘤细胞中具有抗增殖作用，可诱导全基因组 H3K4me3 水平升高。
T28958	TG6-129 TG6 129	Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation
	TG6-129 是有效的EP2受体选择性拮抗剂，可降低 butaprost 诱导的 P388D1 巨噬细胞中炎症因子的表达。
T10595	BQ-788 BQ788	Endothelin Receptor	GPCR/G Protein
	BQ-788 是一种具有选择性和有效性的 ETB 受体拮抗剂，具有潜在的高血压活性，抑制 ET-1 与 ETB 受体结合，抑制外源性 ET-1 诱导的冠状动脉灌注压升高。
T21704	5-fluoro 203 5F-203,NSC-703786	Others	Others
	5-fluoro 203 (NSC-703786) 是一种细胞毒性分子。它可激活芳香烃受体(AhR) 信号传导，诱导 CYP1A1 的转录，从而形成 DNA 加合物以及细胞周期阻滞。它可以提高活性氧水平，并激活 ERK、p38以及JNK。
T1577	Midodrine hydrochloride Pro-Amatine,盐酸米多君	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Midodrine hydrochloride (Pro-Amatine) 通过去甘氨酸反应转化为其活性代谢物 desglymidodrine。Desglymidodrine 选择性地结合并激活小动脉和静脉血管系统的 α-1-肾上腺素能受体。这会导致平滑肌收缩并导致血压升高。 Desglymidodrine 在血脑屏障中的扩散很差，因此与对中枢神经系统的影响无关。Midodrine hydrochloride 是 midodrine 的盐酸盐形式，是一种直接作用的前药和拟交感神经药，具有抗低血压特性。
T15017	CU-T12-9	TLR	Immunology/Inflammation
	CU-T12-9 是特异性 TLR1/2激动剂，可激活先天免疫系统和适应性免疫系统。它选择性激活 TLR1/2 异二聚体，可通过促进 TLR1 和 TLR2 二聚而激活 NF-κB 信号，引起下游 TNF-α、IL-10 和 iNOS 增加。
T41005	PA-8	PACAP	GPCR/G Protein
	PA-8是一种小分子的的 PACAP I 型(PAC1)受体拮抗剂，有选择性、有效性和口服活性。PA-8抑制PACAP 诱导的CREB 在PAC1-受体上的磷酸化，但对VPAC11或VPAC2受体无抑制作用。PA-8也抑制pacap 诱导的体外cAMP 水平升高(IC50 = 2 nM)和体内鞘内注射后pacap 诱导的厌恶反应和机械异位性痛。
T70993	WO-459
	WO-459 is a novel GPR52 agonist, dose-dependently inducing elevation of intracellular cAMP in HEK293/GPR52 cells.
T14068	A-192621	Others	Others
	A-192621 is a potent, nonpeptide, orally active and selective endothelin B (ETB) receptor antagonist with an IC50 of 4.5 nM and a Ki of 8.8 nM. A-192621 promotes apoptosis in PASMCs and it also causes elevation of arterial blood pressure and an elevation
T61137	VEGFR-2-IN-19
	VEGFR-2-IN-19 (Compound 15b) is a highly efficacious inhibitor of VEGFR2, a receptor involved in angiogenesis. Its mechanism of action involves the induction of cellular apoptosis and elevation of intracellular reactive oxygen species. Due to these properties, VEGFR-2-IN-19 holds promise as an effective anticancer agent [1].
T23583	58-G3 58G3
	58-G3 is an agonist of methuselah (Mth)-specific that acts by inducing dose-dependent calcium elevation and membrane translocation of β-arrestin2.
T69991	Difenamizole HCl
	Difenamizole HCl is the salt form of Difenamizole, a non-steroidal anti-inflammatory drug (NSAID) and analgesic of the pyrazolone group related to metamizole. It has monoaminergic properties, including inhibition of monoamine oxidase, augmentation of pargyline-induced elevation of striatal dopamine levels, inhibition of K+-induced striatal dopamine release, and inhibition of the reuptake of dopamine.
T70865	BMY-42393
	BMY-42393 is orally active and selective platelet aggregation inhibitor. BMY-42393 is also a prostacyclin partial agonist that inhibited ADP, collagen and thrombin-induced platelet aggregation (IC50 range 0.3 - 2.0 microM). BMY-42393 stimulated platelet adenylate cyclase activity (EC50 = 25 nM). Platelets treated with BMY 42393 showed an elevation of cAMP levels and activation of cAMP-dependent protein kinase. BMY 42393 also inhibited thrombin-induced elevation of intracellular free calcium. B...
T27331	Flerobuterol HCl CRL-40996,CRL40996,CRL 40996,Flerobuterol hydrochloride
	Flerobuterol is a β adrenergic receptor agonist potentially for the treatment of major depressive disorder. Flerobuterol enhances serotonergic neurotransmission. Flerobuterol acutely increases 5-HT synthesis, in part, through an elevation of brain Trp ava
T68364	GS-9160
