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191

抑制剂 & 化合物

111

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T14367	AZ1495	IRAK; CDK; Haspin Kinase	Cell Cycle/Checkpoint; Immunology/Inflammation; NF-κB
	AZ1495 是一种口服有活性的白介素-1受体相关激酶 4(IRAK4)抑制剂，能够作用于 IRAK4 (IC50:5 nM)和 IRAK1 (IC50:23 nM)。可用于研究突变型 MYD88L265P 弥漫性 B 细胞淋巴瘤 (DLBCL) 。
T37015	Iprindole	5-HT Receptor	GPCR/G Protein; Neuroscience
	Iprindole, a tricyclic indole antidepressant, is a dual weak inhibitor of noradrenaline and 5-HT uptake [1].
T24661	Pridefine Pridefina
	Pridefine is an antidepressant drug. It acts as a balanced reuptake inhibitor of serotonin, dopamine, and norepinephrine. It also has some weak releasing activity.
T26016	R 56865 R-56865,R56865	Sodium Channel	Membrane transporter/Ion channel
	R 56865 是一种弱电位操作通道抑制剂，抑制人分离心肌细胞的晚期钠电流。
T19073	Tris(4-aminophenyl)methane 4,4’,4"-三氨基三苯甲烷,Leucopararosaniline	HCV Protease	Microbiology/Virology; Proteases/Proteasome
	Tris(4-aminophenyl)methane (Leucopararosaniline) 是一种三苯甲烷类染料，是一种 HCV 解旋酶抑制剂。
T5887	7-Hydroxy-3,4-dihydro-2(1H)-quinolinone 3,4-Dihydro-7-hydroxy-2(1H)-quinolinone,3,4-二氢-7-羟基-2(1H)-喹啉酮	MAO; Monoamine Oxidase	Metabolism; Neuroscience
	7-Hydroxy-3,4-dihydro-2(1H)-quinolinone 是弱MAO-A 抑制剂，IC50=183 μM，对 MAO-B 无作用。
T12597	5-HT2 antagonist 1	5-HT Receptor	GPCR/G Protein; Neuroscience
	5-HT2 antagonist 1 是一种有效的 5-HT2 receptor 拮抗剂，同时对 α1 adrenoceptor 有微弱地抑制作用。
T11021	DHODH-IN-12	Dehydrogenase	Metabolism
	DHODH-IN-12 是一种 Leflunomide 衍生物，也是一种二氢乳清酸脱氢酶 (DHODH) 的弱抑制剂，其 pKa 为 5.07。
T7778L	Glypromate acetate(32302-76-4 free base)	NMDAR	Neuroscience
	Glypromate acetate(32302-76-4 free base) 是一种神经保护剂，是一种弱 NMDA 受体激动剂。
T6008	CNX-2006 CNX 2006,CNX2006	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	CNX-2006 是一种新型的不可逆突变选择性 EGFR 抑制剂，对 EGFRT790M 的IC50值小于 20 nM。
T2405	Revaprazan hydrochloride 盐酸瑞伐拉赞,YH1885	ATPase; COX; Antibacterial	Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience
	Revaprazan hydrochloride (YH1885) 是一种新型酸泵拮抗剂，可降低COX-2的表达，在幽门螺杆菌感染中，显著抑制炎症。
T0941	Cyclamic acid Cyclamate,NSC 220327,Cyclohexylsulfamic acid,环己基氨基磺酸,环拉酸	Others	Others
	Cyclamic acid (NSC-220327) 是食品和药品中应用最广泛的一种人造甜味剂。
T11020	DHODH-IN-11	Dehydrogenase; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism
	DHODH-IN-11 是一种来氟米特衍生物和弱二氢乳清酸脱氢酶 (DHODH) 抑制剂，pKa 为 5.03
T10359	AR antagonist 1	Androgen Receptor; Ligand for E3 Ligase; Ligands for Target Protein for PROTAC	Endocrinology/Hormones; PROTAC
	AR antagonist 1 是 AR 拮抗剂，能够与 E3 连接酶配体结合，与 VHL 蛋白结合亲和力较弱，用于 PROTACARD-266 合成。
T11011	Dexpramipexole dihydrochloride 普拉克索杂质D,KNS-760704 dihydrochloride,R-(+)-Pramipexole dihydrochloride,右旋普拉克索二盐酸盐,(R)-Pramipexole dihydrochloride	Dopamine Receptor	GPCR/G Protein; Neuroscience
	Dexpramipexole dihydrochloride (KNS-760704 dihydrochloride) 是一种神经保护剂，是一种弱的非麦角类多巴胺受体激动剂。
T67856	GSK-3β inhibitor 14 1,5-Benzothiazepin-4(5H)-one, 2,3-dihydro-2-methyl-5-(phenylmethyl)-	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	GSK-3β inhibitor 14 (1,5-Benzothiazepin-4(5H)-one, 2,3-dihydro-2-methyl-5-(phenylmethyl)-) 是一种较弱的 GSK-3β 抑制剂，IC50﹥ 100μM。
T16289	NE 10790 3-PEHPC	Others	Others
	NE 10790 (3-PEHPC) 是一种二磷酸利塞磷酸盐的磷酸酯类似物，是一种法尼焦磷酸合成酶的弱抑制剂，也是一种弱抗吸收剂。
