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203

抑制剂 & 化合物

28

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T13561	AT6	Others	Others
	AT6 is a PROTAC AT1 analog which is a highly selective bromodomain (Brd4) degrader.
T3725	K-Ras(G12C) Inhibitor 6	Raf	MAPK
	KRas(G12C) inhibitor 6 是一种变构的，选择性的 K-Ras(G12C)抑制剂。
T0717	Enoxacin hydrate CI-919 hydrate,Enoxacin Sesquihydrate,依诺沙星半水合物,AT-2266 hydrate,依诺沙星倍半水合物	DNA gyrase; DNA/RNA Synthesis; Topoisomerase; Antibacterial; Antibiotic	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology
	Enoxacin hydrate (AT-2266 hydrate) 是氟喹诺酮，可干扰DNA 复制，抑制细菌 DNA 促旋酶 (IC50=126 µg/ml) 和拓扑异构酶 IV (IC50=26.5 µg/ml)。它是特异性癌症生长抑制剂，抑制革兰氏阳性和阴性细菌。
T16435	PBIT	Histone Demethylase; Histone Methyltransferase	Chromatin/Epigenetic
	PBIT 是一种特异性 Jumonji/AT 富集互作结构域 1 抑制剂，抑制JARID1A 和JARID1C，IC50分别为 6 和 4.9 μM。它抑制JARID1B(KDM5B 或PLU1) 组蛋白去甲基化酶，IC50值约为 3 μM。
T6598	MPEP	GluR	Neuroscience
	MPEP 是一种选择性 mGlu5 受体拮抗剂，IC50 为 36 nM，有抗焦虑和抗抑郁活性。
TD0101	AQC 6-Aminoquinolyl-N-hydroxysccinimidyl carbamate	Others	Others
	AQC (6-Aminoquinolyl-N-hydroxysccinimidyl carbamate) 是一种高效液相色谱荧光检测氨基酸或蛋白质序列的试剂。它能够与一级和二级氨基酸反应生成荧光衍生物，在皮摩尔水平下能够检测氨基酸。
T10781	CGP 78608 hydrochloride PAMQX	NMDAR; iGluR	Membrane transporter/Ion channel; Neuroscience
	CGP 78608 hydrochloride 是 NMDA 受体甘氨酸结合位点的特异性拮抗剂 (IC50 = 6 nM)。 CGP 78608 hydrochloride 具有抗惊厥活性。 CGP 78608 hydrochloride 增强 GluN1/GluN3A 介导的甘氨酸电流（估计 EC50 = 26.3 nM）。
T22735	DMAB-anabaseine dihydrochloride N,N-dimethyl-4-[(E)-(6-pyridin-3-yl-3,4-dihydro-2H-pyridin-5-ylidene)methyl]aniline;dihydrochloride	AChR	Neuroscience
	DMAB-anabaseine dihydrochloride (N,N-dimethyl-4-[(E)-(6-pyridin-3-yl-3,4-dihydro-2H-pyridin-5-ylidene)methyl]aniline;dihydrochloride) 是一种含有 α7 的神经元烟碱受体部分激动剂和 α4β2 和其他烟碱受体的拮抗剂。
T10432L	AZD-8529 mesylate	GluR	Neuroscience
	AZD-8529 mesylate 是高度选择性的可口服mGluR2正向调节剂，EC50值为 285 nM。它在 20-25 M 时，对 mGluR1、3、4、5、6、7 和 8 亚型没有显示正变构调节剂反应。
T16962	SW-100	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	SW-100 是一种选择性组蛋白去乙酰化酶 6 抑制剂，IC50为2.3 nM。它有提高的穿过血脑屏障的能力，相对于其他 HDAC 同工酶，还显示出对 HDAC6 的至少高 1000 倍的选择性。
T15728	LDN-212320 LDN-0212320,LDN/OSU-0212320,OSU-0212320	transporter	Metabolism
	LDN-212320 (OSU-0212320) 是兴奋性氨基酸转运体 2(EAAT2)/谷氨酸转运体(GLT-1)的激活剂。它通过上调海马和 ACC 星形胶质细胞 GLT-1 的水平来预防伤害性疼痛。
T50111	6-Fluorotryptamine hydrochloride	Others	Others
	6-Fluorotryptamine hydrochloride 是一种用作分子结构单元的化合物，是天然色胺生物碱血清素的衍生物。它是5-HT2A 和5-HT2C 血清素受体的激动剂，使其成为开发治疗各种精神和神经疾病的新药的潜在候选者。
T12574	PTC299 Emvododstat,(4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate	VEGFR; Dehydrogenase	Angiogenesis; Metabolism; Tyrosine Kinase/Adaptors
	PTC299 ((4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate) 是一种口服活性的 VEGFA mRNA 翻译抑制剂，可选择性地抑制转录后水平的 VEGF 蛋白合成。它还是二氢乳酸脱氢酶 (DHODH) 的有效抑制剂，可研究血液系统恶性肿瘤。
T40443	JAK2-IN-6 JAK2-IN-6	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	JAK2-IN-6是一种有效的、有选择性的 JAK2抑制剂(ic50为22.86 μg/mL),是一种多取代氨基噻唑衍生物。JAK2-IN-6抑制 JAK2酶的活性，通过干扰与 JAK2相关的信号通路，从而对 JAK2失调的特定疾病产生治疗作用，对 JAK1和JAK3不显示出活性。JAK2是一种参与调节细胞生长和分裂的信号通路的蛋白质。JAK2的异常激活与多种疾病有关，包括某些类型的癌症和炎症性疾病。JAK2-IN-6对癌细胞具有抗增殖活性。
T14775	Bragsin2 6-methoxy-5-nitro-2-(trifluoromethyl)chromen-4-one,Bragsin 2	Others	Others
	Bragsin2 (6-methoxy-5-nitro-2-(trifluoromethyl)chromen-4-one) 是非竞争性的核苷酸交换因子 BRAG2选择性抑制剂，其 IC50值为 3 μM。它能够结合到 BRAG2 的 PH 结构域和磷脂双分子层的界面处，使 BRAG2 无法激活磷脂化的 Arf GTPase。它能够影响乳腺癌干细胞。
T16500	PF-3450074 PF-74	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	PF-3450074 (PF-74)是 HIV-1 衣壳蛋白的特异性抑制剂，可广谱抑制 HIV 分离株。它在 HIV-1 感染的早期阶段起作用，通过与 CPSF6 和 NUP153 的结合直接竞争来抑制病毒复制，并阻断病毒生命周期的脱膜，组装和逆转录步骤。
T20187	Alizarin Cyanine Green F NSC41838,NSC-41838,酸性绿 25,NSC 41838	Others	Others
	Alizarin Cyanine Green F (NSC-41838) 是一种绿色染料。它用于为普通外科手术中使用的尼龙 66 和尼龙 6 不可吸收的手术缝合线着色，并用于一般药物的着色，包括用于眼部区域的药物。它也被提议用于半永久性染发剂配方中，作为化妆品成品中最大浓度为 0.3% 的直接染料。
TP1930L1	Spexin acetate(1370290-58-6 free base)	Neuropeptide Y Receptor	GPCR/G Protein; Neuroscience
