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787

抑制剂 & 化合物

33

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T9044	SORT-PGRN interaction inhibitor 1	Neurotensin Receptor	GPCR/G Protein
	SORT-PGRN interaction inhibitor 1 是一种 sortilin-progranulin 相互作用抑制剂，IC50为 2 μM。
T3189	B7/CD28 interaction inhibitor 1 CTLA-4 inhibitor	Others	Others
	B7/CD28 interaction inhibitor 1 (CTLA-4 inhibitor) 是B7.1-CD28相互作用抑制剂(IC50:50 nM)。
T12351	p53 and MDM2 proteins-interaction-inhibitor (racemic) p53-and-mdm2-proteins-interaction-inhibitor-racemic	Others	Others
	p53 and MDM2 proteins-interaction-inhibitor (racemic) is an inhibitor of the interaction between p53 and MDM2 proteins.
T28219	NusB-NusE interaction inhibitor-1
	NusB-NusE interaction inhibitor-1 is a modulator of the NusB-NusE interaction.
T12350	p53 and MDM2 proteins-interaction-inhibitor dihydrochloride	Others	Others
	p53 and MDM2 proteins-interaction-inhibitor dihydrochloride is a interaction inhibitor between p53 and MDM2 proteins.
T82244	HA-CD44 interaction inhibitor 2
	Antitumor agent-108作为一种Hyaluronic acid (HA)-CD44相互作用抑制剂，能够破坏癌症球体的完整性并显示出抗增殖活性。
T79106	SORT-PGRN interaction inhibitor 3	Neurotensin Receptor	GPCR/G Protein
	SORT-PGRN interaction inhibitor 3（Compound 13），一种IC50为0.17 μM的SORT-PGRN相互作用抑制剂，适用于神经退行性疾病研究。
T81126	SORT-PGRN interaction inhibitor 2
	SORT-PGRN interaction inhibitor 2为一种SORT-PGRN抑制剂，能降低哺乳动物细胞中SORT1蛋白水平并提升PGRN在细胞外的分泌，适于神经系统疾病研究之用。
T79756	Beclin1-ATG14L interaction inhibitor 1	Autophagy	Autophagy
	Beclin1-ATG14L interaction inhibitor 1 (com 19) 作为一种选择性抑制剂，特定抑制脂质激酶VPS34的复合物 I 中Beclin1与ATG14L的相互作用，而对Beclin 1-UVRAG作用重要的VPS34复合物 II 无影响。由此，其阻断VPS34复合物 I 形成，抑制自噬过程，但不干扰复合物 II 介导的囊泡运输。
T82245	HA-CD44 interaction inhibitor 1
	Antitumor agent-109（compound 6）是一款针对CD44的透明质酸抑制剂，具有抗肿瘤作用。它能够抑制MDA-MB-231细胞，EC50值仅为0.59 μM，显示出通过阻断透明质酸与CD44的相互作用，从而干预肿瘤的生长与侵袭的潜力。
T5697	BMS-1166	PD-1/PD-L1	Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation
	BMS-1166 是 PD-1/PD-L1免疫检查点抑制剂。它促使 PD-L1 形成 PD-L1 同源二聚体，进而阻断其与 PD-1 的相互作用，其 IC50为 1.4 nM。它阻断了 PD-1/PD-L1 免疫检查点对 T 细胞活化的抑制作用。
T82902	Beclin1-Bcl-2 interaction inhibitor 1
	Beclin1-Bcl-2 interaction inhibitor 1，有效地抑制Beclin 1/Bcl-2的结合作用，适用于癌症和神经退行性疾病的研究领域。
T3624	A-366 A 366,A366	Epigenetic Reader Domain; Histone Methyltransferase	Chromatin/Epigenetic
	A-366 是一种高选择性的肽竞争性组蛋白甲基转移酶 G9a 抑制剂，对 G9a 和 GLP 的 IC50分别为 3.3 和 38 nM。它比其他 21 种甲基转移酶具有 1000 倍以上的选择性。它是 Spindlin1-H3K4me3相互作用的抑制剂，IC50为182.6 nM。它对人 H3R 表现出很高的亲和力，Ki 值为 17 nM，在组胺能和多巴胺能受体家族的亚群间表现出亚型选择性。
T10860	Col003	HSP	Cytoskeletal Signaling; Metabolism
	Col003 是一种选择性和有效的 Hsp47 抑制剂，可竞争性结合 Hsp47 上的胶原蛋白结合位点，IC50为1.8 μM。它通过破坏胶原蛋白三螺旋的稳定性来抑制胶原蛋白的分泌，可用于肺纤维化的相关研究。
T4647	M2I-1 M2I 1	Others	Others
	M2I-1 是Mad2抑制剂，靶向的 Mad2 与 Cdc20 的结合，该结合是纺锤体装配检查点内必不可少的蛋白-蛋白相互作用。
T12979	BI-3406	p38 MAPK; MAPK; Ras	GPCR/G Protein; MAPK