	GS-9160 is a novel and potent inhibitor of human immunodeficiency virus type 1 (HIV-1) integrase (IN) that specifically targets the process of strand transfer. It is an authentic inhibitor of HIV-1 integration, since treatment of infected cells results in an elevation of two-long terminal repeat circles and a decrease of integration junctions.
T40750	12,14-Dichlorodehydroabietic acid
	12,14-Dichlorodehydroabietic acid, a chlorinated resin acid, exhibits potent calcium-activated potassium (BK) channel opening activity. It effectively inhibits GABA-dependent chloride influx in the mammalian brain, functioning as a non-competitive antagonist of GABA A receptors. Moreover, 12,14-Dichlorodehydroabietic acid induces an elevation in cytosolic free calcium levels and promotes the release of neurotransmitters.
T81249	Ru3	PARP	Chromatin/Epigenetic; DNA Damage/DNA Repair
	Ru3是一种poly(ADP-ribose)polymerase 1抑制剂，能够通过诱导DNA损伤、抑制DNA修复机制、扰乱细胞周期、降低线粒体膜电位及增加reactive oxygen species水平来诱导MCF-7细胞的apoptosis。
T68760	Luminespib mesylate
	Luminespib, also known as AUY-922, NVP-AUY922, VER52296, is a derivative of 4,5-diarylisoxazole and a third-generation heat shock protein 90 (Hsp90) inhibitor with potential antineoplastic activity. Hsp90 inhibitor AUY922 has been shown to bind with high affinity to and inhibit Hsp90, resulting in the proteasomal degradation of oncogenic client proteins; the inhibition of cell proliferation; and the elevation of heat shock protein 72 (Hsp72) in a wide range of human tumor cell lines.
T77026	Goflikicept
	Goflikicept (RPH 104) 是一种可选择性结合并灭活循环中的 IL-1ß 和 IL-1α 的杂合蛋白。此化合物在研究ST段抬高型心肌梗死（STEMI）方面具有潜力。
T70763	KR-67607
	KR-67607, also known as NTX-101 is novel selective 11β-hydroxysteroid dehydrogenase 1 (11β-HSD1) inhibitor. KR-67607 decreased 4-hydroxynonenal expression and increased antioxidant and mucus secretion in BAC-treated rat eyes. KR-67607 showed its protective effects against ischemia-reperfusion-induced eye injury. KR-67607 effectively reduced cortisol levels in mouse eyes and maintained the trabecular meshwork (TM) structure in the presence of transient ischemic stress. Furthermore, KR-67607 rever...
T63088	NOD2 antagonist 1
	NOD2 antagonist 1 (compound 32) 是一种有效的、选择性的 NOD2 拮抗剂 (IC50: 5.23 μM)。NOD2 antagonist 1 在 THP-1 细胞，对 Muramyl dipeptide (MDP) 诱导的 IL-8 分泌表现出抑制作用。NOD2 antagonist 1 在 PBMCs 细胞，可以抑制 MDP 诱导的 IL-6、IL-10 和 TNF-α 的水平升高。
T27228	E-3030 free acid E-3030,E3030,E 3030
	E-3030 free acid is a peroxisome proliferator-activated receptor (PPAR) agonist. E-3030 decreased blood glucose, triglyceride, non-esterified fatty acids, and insulin levels and increased blood adiponectin levels. Triglyceride- and non-high-density lipopr
T63248	NTU281
	NTU281 是转谷氨酰胺酶-2 (transglutaminase-2) 的有效抑制剂，能够减少糖尿病大鼠血清肌酐和蛋白尿的升高，并降低肾小球 I 型胶原积累、Hic-5 和α-SMA 表达，以及减少细胞凋亡 (apoptosis)，能够用于糖尿病引起的肾小球硬化的研究。
T73083	Nipradolol KT 210 ; K 351 ; Hypadil,Hypadil,KT 210,K 351
	Nipradolol (KT-210; K-351) 是一种有效的 α-1-肾上腺素能受体的阻滞剂。Nipradolol 还抑制白化兔模型中 Phenylephrine 诱导的眼压升高 (IOP)。Nipradolol 抑制去甲肾上腺素 (NA) 引起的肌肉收缩，对犬冠状动脉也有血管扩张剂活性。
T65252	Pepsin
	Pepsin is an endopeptidase that breaks down proteins into smaller peptides and amino acids that can be easily absorbed in the small intestine[1]. Pepsin is stable at pH ranges as high as pH 6. Above this pH, pepsin is rapidly irreversibly inactivated and elevation of pH of the reaction mixture to pH 8 results in complete inactivation of pepsin[2]. Pepsin has been posited to be a reliable biological marker of EER. An immunologic pepsin assay of combined sputum and saliva was determined to be 100%...

