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Search Results for " antagonistic "

Targets Recommended: Others

51

抑制剂 & 化合物

19

天然产物

2

重组蛋白

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Cat. No.	Product Name	Target	Signaling Pathways
T23101	o-3M3FBS	Others	Others
	o-3M3FBS 是 m-3M3FBS 的阴性对照。它以独立于 PLC 的机制及拮抗方式抑制内向和外向电流。它以与 m-3M3FBS 竞争的方式增加 [Ca2+]i 增加。
T3630	Relugolix RVT-601,瑞卢戈利,TAK-385	GNRH Receptor	GPCR/G Protein
	Relugolix (RVT-601) 是口服有活性的非肽性促性腺激素释放激素的拮抗剂。同 TAK-013 相比，它对人和猴子的受体具有高亲和力和强拮抗活性，它们的 IC50值分别为0.33 nM 和0.32 nM。它可用于研究性激素依赖性疾病，如子宫肌瘤、子宫内膜异位症、前列腺癌等。
T0147	Clemastine fumarate HS-592 (fumarate),富马酸氯马斯汀,Meclastine fumarate,Meclastine (fumarate)	Autophagy; Histamine Receptor	Autophagy; GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Clemastine fumarate (Meclastine (fumarate)) 是一种合成乙醇胺，具有抗胆碱能、镇静和组胺 H1 拮抗作用。
T67957	Pipoxizine	Others	Others
	Pipoxizine 对组胺所致的支气管收缩具有拮抗作用，可用于研究哮喘疾病。
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。
T67811	Tefludazine	Others	Others
	Tefludazine 一种具有苯茚酮结构的新型神经抑制剂，是一种具有良好口服活性且与多巴胺和5-羟色胺受体有拮抗作用的化合物。Tefludazine 在小鼠、大鼠和狗的体外和体内测试模型中表现出强大的多巴胺（DA）拮抗活性。Tefludazine 是一种用来治疗精神类疾病的潜在化合物。
T2623	PD98059 PD 98059	ERK; Aryl Hydrocarbon Receptor; MEK; Autophagy	Autophagy; Immunology/Inflammation; MAPK
	PD98059 是一种 MEK 抑制剂，抑制 MEK1 和 MEK2 (IC50=2/50 μM)，具有非 ATP 竞争性。PD98059 也是一种 AHR 的配体而起拮抗作用。PD98059 可以抑制细胞自噬。
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。
T23380	Sonepiprazole	Dopamine Receptor	GPCR/G Protein; Neuroscience
	Sonepiprazole 是D4多巴胺受体选择性拮抗剂，与rD4多巴胺受体，hD4.2多巴胺受体，rD2多巴胺受体和组胺H1受体结合的Ki 分别为 3.6、10.1、5147 和 7430 nM。
T60536	Terodiline	Calcium Channel; HER; AChR	Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Neuroscience; Tyrosine Kinase/Adaptors
	Terodiline 是一种具有抗胆碱能和钙拮抗特性的仲胺，可阻断 hERG 电流（IC50：375 nM）。Terodiline 具有心脏毒性，可用于研究逼尿肌不稳定引起的疾病。
T23283	2-Methoxyidazoxan monohydrochloride RX 821002 hydrochloride	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	L-Albizziin (2-Methoxyidazoxan monohydrochloride) 是高效的 alpha 2r 肾上腺素受体选择性拮抗剂，对 imidazoline 拮抗作用很小或没有。它对 (豚鼠) alpha 2D 肾上腺素受体 (pKd9.7) 的亲和力明显高于 (兔子) alpha 2A 肾上腺素受体 (pKd8.2)。
T31195	Dalcotidine KU 1257,KU-1257	Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Dalcotidine (KU 1257) 是一种新型组胺H2受体拮抗剂，具有组胺H9受体拮抗活性和抗分泌作用，与豚鼠大脑皮层结合的Ki 值为0.040 对分离性豚鼠右心房组胺诱导的正变时反应的拮抗作用的KB 值为0.041。Dalcotidine 提高了溃疡愈合的质量，可能有助于降低溃疡的复发率和复发率。
T9524	Lanthanum trichloride	Others	Others
	Lanthanum trichloride 可用作分析试剂，可用作提取金属镧的原料和石油裂化催化剂。它在医药领域也有一定的作用。例如，研究表明，它对内毒素（LPS）体内作用的拮抗作用对寻找新的有效内毒素拮抗剂有一定的影响，为防治内毒素血症提供了实验依据。