	BI-3406 是一种可口服、高效且选择性的 KRAS-SOS1 抑制剂，具有抗癌活性。它有效减少 GTP 加载的 KRAS 的形成，抑制 MAPK 信号通路。它还抑制 KRAS 与 SOS1之间相互作用，IC50为 6 nM。
T8727	TH1020	TLR; Antibacterial	Immunology/Inflammation; Microbiology/Virology
	TH1020 是一种选择性 Toll 样受体 5 /鞭毛蛋白复合拮抗剂，IC50为 0.85 μM。它抑制鞭毛蛋白诱导的TLR5信号传导。
T11857	LIT-001	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	LIT-001 是非肽类催产素受体激动剂，EC50为55 nM，Ki 为226 nM。它可改善孤独症小鼠模型的社交互动。
T9986	(E/Z)-ZINC09659342	Rho	Cell Cycle/Checkpoint
	(E/Z)-ZINC09659342 是 Lbc-RhoA 相互作用的抑制剂。
T9461	AZ194	Sodium Channel	Membrane transporter/Ion channel
	CRMP2-Ubc9-NaV1.7 inhibitor 194 是一流的CRMP2-Ubc9相互作用抑制剂及NaV1.7抑制剂 (IC50=1.2 μM)，口服有活性，具有抗伤害作用。AZ194 阻断 CRMP2 的 SUMOylation 以选择性地减少表面表达 NaV1.7 的量。
T13349	WS-383	E1/E2/E3 Enzyme	Ubiquitination
	WS-383 是高效、选择性、可逆的DCN1-UBC12相互作用抑制剂，IC50为11 nM。它抑制 Cul3/1 的类泛素化修饰，引起 NRF2，p21和p27 的积累。
T28036	MI-2-2 MI22,MI 2 2	Histone Methyltransferase	Chromatin/Epigenetic
	MI-2-2 是一种抑制 menin 和 MLL 之间二价蛋白质-蛋白质相互作用的抑制剂，IC50 为 46 nM。 MI-2-2 与 menin 结合，Kd 为 22 nM。
T8421	TED-347	YAP	Stem Cells
	TED-347 是不可逆的、共价的 YAP-TEAD 蛋白质-蛋白质相互作用变构抑制剂，对 TEAD4•Yap1 蛋白质-蛋白质相互作用的 EC50为 5.9 μM。它与 TEAD4 中央口袋内的 Cys-367 特异性共价结合(Ki:10.3 μM)。它可以抑制 TEAD 的转录活性，并且具有抗肿瘤作用。
T22698	TLR3-IN-1 CU CPT 4a	TLR	Immunology/Inflammation
	TLR3-IN-1 (CU CPT 4a) 是一种选择性的TLR3信号抑制剂，在 RAW 264.7 细胞中 IC50 为 3.44 μM。它可以抑制 TLR3/dsRNA 复合物介导的下游信号通路，并抑制全细胞中 TNF-α 和 IL-1β 的产生。
T9317	TAK-041 NBI-1065846	GPR	Endocrinology/Hormones; GPCR/G Protein
	TAK-041 (NBI-1065846) 是一种选择性 GPR139激动剂，EC50为 22 nM，有用于精神分裂症阴性症状的研究潜力。
T13244	Ubiquitination-IN-1	Others	Others
	Ubiquitination-IN-1 是一种有效的泛素化和Cksl-Skp2蛋白互作抑制剂 (IC50=0.17 μM) 抑制剂，增加 p27 水平，可通过阻断肿瘤抑制因子的降解发挥作用。
T8564	BC-1382	Others; E1/E2/E3 Enzyme	Others; Ubiquitination
	BC-1382 是E3泛素连接酶HECTD2抑制剂，能够特异性破坏 HECTD2/PIAS1 相互作用 (IC50≈ 5 nM)。BC-1382具有抗炎活性。
T15022	CVT-10216 3-[[[3-[4-[(甲基磺酰基)氨基]苯基]-4-氧代-4H-苯并吡喃-7-基]氧基]甲基]苯甲酸	Dehydrogenase	Metabolism
	CVT-10216 是可逆的、选择性的醛脱氢酶 2（ALDH-2）抑制剂，IC50为 29 nM。对 ALDH-1的抑制作用较弱，IC50为 1.3 μM。它可以减少偏爱酒精的大鼠过量饮酒，并表现出抗焦虑作用。
T4687	Ro5-3335 CBFβ-Runx1 inhibitor II,Ro 5-3335	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Ro5-3335 (CBFβ-Runx1 inhibitor II) 是苯二氮化合物，是RUNX1-CBFβ 相互作用抑制剂，可抑制 RUNX1/CBFB 依赖性反式激活，能作为核心结合因子 (CBF) 白血病抑制剂。
T19663	Triheptanoin UX 007,IND106011,三庚酸甘油脂,UX007,UX-007,IND 106011,IND-106011	Others	Others
	Triheptanoin (IND 106011) 是合成的中链甘油三酯 (MCT)，由甘油主链上的三个奇数链 7-碳(庚酸)脂肪酸组成，可以用于研究遗传代谢紊乱。
T9093	NY2267 Acetic acid, 2-[[6-[2-(cyclohexylamino)-1-[[(4-methoxyphenyl)methyl](2-pyridinylcarbonyl)amino]-2-oxoethyl]-2-naphthalenyl]oxy]-, 1,1-dimethylethyl ester	c-Myc	Cell Cycle/Checkpoint
	NY2267 (Acetic acid, 2-[[6-[2-(cyclohexylamino)-1-[[(4-methoxyphenyl)methyl](2-pyridinylcarbonyl)amino]-2-oxoethyl]-2-naphthalenyl]oxy]-, 1,1-dimethylethyl ester) 是一种 Myc-Max 相互作用干扰物，抑制 Myc 和 Jun 诱导的转录激活，其 IC50值为 36.5 μM。