T40377	Nicotredole Tryptamide,尼可曲多；尼可曲朵	Others	Others
	Nicotredole (Tryptamide) 是一种口服有效的消炎剂，与 Phenylbutazone 的抗炎作用相当。它仅具有弱的致溃疡活性。它可用于缓解疼痛方面的研究。
T28829	Soquinolol Soquinolol mucate	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Soquinolol (Soquinolol mucate) 是一种β肾上腺素能受体拮抗剂，具有较弱的局部麻醉活性。Soquinolol 具有良好的肠内疗效和较长的作用持续时间。
T8890	653-47 hydrochloride	Epigenetic Reader Domain	Chromatin/Epigenetic
	653-47 hydrochloride 是一种增强剂，能显著增强 666-15 的 cAMP 反应元件结合蛋白 (CREB) 抑制活性。它也是 CREB 抑制剂，IC50为 26.3 μM。
T22545	Acephate acetylphosphoramidothioicacido,s-dimethylester,Ortran,Orthene,Acetamidophos,chevronorthene,乙酰甲胺磷	AChE	Neuroscience
	Acephate (Orthene) 是能产生胆碱毒性的抗胆碱酯酶杀虫剂。它能够有效抑制蟑螂的 AChE，但对大鼠 AChE 的抑制作用较弱。
T21371	Apraclonidine hydrochloride Iopidine,ALO 2145,Apraclonidina,P-aminoclonidine,4-Aminoclonidine,Apraclonidine HCl,Apraclonidinum	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Apraclonidine hydrochloride (ALO 2145) 是一种 α2-肾上腺素能激动剂和弱的 α-1 肾上腺素能受体激动剂。 Apaclonidine hydrochloride 可降低人眼的眼内压，可用于青光眼治疗的研究。
T12306	OMDM-5	Cannabinoid Receptor; Endogenous Metabolite; TRP/TRPV Channel	GPCR/G Protein; Membrane transporter/Ion channel; Metabolism
	OMDM-5 是有效的、选择性的anandamide 细胞摄取抑制剂，Ki 为 4.8 μM。它是VR1 (TRPV1)激动剂，EC50为 75 nM，显示出对大麻素 1 型受体 (CB1) 的弱配体活性 (Ki=4.9 μM)。
T3046	BMY 7378 dihydrochloride BMY7378 HCl	Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor	GPCR/G Protein; Neuroscience
	BMY 7378 dihydrochloride (BMY7378 HCl) 是选择性 α1D 肾上腺素受体拮抗剂，也是5-HT1A 受体部分激动剂。它同表达克隆大鼠 α1D-AR 的膜结合的亲和力 (Ki=2 nM) 是同克隆大鼠 α1A-AR (Ki=800 nM) 或仓鼠 α1B-AR (Ki=600 nM) 结合的亲和力的100 以上。
T10682L	CARM1-IN-1 CARM1-IN-7G	Histone Methyltransferase	Chromatin/Epigenetic
	CARM1-IN-1 (CARM1-IN-7G) 是 CARM1 的选择性抑制剂，IC50 为 8.6 μM。 CARM1-IN-1 对 PRMT1 和 SET7 的活性较弱，IC50 > 600 μM。
T77564	Coumarin102 Exciton 480
	Coumarin102 (Exciton 480)是一种荧光染料。Coumarin102对Monoamine oxidase B、MAO-B和MAO-A具有较弱的抑制活性，可用来研究神经系统疾病。
T23303	S-Sulfo-L-cysteine sodium salt	Antioxidant; GluR	Neuroscience; oxidation-reduction
	S-Sulfo-L-cysteine sodium salt 在高浓度下对 mGluR1α 和 mGluR5a 显示出较弱的亲和力且具有潜在的抗氧化活性。
T8634	8-Bromotheophylline Bromotheophylline,8-溴茶碱	Others	Others
	8-Bromotheophylline (Bromotheophylline) 是 Pamabrom 的活性部分，用于 Oxazolo[2,3-f]purinediones 的合成。Oxazolo[2,3-f]purinediones 可用于腺苷 A1和 A2A 受体上的亲和力评估。
T6592	ML133 hydrochloride ML133 HCl,(4-甲氧基苄基)(1-萘基甲基)胺盐酸盐	Potassium Channel	Membrane transporter/Ion channel
	ML133 hydrochloride (ML133 HCl) 是选择性的Kir2家族通道抑制剂，在pH 7.4 和pH 8.5 时的IC50值分别为1.8 μM 和290 nM。
T1514	Norethindrone Norethisterone,炔诺酮	Estrogen/progestogen Receptor; Progesterone Receptor	Endocrinology/Hormones; Others
	Norethindrone (Norethisterone) 是孕激素，能够用于子宫内膜异位症、由激素水平异常引起的子宫出血和继发性闭经的研究。
T7350	Nelotanserin 1-[3-(4-溴-1-甲基-1H-吡唑-5-基)-4-甲氧基苯基]-3-(2,4-二氟苯基)脲,APD125	5-HT Receptor	GPCR/G Protein; Neuroscience
	Nelotanserin (APD125) 是5-HT2A 强完全逆向激动剂，5-HT2C 中等强度的部分反向激动剂和5-HT2B 的弱反向激动剂，IC50s 值分别为 1.7、79 和 791 nM。
TP1244L1	Adrenocorticotropic Hormone (ACTH) (1-10), human acetate Adrenocorticotropic Hormone (ACTH) (1-10), human acetate(2791-05-1 Free base)	Others	Others
	Adrenocorticotropic Hormone (ACTH) (1-10), human acetate 是促肾上腺皮质激素的一个片段。 Adrenocorticotropic Hormone (ACTH) (1-10), human acetate 仅在 100 和 1000 nM 时具有较弱的 α-MSH 效力。