	Spexin acetate(1370290-58-6 free base) 是一种有效的甘丙肽受体 2/3 (GAL2/GAL3) 激动剂（EC50 值分别为 45.7 和 112.2 nM）。对甘丙肽受体 1 没有显着的活性。抑制脂肪细胞对长链脂肪酸的摄取并减少饮食诱导的肥胖小鼠和大鼠的食物消耗。减少金鱼的 LH 分泌。在体内表现出抗焦虑作用。
T36141	Boscalid	Mitochondrial Metabolism	Metabolism
	Boscalid 是一种广谱羧酰胺类杀菌剂，通过与线粒体复合物 II/琥珀酸脱氢酶的泛醌位点结合来抑制真菌呼吸。
T36944	Ara-G	Nucleoside Antimetabolite/Analog	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Ara-G 是一种脱氧鸟苷 (GdR) 类似物和核苷类似物，可被 T 淋巴谱系细胞迅速转化为其相应的阿拉伯糖基鸟嘌呤核苷酸三磷酸 (araGTP)，从而抑制 DNA 合成和对 T 淋巴母细胞的选择性体外毒性细胞系以及来自 T 细胞急性淋巴细胞白血病 (ALL) 患者的新鲜分离的白血病细胞。
T36949	Niaprazine	5-HT Receptor; Adrenergic Receptor; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Niaprazine 是有效的组胺 H1 受体拮抗剂，具有抗组胺和抗血清素活性。Niaprazine 在睡眠障碍方面有研究的价值。
T70181	FFA3-Antagonist-6
	FFA3-Antagonist-6 is a PAM-antagonist of the function of C3 at FFA3.
T31631	Enkephalin-leu, ala(2)-ser(6)- DALES,2-Ala-6-ser-leu-enkephalin
	Enkephalin-leu, ala(2)-ser(6)- is an active compound at the delta (non-complexed) opioid receptor.
T10187	6-Raloxifene-β-D-glucopyranoside	Others	Others
	6-Raloxifene-β-D-glucopyranoside is a benzothiophene glucuronidated at the 6' position. It is a selective and orally active estrogen receptor antagonist. 6-Raloxifene-β-D-glucopyranoside can be used for inhibiting bone loss, resorption, and lowering lipid
T73811	AT-1002 TFA
	AT-1002 TFA 是一种 6 聚体合成肽，是一种紧密连接 (junction) 的调节剂和吸收增强剂。
T62185	GABA-AT-IN-1
	GABA-AT-IN-1 (Compound 6) 是一种能够透过血脑屏障的 γ-氨基丁酸转氨酶（GABA-AT）抑制剂。GABA-AT-IN-1 可以明显增加小鼠大脑 GABA 水平，能够用作抗惊厥药物。
T28563	Ro 18-5364 Ro-18-5364,Ro 185364
	Ro 18-5364 is a potent inhibitor of the gastric (H+ + K+)-ATPase with an apparent Ki of 0.1 μM at pH 6.
T2344	LY 344864 LY344864	5-HT Receptor	GPCR/G Protein; Neuroscience
	LY 344864 是一种特异性受体激动剂，有对克隆 5-HT1F 受体的亲和力，Ki 为6 nM。
T37240	(±)4(5)-DiHDPA lactone
	(±)5(6)-DiHET lactone is a 1,5 cyclic ester derived from (±)5(6)-DiHET , which, in turn, is a potential derivative of epoxidation of arachidonic acid at the α-5 double bond. (±)4(5)-DiHDPA lactone is a derivative of docosahexaenoic acid that is analogous to (±)5(6)-DiHET lactone. It is the 1,4 cyclic ester derived from (±)4(5)-DiHDPA, which is produced by epoxidation of DHA at the α-4 double bond. Its biological activity is unknown.
T13560	AT-1002	Others	Others
	AT-1002 is a tight junction regulator and absorption enhancer. It is a 6-mer synthetic peptide.
T28891	SW106
	SW106 is a selective antagonist of PTHR1-mediated cAMP signaling, not functioning as an inverse agonist on either PTHR1-T410P or PTHR1-H223R, which have activating mutations at the cytoplasmic ends of TMD helices-2 and -6, respectively.
T13560L	AT-1002 TFA (835872-35-0 free base) AT-1002 TFA	Others	Others
	AT-1002 TFA is a tight junction regulator and absorption enhancer. It is a 6-mer synthetic peptide.
T38186	6-Amino-8-trifluoromethylphenanthridine
	6-Amino-8-trifluoromethylphenanthridine (6A-8tFP) is an antiprion agent and a derivative of 6-aminophenanthridine . It inhibits protein folding activity of the ribosome (PFAR) when used at a concentration of 150 μM. 6A-8tFP directly competes with protein substrates for the ribosomal active site.
T83363	3-Acetyl-6-bromocoumarin
	3-Acetyl-6-bromocoumarin，一种香豆素，具有约56%的强抗氧化活性。
T72928	CDK4/6-IN-15
	CDK4/6-IN-15 是一种口服有效和选择性 CDK4/6抑制剂。CDK4/6-IN-15 能有效抑制癌细胞生长。CDK4/6-IN-15 将细胞周期阻滞在 G1 期，并抑制视网膜母细胞瘤肿瘤抑制蛋白 (Rb) 在 S780 位点的磷酸化和 E2 因子 (E2F) 调控的基因表达。
T75405	GlcNAc kinase (EcNagK)
	GlcNAc kinase (EcNagK) (N-Acetylglucosamine kinase) 为GlcNAc代谢过程中的关键酶。通过将ATP的γ-磷酰基转移到GlcNAc的C-6位羟基，生成GlcNAc-6-P。
T41295	LY 344864 hydrochloride
	LY 344864 hydrochloride 是选择性的受体激动剂，对5-HT1F 受体具有6 nM(Ki)的亲和力。
T10432	AZD-8529	Others	Others
	AZD-8529 is a highly selective, and orally bioavailable positive allosteric modulator of mGluR2 (EC50: 285 nM). It shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 subtypes.
T25481	H 77 H77,H-77
