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Search Results for " chemotaxis "

82

抑制剂 & 化合物

4

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T16111	ML604086	CCR	Immunology/Inflammation; Microbiology/Virology
	ML604086 是选择性CCR8抑制剂，抑制循环T 细胞上 CCL1 与 CCR8 结合，还抑制 CCL1 介导的趋化性并提高细胞内 Ca2 浓度。
T17250	W-54011	ROS; Complement System	Immunology/Inflammation
	W-54011 是口服有效的非肽 C5a 受体拮抗剂，抑制125I 标记的 C5a 与人嗜中性白细胞的结合，Ki 为 2.2 nM。它还抑制C5a 诱导的人嗜中性粒细胞的细胞内 Ca2+动员，趋化性和ROS 的生成，IC50分别为 3.1 nM、2.7 nM 和1.6 nM。
T10639	C-021 dihydrochloride	CCR	Immunology/Inflammation; Microbiology/Virology
	C-021 dihydrochloride 是一种有效的 CCR4 拮抗剂。它有效抑制人和小鼠的功能趋化性，IC50 为 140 nM 和 39 nM。
T11699	J-113863	CCR	Immunology/Inflammation; Microbiology/Virology
	J-113863 是选择性的 CCR1 (CD18)拮抗剂，有抗炎作用，对人和小鼠 CCR1受体的 IC50值分别为 0.9 和 5.8 nM。它是人 CCR3的强效拮抗剂，还是小鼠 CCR3的弱效拮抗剂，IC50分别为 0.58 和 460 nM。
T13114	CCR2 antagonist 4 Teijin compound 1	CCR	Immunology/Inflammation; Microbiology/Virology
	CCR2 antagonist 4 (Teijin compound 1) 是高效的、特异性的CCR2拮抗剂，对 CCR2b 的IC50为 180 nM，抑制 MCP-1 诱导的趋化作用的 IC50为 24 nM。
T17225	Vercirnon CCX282-B,维塞诺,GSK-1605786,Traficet-EN	CCR	Immunology/Inflammation; Microbiology/Virology
	Vercirnon (Traficet-EN) 是可口服的选择性 CCR9拮抗剂，可抑制 CCR9 介导的 Molt-4 细胞上 Ca2+移动和趋化性，用于炎症性肠病的研究。
T39789	BMS-986235 BMS-986235,LAR-1219	Others	Others
	BMS-986235 (LAR-1219) 是一种特异性和口服活性的甲酰肽受体 2 (FPR2) 激动剂，对 hFPR2 和 mFPR2 的 EC50 分别为 0.41 nM 和 3.4 nM。 BMS-986235 可用于预防心力衰竭的研究。
T2690	Tranilast 曲尼司特,MK 341,SB 252218	RAAS; Prostaglandin Receptor	Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation
	Tranilast (SB 252218) 是一种抗过敏药物，可抑制炎症细胞释放脂质介质和细胞因子，抑制前列腺素 D2 (PGD2)产生，IC50为 0.1 mM。它拮抗血管紧张素 II 并抑制其在血管平滑肌细胞中的生物学作用，具有抗炎和免疫调节作用。
T21870	C-021 4-Quinazolinamine, 2-[1,4'-bipiperidin]-1'-yl-N-cycloheptyl-6,7-dimethoxy-	CCR	Immunology/Inflammation; Microbiology/Virology
	C 021 dihydrochloride 是一种 CC 趋化因子受体 4 (CCR4) 拮抗剂，抑制人和小鼠的功能趋化性，IC50分别为 140 和 39 nM。C-021 (4-Quinazolinamine, 2-[1,4'-bipiperidin]-1'-yl-N-cycloheptyl-6,7-dimethoxy-) 可有效阻止人 CCL22 衍生的 [35S]GTPγS 与受体结合，IC50为 18 nM。
T2036	6-OAU GTPL5846	GPR	Endocrinology/Hormones; GPCR/G Protein
	6-OAU (GTPL5846) 是 GPR84 的替代激动剂，在 Gqi5 嵌合体存在的情况下，在 HEK293 细胞中激活人 GPR84，在 PI 测定中 EC50 为 105 nM。
T1615	Irbesartan 厄贝沙坦,SR-47436,BMS-186295	Apoptosis; RAAS	Apoptosis; Endocrinology/Hormones
	Irbesartan (SR-47436) 是一种 1 型血管紧张素 II 受体拮抗剂，IC50为1.3 nM。
T16850	SB-265610 GSK-CXCR2	CXCR	Autophagy; GPCR/G Protein; Immunology/Inflammation
	SB-265610 (GSK-CXCR2) 是竞争性非肽变构CXCR2选择性拮抗剂，可阻断大鼠 CINC-1 诱导的钙动员和中性粒细胞趋化性，IC50分别为 3.7 和 70 nM。
T40446	AG-09/1	Others	Others
	AG-09/1 是一种具有选择性和有效性的甲酰基肽受体 1 (FPR1) 激动剂，可激活人中性粒细胞的趋化作用。
T24700	R243 R 243,R-243	CCR	Immunology/Inflammation; Microbiology/Virology
	R243 是选择性的CCR8拮抗剂，可抑制CCL1/CCR8的相互作用，以及CCR8信号传导和趋化性，具有抗伤害感受和抗炎作用。
T3580	FIPI 5-Fluoro-2-indolyl deschlorohalopemide	Phospholipase; Autophagy	Autophagy; Metabolism