化合物

Cat.No: T7127

Target: Apoptosis, GPR

Cat.No: T69795

Synonym: BIII 890 CL,Crobenetine Free Base

Target: Calcium Channel, Sodium Channel

Cat.No: T3543

Synonym: NS 638

Target: Calcium Channel

Cat.No: T15648

Target: Histone Demethylase

Cat.No: T28958

Synonym: TG6 129

Target: Prostaglandin Receptor

Cat.No: T10595

Synonym: BQ788

Target: Endothelin Receptor

Cat.No: T21704

Synonym: 5F-203,NSC-703786

Target: Others

Midodrine hydrochloride

Cat.No: T1577

Synonym: Pro-Amatine,盐酸米多君

Target: Adrenergic Receptor

Cat.No: T15017

Target: TLR

Cat.No: T41005

Target: PACAP

Cat.No: T70993

Cat.No: T14068

Target: Others

Cat.No: T61137

Cat.No: T23583

Synonym: 58G3

Difenamizole HCl

Cat.No: T69991

Cat.No: T70865

Flerobuterol HCl

Cat.No: T27331

Synonym: CRL-40996,CRL40996,CRL 40996,Flerobuterol hydrochloride

Cat.No: T68364

12,14-Dichlorodehydroabietic acid

Cat.No: T40750

Cat.No: T81249

Target: PARP

Luminespib mesylate

Cat.No: T68760

Cat.No: T77026

Cat.No: T70763

NOD2 antagonist 1

Cat.No: T63088

E-3030 free acid

Cat.No: T27228

Synonym: E-3030,E3030,E 3030

Cat.No: T63248

Cat.No: T73083

Synonym: KT 210 ; K 351 ; Hypadil,Hypadil,KT 210,K 351

Cat.No: T65252

Cat. No.	Product Name	Target	Signaling Pathways
T3273	Bifendate 联苯双酯,Bifendatatum	HBV; Reverse Transcriptase	Microbiology/Virology
	Bifendate (Bifendatatum) 是 Schisandrin C 的合成中间体，在慢性 B 型肝炎的研究中具有抗HBV 功效，用于治疗病毒性肝炎和药物性肝损伤引起的转氨酶升高。
T19924	Rhododendrol Betuligenol,Frambinol,杜鹃醇	Others	Others
	Rhododendrol (Frambinol) 是一种黑色素合成物，防止雄性小鼠高脂饮食引起的体重升高和增加雄性小鼠白色脂肪细胞的脂肪分解。Rhododendrol 可用作美白/美白化妆品抑制剂。
T21344	1-Deoxynojirimycin hydrochloride Moranoline,去氧野艽霉素盐酸盐,AT2220,Duvoglustat hydrochloride,1-Deoxynojirimycin,DNJ,deoxynojirimycin	PI3K; Antibacterial; Antibiotic; Glucosidase	Metabolism; Microbiology/Virology; PI3K/Akt/mTOR signaling
	1-Deoxynojirimycin hydrochloride (Moranoline) 是一种口服有效的 α-葡萄糖苷酶抑制剂，具有降血糖、减肥和抗病毒的作用，可抑制餐后血糖，预防糖尿病。
T0611	Vanillylmandelic acid 4-Hydroxy-3-methoxymandelic acid,3-甲氧基-4-羟基扁桃酸	Others	Others
	Vanillylmandelic acid (4-Hydroxy-3-methoxymandelic acid) 是儿茶酚胺、肾上腺素和去甲肾上腺素代谢的最终产物，常用于帮助诊断嗜铬细胞瘤，以及其升高与抑郁症状有关。
T2S1778	DL-Goitrin DL-甲状腺肿素,板蓝根,Goitrin,(R,S)-告依春	Others	Others
	DL-Goitrin 也称为 (R,S)-Goitrin，由 epigoitrin (R-Goitrin) 和告依春 (S-Goitrin) 两种异构体组成，是板蓝根的成分。
T4713	Phosphorylcholine chloride calcium salt tetrahydrate Phosphocholine chloride calcium salt tet,胆碱磷酸氯化钙四水,CalciuM Phosphorylcholine Tetrahydrate	Others; Endogenous Metabolite	Metabolism; Others
	Phosphorylcholine chloride calcium salt tetrahydrate (Phosphocholine chloride calcium salt tet) 是内源性代谢产物的一种。
TN1011	Rhodionin	P450; AChE	Metabolism; Neuroscience
	Rhodionin 是从红景天的根中分离的特异性非竞争性细胞色素 P450 2D6 抑制剂，IC50=0.761 μM，Ki=0.769 μM。它有 DPPH 自由基清除活性，IC50为 19.49 μM。它抑制乙酰胆碱酯酶，IC50范围为 57.50 至 2.43 μg/mL。