T1197	Trimebutine maleate Debridat,Polibutin,马来酸曲美布汀	Calcium Channel; Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience
	Trimebutine maleate (Polibutin) 是一种外周 μ、δ 和 kappa 阿片受体激动剂，用作治疗慢性和急性腹痛的解痉药物。
T10466	BAY-1797	P2X Receptor	Membrane transporter/Ion channel; Neuroscience
	BAY-1797 是具有口服活性的选择性P2X4高效拮抗剂，对人 P2X4 的IC50为 211 nM，具有抗伤害和抗炎作用。
TP1245L	ACTH 4-11 acetate ACTH 4-11 acetate (67224-41-3 Free base)	Others	Others
	ACTH 4-11 acetate 是一种促肾上腺皮质激素片段，具有与 α-黑素细胞刺激素 (MSH) 相同的氨基酸序列。 ACTH 4-11 acetate 仅在高剂量时表现出微弱的 MSH 效力。
T16378	Ogerin	Others; 5-HT Receptor; Adenosine Receptor	GPCR/G Protein; Neuroscience; Others
	Ogerin 是选择性 GPR68正向别构调节剂(pEC50:6.83)。它能够抑制小鼠对恐惧记忆的回忆。它对 A2A 受体具有适中的拮抗作用(Ki:220 nM)。对 5-HT2B 受体的拮抗作用较弱(Ki:736 nM)。
TP1927L1	d[Leu4,Lys8]-VP acetate d[Leu4,Lys8]-VP acetate(42061-33-6 free base)	Vasopressin Receptor	GPCR/G Protein
	d[Leu4,Lys8]-VP acetate 是一种选择性加压素 V1b 受体激动剂。大鼠、人和小鼠 V1b 受体的 Kis 分别为 0.16 nM、0.52 nM 和 0.1.38 nM。 d[Leu4,Lys8]-VP acetate 表现出较弱的抗利尿、血管加压和体外催产活性。
T9552	BAZ1A-IN-1	Epigenetic Reader Domain	Chromatin/Epigenetic
	BAZ1A-IN-1 是BAZ1A（含溴结构域蛋白）抑制剂(Kd:0.52 μM)。它对低表达BAZ1A 的癌细胞表现出弱活性或无活性，但对高表达BAZ1A 的癌细胞系显示出良好的抗生存作用。
T23543	YIL 781	GHSR	GPCR/G Protein
	YIL 781是一种选择性ghrelin 受体拮抗剂(GHS-R1a) (Ki = 17 nM))，对运动素受体显示出较弱的亲和力(K = 6 μ M)。YIL 781通过阻断胃饥饿素分泌对体内和体外胰岛素分泌改善体内葡萄糖稳态。
TP2018L	GIP (human) acetate GIP (human) acetate(100040-31-1 Free base)	IGF-1R	Tyrosine Kinase/Adaptors
	GIP (human) acetate 是葡萄糖依赖性胰岛素分泌的刺激剂和胃酸分泌的弱抑制剂。 GIP (human) acetate 在脂质代谢和肥胖的发展中起着至关重要的作用。
T15129	DiI DiIC18(3)	Others	Others
	DiI (DiIC18(3)) 是一种亲脂性膜染料，通常用作神经元和其它细胞的长期示踪剂。它在进入细胞膜之前荧光非常弱，仅当进入到细胞膜后才可以被激发出很强的橙红色荧光 (λex=549 nm，λem=565 nm)。
T6066	SCH772984	ERK; MEK	MAPK
	SCH772984 是高选择性和 ATP 竞争性ERK 抑制剂，对 ERK1 和 ERK2 的IC50分别为 4 和 1 nM。它在含有 BRAF 或 RAS 突变的 MAPK 抑制剂初治和 MAPK 抑制剂耐药细胞中具有抗肿瘤活性。
TP2252	GLP-1 (9-36) amide	Glucagon Receptor	GPCR/G Protein
	GLP-1(9-36)amide 是胰高血糖素样肽-1 (7-36) amide 的主要代谢产物，对人胰腺 GLP-1受体具有拮抗作用。
T12196	NCT-505	Dehydrogenase	Metabolism
	NCT-505是乙醛脱氢酶的选择性抑制剂，IC50为 7 nM。对 hALDH1A2，hALDH1A3，hALDH2，hALDH3A1的抑制作用较弱，IC50分别为 >57，22.8，20.1，>57 μM。
T74696	SpdSyn binder-1	Parasite	Microbiology/Virology
	SpdSyn binder-1 是一种弱结合剂，结合在恶性疟原虫亚精胺合酶的活性位点，对疟疾有部分抑制作用，可用于研究疟疾。
T10152	4-Methylamino antipyrine	COX; Drug Metabolite	Immunology/Inflammation; Metabolism; Neuroscience
	4-Methylamino antipyrine 是 Metamizole 的活性代谢产物，可用于疼痛和发烧的研究。Metamizole 是吡唑啉酮类非甾体抗炎药，可抑制COX。
T3483	FTIDC	GluR	Neuroscience
	FTIDC 是非竞争性和选择性的口服变构代谢型谷氨酸受体 1 拮抗剂，对人 mGluR1a 的IC50为 5.8 nM。
T60248	4-Aminobenzamidine dihydrochloride p-Aminobenzamidine dihydrochloride	Serine Protease	Proteases/Proteasome
	4-Aminobenzamidine dihydrochloride (p-Aminobenzamidine dihydrochloride) 是一种强胰蛋白酶 (trypsin)抑制剂，也是一种相对较弱的尿激酶型纤溶酶原激活剂 (uPA) 抑制剂 (Ki=82 μM)。4-Aminobenzamidine 可抑制 SCID 小鼠体内前列腺肿瘤的生长。
T21593	AAL-993	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	AAL-993 是口服有效的VEGFR 选择性抑制剂，抑制 VEGFR1、VEGFR2 和 VEGFR3 的IC50分别为 130 nM、23 nM 和 18 nM，对其他酪氨酸激酶的抑制作用较弱。AAL-993 具有抗血管生成和抗肿瘤的活性。
T16154	MS417 GTPL7512	Epigenetic Reader Domain; HIV Protease	Chromatin/Epigenetic; Microbiology/Virology; Proteases/Proteasome
	MS417 (GTPL7512) 是一种 BET 特异性 BRD4 抑制剂，与 BRD4-BD1 和 BRD4-BD2 结合，Kd 值分别为 36.1和25.4 nM，IC50值分别为 30和46 nM。它对 CBP BRD 的选择性较低，IC50值为 32.7 μM。