	FIPI (5-Fluoro-2-indolyl deschlorohalopemide) 是 halopemide 的衍生物，抑制PLD1和PLD2，IC50值分别为 25 nM 和 20 nM。它防止 PLD 调节 F-肌动蛋白细胞骨架重组、细胞扩散和趋化性。
T9239	RS-25344	PDE	Metabolism
	RS-25344 是一种有效的选择性磷酸二酯酶 (PDE) 4 抑制剂。它在体外抑制嗜酸性粒细胞趋化性并增加精子的进行性运动。
T27682	CCR2 antagonist 5 JNJ-41443532,JNJ-41443532 Free Base,JNJ 41443532,JNJ41443532	CCR	Immunology/Inflammation; Microbiology/Virology
	CCR2 antagonist 5 (JNJ-41443532) 是一种具有选择性和口服活性的 hCCR2 抑制剂，具有良好的结合亲和力 (IC50=37 nM) 和有效的功能拮抗作用 (chemotaxis IC50=30 nM)。JNJ-41443532 对 mCCR2 结合的 Ki 为 9.6 µM，可用于研究炎症性疾病和糖尿病。
T26861	BMS-817399 BMS817399	CCR	Immunology/Inflammation; Microbiology/Virology
	BMS-817399 是一种具有口服活性的 CCR1 拮抗剂，具有结合亲和力和趋化性抑制效力的 IC50，可用于类风湿性关节炎的研究。
T14688	BMS CCR2 22	CCR	Immunology/Inflammation; Microbiology/Virology
	BMS CCR2 22 是一种有效的选择性 CC 型趋化因子受体2拮抗剂，钙通量 IC50为 18 nM，趋化性 IC50为1 nM，结合 IC50为5.1 nM。
T22879	JNJ 10191584 maleate JNJ 10191584 maleate salt,VUF6002 maleate	Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	JNJ 10191584 maleate (VUF6002 maleate) 是一种具有口服活性的选择性 H4 受体拮抗剂 (Ki = 26 nM)。 JNJ 10191584 maleate 抑制嗜酸性粒细胞和肥大细胞的趋化性(IC50 = 530 nM 和 138 nM)。
T4163	Reparixin DF 1681Y,Repertaxin,瑞帕利辛	CXCR	Autophagy; GPCR/G Protein; Immunology/Inflammation
	Reparixin (Repertaxin) 是两种 CXCL8 受体 CXCR1/2 的强效抑制剂，它对 CXCR2 介导的细胞迁移具有微弱的抑制作用，IC50为 100 nM。它强烈阻断 CXCR1 介导的趋化性，IC50为 1 nM。
TQ0103	INCB3344	CCR	Immunology/Inflammation; Microbiology/Virology
	INCB3344 是一种有效、特异性和口服生物可利用的 CCR2 拮抗剂，结合拮抗作用的 IC50 值为 9.5 nM (mCCR2) 和 5.1 nM (hCCR2)，趋化活性拮抗作用的 IC50 值为 7.8 nM (mCCR2) 和 3.8 nM (hCCR2)。
T0944	Levamisole hydrochloride (-)-Tetramisole hydrochloride,盐酸左旋咪唑	Phospholipase; AChR; Parasite; HSV	Metabolism; Microbiology/Virology; Neuroscience
	Levamisole hydrochloride ((-)-Tetramisole hydrochloride) 是驱虫剂和免疫调节剂。它对HSV 病毒有明显抗病毒作用。
TP2334	PMX 53 acetate(219639-75-5 free base)	Complement System	Immunology/Inflammation
	PMX 53 acetate(219639-75-5 free base) 是一种有效的口服活性 CD88 (C5aR) 拮抗剂 (IC50: 20 nM)，抑制 C5a 诱导的中性粒细胞髓过氧化物酶释放和趋化性，IC50 值分别为 22 nM 和 75 nM。 PMX-53 也是 Mas 相关基因 2 (MrgX2) 的激动剂。
T9084	Cetirizine Impurity B dihydrochloride De(carboxymethoxy) Cetirizine Acetic Acid Dihydrochloride,西替利嗪杂质B二盐酸盐,西替利嗪杂质04	Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Cetirizine Impurity B dihydrochloride (De(carboxymethoxy) Cetirizine Acetic Acid Dihydrochloride) 是 Cetirizine dihydrochloride 的杂质。Cetirizine 是一种抗组胺剂，是口服有活力的、特异性 H1受体拮抗剂。它能够抑制过敏反应期间嗜酸性粒细胞趋化，可以标记抗过敏特性。
T3520	Setipiprant KYTH-105,塞替匹仑,ACT-129968	GPR; Prostaglandin Receptor	Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation
	Setipiprant (ACT-129968) 是一种口服的选择性 CRTH2 拮抗剂，IC50为6.0 nM。
T15641	K777 APC-3316	P450; Cysteine Protease; CCR	Immunology/Inflammation; Metabolism; Microbiology/Virology; Proteases/Proteasome
	K777 是有效的，具有口服活性的，不可逆的半胱氨酸蛋白酶 (cysteine protease) 抑制剂。K777是有效的 CYP3A4 抑制剂(IC50= 60 nM)。K777也是选择性的 CCR4 拮抗剂，显示出强的趋化性抑制作用。K777 对 Cruzain（克鲁斯锥虫的主要半胱氨酸蛋白酶）和组织蛋白酶 B 和 L 具有不可逆的抑制作用。K777 通过靶向组织蛋白酶介导的细胞进入，显示出广谱的抗病毒作用。K777 抑制 EBOV 和 SARS-CoV 病毒的进入，IC50 值分别为 0.87 nM 和 0.68 nM。