T2860	Vanillyl Alcohol 4-Hydroxy-3-methoxybenzenemethanol,3-Methoxy-4-hydroxybenzyl alcohol,4-Hydroxy-3-methoxybenzyl alcohol,香兰醇,Vanillin alcohol,Vanillic alcohol	Apoptosis; Others	Apoptosis; Others
	Vanillyl Alcohol (3-Methoxy-4-hydroxybenzyl alcohol) 是一种酚类醇，具有抗血管生成、抗惊厥、抗炎、抗氧化、神经保护和抗伤害活性。它由香兰素衍生而来，在食品和饮料中用作调味剂。
T4877	L-Homocystine	Endogenous Metabolite	Metabolism
	L-Homocystine 是一种 L-homocysteine 的氧化物。其中 L-homocysteine 是抗血栓因子、血管舒张损害剂、促炎因子，也是研究心血管疾病发生机制的内质网应激反应的诱导剂。
T5S1632	Barlerin 8-O-乙酰山栀苷甲酯,8-O-Acetylshanzhiside methyl ester,ND01	VEGFR; TNF; NF-κB; Akt; Caspase	Angiogenesis; Apoptosis; Cytoskeletal Signaling; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Tyrosine Kinase/Adaptors
	Barlerin (8-O-Acetylshanzhiside methyl ester) 是一种环孢菌素葡萄糖苷，从中国西藏民间药用植物中分离得到，能够抑制NF-κB 活性。
T4S2326	Cornuside 7-Galloylsecologanol,7-O-Galloylsecologanol,山茱萸新苷,Comuside	ERK; p38 MAPK; NF-κB; JNK	MAPK; NF-κB
	Cornuside (Comuside) 是从山茱萸的果实中分离出的环烯醚萜苷，可用于炎症疾病的研究和促进血液循环。它通过下调 MAPK 和 NF-κB 信号通路抑制肥大细胞介导的过敏反应，用于炎性过敏性疾病中的潜能。
T13752	L-(+)-Arabinose	Endogenous Metabolite	Metabolism
	L-(+)-Arabinose 能够选择性抑制肠道蔗糖酶，并抑制因蔗糖摄入而导致的血浆葡萄糖提高。
TN2224	Soyasapogenol A 大豆甾醇A,大豆甾醇 A	TNF	Apoptosis
	Soyasapogenol A shows estrogenic and hepatoprotective activities, it directly prevents apoptosis of hepatocytes, and secondly, inhibits the elevation of plasma TNF-α±, which consequently resulted in the prevention of liver damage in the concanavalin A-induced hepatitis model.
TN4317	Isopedicin	NADPH-oxidase; cAMP; p38 MAPK; PKA; JNK; PDE	GPCR/G Protein; Immunology/Inflammation; MAPK; Metabolism; Tyrosine Kinase/Adaptors
	Isopedicin has anti-inflammatory functions, it inhibits the O(2)()(-) production in human neutrophils by an elevation* of cellular cAMP and activation of PKA through its inhibition of cAMP-specific PDE.
T27564	Hymenidin	5-HT Receptor	GPCR/G Protein; Neuroscience
	Hymenidin是一种从冲绳海绵Hymeniacidon sp。中分离出的生物碱，是一种5-羟色胺能受体拮抗剂和电压门控钾通道抑制剂，具有潜在的抗原生动物作用，可选择性结合 FOXO1 DNA ，可降低去极化诱导的细胞钙升高。
TN2169	Saikogenin D 柴胡皂甙元 D,皂苷元 D	IL Receptor; Calcium Channel; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism
	Saikogenin D possesses a dual effect: an inhibition of A23187-induced PGE2 production without a direct inhibition of cyclooxygenase activity; and an elevation of [Ca2+]i that is attributed to Ca2+ release from intracellular stores. Saikogenin D has immuno
TN4582	Moracin T	c-Myc; COX	Cell Cycle/Checkpoint; Immunology/Inflammation; Neuroscience
	Moracin treatment can inhibit the double 12-O-tetradecanoylphorbol 13-acetate (TPA) treatment-induced morphological changes reflecting inflammatory response, including leucocyte infiltration, hyperplasia and cell proliferation; moracin treatment furthermo