T67894	Butyzamide	Thrombopoietin Receptor; JAK	Angiogenesis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Stem Cells
	Butyzamide 是一种有效的可口服的Mpl 激活剂，是一种对血小板生成素(TPO)受体具有拮抗作用的新型非肽基分子，促进表达人Mpl (hMpl)的和小鼠pro B 细胞株Ba/F3的增殖，诱导JAK2、STAT3、STAT5和MAPK 的磷酸化。Butyzamide 在小鼠异种移植试验中有助于提升血小板水平。
T67959	Pirodomast	Thrombin; Serine Protease	Proteases/Proteasome
	Pirodomast 是血栓素 A（TXA2）合成酶抑制剂。Pirodomast 能抑制白三烯（LT）D4、C4、E4 的形成和血栓素 B2（TXB2）的活性，但对组胺、甲氧胆碱、血清素、LTC4 或血小板活化因子诱导的豚鼠支气管痉挛的拮抗作用较弱或无效。Pirodomast 在体外对豚鼠气管只有微弱的松弛活性。Pirodomast 是一种潜在的抗过敏化合物，在体外可抑制胰蛋白酶的蛋白水解活性，在体内可阻止抗原诱发过敏绵羊的即时和晚期哮喘反应，抑制抗原诱导的过敏绵羊对组胺和卡巴胆碱的气道高反应性。
T71159	F-0401	Others	Others
	F-0401 is a novel calcium antagonist with platelet-activating factor-antagonistic action.
T68838	Medroxalol hydrochloride	Others	Others
	Medroxalol hydrochloride is an antihypertensive agent that possesses both alpha and beta-adrenergic antagonistic properties.
T68690	Temiverine hydrochloride monohydrate	Others	Others
	Temiverine hydrochloride monohydrate is an anticholinergic drug with calcium antagonistic activity.
T68871	Pipradimadol	Others	Others
	Pipradimadol is a 4,4-disubstituted piperidine derivative with antidepressive and serotonin antagonistic activity.
T23580	20681-S 20681 S	Others	Others
	20681-S has narcotic antagonistic properties and antinociceptive.
T38139	Orexin receptor antagonist 2	Others	Others
	Orexin Receptor Antagonist 2 (compound 30), characterized by its potent antagonistic activity with pKis of 7.69 and 9.78, holds promise for insomnia research[1].
T69021	Nifedipine HCl	Others	Others
	Nifedipine HCl is a potent vasodilator agent with calcium antagonistic action. It is a useful anti-anginal agent that also lowers blood pressure.
T71029	RCC-36 HCl	Others	Others
	Rcc 36 is an active metabolite of temiverine that has inhibitory actions toward the atropine-resistant part of contractions, which may be related to the calcium antagonistic actions of these compounds.
T28795	SKI2496 SKI 2496,SKI-2496	Others	Others
	SKI2496 is a potent and orally bioavailableantagonist of Gonadotropin-Releasing Hormone Receptor (hGnRHR IC50 = 0.46 nM; max. LH inh. inh. (%, h)= 84%, 12h; LH inh. (24h) = 76%.). SKI2496 exhibits more selective antagonistic activity toward the human GnRH
T36597	ISPA-28	Others	Others
	ISPA-28 is a specific antagonist of the plasmodial surface anion channel (PSAC). It exerts its antagonistic effects by direct and reversible binding to CLAG3[1][2].
T70634	Psycholeine	Others	Others