T0788L	Spectinomycin dihydrochloride pentahydrate 盐酸大观霉素五水合物,Trobicin,Spectogard,Spectinomycin hydrochloride hydrate	ribosome; Antibacterial; Antibiotic	Microbiology/Virology
	Spectinomycin dihydrochloride pentahydrate (Spectogard) 是一种广谱氨基环糊精抗生素，可以抑制多种革兰氏阳性和革兰氏阴性生物的生长。
T36573	NHWD-870	Apoptosis; Epigenetic Reader Domain	Apoptosis; Chromatin/Epigenetic
	NHWD-870 是一种有效且特异性的 BET 家族溴结构域抑制剂，仅与 BRD2、BRD3、BRD4 (IC50 = 2.7 nM) 和 BRDT 结合。 NHWD-870 具有强大的抗肿瘤功效，并通过增加肿瘤细胞凋亡和抑制肿瘤增殖来抑制癌细胞-巨噬细胞相互作用。
T6023	Nutlin-3a (-)-Nutlin-3,Nutlin-3a chiral,(−)-Nutlin-3	Apoptosis; E1/E2/E3 Enzyme; Autophagy	Apoptosis; Autophagy; Ubiquitination
	Nutlin-3a ((−)-Nutlin-3) 是 Nutlin-3 的活性对映体，是一种 MDM2抑制剂，可抑制 MDM2-p53相互作用，稳定 p53 蛋白，从而诱导细胞自噬和凋亡，有潜力研究 TP53野生型卵巢癌。
T76089	Pepinh-TRIF TFA	Raf; TLR	Immunology/Inflammation; MAPK
	Pepinh-TRIF TFA 是一种 30 aa 肽，与免疫系统有关，通过干扰 TLR-TRIF 的相互作用 (TLR-TRIF interaction ) 来阻断 TRIF 信号。
T13173	TMPA	Others; AMPK	Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling
	TMPA 是一种核受体 Nur77 和 LKB1 相互作用的拮抗剂。
T10601	BRCA1-IN-2	Others	Others
	BRCA1-IN-2 是一种可穿过细胞膜的 BRCA1 蛋白-蛋白相互作用（PPI）抑制剂，具有抗肿瘤活性，通过破坏 BRCA1 (BRCT)2 与蛋白质的相互作用来发挥作用。
T21578	NSC 66811	Mdm2	Apoptosis
	NSC 66811 是一种MDM2-p53抑制剂，其结合到 MDM2 的Ki 值为 120 nM。
T9902	Atezolizumab 阿特朱单抗,阿特珠单抗	Apoptosis; PD-1/PD-L1; Autophagy	Apoptosis; Autophagy; Cell Cycle/Checkpoint; Immunology/Inflammation
	Atezolizumab 是一种人源化单克隆抗体 IgG1，能抵抗程序性死亡因子配体1 ，可用于癌症研究。
T6691	TAI-1	Apoptosis; Microtubule Associated	Apoptosis; Cytoskeletal Signaling
	TAI1 是一种具有口服活性的特异性 Hec1 抑制剂，有抗肿瘤活性，在 K562 细胞中的 GI50值为 13.48 nM。
T24557	NSC756093 NSC-756093,NSC 756093	Others	Others
	NSC756093 可能抑制 GBP1:PIM1 相互作用。 NSC756093 可用于卵巢癌研究。
T5108	ML311	BCL	Apoptosis
	ML311 是 Mcl-1/Bim 相互作用的一种选择性抑制剂。
T11851	Lin28-let-7a antagonist 1	Others	Others
	Lin28-let-7a antagonist 1 对 Lin28A-let-7a-1 相互作用的 IC50 为 4.03 μM，对 Lin28-let-7a 相互作用有明显的拮抗作用。
T9156	CDC25B-IN-2	Phosphatase; mTOR	Metabolism; PI3K/Akt/mTOR signaling
	BIA 是一种 cdc25B 抑制剂。
T5374	NAcM-OPT	E1/E2/E3 Enzyme; NEDD8	Metabolism; Ubiquitination
	NAcM-OPT 是口服活性、有效的 cullin neddylation 1 抑制剂，可以抑制 DCN1-UBE2M 相互作用。
TQ0069	MI-503	Epigenetic Reader Domain; Histone Methyltransferase	Chromatin/Epigenetic
	MI-503 是一种高效且可口服的 menin-mLL 相互作用抑制剂。
T4311	HAMNO NSC111847	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	HAMNO (NSC-111847) 是一种复制蛋白 A 的新型蛋白质相互作用抑制剂。
T4021	UNC3866	Histone Methyltransferase	Chromatin/Epigenetic
	UNC3866 CBX7-H3 相互作用的有效拮抗剂，IC50为 66±1.2 nM。
T8784	IGS-1.76	Others	Others
	IGS-1.76 exhibits pronounced affinity towards hNCS-1 and effectively modulates the interaction between hNCS-1 and Ric8a. Moreover, IGS-1.76 proficiently inhibits the complex formed by human NCS-1 and Ric8a.
T6462	Deltarasin	PDE; Ras	GPCR/G Protein; MAPK; Metabolism
	Deltarasin 是一种 KRAS-PDEδ 相互作用的小分子抑制剂，与纯化的 PDEδ 结合，Kd 值为 38 nM。