化合物

Cat.No: T14367

Target: IRAK, CDK, Haspin Kinase

Cat.No: T37015

Target: 5-HT Receptor

Cat.No: T24661

Synonym: Pridefina

Cat.No: T26016

Synonym: R-56865,R56865

Target: Sodium Channel

Tris(4-aminophenyl)methane

Cat.No: T19073

Synonym: 4,4’,4"-三氨基三苯甲烷,Leucopararosaniline

Target: HCV Protease

7-Hydroxy-3,4-dihydro-2(1H)-quinolinone

Cat.No: T5887

Synonym: 3,4-Dihydro-7-hydroxy-2(1H)-quinolinone,3,4-二氢-7-羟基-2(1H)-喹啉酮

Target: MAO, Monoamine Oxidase

5-HT2 antagonist 1

Cat.No: T12597

Target: 5-HT Receptor

Cat.No: T11021

Target: Dehydrogenase

Glypromate acetate(32302-76-4 free base)

Cat.No: T7778L

Target: NMDAR

Cat.No: T6008

Synonym: CNX 2006,CNX2006

Target: EGFR

Revaprazan hydrochloride

Cat.No: T2405

Synonym: 盐酸瑞伐拉赞,YH1885

Target: ATPase, COX, Antibacterial

Cat.No: T0941

Synonym: Cyclamate,NSC 220327,Cyclohexylsulfamic acid,环己基氨基磺酸,环拉酸

Target: Others

Cat.No: T11020

Target: Dehydrogenase, DNA/RNA Synthesis

AR antagonist 1

Cat.No: T10359

Target: Androgen Receptor, Ligand for E3 Ligase, Ligands for Target Protein for PROTAC

Dexpramipexole dihydrochloride

Cat.No: T11011

Synonym: 普拉克索杂质D,KNS-760704 dihydrochloride,R-(+)-Pramipexole dihydrochloride,右旋普拉克索二盐酸盐,(R)-Pramipexole dihydrochloride

Target: Dopamine Receptor

GSK-3β inhibitor 14

Cat.No: T67856

Synonym: 1,5-Benzothiazepin-4(5H)-one, 2,3-dihydro-2-methyl-5-(phenylmethyl)-

Target: GSK-3

Cat.No: T16289

Synonym: 3-PEHPC

Target: Others

Cat.No: T40377

Synonym: Tryptamide,尼可曲多；尼可曲朵

Target: Others

Cat.No: T28829

Synonym: Soquinolol mucate

Target: Adrenergic Receptor

653-47 hydrochloride

Cat.No: T8890

Target: Epigenetic Reader Domain

Cat.No: T22545

Synonym: acetylphosphoramidothioicacido,s-dimethylester,Ortran,Orthene,Acetamidophos,chevronorthene,乙酰甲胺磷

Target: AChE

Apraclonidine hydrochloride

Cat.No: T21371

Synonym: Iopidine,ALO 2145,Apraclonidina,P-aminoclonidine,4-Aminoclonidine,Apraclonidine HCl,Apraclonidinum

Target: Adrenergic Receptor

Cat.No: T12306

Target: Cannabinoid Receptor, Endogenous Metabolite, TRP/TRPV Channel

BMY 7378 dihydrochloride

Cat.No: T3046

Synonym: BMY7378 HCl

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

Cat.No: T10682L

Synonym: CARM1-IN-7G

Target: Histone Methyltransferase

Cat.No: T77564

Synonym: Exciton 480

S-Sulfo-L-cysteine sodium salt

Cat.No: T23303

Target: Antioxidant, GluR

8-Bromotheophylline

Cat.No: T8634

Synonym: Bromotheophylline,8-溴茶碱

Target: Others

ML133 hydrochloride

Cat.No: T6592

Synonym: ML133 HCl,(4-甲氧基苄基)(1-萘基甲基)胺盐酸盐

Target: Potassium Channel

Cat.No: T1514

Synonym: Norethisterone,炔诺酮

Target: Estrogen/progestogen Receptor, Progesterone Receptor

Cat.No: T7350

Synonym: 1-[3-(4-溴-1-甲基-1H-吡唑-5-基)-4-甲氧基苯基]-3-(2,4-二氟苯基)脲,APD125

Target: 5-HT Receptor

Adrenocorticotropic Hormone (ACTH) (1-10), human acetate

Cat.No: TP1244L1

Synonym: Adrenocorticotropic Hormone (ACTH) (1-10), human acetate(2791-05-1 Free base)