天然产物

Cat.No: T3273

Synonym: 联苯双酯,Bifendatatum

Target: HBV, Reverse Transcriptase

Cat.No: T19924

Synonym: Betuligenol,Frambinol,杜鹃醇

Target: Others

1-Deoxynojirimycin hydrochloride

Cat.No: T21344

Synonym: Moranoline,去氧野艽霉素盐酸盐,AT2220,Duvoglustat hydrochloride,1-Deoxynojirimycin,DNJ,deoxynojirimycin

Target: PI3K, Antibacterial, Antibiotic, Glucosidase

Vanillylmandelic acid

Cat.No: T0611

Synonym: 4-Hydroxy-3-methoxymandelic acid,3-甲氧基-4-羟基扁桃酸

Target: Others

Cat.No: T2S1778

Synonym: DL-甲状腺肿素,板蓝根,Goitrin,(R,S)-告依春

Target: Others

Phosphorylcholine chloride calcium salt tetrahydrate

Cat.No: T4713

Synonym: Phosphocholine chloride calcium salt tet,胆碱磷酸氯化钙四水,CalciuM Phosphorylcholine Tetrahydrate

Target: Others, Endogenous Metabolite

Cat.No: TN1011

Target: P450, AChE

Vanillyl Alcohol

Cat.No: T2860

Synonym: 4-Hydroxy-3-methoxybenzenemethanol,3-Methoxy-4-hydroxybenzyl alcohol,4-Hydroxy-3-methoxybenzyl alcohol,香兰醇,Vanillin alcohol,Vanillic alcohol

Target: Apoptosis, Others

Cat.No: T4877

Target: Endogenous Metabolite

Cat.No: T5S1632

Synonym: 8-O-乙酰山栀苷甲酯,8-O-Acetylshanzhiside methyl ester,ND01

Target: VEGFR, TNF, NF-κB, Akt, Caspase

Cat.No: T4S2326

Synonym: 7-Galloylsecologanol,7-O-Galloylsecologanol,山茱萸新苷,Comuside

Target: ERK, p38 MAPK, NF-κB, JNK

L-(+)-Arabinose

Cat.No: T13752

Target: Endogenous Metabolite

Soyasapogenol A

Cat.No: TN2224

Synonym: 大豆甾醇A,大豆甾醇 A

Target: TNF

Cat.No: TN4317

Target: NADPH-oxidase, cAMP, p38 MAPK, PKA, JNK, PDE

Cat.No: T27564

Target: 5-HT Receptor

Cat.No: TN2169

Synonym: 柴胡皂甙元 D,皂苷元 D

Target: IL Receptor, Calcium Channel, Prostaglandin Receptor

Cat.No: TN4582

Target: c-Myc, COX

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