化合物

SORT-PGRN interaction inhibitor 1

Cat.No: T9044

Target: Neurotensin Receptor

B7/CD28 interaction inhibitor 1

Cat.No: T3189

Synonym: CTLA-4 inhibitor

Target: Others

p53 and MDM2 proteins-interaction-inhibitor (racemic)

Cat.No: T12351

Synonym: p53-and-mdm2-proteins-interaction-inhibitor-racemic

Target: Others

NusB-NusE interaction inhibitor-1

Cat.No: T28219

p53 and MDM2 proteins-interaction-inhibitor dihydrochloride

Cat.No: T12350

Target: Others

HA-CD44 interaction inhibitor 2

Cat.No: T82244

SORT-PGRN interaction inhibitor 3

Cat.No: T79106

Target: Neurotensin Receptor

SORT-PGRN interaction inhibitor 2

Cat.No: T81126

Beclin1-ATG14L interaction inhibitor 1

Cat.No: T79756

Target: Autophagy

HA-CD44 interaction inhibitor 1

Cat.No: T82245

Cat.No: T5697

Target: PD-1/PD-L1

Beclin1-Bcl-2 interaction inhibitor 1

Cat.No: T82902

Cat.No: T3624

Synonym: A 366,A366

Target: Epigenetic Reader Domain, Histone Methyltransferase

Cat.No: T10860

Target: HSP

Cat.No: T4647

Synonym: M2I 1

Target: Others

Cat.No: T12979

Target: p38 MAPK, MAPK, Ras

Cat.No: T8727

Target: TLR, Antibacterial

Cat.No: T11857

Target: Oxytocin Receptor

(E/Z)-ZINC09659342

Cat.No: T9986

Target: Rho

Cat.No: T9461

Target: Sodium Channel

Cat.No: T13349

Target: E1/E2/E3 Enzyme

Cat.No: T28036

Synonym: MI22,MI 2 2

Target: Histone Methyltransferase

Cat.No: T8421

Target: YAP

Cat.No: T22698

Synonym: CU CPT 4a

Target: TLR

Cat.No: T9317

Synonym: NBI-1065846

Target: GPR

Ubiquitination-IN-1

Cat.No: T13244

Target: Others

Cat.No: T8564

Target: Others, E1/E2/E3 Enzyme

Cat.No: T15022

Synonym: 3-[[[3-[4-[(甲基磺酰基)氨基]苯基]-4-氧代-4H-苯并吡喃-7-基]氧基]甲基]苯甲酸

Target: Dehydrogenase

Cat.No: T4687

Synonym: CBFβ-Runx1 inhibitor II,Ro 5-3335

Target: DNA/RNA Synthesis

Cat.No: T19663

Synonym: UX 007,IND106011,三庚酸甘油脂,UX007,UX-007,IND 106011,IND-106011

Target: Others

Cat.No: T9093

Synonym: Acetic acid, 2-[[6-[2-(cyclohexylamino)-1-[[(4-methoxyphenyl)methyl](2-pyridinylcarbonyl)amino]-2-oxoethyl]-2-naphthalenyl]oxy]-, 1,1-dimethylethyl ester