	Psycholeine is isolated from the tropical plant Psychotria oleoides; exhibits somatostatin antagonistic activity on growth hormone secretion.
T78013	Pep2-8 TFA
	Pep2-8是增强PCSK9拮抗活性的肽，作用于前蛋白转化酶枯草杆菌蛋白酶/可辛9型(PCSK9)。
T71466	Sdz 210-096	Others	Others
	Sdz 210-096 is a novel opiate antagonist. It is a novel 14 beta-benzyl morphinan derivative with antagonistic actions at mu and kappa opiate receptors. This compound has been characterized for luteinizing hormone (LH) secretion-stimulating effects in a variety of experimental paradigms in the rat.
T79266	Antihypertensive agent 2	Others	Others
	Antihypertensive agent 2 (Compound 4g) 为一种有效的血管紧张素 II 受体 1 拮抗剂，其降血压效能可与Losartan媲美或更胜一筹。
T78778	D3R/MOR antagonist 1	Dopamine Receptor	GPCR/G Protein; Neuroscience
	D3R/MOR antagonist 1 (Compound 114) 为D3R/MOR拮抗剂，其对D3R和MOR的Ki值分别为46.5 nM和691 nM。该化合物通过MOR的部分激动作用可能具有镇痛效果，同时通过D3R的拮抗作用有助于降低阿片类药物的滥用风险。
T80183	Muscarinic toxin 7
	Muscarinic toxin 7，一种肽类毒素，特异性地针对毒蕈碱M1受体表现出选择性和非竞争性的拮抗活性。
T82901	Belrestotug GSK4428859A,EOS884448,EOS-448
	Belrestotug (EOS-448) 是一种抗TIGIT (VSIG9, VSTM3) 的拮抗性人免疫球蛋白 G1 kappa (hIgG1 kappa) 抗体，具备抗肿瘤活性。
T25911	Oxycinchophen Magnophenyl,Sintofene,Reumartril,Chinoxone	Others	Others
	Oxycinchophen 是一种喹啉类的有机物，抗风湿病的化合物。它已被用于研究 P- 选择素拮抗活性，DHOD 抑制活性，以及抗炎药对血管平滑肌的作用。
T61347	D4R antagonist-1	Others	Others
	D4R antagonist-1 是一种有效的选择性 D4R 拮抗剂，IC50为 6.87 μM。D4R antagonist-1 具有帕金森病研究潜力。
TP1075	AUNP-12 TFA (1353563-85-5 free base) AUNP-12 TFA,NP-12 TFA
	AUNP-12 TFA (NP-12 TFA) is a polypeptide antagonist in the pd-1 signaling pathway, which has the same antagonistic effect on pd-l1 and pd-l2, and can protect the proliferation and effector function of lymphocytes.
T83487	[Pmp1,Tyr(OEt)2] AVP
	[Pmp1,Tyr(OEt)2] AVP为环状加压素(AVP)的线性拮抗剂，具备相似结构。
T26751	BBR 2160 BBR-2160,BBR2160	Others	Others
	BBR 2160 is a dihydropyridine derivative belonging to the group of the so-called tiampidine. BBR 2160 has calcium-antagonistic properties in cardiac tissue. Intracellular microelectrodes have been used to characterize the electrophysiological properties o
T61145	Topiramate lithium	Others	Others
	Topiramate lithium (McN 4853) is a wide-ranging antiepileptic compound with GluR5 receptor antagonistic properties. Its mechanism of action involves enhancing GABAergic activity, inhibiting kainate/AMPA receptors, voltage-sensitive sodium and calcium channels, and increasing potassium conductance. Additionally, this compound inhibits carbonic anhydrase. [1][2][3]
T75834	Antagonist G TFA