Target: Others

Trimebutine maleate

Cat.No: T1197

Synonym: Debridat,Polibutin,马来酸曲美布汀

Target: Calcium Channel, Opioid Receptor

Cat.No: T10466

Target: P2X Receptor

ACTH 4-11 acetate

Cat.No: TP1245L

Synonym: ACTH 4-11 acetate (67224-41-3 Free base)

Target: Others

Cat.No: T16378

Target: Others, 5-HT Receptor, Adenosine Receptor

d[Leu4,Lys8]-VP acetate

Cat.No: TP1927L1

Synonym: d[Leu4,Lys8]-VP acetate(42061-33-6 free base)

Target: Vasopressin Receptor

Cat.No: T9552

Target: Epigenetic Reader Domain

Cat.No: T23543

Target: GHSR

GIP (human) acetate

Cat.No: TP2018L

Synonym: GIP (human) acetate(100040-31-1 Free base)

Target: IGF-1R

Cat.No: T15129

Synonym: DiIC18(3)

Target: Others

Cat.No: T6066

Target: ERK, MEK

GLP-1 (9-36) amide

Cat.No: TP2252

Target: Glucagon Receptor

Cat.No: T12196

Target: Dehydrogenase

SpdSyn binder-1

Cat.No: T74696

Target: Parasite

4-Methylamino antipyrine

Cat.No: T10152

Target: COX, Drug Metabolite

Cat.No: T3483

Target: GluR

4-Aminobenzamidine dihydrochloride

Cat.No: T60248

Synonym: p-Aminobenzamidine dihydrochloride

Target: Serine Protease

Cat.No: T21593

Target: VEGFR

Cat.No: T16154

Synonym: GTPL7512

Target: Epigenetic Reader Domain, HIV Protease

Cat. No.	Product Name	Target	Signaling Pathways
T80778	weak Hepatoprotective agent-1
	Weak Hepatoprotective agent-1 (Compound 11)，一种从Arctium lappa L. 分离得到的天然产物，在10 μM浓度下具有弱肝保护活性。
T4811	D-Alanine D-α-Alanine,Ba 2776,(R)-Alanine,D-丙氨酸,(R)-2-Aminopropionic acid	Chloride channel; Endogenous Metabolite	Membrane transporter/Ion channel; Metabolism
	D-Alanine ((R)-Alanine) 是一种GlyR 和PMBA 的弱激动剂，其对GlyR 的EC50=9 mM。
T25114	Ascaridole NSC-406266,NSC 406266,NSC406266	Parasite	Microbiology/Virology
	Ascaridole (NSC-406266) 可作为驱虫化合物，能驱除人体和植物中的寄生蠕虫(蠕虫)，具有较弱的抗疟活性。
T21504	γ-Linolenic Acid methyl ester Methyl gamma-linolenate,γ-亚麻酸甲酯	LTR	Immunology/Inflammation
	γ-Linolenic Acid methyl ester (Methyl gamma-linolenate) 是一种弱白三烯 B4 (LTB4) 受体拮抗剂。
T7029	Pseudolaric Acid C	Antifungal	Microbiology/Virology
	Pseudolaric Acid C 是一种从Pseudolarix kaempferiGorden 根皮部中分离的二萜酸，对白色念珠菌有较弱的抗真菌活性。
T1704	Diosmetin Luteolin 4-methyl ether,香叶木素	P450; Trk receptor	Metabolism; Tyrosine Kinase/Adaptors
	Diosmetin (Luteolin 4-methyl ether) 是一种天然类黄酮，能够抑制人CYP1A 酶活性，在HepG2细胞的IC50值为40 μM。
TN7094	Coreoside B	Antibacterial	Microbiology/Virology
	Coreoside B 是从coreoside 中分离出来的，对金黄色葡萄球菌和炭疽杆菌显示出较弱的抗菌活性。
T7060	Amantadine 1-Aminoadamantane,1-金刚烷胺,金刚烷胺,1-Adamantanamine,1-Adamantylamine	Others	Others
	Amantadine (1-Aminoadamantane) 是抗病毒药物，也是是 NMDA 型谷氨酸受体的弱拮抗剂，能促进高多巴胺的释放，并阻断多巴胺的再摄取。
T4854	Acetoacetic acid lithium salt LithoTab acetoacetate,Lithium acetoacetate,Lithium 3-Oxobutyrate,乙酰乙酸锂	Others; Endogenous Metabolite	Metabolism; Others
	Acetoacetic acid lithium salt (Lithium 3-Oxobutyrate) 是内源性代谢产物的一种。
T6S0325	Glycitein 黄豆黄素,Glycetein	Apoptosis; Others	Apoptosis; Others
	Glycitein (Glycetein) 是一种大豆异黄酮，可研究抗氧化和细胞凋亡。
T0065	Acetaminophen 对乙酰氨基酚,醋氨酚,4-Acetamidophenol,4'-Hydroxyacetanilide,APAP,Paracetamol	COX; Endogenous Metabolite; Histone Acetyltransferase	Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; Neuroscience
	Acetaminophen (APAP) 是一种 COX 抑制剂，抑制 COX-1 和 COX-2 (IC50=113.7/25.8 μM)。Acetaminophen 具有解热镇痛活性，以及较弱的抗炎活性。
T8087	Tropolone	Tyrosinase	Proteases/Proteasome
	Tropolone 是一种 mushroom tyrosinase 抑制剂，IC50=0.4 μM，它的抑制作用可以通过透析或过量的 CU2+逆转。它是 2 位上带有羟基的 tropone 衍生物，是许多 Azulene 衍生物的前体，如 2-methylazulene-1-carboxylate。