Target: c-Myc

Spectinomycin dihydrochloride pentahydrate

Cat.No: T0788L

Synonym: 盐酸大观霉素五水合物,Trobicin,Spectogard,Spectinomycin hydrochloride hydrate

Target: ribosome, Antibacterial, Antibiotic

Cat.No: T36573

Target: Apoptosis, Epigenetic Reader Domain

Cat.No: T6023

Synonym: (-)-Nutlin-3,Nutlin-3a chiral,(−)-Nutlin-3

Target: Apoptosis, E1/E2/E3 Enzyme, Autophagy

Pepinh-TRIF TFA

Cat.No: T76089

Target: Raf, TLR

Cat.No: T13173

Target: Others, AMPK

Cat.No: T10601

Target: Others

Cat.No: T21578

Target: Mdm2

Cat.No: T9902

Synonym: 阿特朱单抗,阿特珠单抗

Target: Apoptosis, PD-1/PD-L1, Autophagy

Cat.No: T6691

Target: Apoptosis, Microtubule Associated

Cat.No: T24557

Synonym: NSC-756093,NSC 756093

Target: Others

Cat.No: T5108

Target: BCL

Lin28-let-7a antagonist 1

Cat.No: T11851

Target: Others

Cat.No: T9156

Target: Phosphatase, mTOR

Cat.No: T5374

Target: E1/E2/E3 Enzyme, NEDD8

Cat.No: TQ0069

Target: Epigenetic Reader Domain, Histone Methyltransferase

Cat.No: T4311

Synonym: NSC111847

Target: DNA/RNA Synthesis

Cat.No: T4021

Target: Histone Methyltransferase

Cat.No: T8784

Target: Others

Cat.No: T6462

Target: PDE, Ras

Cat. No.	Product Name	Target	Signaling Pathways
T0788	Spectinomycin dihydrochloride 淋必治,Spectinomycin 2HCl,盐酸奇霉素,Actinospectacin	ribosome; Antibacterial; Antibiotic	Microbiology/Virology
	Spectinomycin dihydrochloride (Actinospectacin) 是一种能与细菌核糖体的30S 亚基结合，干扰蛋白质合成的抗生素。
TN5118	Taxol C	P-gp	Membrane transporter/Ion channel; Neuroscience
	Taxol C 可以减少与 P-糖蛋白转运蛋白的相互作用，从而增加紫杉烷类向大脑的渗透。
T19418	Methionine sulfoxide	Endogenous Metabolite	Metabolism
	Methionine sulfoxide 是具有特性氧的甲硫氨酸的氧化产物，能够用作体内氧化应激的生物标记。
TN1074	GL3 女贞苷G13	Others	Others
	GL3 是一种基于苯基乙醛醇和甲基油苷的衍生物，也是苦瓜种子的主要成分。
T23735	Jamaicin An-Co-A4,AnCoA-4,An Co A4,AnCoA4	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Jamaicin (AnCoA4) 是一种从鸡血藤植物中提取的异黄酮，是一种 STIM1-Orai1 通道的抑制剂，可阻断钙离子流入，减少其与 STIM1 的相互作用，抑制 T 细胞的活化。
T7210	Guanosine 5'-diphosphate GDP,鸟苷-5ˊ-二磷酸	Endogenous Metabolite	Metabolism
	Guanosine 5'-diphosphate (GDP) 是核苷二磷酸，是潜在的铁动员剂，能够阻断铁调素-铁转运蛋白相互作用并调节白细胞介素-6 (IL-6)/stat-3 途径。
T4S1990	Carvacrol 香荆芥酚,Karvakrol,O-Thymol,cymophenol,香芹酚	Apoptosis; Others; Gamma-secretase; Endogenous Metabolite; Antifungal	Apoptosis; Metabolism; Microbiology/Virology; Neuroscience; Others; Proteases/Proteasome; Stem Cells
	Carvacrol (O-Thymol) 是唇形科植物中的一种单萜酚类天然产物，具有镇痛、抗焦虑、抗抑郁、抗氧化、抗炎和抗癌作用。
TN4761	Phellamurin	P-gp	Membrane transporter/Ion channel; Neuroscience
	Phellamurin 是一种来自黄檗叶的黄酮糖苷，可诱导细胞凋亡，具有抗肿瘤活性。它抑制肠道 P-糖蛋白，还抑制凤蝶的产卵。
T8189	Dihydroberberine	Potassium Channel; HSP; HER	Angiogenesis; Cytoskeletal Signaling; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Tyrosine Kinase/Adaptors
	Dihydroberberine 可抑制人类 ether-a-go-go 相关基因 (hERG) 通道并显着降低 Hsp90 表达及其与 hERG 的相互作用，具有抗动脉粥样硬化、抗炎、降血脂和抗肿瘤活性。
T3669	Curcumenol (+)-Curcumenol,莪术醇	P450	Metabolism
	Curcumenol ((+)-Curcumenol) 提取具有药用价值的 Curcuma zedoaria，是高效的 CYP3A4抑制剂(IC50=12.6 μM)，具有神经抗肿瘤、保护、抗炎、和保肝的作用。它在 LPS 刺激的 BV-2 小胶质细胞中，抑制 Akt 介导的 NF-κB 活化及 p38 MAPK 信号通路。
T5803	D(-)-Tartaric acid	Others	Others
	D(-)-Tartaric acid 存在于许多植物中，特别是罗望子和葡萄，口服后通过与碳酸氢钠相互作用产生二氧化碳。二氧化碳会延伸胃部并在双造影射线照相期间提供负造影剂。
T3363	Jervine 蒜黎芦碱,Iervin,11-Ketocyclopamine,Jerwiny	Hedgehog/Smoothened; Smo	GPCR/G Protein; Stem Cells
	Jervine (Jerwiny) 是一种有效的刺猬 (Hh) 抑制剂(IC50:500-700 nM)。它是一种天然致畸性甾体生物碱，来自于 Veratrumalbum 的根茎，具有抗炎和抗氧化作用。
T14140	Agaric acid 落叶松蕈酸,Agaricinic Acid	Mitochondrial Metabolism; AChR	Metabolism; Neuroscience