T3360	ZK 756326 ZK756326 2HCl	CCR	Immunology/Inflammation; Microbiology/Virology
	ZK 756326 是一种选择性的非肽 CCR8 趋化因子受体激动剂（IC50：1.8 μM，在人体内；2.6 μM，在小鼠体内）。对 CCR4/5 和 CXCR3/4 没有活性，比其他 26 种 GPCR 的选择性高 28 倍（对 α2A 和 5-HT 受体的选择性较低）。诱导趋化性并抑制 Env 介导的 (HIV) 细胞-细胞融合。
T1544	Olsalazine disodium Dipentum,奥沙拉秦钠,Olsalazine Sodium	Others; COX; Antibacterial; Antibiotic	Immunology/Inflammation; Microbiology/Virology; Neuroscience; Others
	Olsalazine disodium (Dipentum) 是抗炎化合物，可作用于溃疡性结肠炎和炎症性肠病。
T23920	CX4338 CX-4338,CX 4338
	CX4338 is a CXCL8-mediated chemotaxis inhibitor.
T22526	BML-111 5(S),6(R)-7-trihydroxymethyl Heptanoate	Others	Others
	inhibits leukotriene B4 (LTB4)-induced polymorphonuclear neutrophils (PMN) chemotaxis
TP2466	Platelet factor 4 (59-70) PF4 (59-70)
	Platelet factor 4 (59-70) elicits human neutrophil & monocyte chemotaxis.
T24156	ICI 195739 DO870,D0870,D 0870,D-0870
	ICI 195739 is a newer antifungal agent. It inhibits neutrophil random migration, chemotaxis, and hexose monophosphate shunt activity.
T30535	BMS-639623 UNII-PON9OFP69G,PON9OFP69G,BMS 639623,CHEMBL399495
	BMS-639623 is a CCR3 antagonist with a picomolar inhibitory effect on eosinophilic chemotaxis and can be used in the treatment of asthma.
T19230	CCR2 antagonist 4 hydrochloride Teijin compound 1 hydrochloride	Others	Others
	CCR2 antagonist 4 hydrochloride is a specific CCR2 antagonist (IC50s: 180 nM for CCR2b). It potently inhibits MCP-1-induced chemotaxis (IC50: 24 nM).
T11862	LMD-009	Others	Others
	LMD-009 mediates chemotaxis, inositol phosphate accumulation, and calcium release in high potencies with EC50s from 11 to 87 nM. LMD-009 is a selective CCR8 nonpeptide agonist.
T40430	Cetirizine Impurity D
	Cetirizine Impurity D is an impurity of Cetirizine. Cetirizine is a second-generation antihistamine that acts as a specific, orally active, and long-acting antagonist of the histamine H1-receptor. Cetirizine exhibits antiallergic properties and inhibits eosinophil chemotaxis in response to allergies.
T0260L	Meclofenamate sodium hydrate INF 4668,CI583,CI-583,INF-4668,CI 583,INF4668
	Meclofenamate sodium is a potent non-steroidal anti-inflammatory agent, which can specifically inhibit chemokine-induced human polymorphonuclear leukocyte function: chemotaxis, degranulation, and superoxide anion free radical production.
T38227	Quin C1
	Potent and selective FPR2 agonist (EC50 = 15 nM). Induces Ca2+ mobilization in FPR2 but not FPR1-transfected mast cells. Induces neutrophil chemotaxis and degranulation in vitro. Reduces neutrophil and lymphocyte counts in bronchoalveolar lavage fluid in a mouse lung injury model. Anti-inflammatory. Zhou et al (2007) Pharmacological characterization of a novel nonpeptide antagonist for formyl peptide receptor-like 1. Mol.Pharmacol. 72 976 PMID:17652444 \|Corminboeuf et al (2014) FPR2/ALXR agonist...