TN5845	Neochlorogenic acid methyl ester 5-O-Caffeoylquinic acid methyl ester,Methyl 3-caffeoylquinate,GIP (1-39) acetate(725474-97-5 Free base),Methyl neochlorogenate,新绿原酸甲酯	Antioxidant; HBV	Microbiology/Virology; oxidation-reduction
	Neochlorogenic acid methyl ester (5-O-Caffeoylquinic acid methyl ester) 来源于毛蒿和黑色苦莓(Aronia melanocarpa)果实。Neochlorogenic acid methyl ester 显示出抗 HBV 活性、抗氧化活性和醌还原酶活性，CD 为 6.7 μM。
T4S2084	3'-Methoxypuerarin 3'-甲氧基葛根素,3’- Methoxy Puerarin	Antioxidant	oxidation-reduction
	3'-Methoxypuerarin 是一种提取自葛根中的异黄酮，具有神经元保护作用。
T5S2017	Ingenol (-)-Ingenol,巨大戟二萜醇,巨大戟醇	PKC	Chromatin/Epigenetic; Cytoskeletal Signaling
	Ingenol ((-)-Ingenol) 是一种PKC 激活剂，Ki 值为 30 μM，具有抗肿瘤活性。从 Ingenol 酯中配制新的衍生物可能是开发新的先导化合物以重新激活潜伏 HIV 的创新方法。Ingenol mebutate 是治疗光化性角化病的有效方法。
TN6675	Cyclo(Pro-Val) Cyclo(prolylvalyl)	Antibacterial; Antifungal	Microbiology/Virology
	Cyclo(Pro-Val) (Cyclo(prolylvalyl)) 是从海洋真菌中获得的，具有中等的抗真菌活性和较弱的抗肿瘤活性。 Cyclo(Pro-Val) 抑制枯草芽孢杆菌的生长，MIC 为 0.8 g/L。
T3739	2,6-Dimethoxyquinone 2,6-Dimethoxy-1,4-benzoquinone,2,6-Dimethoxy-p-benzoquinone,2,6-Dimethoxybenzoquinone,2,6-二甲氧基-1,4-苯醌	Others	Others
	2,6-Dimethoxyquinone (2,6-Dimethoxy-p-benzoquinone) 是一种植物中提取吸脂诱导因子。它具有抗脂肪、抗癌、抗菌、抗疟疾和抗炎的作用。
T6S0071	Fraxinellone	HIF/HIF Prolyl-Hydroxylase; STAT; PD-1/PD-L1	Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Metabolism; Stem Cells
	Fraxinellone 是从白鲜的根皮中分离出来的一种天然产物，是PD-L1抑制剂，可抑制HIF-1α蛋白质合成。它通过靶向 PD-L1，有用于癌症免疫的潜力。
T2835	Morin 桑色素,Toxylon pomiferum,Aurantica,Calico Yellow,Al-Morin	Others	Others
	Morin (Calico Yellow) 是植物性黄酮类化合物，具有较弱的抗氧化活性，是用于铝物种形成的荧光螯合剂。
TN1594	DL-Syringaresinol (±)-Syringaresinol	Antioxidant; Antifungal	Microbiology/Virology; oxidation-reduction
	DL-Syringaresinol ( (±)-Syringaresinol) 是一种来自与人参浆果的木质素，具有抗炎、抗氧化、镇痛活性和较弱的抗分枝杆菌活性。DL-Syringaresinol 可通过自噬延缓氧化应激诱导的皮肤老化，通过抑制炎症反应来缓解奥沙利铂诱导的神经性疼痛和脓毒症引起的心功能障碍。
T3834	8-Epideoxyloganic acid 8-表去氧马钱酸	ROS; Immunology/Inflammation related	Immunology/Inflammation
	8-Epideoxyloganic acid 是从 Incarvillea delavayi 中分离得到的一种环烯醚萜苷。它具有微弱的缓解疼痛活性。
T2834	Nobiletin Hexamethoxyflavone,川陈皮素,川皮苷	Apoptosis; MMP; Reactive Oxygen Species; ROR; Autophagy	Apoptosis; Autophagy; Immunology/Inflammation; Metabolism; NF-κB; Proteases/Proteasome
	Nobiletin (Hexamethoxyflavone) 是一种来自柑橘皮的聚甲氧基黄酮，是RORs 激动剂，可改善记忆力丧失。它可降低分化的 C2C12 肌管中的ROS 水平，并具有抗炎，抗癌，抗血管生成，抗增殖，抗转移和诱导细胞凋亡作用。
T4429	Rauwolscine hydrochloride Corynanthidine hydrochloride,盐酸育亨宾碱,萝芙素盐酸盐,α-Yohimbine hydrochloride,Isoyohimbine hydrochloride	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Rauwolscine hydrochloride (Isoyohimbine hydrochloride) 是一种高选择性的 α2 adrenergic 受体拮抗剂，Ki=12 nM。
T8105	Indole-3-carboxaldehyde 3-Formylindole,3-吲哚甲醛	Endogenous Metabolite	Metabolism
	Indole-3-carboxaldehyde (3-Formylindole) 是由黄化豌豆幼苗的粗酶制剂氧化降解IAA 的产物，是一种卷心菜提取物。它可用于制备吲哚类植物抗毒素环芸香素类似物。
T6491	(-)-(S)-Equol (−)-Equol,Equol,4',7-Dihydroxyisoflavan,4',7-Isoflavandiol,雌马酚	Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Endogenous Metabolite	Endocrinology/Hormones; Metabolism
	(-)-(S)-Equol (4',7-Dihydroxyisoflavan) 是雌激素受体β的高亲和力配体。
T5S2343	Acetylshikonin 乙酰紫草素,Acetyl shikonin	Others; P450; AChE	Metabolism; Neuroscience; Others
	Acetylshikonin 来源于紫草根，具有抗癌、抗炎作用。它是一种 AChE 抑制剂，具有很强的抗凋亡活性。它是一种非选择性的细胞色素 P450抑制剂，对所有 P450 亚型抑制的 IC50值范围为 1.4-4.0 μM。
T4776	Glycerol Glycerin,甘油	Endogenous Metabolite	Metabolism