	H 77 is a new effective renin inhibitor. H 77 is angiotensinogen (6-13)-octapeptide in which the peptide bond -CO-NH- at the Leu(9)-Leu(11) linkage is replaced by a -CH2-NH- bond.
T62710	Antitrypanosomal agent 6
	Antitrypanosomal agent 6 (compound 18a) 是一种有效的抗锥体虫剂，表现出良好的 ADME 特性。Antitrypanosomal agent 6 抗布氏锥虫 (T. brucei) 的活性比 Nifurtimox 高两倍以上，IC50为 0.47 μM。Antitrypanosomal agent 6 与 DNA 具有很强的相互作用，可以选择性的结合富含 AT 碱基的 DNA。
T36882	CAY10773
	CAY10773 is a derivative of the ferroptosis inducer sorafenib .1It selectively inhibits proliferation of BEL-7402, MGC803, and T24 bladder cancer cells (IC50s = 5.77, 5.21 and 3.97 μM, respectively) over non-cancerous HCV-29 cells (IC50= 23.19 μM). CAY10773 induces apoptosis in T24 cells when used at concentrations ranging from 2 to 6 μM but induces ferroptosis at concentrations greater than or equal to 6 μM with 10 hour or longer incubation times. It increases the production of reactive oxygen ...
T36908	Bimatoprost grenod 15-(6-nitroxyhexanoyl)-17-phenyl trinor Prostaglandin F2α
	Bimatoprost grenod(15-(6-nitroxyhexanoyl)-17-phenyl trinor PGF2α) is a nitric oxide-donating derivative of 17-phenyl trinor PGF2α.1It increases cGMP levels in rabbit aqueous humor and iris ciliary body when topically administered at a concentration of 0.042%. Topical administration of 15-(6-nitroxylhexanoyl)-17-phenyl trinor PGF2α(0.14%) reduces intraocular hypertension (IOP) in a rabbit model of hypertonic saline-induced transient ocular pressure. It also reduces IOP in a cynomolgus monkey mode...
T36070	(±)5(6)-EET
	5(6)-EET is a fully racemic version of the enantiomeric forms biosynthesized from arachidonic acid by cytochrome P450 enzymes. In solution, 5(6)-EET degrades into 5,6-DiHET and 5(6)-δ-lactone, which can be converted to 5(6)-DiHET and quantified by GC-MS. In neuroendocrine cells, such as the anterior pituitary and pancreatic islets, 5(6)-EET has been implicated in the mobilization of calcium and hormone secretion. 5(6)-EET is an inhibitor of T-type voltage-gated calcium channels (Cav3) that inhib...
T40061	DDR1-IN-6 DDR1-IN-6
	DDR1-IN-6 is a potent and selective inhibitor of Discoidin Domain Receptor family member 1 (DDR1), exhibiting remarkable inhibitory activity at an IC50 of 9.72 nM. It effectively suppresses the auto-phosphorylation of DDR1b (Y513) with an IC50 value of 9.7 nM. Furthermore, DDR1-IN-6 displays strong anti-cancer activity.
T83285	5-n-Heptyl-6-hydroxy-4,7-dioxobenzothiazole
	5-n-Heptyl-6-hydroxy-4,7-dioxobenzothiazole 是酿酒酵母细胞色素 bc1 复合物（细胞色素c氧化还原酶）Qo位点的竞争性抑制剂。
T35682	2-deoxy-2-fluoro-D-Glucose
	2-deoxy-2-fluoro-D-Glucose (2-FG) is a derivative of glucose with anticancer activity.1It inhibits the growth of 143B osteosarcoma cells grown under normoxic and hypoxic conditions when used at concentrations of 6 and 24 mM.
T79726	RET-IN-25
	RET-IN-25（化合物6b）是一种具有抗癌活性的RET激酶抑制剂。该化合物能够抑制甲状腺髓样癌（MTC），在TT(C634R) MTC细胞系中的IC50值分别为3.6 μM（3天）和3.0 μM（6天）。
T25888	NSC-670224 NSC 670224
	NSC-670224 is an inhibitor of histone deacetylases-6 (HDAC6) and nuclear factor-κB (NF-κB) activation blocker. It has been shown to be toxic to Saccharomyces cerevisiae at low micromolar concentrations, potentially acts via a mechanism of action related t
T40289	CDK12-IN-6 CDK12-IN-6
	CDK12-IN-6, a pyrazolotriazine compound, is a powerful inhibitor of CDK12. Its inhibitory activity is significant with an IC50 value of 1.19 μM when tested at high ATP concentration (2 mM). Notably, CDK12-IN-6 does not exhibit any inhibitory effect on CDK2/Cyclin E (IC50 >20 μM) and CDK9/Cyclin T1 (IC50 >20 μM) when tested under the same high ATP conditions (2 mM) (WO2021116178A1).
T61644	α-Synuclein inhibitor 6
	α-Synuclein inhibitor 6 (compound 3ge) is a highly effective and blood-brain barrier-permeable inhibitor that targets the aggregation of α-Synuclein (α-Syn). It exhibits a potent inhibitory activity, with an IC50 value of 1.70 μM, leading to a remarkable inhibition ratio of 94.4% at 30 μM [1].