T76504	CKLF1-C19
	CKLF1-C19 是人类趋化因子样因子 1 (CKLF1) 的 C 端肽。CKLF1-C19 与 CCR4相互作用，抑制 CKLF1 和 CCL17诱导的趋化性。CKLF1-C19 可以通过抑制 CCR3和 CCR4介导的趋化性来抑制过敏性肺部炎症。
T62660	MLN3126
	MLN3126 是一种口服具有活力的强效 CCR9 拮抗剂。 MLN3126 抑制 CCL25 诱导的钙动员 (calcium mobilization) 和小鼠初级胸腺细胞趋化 (chemotaxis) (IC50: 6.3 nM)。
T41016	Vercirnon sodium GSK-1605786 sodium,CCX282-Bsodium,维塞诺钠盐,Traficet-ENsodium
	Vercirnon (GSK1605786A) sodium is an orally bioavailable, selective, and potent antagonist of CCR9 . Vercirnon sodium inhibits CCR9-mediated Ca 2+ mobilization and chemotaxis on Molt-4 cells with IC 50 values of 5.4 and 3.4 nM, respectively. Vercirnon sodium is selective for CCR9 over CCR1-12 and CX3CR1-7 (IC 50 s>10 μM for all). Vercirnon sodium is an equipotent inhibitor of CCL25-directed chemotaxis of both splice forms of CCR9 (CCR9A and CCR9B) with IC 50 values of 2.8 and 2.6 nM, respectivel...
T81078	Substance P (3-11)
	Substance P (3-11)，作为P 物质 (SP) 的片段肽，具备穿透血脑屏障的能力，且对豚鼠回肠显示出收缩活性。
T71913	Bourgeonal
	Bourgeonal is an agonist of human testicular olfactory receptor hOR17-4. It increases cytosolic calcium levels in human spermatozoa, acts as a chemoattractant, and increases swimming speed in sperm chemotaxis assays in a concentration-dependent manner.
T37617	Leukotriene B3
	LTB3 is the LTA hydrolase metabolite of LTA3 in the leukotriene biosynthetic pathway. LTB3 and LTB4 are equipotent in their pro-inflammatory effects. However, LTB3 is five times less potent than LTB4 in eliciting chemotaxis of human neutrophils.
T41145	TASP 0277308
	TASP 0277308 is a potent and selective sphingosine 1-phosphate 1 (S1P1) receptor antagonist (IC50 = 7.8 nM). TASP 0277308 inhibits S1P-induced chemotaxis (IC50 = 1.1-1.6 nM), HUVEC cell proliferation (IC50 = 3-3.6 nM) and suppresses angiogenesisin vivo. TASP 0277308 also blocks VEGF-induced tube-formation of HUVECsin vitroand reverses or impairs the development of arthritis or mechano-allodynia.
T60262	Cholera autoinducer 1
	Cholera autoinducer 1 是霍乱弧菌的自诱导剂。Cholera autoinducer 1 影响秀丽隐杆线虫的趋化性。
T37264	15(R)-15-methyl Prostaglandin D2 15(R)15methyl PGD2	GPR	Endocrinology/Hormones; GPCR/G Protein
	15(R)-15-methyl Prostaglandin D2 (15(R)15methyl PGD2) 是一种 PGD2 合成类似物，也是一种具有选择性和强效性的 CRTH2/DP2 受体激动剂，可调节嗜酸性粒细胞 CD11b 表达、肌动蛋白聚合和趋化。
T79418	BLT2 antagonist-1	Leukotriene Receptor	GPCR/G Protein
	BLT2 agonist-1 (compound 15b) 是选择性BLT2拮抗剂，能在224 nM IC50下抑制CHO-BLT2细胞趋化性。它不影响CHO-BLT1细胞趋化性，并在132 nM Ki值下抑制LTB4与BLT2结合。BLT2 agonist-1适用于哮喘、慢性阻塞性肺病等炎症性气道疾病研究。
TQ0032L	Rosiptor acetate AQX-1125,AQX 1125,AQX1125,AQX-1125 acetate
	Rosiptor is a potent and selective SHIP1 activator. AQX-1125 inhibits Akt phosphorylation in SHIP1-proficient but not in SHIP1-deficient cells, reduces cytokine production in splenocytes, inhibits the activation of mast cells and inhibits human leukocyte