	Glycerol 是甘油三酯（即脂肪和油）和磷脂的重要成分。它在食品工业中被广泛用作甜味剂和保湿剂以及药物制剂。
TN5597	Gopherenediol
	Gopherenediol shows weak antifeedant activity.
T28019	(-)-Mesembrine Mesembrin,Mesembrine,Mesembranone
	Mesembrine is a serotonin reuptake inhibitor and is also a weak inhibitor of the enzyme phosphodiesterase 4 (PDE4).
TN5937	Walsuronoid B
	Walsuronoid B shows weak antimalarial activity.
TN3710	Coronarin E	Antifection	Microbiology/Virology
	Coronarin E exhibits weak antimicrobial activity.
TN4298	Isohyenanchin	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Isohyenanchin is the potent antagonist of RDLac homo-oligomers, it is also a weak antagonist of ionotropic GABA receptors.
TN2380	Glycerol 1-(26-hydroxyhexacosanoate)	Others	Others
	Glycerol 1-(26-hydroxyhexacosanoate) has weak activities antiplasmodial
TN2892	3,5,7-Trihydroxychromone	Others	Others
	3,5,7-Trihydroxychromone exhibits weak antiangiogenic activity.
TN4539	Methyl chanofruticosinate	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Methyl chanofruticosinate has weak anti-HIV-1 activity.
TN5373	Ustusolate A
	1. Ustusolate A shows weak cytotoxicity against HL-60 and A549 cells with IC50 values of 20.6 and 30.0 microM, respectively.
T41138	Prosaikogenin H
	Prosaikogenin H, an intestinal metabolite derived from saikosaponin, exhibits weak hemolytic activity.
TN6446	Cyclo(Ile-Val)
	Cyclo(Ile-Val) shows moderate antifungal and weak antitumor activities in vitro.
TN5191	Tsugafolin	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Tsugafolin has weak anti-HIV activity.
T81996	Kadsuphilin A
	Kadsuphilin A, 提取自Kadsura coccinea (Lem.), 展现出较弱的抗增殖活性。
TN3677	Cleroindicin B	Others	Others
	Cleroindicin B shows weak scavenging action on 2,2-diphenyl-l-picrylhydrazyl and hydroxyl radicals.
TN2820	24-Methylenecycloartan-3-ol	Antifection	Microbiology/Virology
	24-Methylenecycloartan-3-ol and methyl caffeate show weak activity against Staphylococcus aureus and Escherichia coli.
TN6536	Decuroside I
	Decuroside I shows weak inhibiting activity against the primary and secondary wave aggregation of human platelet.
TN3550	Buxbodine B	AChR	Neuroscience
	Buxbodine B has weak anti-AChE activity with IC50 values in the range of 10.8-98μM.
TN3943	ent-17-Hydroxykauran-3-one	Antifection	Microbiology/Virology
	ent-17-Hydroxy-16α-kauran-3-one shows weak antimicrobial activity when tested against Staphylococcusaureus.
TN4976	Scutebata E	Others	Others
	Scutebata E shows weak cytotoxicity with IC50 values ranging from 35.11 to 42.73 μM against K562 cell lines.
TN4630	Nemoralisin	Others	Others
	Nemoralisin exhibits weak cytotoxicities (IC50>10 uM) against HepG2, AGS, MCF-7, and A-549 cancer cell lines.
TN3547	Bullatantriol	Antifection	Microbiology/Virology
	Bullatantriol has a stimulative effect on significantly proliferation and differentiation of culture osteoblasts. It may have weak antibacterial activities.
TN3465	Atalantoflavone	Antifection	Microbiology/Virology
	Atalantoflavone shows urease inhibitory potential. It displays weak cytotoxic activity against the human Caucasian prostate adenocarcinoma cell line PC-3.
TN2192	Scutebarbatine B	Others	Others
	Scutebarbatine B shows weak cytotoxicity with IC50 values ranging from 35.11 to 42.73 μM against K562 cell lines and HL60 cell lines.
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天然产物