	Antagonist G TFA 作为后叶加压素（vasopressin）的有效拮抗剂，同时对GRP和缓激肽具有弱拮抗作用。此外，Antagonist G 能够诱导AG-1转录，增强癌细胞对化疗的敏感性。
T73132	DS69910557	Others	Others
	DS69910557为高效、选择性的hPTHR1拮抗剂，口服有效。其对PTHR1的拮抗IC50值为0.08 μM。适用于甲状旁腺功能亢进症、恶性肿瘤引起的高钙血症及骨质疏松症研究。
T80561	Atrosab
	Atrosab是一种人源化IgG1抗TNFR1抗体，具有拮抗作用。它能够抑制TNF诱导的细胞凋亡(apoptosis)，并减少IL-6和IL-8的生成，有助于研究炎症性疾病。
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。
T80787	WAY-649123	Others	Others
	WAY-649123为一有活性分子，适用于生化反应研究。
T62918	GPR84 antagonist 3	Others	Others
	GPR84antagonist 3 (compound 42)为一种高效GPR84(G 蛋白偶联受体 84)拮抗剂，具pIC50值为8.28，表现出对GTPγS的抑制作用，并拥有良好的药代动力学特性。
T60249	RhlR antagonist 1	Others	Others
	RhlR antagonist 1 is a highly effective antagonist of the RhlR protein, showing an IC50 value of 26 μM. It exhibits selective antagonistic activity against RhlR, with minimal effect on LasR and PqsR. RhlR antagonist 1 strongly inhibits biofilm formation in both static and dynamic environments and reduces the production of virulence factors, such as rhamnolipid and pyocyanin, in P. aeruginosa. These characteristics make RhlR antagonist 1 a valuable tool for the development of molecules that modul...
T79547	MOR agonist-2	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	MOR agonist-2 (Compound 46) 为D3R拮抗剂及MOR激动剂，其Ki值分别为7.26 nM和564 nM。MOR agonist-2潜在以MOR部分激动机制实现镇痛效果，并通过D3R拮抗降低阿片类药物的滥用风险。
T72492	GnRH-R antagonist 1	GNRH Receptor	GPCR/G Protein
	GnRH-R antagonist 1 (化合物 21a) 是GnRH-R拮抗剂，具有优良口服安全性及膜透性，高亲和力结合GnRH-R（IC50=0.57 nM），并展现出有效体外拮抗活性（IC50=2.18 nM）。该化合物适用于晚期前列腺癌治疗和预防过早LH峰出现的研究。
T78734	Sigma-1 receptor antagonist 5	Sigma receptor	GPCR/G Protein
	Sigma-1 receptor antagonist 5 (compound 12) 是一种 4-吡啶衍生物，既有镇痛活性也是 sigma 受体 (Ki=4.5 nM (σ1R)，10 nM (σ2R)) 及组胺 H3 (hH3R，Ki=7.7 nM，IC50=215 nM) 的拮抗剂。它能够抑制辣椒素引起的痛觉，并展现出对伤害性和神经性疼痛模型的显著疗效。
T74415	Imlunestrant tosylate	Others	Others
	Imlunestrant (LY-3484356) tosylate 是口服有效且选择性的雌激素受体(estrogen receptor, ER)降解剂(SERD)，具纯拮抗性。该化合物能持续抑制ER依赖的基因转录与细胞生长，适用于研究ER阳性(ER+)晚期乳腺癌(aBC)与子宫内膜样癌(EEC)。
T70309	Dicetrorelix pamoate	Others	Others
	Dicetrorelix pamoate is a synthetic decapeptide with gonadotropin-releasing hormone (GnRH) antagonistic activity. GnRH induces the production and release of luteinizing hormone (LH) and follicle stimulating hormone (FSH) from the gonadotrophic cells of the anterior pituitary. Due to a positive estradiol (E2) feedback at midcycle, GnRH liberation is enhanced resulting in an LH-surge. This LH-surge induces the ovulation of the dominant follicle, resumption of oocyte meiosis and subsequently lutein...