化合物

Cat.No: T16111

Target: CCR

Cat.No: T17250

Target: ROS, Complement System

C-021 dihydrochloride

Cat.No: T10639

Target: CCR

Cat.No: T11699

Target: CCR

CCR2 antagonist 4

Cat.No: T13114

Synonym: Teijin compound 1

Target: CCR

Cat.No: T17225

Synonym: CCX282-B,维塞诺,GSK-1605786,Traficet-EN

Target: CCR

Cat.No: T39789

Synonym: BMS-986235,LAR-1219

Target: Others

Cat.No: T2690

Synonym: 曲尼司特,MK 341,SB 252218

Target: RAAS, Prostaglandin Receptor

Cat.No: T21870

Synonym: 4-Quinazolinamine, 2-[1,4'-bipiperidin]-1'-yl-N-cycloheptyl-6,7-dimethoxy-

Target: CCR

Cat.No: T2036

Synonym: GTPL5846

Target: GPR

Cat.No: T1615

Synonym: 厄贝沙坦,SR-47436,BMS-186295

Target: Apoptosis, RAAS

Cat.No: T16850

Synonym: GSK-CXCR2

Target: CXCR

Cat.No: T40446

Target: Others

Cat.No: T24700

Synonym: R 243,R-243

Target: CCR

Cat.No: T3580

Synonym: 5-Fluoro-2-indolyl deschlorohalopemide

Target: Phospholipase, Autophagy

Cat.No: T9239

Target: PDE

CCR2 antagonist 5

Cat.No: T27682

Synonym: JNJ-41443532,JNJ-41443532 Free Base,JNJ 41443532,JNJ41443532

Target: CCR

Cat.No: T26861

Synonym: BMS817399

Target: CCR

Cat.No: T14688

Target: CCR

JNJ 10191584 maleate

Cat.No: T22879

Synonym: JNJ 10191584 maleate salt,VUF6002 maleate

Target: Histamine Receptor

Cat.No: T4163

Synonym: DF 1681Y,Repertaxin,瑞帕利辛

Target: CXCR

Cat.No: TQ0103

Target: CCR

Levamisole hydrochloride

Cat.No: T0944

Synonym: (-)-Tetramisole hydrochloride,盐酸左旋咪唑

Target: Phospholipase, AChR, Parasite, HSV

PMX 53 acetate(219639-75-5 free base)

Cat.No: TP2334

Target: Complement System

Cetirizine Impurity B dihydrochloride

Cat.No: T9084

Synonym: De(carboxymethoxy) Cetirizine Acetic Acid Dihydrochloride,西替利嗪杂质B二盐酸盐,西替利嗪杂质04

Target: Histamine Receptor

Cat.No: T3520

Synonym: KYTH-105,塞替匹仑,ACT-129968

Target: GPR, Prostaglandin Receptor

Cat.No: T15641

Synonym: APC-3316

Target: P450, Cysteine Protease, CCR

Cat.No: T3360

Synonym: ZK756326 2HCl

Target: CCR

Olsalazine disodium

Cat.No: T1544

Synonym: Dipentum,奥沙拉秦钠,Olsalazine Sodium

Target: Others, COX, Antibacterial, Antibiotic

Cat.No: T23920

Synonym: CX-4338,CX 4338

Cat.No: T22526

Synonym: 5(S),6(R)-7-trihydroxymethyl Heptanoate

Target: Others

Platelet factor 4 (59-70)