weak Hepatoprotective agent-1

Cat.No: T80778

Cat.No: T4811

Synonym: D-α-Alanine,Ba 2776,(R)-Alanine,D-丙氨酸,(R)-2-Aminopropionic acid

Target: Chloride channel, Endogenous Metabolite

Cat.No: T25114

Synonym: NSC-406266,NSC 406266,NSC406266

Target: Parasite

γ-Linolenic Acid methyl ester

Cat.No: T21504

Synonym: Methyl gamma-linolenate,γ-亚麻酸甲酯

Target: LTR

Pseudolaric Acid C

Cat.No: T7029

Target: Antifungal

Cat.No: T1704

Synonym: Luteolin 4-methyl ether,香叶木素

Target: P450, Trk receptor

Cat.No: TN7094

Target: Antibacterial

Cat.No: T7060

Synonym: 1-Aminoadamantane,1-金刚烷胺,金刚烷胺,1-Adamantanamine,1-Adamantylamine

Target: Others

Acetoacetic acid lithium salt

Cat.No: T4854

Synonym: LithoTab acetoacetate,Lithium acetoacetate,Lithium 3-Oxobutyrate,乙酰乙酸锂

Target: Others, Endogenous Metabolite

Cat.No: T6S0325

Synonym: 黄豆黄素,Glycetein

Target: Apoptosis, Others

Cat.No: T0065

Synonym: 对乙酰氨基酚,醋氨酚,4-Acetamidophenol,4'-Hydroxyacetanilide,APAP,Paracetamol

Target: COX, Endogenous Metabolite, Histone Acetyltransferase

Cat.No: T8087

Target: Tyrosinase

Neochlorogenic acid methyl ester

Cat.No: TN5845

Synonym: 5-O-Caffeoylquinic acid methyl ester,Methyl 3-caffeoylquinate,GIP (1-39) acetate(725474-97-5 Free base),Methyl neochlorogenate,新绿原酸甲酯

Target: Antioxidant, HBV

3'-Methoxypuerarin

Cat.No: T4S2084

Synonym: 3'-甲氧基葛根素,3’- Methoxy Puerarin

Target: Antioxidant

Cat.No: T5S2017

Synonym: (-)-Ingenol,巨大戟二萜醇,巨大戟醇

Target: PKC

Cat.No: TN6675

Synonym: Cyclo(prolylvalyl)

Target: Antibacterial, Antifungal

2,6-Dimethoxyquinone

Cat.No: T3739

Synonym: 2,6-Dimethoxy-1,4-benzoquinone,2,6-Dimethoxy-p-benzoquinone,2,6-Dimethoxybenzoquinone,2,6-二甲氧基-1,4-苯醌

Target: Others

Cat.No: T6S0071

Target: HIF/HIF Prolyl-Hydroxylase, STAT, PD-1/PD-L1

Cat.No: T2835

Synonym: 桑色素,Toxylon pomiferum,Aurantica,Calico Yellow,Al-Morin

Target: Others

DL-Syringaresinol

Cat.No: TN1594

Synonym: (±)-Syringaresinol

Target: Antioxidant, Antifungal

8-Epideoxyloganic acid

Cat.No: T3834

Synonym: 8-表去氧马钱酸

Target: ROS, Immunology/Inflammation related

Cat.No: T2834

Synonym: Hexamethoxyflavone,川陈皮素,川皮苷

Target: Apoptosis, MMP, Reactive Oxygen Species, ROR, Autophagy

Rauwolscine hydrochloride

Cat.No: T4429

Synonym: Corynanthidine hydrochloride,盐酸育亨宾碱,萝芙素盐酸盐,α-Yohimbine hydrochloride,Isoyohimbine hydrochloride

Target: Adrenergic Receptor

Indole-3-carboxaldehyde

Cat.No: T8105

Synonym: 3-Formylindole,3-吲哚甲醛

Target: Endogenous Metabolite

Cat.No: T6491

Synonym: (−)-Equol,Equol,4',7-Dihydroxyisoflavan,4',7-Isoflavandiol,雌马酚

Target: Estrogen Receptor/ERR, Estrogen/progestogen Receptor, Endogenous Metabolite

Cat.No: T5S2343

Synonym: 乙酰紫草素,Acetyl shikonin

Target: Others, P450, AChE

Cat.No: T4776

Synonym: Glycerin,甘油

Target: Endogenous Metabolite

Cat.No: TN5597

Cat.No: T28019

Synonym: Mesembrin,Mesembrine,Mesembranone

Cat.No: TN5937

Cat.No: TN3710

Target: Antifection

Cat.No: TN4298

Target: GABA Receptor

Glycerol 1-(26-hydroxyhexacosanoate)

Cat.No: TN2380

Target: Others

3,5,7-Trihydroxychromone

Cat.No: TN2892

Target: Others

Methyl chanofruticosinate

Cat.No: TN4539

Target: HIV Protease

Cat.No: TN5373

Prosaikogenin H

Cat.No: T41138

Cat.No: TN6446

Cat.No: TN5191

Target: HIV Protease

Cat.No: T81996

Cat.No: TN3677

Target: Others

24-Methylenecycloartan-3-ol

Cat.No: TN2820

Target: Antifection

Cat.No: TN6536

Cat.No: TN3550

Target: AChR

ent-17-Hydroxykauran-3-one

Cat.No: TN3943

Target: Antifection

Cat.No: TN4976

Target: Others

Cat.No: TN4630

Target: Others

Cat.No: TN3547

Target: Antifection

Atalantoflavone

Cat.No: TN3465

Target: Antifection

Scutebarbatine B

Cat.No: TN2192

Target: Others

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