化合物

Cat.No: T23101

Target: Others

Cat.No: T3630

Synonym: RVT-601,瑞卢戈利,TAK-385

Target: GNRH Receptor

Clemastine fumarate

Cat.No: T0147

Synonym: HS-592 (fumarate),富马酸氯马斯汀,Meclastine fumarate,Meclastine (fumarate)

Target: Autophagy, Histamine Receptor

Cat.No: T67957

Target: Others

Lin28-let-7a antagonist 1

Cat.No: T11851

Target: Others

Cat.No: T67811

Target: Others

Cat.No: T2623

Synonym: PD 98059

Target: ERK, Aryl Hydrocarbon Receptor, MEK, Autophagy

Opiranserin hydrochloride

Cat.No: T9833

Target: P2X Receptor, GlyT, 5-HT Receptor

Cat.No: T23380

Target: Dopamine Receptor

Cat.No: T60536

Target: Calcium Channel, HER, AChR

2-Methoxyidazoxan monohydrochloride

Cat.No: T23283

Synonym: RX 821002 hydrochloride

Target: Adrenergic Receptor

Cat.No: T31195

Synonym: KU 1257,KU-1257

Target: Histamine Receptor

Lanthanum trichloride

Cat.No: T9524

Target: Others

Cat.No: T67894

Target: Thrombopoietin Receptor, JAK

Cat.No: T67959

Target: Thrombin, Serine Protease

Cat.No: T71159

Target: Others

Medroxalol hydrochloride

Cat.No: T68838

Target: Others

Temiverine hydrochloride monohydrate

Cat.No: T68690

Target: Others

Cat.No: T68871

Target: Others

Cat.No: T23580

Synonym: 20681 S

Target: Others

Orexin receptor antagonist 2

Cat.No: T38139

Target: Others

Cat.No: T69021

Target: Others

Cat.No: T71029

Target: Others

Cat.No: T28795

Synonym: SKI 2496,SKI-2496

Target: Others

Cat.No: T36597

Target: Others

Cat.No: T70634

Target: Others

Cat.No: T78013

Cat.No: T71466

Target: Others

Antihypertensive agent 2

Cat.No: T79266

Target: Others

D3R/MOR antagonist 1

Cat.No: T78778

Target: Dopamine Receptor

Muscarinic toxin 7

Cat.No: T80183

Cat.No: T82901

Synonym: GSK4428859A,EOS884448,EOS-448

Cat.No: T25911

Synonym: Magnophenyl,Sintofene,Reumartril,Chinoxone

Target: Others

D4R antagonist-1

Cat.No: T61347

Target: Others

AUNP-12 TFA (1353563-85-5 free base)