Cat.No: TP2466

Synonym: PF4 (59-70)

Cat.No: T24156

Synonym: DO870,D0870,D 0870,D-0870

Cat.No: T30535

Synonym: UNII-PON9OFP69G,PON9OFP69G,BMS 639623,CHEMBL399495

CCR2 antagonist 4 hydrochloride

Cat.No: T19230

Synonym: Teijin compound 1 hydrochloride

Target: Others

Cat.No: T11862

Target: Others

Cetirizine Impurity D

Cat.No: T40430

Meclofenamate sodium hydrate

Cat.No: T0260L

Synonym: INF 4668,CI583,CI-583,INF-4668,CI 583,INF4668

Cat.No: T38227

Cat.No: T76504

Cat.No: T62660

Vercirnon sodium

Cat.No: T41016

Synonym: GSK-1605786 sodium,CCX282-Bsodium,维塞诺钠盐,Traficet-ENsodium

Substance P (3-11)

Cat.No: T81078

Cat.No: T71913

Cat.No: T37617

Cat.No: T41145

Cholera autoinducer 1

Cat.No: T60262

15(R)-15-methyl Prostaglandin D2

Cat.No: T37264

Synonym: 15(R)15methyl PGD2

Target: GPR

BLT2 antagonist-1

Cat.No: T79418

Target: Leukotriene Receptor

Rosiptor acetate

Cat.No: TQ0032L

Synonym: AQX-1125,AQX 1125,AQX1125,AQX-1125 acetate

Cat. No.	Product Name	Target	Signaling Pathways
T9218	Andrograpanin 19-HYDROXY-8(17),13-LABDADIEN-16,15-OLIDE,新穿心莲内酯苷元	p38 MAPK	MAPK
	Andrograpanin (19-HYDROXY-8(17),13-LABDADIEN-16,15-OLIDE) 是来自穿心莲的一种天然产物，具有抗炎和抗感染活性。
T0508	γ-Aminobutyric acid Gamma-aminobutyric acid,4-Aminobutyric acid,4-氨基丁酸,γ-氨基丁酸,GABA,4-Aminobutanoic acid,Piperidic acid	GABA Receptor; Endogenous Metabolite	Membrane transporter/Ion channel; Metabolism; Neuroscience
	γ-Aminobutyric acid (4-Aminobutyric acid) 是成年哺乳动物大脑中主要的抑制性神经递质，能够与离子移变 GABA 受体(GABAA) 受体和促代谢受体 (GABAB) 受体结合发挥作用。
TMS1461	Qingyangshengenin B 青阳参甙元B,青阳参苷元B,Otophylloside B	Beta Amyloid	Neuroscience
	Qingyangshengenin B (Otophylloside B) 是一种分离自 Qingyangshen 的 C-21 甾体苷。它能够在 mRNA 水平上抑制 Aβ 的表达来减少 Aβ 的沉积，对 Aβ 的毒性有保护作用。它具有抗癫痫作用。
T36051	Lipoxin A4 脂氧素 A4,LXA4
	Lipoxin A4 (LXA4) is a trihydroxy fatty acid containing a conjugated tetraene, produced by the metabolism of (±)15-HETE or 15-HpETE with human leukocytes.[1] LXA4 is equipotent to leukotriene B4 in inducing superoxide generation in human neutrophils at 0.1 μM.2 LXA4 is associated with several other biological functions including leukocyte activation, chemotaxis effects, natural killer cell inhibition, and monocyte migration and adhesion.[2],[3],[4] Analytical and biological comparisons of synth...

天然产物

Cat.No: T9218

Synonym: 19-HYDROXY-8(17),13-LABDADIEN-16,15-OLIDE,新穿心莲内酯苷元

Target: p38 MAPK

γ-Aminobutyric acid

Cat.No: T0508

Synonym: Gamma-aminobutyric acid,4-Aminobutyric acid,4-氨基丁酸,γ-氨基丁酸,GABA,4-Aminobutanoic acid,Piperidic acid

Target: GABA Receptor, Endogenous Metabolite

Qingyangshengenin B

Cat.No: TMS1461

Synonym: 青阳参甙元B,青阳参苷元B,Otophylloside B

Target: Beta Amyloid

Cat.No: T36051

Synonym: 脂氧素 A4,LXA4

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