	Agaric acid (Agaricinic Acid) 来一种自真菌部落的Polyporus officinalis 和Polyporus igniarius。它可促进积累的 Ca2+流出，跨膜电位的破坏和线粒体肿胀。它通过其与腺嘌呤核苷酸转位酶的相互作用诱导线粒体通透性转变。它用于调节脂类代谢。
T2S2173	(E)-Naringenin chalcone Isosalipurpol,柚皮苷查尔酮,Chalconaringenin,trans-2'4'6'4-tetrahydroxychalcone,柚皮素查耳酮	Others	Others
	Naringenin chalcone (Isosalipurpol) 是一种黄酮醇生物合成的中间体，在查耳酮异构酶的作用下，自发代谢成柚皮素。它具有抗炎和抗过敏活性。
T5079	Adenosine 5'-diphosphate sodium salt 腺苷-5‘-二磷酸钠盐,Adenosine-5'-diphosphate trisodium salt,ADP sodium salt	Others; Endogenous Metabolite	Metabolism; Others
	Adenosine 5'-diphosphate sodium salt (ADP sodium salt) 是一种核苷二磷酸，是一种 ATP 酶对 ATP 去磷酸化的产物。它通过在 P2T-嘌呤受体上的作用诱导人血小板聚集并抑制刺激的腺苷酸环化酶。
TN6872	Trypsin	Protease-activated Receptor	GPCR/G Protein
	Trypsin 是一种可从鱼类分离出的丝氨酸蛋白酶，可水解赖氨酸或精氨酸羧基侧蛋白质。Trypsin 具有抗炎活性，可通过 PDCoV 的 S 糖蛋白与 pAPN 的相互作用诱导 PDCoV 感染的细胞膜融合，可激活 PAR2 和 PAR4，促进细胞增殖和分化。Trypsin 可用于促进伤口愈合和研究神经源性炎症。
T4707	3-Hydroxyanthranilic acid 3-HYDROXY-2-AMINOBENZOIC ACID,3-羟基-2-氨基苯甲酸	Others; Endogenous Metabolite	Metabolism; Others
	3-Hydroxyanthranilic acid (3-HYDROXY-2-AMINOBENZOIC ACID) 是犬尿氨酸途径中的色氨酸代谢物。它已在人类表皮和膀胱组织中发现，并且在多种生物体液中也已检测到，例如尿液和血液。在细胞内，它主要位于细胞质中。它存在于从酵母到人类的所有真核生物中。
T4S1419	(±)-Praeruptorin A Praeruptorin A,(±)-白花前胡甲素,白花前胡甲素,(-)-Praeruptorin A	p38 MAPK; Calcium Channel; Akt	Cytoskeletal Signaling; MAPK; Membrane transporter/Ion channel; Metabolism; PI3K/Akt/mTOR signaling
	(±)-Praeruptorin A 是来自白花前胡的干燥根中的一种主要成分，用于研究伴有厚痰和呼吸困难的咳嗽，非天生性咳嗽和上呼吸道感染。它是顺式-内酯 (CKL) 的二酯化产物，可作为 Ca2+-反流阻滞剂，用于高血压的研究。
TN5171	Tricetin	Apoptosis; Others; Nrf2	Apoptosis; Immunology/Inflammation; Others
	Tricetin 是一种从石榴中分离出的类黄酮。Tricetin 是 Keap1-Nrf2 蛋白相互作用（PPI）的强效竞争性抑制剂，通过激活 Nrf2/HO-1 信号通路和阻止线粒体依赖性细胞凋亡通路，保护帕金森病患免受 6-OHDA 诱导的神经毒性的影响。Tricetin 通过 Akt/GSK-1β途径抑制鼻咽癌的迁移和指示性蛋白酶早老素-1（PS-1）表达。Tricetin 抑制由Egr-1介导的氧化LDL 诱导的内皮炎症，保护大鼠软骨细胞免受IL-1β诱导的炎症和细胞凋亡。
TN1518	Cochinchinenin C	Others	Others
	There is a synergistic interaction between loureirin A and Cochinchinenin C, and the fluorescence quenching of HSA by loureirin A (or Cochinchinenin C) is a combined quenching procedure (dynamic and static quenching).
TMA0805	Lupanine	ATPase; Potassium Channel; Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Lupanine has a weak sedative effect on the central nervous system, interaction with specific drugs used for treatment of the CNS and for analgesic activity. Lupanine improves glucose homeostasis by influencing KATP-channels of pancreatic beta cells.
TN1349	9-Hydroxycalabaxanthone	Antifection	Microbiology/Virology
	9-Hydroxycalabaxanthone exhibits cytotoxicity against the HT-29 cell line with ED50 values of 9.1 microM. The combination of 9-hydroxycalabaxanthone with α±-mangostin shows the synergistic antimalarial interaction in both clones.
TN1550	Danshenxinkun A 丹参新醌甲,丹参新醌A	Others	Others
	Danshenxinkun A, Danshenxinkun B and Neocryptotanshinone may intervene thrombotic diseases by adjusting the targets mainly involved in pathways of endocrine system, signal transduction, signaling molecules and interaction, cell motility, environmental ada
TN3627	Chalepensin	ATPase; NADPH-oxidase; P450; Antifection	Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology
	Chalepensin behaves as an energy transfer inhibitor at low concentration, it inhibits multiple P450s and that epoxidation activity is crucial for the potential drug interaction through mechanism-based inhibition. Chalepensin shows antiprotozoal activity; it also can cause significant inhibition of radicle growth of A. hypochondriacus and E. crus-galli.
T11837	Leptomycin A	CRM1	Membrane transporter/Ion channel