Cat.No: TP1075

Synonym: AUNP-12 TFA,NP-12 TFA

[Pmp1,Tyr(OEt)2] AVP

Cat.No: T83487

Cat.No: T26751

Synonym: BBR-2160,BBR2160

Target: Others

Topiramate lithium

Cat.No: T61145

Target: Others

Antagonist G TFA

Cat.No: T75834

Cat.No: T73132

Target: Others

Cat.No: T80561

Cat.No: T16399

Target: P2X Receptor, GlyT, 5-HT Receptor

Cat.No: T80787

Target: Others

GPR84 antagonist 3

Cat.No: T62918

Target: Others

RhlR antagonist 1

Cat.No: T60249

Target: Others

Cat.No: T79547

Target: Opioid Receptor

GnRH-R antagonist 1

Cat.No: T72492

Target: GNRH Receptor

Sigma-1 receptor antagonist 5

Cat.No: T78734

Target: Sigma receptor

Imlunestrant tosylate

Cat.No: T74415

Target: Others

Dicetrorelix pamoate

Cat.No: T70309

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
T2S0271	Voacamine 老刺木胺,Voacanginine	Cannabinoid Receptor; P-gp	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Voacamine (Voacanginine) 是非洲马铃果中的一种吲哚生物碱，可抑制多药耐药肿瘤细胞中的 P-糖蛋白作用，具有强效的大麻素 CB1受体拮抗活性。
T4S1659	Xanthotoxol 8-Hydroxypsoralen,8-Hydroxyfuranocoumarin,Psoralen,花椒毒酚,8-Hydroxypsoralene	Reactive Oxygen Species; 5-HT Receptor; Endogenous Metabolite	GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB
	Xanthotoxol (Psoralen) 是一种具有生物活性的线性呋喃香豆素，具有很强的抗炎、抗氧化、5-HT 拮抗和神经保护作用等药理活性。
T20939	Bimatoprost acid 17-phenyl trinor PGF2α,17-phenyl trinor Prostaglandin F2α	GPR	Endocrinology/Hormones; GPCR/G Protein
	Bimatoprost acid (17-phenyl trinor PGF2α) 是一种代谢稳定的 PGF2α 类似物，对 FP 受体具有潜在的拮抗活性。与 PGF2α 相比，它与绵羊黄体细胞上的 FP 受体结合的相对效力为 756%。
T6S1885	Benzoylmesaconine Mesaconine 14-benzoate,苯甲酰新乌头原碱	Others	Others
	Benzoylmesaconine (Mesaconine 14-benzoate) 是乌头汤最丰富的组分。其中乌头汤可用于研究类风湿性关节炎。
T6S0659	Rhynchophylline 钩藤碱,Rhynchophyllin,Rhyncophylline,Mitrinermine,Mitrinermin	Calcium Channel; NF-κB	Membrane transporter/Ion channel; Metabolism; NF-κB
	Rhynchophylline (Mitrinermine) 是一种生物碱类化合物，从钩藤中分离得到，具有很高的生物活性，被广泛用于抗炎、神经保护等方面的研究。
T15248	Estetrol Donesta	Estrogen Receptor/ERR; Endogenous Metabolite	Endocrinology/Hormones; Metabolism
	Estetrol(Donesta) 是可口服且具有选择性核雌激素受体 (estrogen receptor) 调节剂,是一种在怀孕期间由人类胎儿肝脏合成的天然雌激素。Estetrol 对子宫内膜或中枢神经系统有作用，但对乳房有拮抗作用。Estetrol 在低浓度时可能有助于降低血栓形成。Estetrol 可用于缓解更年期症状。
T3915	Ginsenoside Ro 人参皂苷Ro,Chikusetsusaponin 5,Polysciasaponin P3,人参皂苷 Ro,Chikusetsusaponin V	Calcium Channel; Reductase; Prostaglandin Receptor	Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism
	Ginsenoside Ro (Chikusetsusaponin V) 能降低 TXA2产量，较弱降低 COX-1 和 TXAS 活性，具有 Ca2+拮抗剂的抗血小板作用，IC50为 155 μM。
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。
TN4821	Pregomisin	PAFR	GPCR/G Protein
	Pregomisin shows platelet-activating factor (PAF) antagonistic activity and the IC 50 value is 4.8x10(-5) M.
TN1719	Gymnestrogenin 匙羹藤苷元,(3BETA,4ALPHA,16BETA,21BETA)-齐墩果-12-烯-3,16,21,23,28-五醇	Liver X Receptor	Metabolism
	Gymnestrogenin has a dual LXRα±/α2 antagonistic profile.
TN6500	Microgrewiapine A
	Microgrewiapine A is a selective cytotoxic agent for colon cancer cells over normal colon cells and to exhibit nicotinic receptor antagonistic activity for both the hα3β4 and hα4β2 receptor subtypes.
T3P2855	Chamigrenal	EGFR; NOS; PAFR; COX; Prostaglandin Receptor	Angiogenesis; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Tyrosine Kinase/Adaptors
	β-Chamigrenal has anti-inflammatory activity, it has inhibitory effects on lipopolysaccharide-induced nitric oxide and prostaglandin E2 production in RAW 264.7 macrophages. Chamigrenal shows platelet-activating factor antagonistic activity and the IC(50)
TN6682	Cyclo(Phe-Gly)
	Cyclo(Phe-Gly) shows weak antagonistic activity against VEGFR2 -CD, it also shows strong inhibitory activity against human cancer cells(KB,KBv200) with LD50 at 6.5 and 11.2 umol/L,respectively.
TN6678	Cyclo(Tyr-Pro)
	Cyclo(Tyr-Pro) shows antibacterial activity towards several marine bacterial species, it also shows weak antagonistic activity against VEGFR2 -CD. Cyclo(Tyr-Pro) and cyclo(Pro-Val) are toxic to both suspension cells and seedlings of Pinus thunbergii, whic
TN2763	2-Hydroxy-3-methoxybenzoic acid glucose ester	PAFR	GPCR/G Protein
	2-Hydroxy-3-methoxybenzoic acid glucose ester shows a potent antagonistic activity against platelet activating factor (PAF), it can prevent the mice from the PAF-induced death at a dose of 300 micrograms/mouse.
TN1815	Kadsulignan L	HBV; PAFR	GPCR/G Protein; Microbiology/Virology
	Kadsulignan L shows in vitro antiviral effects on hepatitis B virus. It also shows moderate platelet-activating factor (PAF) antagonistic activities with the IC50 value of 2.6 x 10(-5) M.
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
TN4624	Nantenine	Others	Others
	Nantenine is an acetylcholinesterase inhibitor, it functions as an effective antagonist against a wide range of MDMA-induced effects in mice. Nantenine has anticonvulsant effect, which seems attributable to its stimulation and the resultant decrease of Ca
T35779	Oosporein	Others	Others
	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), ...