化合物

Cat.No: T13561

Target: Others

K-Ras(G12C) Inhibitor 6

Cat.No: T3725

Target: Raf

Enoxacin hydrate

Cat.No: T0717

Synonym: CI-919 hydrate,Enoxacin Sesquihydrate,依诺沙星半水合物,AT-2266 hydrate,依诺沙星倍半水合物

Target: DNA gyrase, DNA/RNA Synthesis, Topoisomerase, Antibacterial, Antibiotic

Cat.No: T16435

Target: Histone Demethylase, Histone Methyltransferase

Cat.No: T6598

Target: GluR

Cat.No: TD0101

Synonym: 6-Aminoquinolyl-N-hydroxysccinimidyl carbamate

Target: Others

CGP 78608 hydrochloride

Cat.No: T10781

Synonym: PAMQX

Target: NMDAR, iGluR

DMAB-anabaseine dihydrochloride

Cat.No: T22735

Synonym: N,N-dimethyl-4-[(E)-(6-pyridin-3-yl-3,4-dihydro-2H-pyridin-5-ylidene)methyl]aniline;dihydrochloride

Target: AChR

AZD-8529 mesylate

Cat.No: T10432L

Target: GluR

Cat.No: T16962

Target: HDAC

Cat.No: T15728

Synonym: LDN-0212320,LDN/OSU-0212320,OSU-0212320

Target: transporter

6-Fluorotryptamine hydrochloride

Cat.No: T50111

Target: Others

Cat.No: T12574

Synonym: Emvododstat,(4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate

Target: VEGFR, Dehydrogenase

Cat.No: T40443

Synonym: JAK2-IN-6

Target: JAK

Cat.No: T14775

Synonym: 6-methoxy-5-nitro-2-(trifluoromethyl)chromen-4-one,Bragsin 2

Target: Others

Cat.No: T16500

Synonym: PF-74

Target: HIV Protease

Alizarin Cyanine Green F

Cat.No: T20187

Synonym: NSC41838,NSC-41838,酸性绿 25,NSC 41838

Target: Others

Spexin acetate(1370290-58-6 free base)

Cat.No: TP1930L1

Target: Neuropeptide Y Receptor

Cat.No: T36141

Target: Mitochondrial Metabolism

Cat.No: T36944

Target: Nucleoside Antimetabolite/Analog

Cat.No: T36949

Target: 5-HT Receptor, Adrenergic Receptor, Histamine Receptor

FFA3-Antagonist-6

Cat.No: T70181

Enkephalin-leu, ala(2)-ser(6)-

Cat.No: T31631

Synonym: DALES,2-Ala-6-ser-leu-enkephalin

6-Raloxifene-β-D-glucopyranoside

Cat.No: T10187

Target: Others

Cat.No: T73811

Cat.No: T62185

Cat.No: T28563

Synonym: Ro-18-5364,Ro 185364

Cat.No: T2344

Synonym: LY344864

Target: 5-HT Receptor

(±)4(5)-DiHDPA lactone

Cat.No: T37240

Cat.No: T13560

Target: Others

Cat.No: T28891

AT-1002 TFA (835872-35-0 free base)

Cat.No: T13560L

Synonym: AT-1002 TFA

Target: Others

6-Amino-8-trifluoromethylphenanthridine

Cat.No: T38186

3-Acetyl-6-bromocoumarin

Cat.No: T83363

Cat.No: T72928

GlcNAc kinase (EcNagK)