	Leptomycin A, a metabolite derived from Streptomyces, acts as an inhibitor of CRM1 (exportin 1) and effectively suppresses HIV-1 replication. Compared to Leptomycin B, it exhibits lesser potency. Leptomycin A hampers the interaction between CRM1 and nuclear export signals, effectively hindering the nuclear export of a wide array of proteins.
TMA1130	2,4-Dihydroxyphenylacetic acid	Others	Others
	2,4-Dihydroxyphenylacetic acid is a functional moiety in the toxin molecule and the biological action of spider toxin is explained by direct interaction with an Fe-S center which is known to play an important role for the glutamate binding.
T39071	Thailanstatin D
	Thailanstatin D, an analogue of Thailanstatin A, inhibits AR-V7 gene splicing by disrupting the interaction between U2AF65 and SAP155, hindering their binding to the polypyrimidine tract situated between the branch point and the 3' splice site. This compound displays potent tumor inhibitory properties in human castration-resistant prostate cancer (CRPC) xenografts, resulting in cellular apoptosis.
T40424	9-cis-Vitamin A palmitate 9-cis-Vitamin A palmitate,9-cis-Retinyl palmitate
	9-cis-Vitamin A palmitate (9-cis-Retinyl palmitate) is a 9-cis isomer resulting from the interaction of vitamin A palmitate in corn flakes. It exhibits a biological activity of 26% compared to all-trans-vitamin A palmitate, which is known to be the most biologically active form of vitamin A.
TMA0291	Dehydroglyasperin D	GSK-3; p38 MAPK; ROS; Akt; COX; PI3K; DNA/RNA Synthesis; Prostaglandin Receptor; JNK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; MAPK; Neuroscience; PI3K/Akt/mTOR signaling; Stem Cells
	Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 human colorectal cancer cells through direct interaction with phosphatidylinositol 3-kinase; it also mediates suppression of both COX-2 expression and the MLK3 signalling pathway through direct binding and inhibition of MLK3. Dehydroglyasperin D shows strong ferric reducing activities and effectively scavenged DPPH, ABTS(+), and singlet o...
TN6570	Daturaolone
	Daturaolone has potency in reducing the harmful effects or in maintaining the normal hepatic physiological mechanisms in both acute and chronic hepato-toxic induced liver damage in rats. Daturaolone also possesses in vivo anti-inflammatory and antinocicep
TN4319	Isopimaric acid	Antifection	Microbiology/Virology
	Isopimaric acid is active against MDR and MRSA strains of S. aureus which are becoming increasingly resistant to antibiotics, the minimum inhibitory concentrations (MIC) are 32-64 microg/mL . Isopimaric acid is also possible that an antagonistic interacti
TN4552	Methyl p-hydroxyphenyllactate	Others	Others
	Methyl para-hydroxyphenyllactate(MeHPLA) can suppress the cellular proliferation of estrogen-sensitive MCF-7 breast cancer cells in vitro and to suppress the growth of rat uteri in vivo, high affinity of MeHPLA for the type II estrogen binding site (EBS)
T36749	Herboxidiene
	Herboxidiene is a polyketide originally isolated from S. chromofuscus that has diverse biological activities.[1],[2,][3],[4],[5] It inhibits growth of HeLa S3, SK-MEL-2, PC3, A549, and EBC-1 cells with GI50 values ranging from 7.4 to 62 nM.3 Herboxidiene is cytostatic against human umbilical vein endothelial cells (HUVECs; (IC50 = 26 nM)) and inhibits VEGF-induced invasion and tube formation of serum-starved HUVECs in a concentration-dependent manner, indicating antiangiogenic activity.[4] Herbo...