天然产物

Cat.No: T2S0271

Synonym: 老刺木胺,Voacanginine

Target: Cannabinoid Receptor, P-gp

Cat.No: T4S1659

Synonym: 8-Hydroxypsoralen,8-Hydroxyfuranocoumarin,Psoralen,花椒毒酚,8-Hydroxypsoralene

Target: Reactive Oxygen Species, 5-HT Receptor, Endogenous Metabolite

Bimatoprost acid

Cat.No: T20939

Synonym: 17-phenyl trinor PGF2α,17-phenyl trinor Prostaglandin F2α

Target: GPR

Benzoylmesaconine

Cat.No: T6S1885

Synonym: Mesaconine 14-benzoate,苯甲酰新乌头原碱

Target: Others

Rhynchophylline

Cat.No: T6S0659

Synonym: 钩藤碱,Rhynchophyllin,Rhyncophylline,Mitrinermine,Mitrinermin

Target: Calcium Channel, NF-κB

Cat.No: T15248

Synonym: Donesta

Target: Estrogen Receptor/ERR, Endogenous Metabolite

Cat.No: T3915

Synonym: 人参皂苷Ro,Chikusetsusaponin 5,Polysciasaponin P3,人参皂苷 Ro,Chikusetsusaponin V

Target: Calcium Channel, Reductase, Prostaglandin Receptor

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: TN4821

Target: PAFR

Cat.No: TN1719

Synonym: 匙羹藤苷元,(3BETA,4ALPHA,16BETA,21BETA)-齐墩果-12-烯-3,16,21,23,28-五醇

Target: Liver X Receptor

Microgrewiapine A

Cat.No: TN6500

Cat.No: T3P2855

Target: EGFR, NOS, PAFR, COX, Prostaglandin Receptor

Cat.No: TN6682

Cat.No: TN6678

2-Hydroxy-3-methoxybenzoic acid glucose ester

Cat.No: TN2763

Target: PAFR

Cat.No: TN1815

Target: HBV, PAFR

Isopimaric acid

Cat.No: TN4319

Target: Antifection

Cat.No: TN4624

Target: Others

Cat.No: T35779

Target: Others

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPH-00589	SpoT Protein, E. coli, Recombinant (His & Myc) Bifunctional (p)ppGpp synthase/hydrolase SpoT,spoT	E. coli	E. coli
	In eubacteria ppGpp (guanosine 3'-diphosphate 5'-diphosphate) is a mediator of the stringent response which coordinates a variety of cellular activities in response to changes in nutritional abundance. This enzyme catalyzes both the synthesis and degradation of ppGpp. The second messengers ppGpp and c-di-GMP together control biofilm formation in response to translational stress; ppGpp represses biofilm formation while c-di-GMP induces it. ppGpp activates transcription of CsrA-antagonistic small ...
TMPY-01812	Enoyl-ACP Reductase Protein, E. coli, Recombinant (His) b1288,JW1281,gts,ECK1283,qmeA,envM	E. coli	E. coli
	Enoyl-ACP reductase, also known as NADH-dependent enoyl-ACP reductase and FABI, is a cell inner membrane and peripheral membrane protein which belongs to theshort-chain dehydrogenases/reductases (SDR) family and FabI subfamily. Microorganisms produce many kinds of antibiotics which function in an antagonistic capacity in nature where they have much competition. Bacterial FAS provides essential fatty acids for use in the assembly of key cellular components. Among them, FABI is an enoyl-ACP...

重组蛋白

SpoT Protein, E. coli, Recombinant (His & Myc)

Cat.No: TMPH-00589

Species: E. coli

Expression System: E. coli

Enoyl-ACP Reductase Protein, E. coli, Recombinant (His)

Cat.No: TMPY-01812

Species: E. coli

Expression System: E. coli

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