Cat.No: T75405

LY 344864 hydrochloride

Cat.No: T41295

Cat.No: T10432

Target: Others

Cat.No: T25481

Synonym: H77,H-77

Antitrypanosomal agent 6

Cat.No: T62710

Cat.No: T36882

Bimatoprost grenod

Cat.No: T36908

Synonym: 15-(6-nitroxyhexanoyl)-17-phenyl trinor Prostaglandin F2α

Cat.No: T36070

Cat.No: T40061

Synonym: DDR1-IN-6

5-n-Heptyl-6-hydroxy-4,7-dioxobenzothiazole

Cat.No: T83285

2-deoxy-2-fluoro-D-Glucose

Cat.No: T35682

Cat.No: T79726

Cat.No: T25888

Synonym: NSC 670224

Cat.No: T40289

Synonym: CDK12-IN-6

α-Synuclein inhibitor 6

Cat.No: T61644

Cat. No.	Product Name	Target	Signaling Pathways
T3S1967	(S)-Indoximod N-ME-Tryptophan,Abrine,相思豆碱,L-Abrine	Others; Indoleamine 2,3-Dioxygenase (IDO)	Metabolism; Others
	(S)-Indoximod (L-Abrine) 是一种吲哚胺-2,3-双加氧酶 (IDO) 抑制剂，可用于研究癌症。
TN1325	(2S)-6-Prenylnaringenin (2S)-6-异戊烯基柚皮素,6-异戊二烯基柚皮素,6-Prenylnaringenin,6-PN	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	(2S)-6-Prenylnaringenin (6-Prenylnaringenin) 是强效植物雌激素 8-prenylnaringenin 的异构体，是前脑中最有效的化合物，在 α+β 结合位点上起GABAA 正变构调节剂的作用。
T19262	D-Glucose 6-phosphate disodium salt D-Glucose 6-phosphate disodium salt	Endogenous Metabolite	Metabolism
	D-Glucose 6-phosphate disodium salt 广泛存在于生物提内的化合物，是葡萄糖第 6 号碳经过磷酸化后生成的分子，参与磷酸戊糖途径与糖酵解途径等体内多种多种代谢调节途径。
T4726	D-Glucose 6-phosphate sodium G6P sodium salt,D-Glucose 6-phosphate sodium salt,D-葡萄糖-6-磷酸钠盐,Sodium Glucose-6-Phosphate	Others; Endogenous Metabolite	Metabolism; Others
	D-Glucose 6-phosphate sodium (G6P sodium salt) 是内源性代谢产物的一种。
T21532	Anisodamine 6-Hydroxyhyoscyamine,6-beta-Hydroxyhyoscyamine	AChR	Neuroscience
	Anisodamine (6-beta-Hydroxyhyoscyamine) 是毒蕈碱和烟碱胆碱受体的拮抗剂，对毒蕈碱受体的亲和力与东莨菪碱和阿托品相似。 Anisodamine 改善休克状态下的微循环，可用于有机磷中毒的研究。
T3794	Pentagalloylglucose Penta-O-galloyl-β-D-glucose,1,2,3,4,6-O-Pentagalloylglucose,1,2,3,4,6-Penta-O-galloyl-beta-D-glucopyranose,1,2,3,4,6-五没食子酰葡萄糖	Influenza Virus	Microbiology/Virology
	1,2,3,4,6-O-Pentagalloylglucose (Penta-O-galloyl-β-D-glucose) 存在于多种植物中，具有重要的药理作用。Pentagalloylglucose 表现出显著的抗狂犬病病毒 (RABV) 活性。
T3398	Icaritin Anhydroicaritin,去水淫羊藿黄素,Cycloicaritin	Apoptosis; JAK; STAT; Autophagy	Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	Icaritin (Anhydroicaritin) 是Epimedium Genusis 的异戊二烯类黄酮衍生物，有效抑制 K562 细胞和原代 CML 细胞的增殖。它可以调节MAPK/ERK/JNK 和JAK2/STAT3/AKT 信号传导，并具有增强成骨的作用。
T5S1981	alpha-Cyperone (+)-α-Cyperone,α-香附酮,α-Cyperone	Others; Endogenous Metabolite	Metabolism; Others
	alpha-Cyperone (α-Cyperone) 与 IL-6, Cox-2, Cdc42, Nck-2, Rac1 的表达下调相关,从而能够抑制炎症反应。
T3926	Echinatin 刺甘草查尔酮,Retrochalcone	Free radical scavengers	oxidation-reduction
	Echinatin (Retrochalcone) 是分离自中草药甘草中，具有保肝和抗炎活性。在大鼠中，它可以被快速吸收和消除，并广泛分布，绝对生物利用度约为 6.81％。
T6S0033	Crotonoside 巴豆苷；异鸟苷,巴豆苷,Isoguanosine,2-HYDROXYADENOSINE	Others; FLT; HDAC	Angiogenesis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Others; Tyrosine Kinase/Adaptors
	Crotonoside (Isoguanosine) 是从中草药巴豆中分离出来的一种天然产物。它抑制 FLT3 和 HDAC3/6，有治疗急性髓性白血病 (AML)的研究潜力。
T5069	D-Glucose 6-phosphate potassium salt	Others	Others
	在细胞中，当葡萄糖被己糖激酶或葡萄糖激酶磷酸化或在糖原分解过程中通过磷酸葡萄糖变位酶转化葡萄糖 1-磷酸时，会产生D-glucose 6-phosphate (G6P)。 G6P 位于糖酵解和戊糖磷酸途径的起点。当血糖水平高时，它也可以作为糖原储存。