天然产物

Spectinomycin dihydrochloride

Cat.No: T0788

Synonym: 淋必治,Spectinomycin 2HCl,盐酸奇霉素,Actinospectacin

Target: ribosome, Antibacterial, Antibiotic

Cat.No: TN5118

Target: P-gp

Methionine sulfoxide

Cat.No: T19418

Target: Endogenous Metabolite

Cat.No: TN1074

Synonym: 女贞苷G13

Target: Others

Cat.No: T23735

Synonym: An-Co-A4,AnCoA-4,An Co A4,AnCoA4

Target: Calcium Channel

Guanosine 5'-diphosphate

Cat.No: T7210

Synonym: GDP,鸟苷-5ˊ-二磷酸

Target: Endogenous Metabolite

Cat.No: T4S1990

Synonym: 香荆芥酚,Karvakrol,O-Thymol,cymophenol,香芹酚

Target: Apoptosis, Others, Gamma-secretase, Endogenous Metabolite, Antifungal

Cat.No: TN4761

Target: P-gp

Dihydroberberine

Cat.No: T8189

Target: Potassium Channel, HSP, HER

Cat.No: T3669

Synonym: (+)-Curcumenol,莪术醇

Target: P450

D(-)-Tartaric acid

Cat.No: T5803

Target: Others

Cat.No: T3363

Synonym: 蒜黎芦碱,Iervin,11-Ketocyclopamine,Jerwiny

Target: Hedgehog/Smoothened, Smo

Cat.No: T14140

Synonym: 落叶松蕈酸,Agaricinic Acid

Target: Mitochondrial Metabolism, AChR

(E)-Naringenin chalcone

Cat.No: T2S2173

Synonym: Isosalipurpol,柚皮苷查尔酮,Chalconaringenin,trans-2'4'6'4-tetrahydroxychalcone,柚皮素查耳酮

Target: Others

Adenosine 5'-diphosphate sodium salt

Cat.No: T5079

Synonym: 腺苷-5‘-二磷酸钠盐,Adenosine-5'-diphosphate trisodium salt,ADP sodium salt

Target: Others, Endogenous Metabolite

Cat.No: TN6872

Target: Protease-activated Receptor

3-Hydroxyanthranilic acid

Cat.No: T4707

Synonym: 3-HYDROXY-2-AMINOBENZOIC ACID,3-羟基-2-氨基苯甲酸

Target: Others, Endogenous Metabolite

(±)-Praeruptorin A

Cat.No: T4S1419

Synonym: Praeruptorin A,(±)-白花前胡甲素,白花前胡甲素,(-)-Praeruptorin A

Target: p38 MAPK, Calcium Channel, Akt

Cat.No: TN5171

Target: Apoptosis, Others, Nrf2

Cochinchinenin C

Cat.No: TN1518

Target: Others

Cat.No: TMA0805

Target: ATPase, Potassium Channel, Calcium Channel

9-Hydroxycalabaxanthone

Cat.No: TN1349

Target: Antifection

Danshenxinkun A

Cat.No: TN1550

Synonym: 丹参新醌甲,丹参新醌A

Target: Others

Cat.No: TN3627

Target: ATPase, NADPH-oxidase, P450, Antifection

Cat.No: T11837

Target: CRM1

2,4-Dihydroxyphenylacetic acid

Cat.No: TMA1130

Target: Others

Thailanstatin D

Cat.No: T39071

9-cis-Vitamin A palmitate

Cat.No: T40424

Synonym: 9-cis-Vitamin A palmitate,9-cis-Retinyl palmitate

Dehydroglyasperin D

Cat.No: TMA0291

Target: GSK-3, p38 MAPK, ROS, Akt, COX, PI3K, DNA/RNA Synthesis, Prostaglandin Receptor, JNK

Cat.No: TN6570

Isopimaric acid

Cat.No: TN4319

Target: Antifection

Methyl p-hydroxyphenyllactate

Cat.No: TN4552

Target: Others

Cat.No: T36749

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