T5S1889	Yunaconitine Guayewuanine B,滇乌头碱	Others	Others
	Yunaconitine (Guayewuanine B) 是一种乌头类生物碱，具有剧毒。
T3891	Oroxylin A-7-O-glucuronide Oroxylin A Glucoronide,千层纸素A-7-0-Β-D-葡萄糖醛酸苷,Oroxyloside,Oroxylin A 7-O-beta-D-glucuronide	Others	Others
	Oroxylin A-7-O-glucuronide (Oroxylin A Glucoronide) 是一种类黄酮葡糖苷酸，提取自 Scutellaria baicalensis 干燥的根中，具有脯氨酰寡肽酶(POP)抑制作用。
T4115	Auraptene 橙皮油内酯,7-geranyloxycoumarin,橙皮油素	MMP; BACE	Neuroscience; Proteases/Proteasome
	Auraptene 是一种丰富的天然香叶氧基香豆素。它能够抑制基质金属蛋白酶 2 以及关键炎症因子，包括 IL-6，IL-8 和趋化因子 (C-C 基序) 配体-5 (CCL5）的分泌。
T5S1172	Tiliroside 银椴甙,Tribuloside,银椴苷；椴树苷	Antioxidant	oxidation-reduction
	Tiliroside (Tribuloside) 是糖苷类黄酮，是 α-淀粉酶的非竞争性抑制剂(Ki:84.2 μM)。它抑制胃肠道中碳水化合物的消化和葡萄糖的吸收，具有抗糖尿病作用。
T2S2215	Crebanine	Apoptosis; Others; Akt	Apoptosis; Cytoskeletal Signaling; Others; PI3K/Akt/mTOR signaling
	Crebanine 是来自于韦诺萨千金藤的一种生物碱，通过抑制 MAPKs 和 Akt 信号通路表现出抗炎活性，还具有抗心律失常的作用。它可诱导人类癌细胞的 G1阻滞和凋亡。
TN3603	Carpinontriol B	IL Receptor; Antifection	Immunology/Inflammation; Microbiology/Virology
	Carpinontriol B has antimicrobial activity, it at 40 ug/disk caused the formation of zones of inhibition. It also has anti-inflammatory activity, it shows considerable inhibition on the production of nitric oxide and reduces the production of interleukin-6 in dose-dependent manner in RAW 264.7 cells.
T79958	Isocrenatoside	Angiotensin-converting Enzyme (ACE)	Metabolism
	Isocrenatoside (compound 6)为环状八肽，具有ACE抑制活性。该化合物可通过乙醇提取Microtoena prainiana茎部分离纯化。研究显示，1 mg/mL浓度下，Isocrenatoside的ACE抑制效率高达99.3%。
T36226	Beauveriolide I
	Beauveriolide I is a cyclodepsipeptide that has been found inBeauveriaand an inhibitor of lipid droplet formation.1It inhibits lipid droplet formation when used at concentrations of 3 and 10 μM, as well as inhibits cholesterol synthesis (IC50= 0.78 μM), in primary mouse peritoneal macrophages.1,2Beauveriolide I also inhibits acyl-coenzyme A:cholesterol acyltransferase (ACAT) activity in mouse macrophage membranes (IC50= 6 μM).2 1.Namatame, I., Tomoda, H., Si, S., et al.Beauveriolides, specific i...
T83876	L-Ascorbic Acid 6-stearate L-Ascorbyl-6-stearate,6-O-Stearoyl-L-Ascorbic Acid
	L-抗坏血酸6硬脂酸酯是L-抗坏血酸与硬脂酸的衍生物，在K. coccinea中发现，具有抗氧化和抗癌作用。在细胞外试验中清除DPPH（IC50 = 3.31 µg/ml）。包裹L-抗坏血酸6硬脂酸酯的脂质纳米颗粒（LNPs）在190 µM浓度下诱导HL-60前髓母细胞凋亡。含有L-抗坏血酸6硬脂酸酯的配方已用于化妆品和个人护理产品中。
T36992	Monocerin
	Monocerin is a fungal metabolite that has been found inF. larvarumand has diverse biological activities.1,2,3It is active against the bacteriaE. coliandB. megaterium, the phytopathogenic fungusM. violaceum, and the algaC. fuscain an agar diffusion assay when used at a concentration of 50 μg/disc.1Monocerin (17.5 μg/ml) induces mortality in adultC. erythrocephala.2It reduces root elongation in pre-germinatedS. halepenseseeds when used at a concentration of 33 ppm.3 1.Zhang, W., Krohn, K., Draeger...
T83916	Cytogenin
	Cytogenin（一种源自S. eurocidicum的香豆素衍生物）具有多种生物活性。在每日给药25 mg/kg剂量下，能减轻Ehrlich鼠自发性腺癌模型的肿瘤重量。在体内，Cytogenin（每日30和100 mg/kg）可减少链脲佐菌素诱导的体重下降和血浆葡萄糖水平上升，以及小鼠糖尿病模型中巨噬细胞胰腺浸润。同时，在每日100 mg/kg的剂量下，能降低小鼠巨噬细胞中zymosan和LPS诱导的一氧化氮产生，及LPS诱导的Il-6水平增加。
T36227	Beauveriolide III
	Beauveriolide III is a cyclodepsipeptide that has been found inBeauveriaand an inhibitor of lipid droplet formation.1It inhibits lipid droplet formation when used at concentrations of 3 and 10 μM, as well as inhibits cholesterol synthesis (IC50= 0.41 μM), in primary mouse peritoneal macrophages.1,2Beauveriolide III also inhibits acyl-coenzyme A:cholesterol acyltransferase (ACAT) activity in mouse macrophage membranes (IC50= 5.5 μM).2Beauveriolide III (25 and 50 mg/kg) reduces the size of aortic ...
T36000	3-Hydroxyterphenyllin
	3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,3,4 It has a 96% scavenging effect on 2,2-diphenyl-1-picrylhydrazyl radicals when used at a concentration of 100 μg/ml.2 3-Hydroxyterphenyllin inhibits the growth of HeLa cervical, A549 lung, and HepG2 liver cancer cells (IC50s = 23, 36, and 32 μM, respectively), as well as methi...
T35741	Gliovirin
	Gliovirin is a fungal metabolite that has been found inT. harzianumand has fungicidal, antimicrobial and anti-inflammatory activities.1It is active against the plant pathogenic fungusP. ultimum(MIC = 60 ng/ml) and the parasiteT. brucei brucei(IC50= 90 ng/ml), but has no effect on the plant pathogenic fungiR. solani,P. omnivorum,T. basicola,R. arrhizus, andV. dahliaeor the bacteriaB. thuringiensis,P. fluorescens, andX. malvacearumwhen used at concentrations up to 1,000 ng/ml.2,3Gliovirin decrease...
T35624	Ajoene
	Ajoene is a disulfide that has been found inA. sativumand has diverse biological activities, including antibacterial, anticancer, antiplatelet, and antioxidant properties.1,2,3,4It is active against Gram-positive (MICs = 5-160 &#181g/ml) and Gram-negative bacteria (MICs = 136-200 &#181g/ml), as well as yeasts (MICs = 10-20 &#181g/ml).1Ajoene is cytotoxic to mouse melanoma cells (IC50= 18 &#181M), as well as human colon, lung, mammary, and pancreatic cancer cells (IC50s = 7-41 &#181M).2It reduces...
T35779	Oosporein
	Oosporein is a mycotoxin that has been found inBeauveriaand has diverse biological activities.1,2It is cytotoxic to Sf9 and Sf21 insect cells with 50% cytotoxic concentration (CC50) values of 4.23 and 10.43 μM, respectively.3Oosporin induces lethality in day-old cockerels (LD50= 6.12 mg/kg).4It inhibits Na+/K+-, Ca2+-, and Mg2+-ATPase activities by 27, 52, and 100%, respectively, in equine erythrocyte ghosts when used at a concentration of 200 μg/ml.2Oosporein inhibits herpes simplex 1 (HSV-1), ...
T36563	(E)-Guggulsterone
	Bile acids are essential for solubilization and transport of dietary lipids, are the major products of cholesterol catabolism, and are physiological ligands for farnesoid X receptor (FXR), a nuclear receptor that regulates genes involved in lipid metabolism.1They are also inherently cytotoxic, as physiological imbalance contributes to increased oxidative stress.2,3Bile acid-controlled signaling pathways are promising novel targets to treat such metabolic diseases as obesity, type II diabetes, hy...

天然产物

Cat.No: T3S1967

Synonym: N-ME-Tryptophan,Abrine,相思豆碱,L-Abrine

Target: Others, Indoleamine 2,3-Dioxygenase (IDO)

(2S)-6-Prenylnaringenin

Cat.No: TN1325

Synonym: (2S)-6-异戊烯基柚皮素,6-异戊二烯基柚皮素,6-Prenylnaringenin,6-PN

Target: GABA Receptor

D-Glucose 6-phosphate disodium salt

Cat.No: T19262

Synonym: D-Glucose 6-phosphate disodium salt

Target: Endogenous Metabolite

D-Glucose 6-phosphate sodium

Cat.No: T4726

Synonym: G6P sodium salt,D-Glucose 6-phosphate sodium salt,D-葡萄糖-6-磷酸钠盐,Sodium Glucose-6-Phosphate

Target: Others, Endogenous Metabolite

Cat.No: T21532

Synonym: 6-Hydroxyhyoscyamine,6-beta-Hydroxyhyoscyamine

Target: AChR

Pentagalloylglucose

Cat.No: T3794

Synonym: Penta-O-galloyl-β-D-glucose,1,2,3,4,6-O-Pentagalloylglucose,1,2,3,4,6-Penta-O-galloyl-beta-D-glucopyranose,1,2,3,4,6-五没食子酰葡萄糖

Target: Influenza Virus

Cat.No: T3398

Synonym: Anhydroicaritin,去水淫羊藿黄素,Cycloicaritin

Target: Apoptosis, JAK, STAT, Autophagy

Cat.No: T5S1981

Synonym: (+)-α-Cyperone,α-香附酮,α-Cyperone

Target: Others, Endogenous Metabolite

Cat.No: T3926

Synonym: 刺甘草查尔酮,Retrochalcone

Target: Free radical scavengers

Cat.No: T6S0033

Synonym: 巴豆苷；异鸟苷,巴豆苷,Isoguanosine,2-HYDROXYADENOSINE

Target: Others, FLT, HDAC

D-Glucose 6-phosphate potassium salt

Cat.No: T5069

Target: Others

Cat.No: T5S1889

Synonym: Guayewuanine B,滇乌头碱

Target: Others

Oroxylin A-7-O-glucuronide

Cat.No: T3891

Synonym: Oroxylin A Glucoronide,千层纸素A-7-0-Β-D-葡萄糖醛酸苷,Oroxyloside,Oroxylin A 7-O-beta-D-glucuronide

Target: Others

Cat.No: T4115

Synonym: 橙皮油内酯,7-geranyloxycoumarin,橙皮油素

Target: MMP, BACE

Cat.No: T5S1172

Synonym: 银椴甙,Tribuloside,银椴苷；椴树苷

Target: Antioxidant

Cat.No: T2S2215

Target: Apoptosis, Others, Akt

Carpinontriol B

Cat.No: TN3603

Target: IL Receptor, Antifection

Cat.No: T79958

Target: Angiotensin-converting Enzyme (ACE)

Beauveriolide I

Cat.No: T36226

L-Ascorbic Acid 6-stearate

Cat.No: T83876

Synonym: L-Ascorbyl-6-stearate,6-O-Stearoyl-L-Ascorbic Acid

Cat.No: T36992

Cat.No: T83916

Beauveriolide III

Cat.No: T36227

3-Hydroxyterphenyllin

Cat.No: T36000

Cat.No: T35741

Cat.No: T35624

Cat.No: T35779

(E)-Guggulsterone

Cat.No: T36563

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