48
22
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T21632 |
Myoseverin
|
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
Myoseverina 是多核肌管可逆分裂成单核片段的诱导剂,影响多种生长因子、免疫调节、细胞外基质重塑和应激反应基因的表达,与伤口愈合和组织再生相关通路的激活一致。 | |||
T8575 |
ENFENAMIC ACID
|
Platelet aggregation | Others |
Enfenamic acid 是一种能够抑制伤口愈合的非甾体抗炎药。 | |||
T21653 |
1,4-DPCA
|
HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism |
1,4-DPCA 是一种脯氨酰羟化酶抑制剂,对人源包皮成纤维细胞中胶原羟基化的 IC50 为 2.4 μM,对因子抑制 HIF (FIH) 的 IC50 为 60 μM。 | |||
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。 | |||
T4478 |
CID 16020046
C390-0219 |
Cannabinoid Receptor | GPCR/G Protein |
CID 16020046 (C390-0219) 是一种选择性 GPR55 拮抗剂,在酵母中抑制 GPR55 组成型活性,IC50 为 0.15 μM。它抑制 GPR55 介导的 Ca2+信号传导和 GPR55 介导的 ERK1/2 磷酸化,可降低内皮细胞的伤口愈合,参与血小板功能的调节。 | |||
T34685 |
Sonedenoson
MRE-0094,MRE0094,MRE 0094 |
||
Sonedenoson( MRE0094) is an adenosine A2A receptor agonist that promotes rapid wound healing. | |||
T2206 |
Quadrol
N,N,N′,N′-Tetrakis(2-hydroxypropyl)ethylenediamine,EDTP,依的托,Edetol |
Others | Others |
Quadrol (EDTP) 是一种免疫刺激剂,是潜在的能够加速伤口愈合的有用药物。 | |||
T13823 |
Polyvinylpyrrolidone
PVP,Povidone,Polyvidone,聚乙烯吡咯烷酮 |
Others | Others |
Polyvinylpyrrolidone (Polyvidone) 与碘和其他化合物结合后,可用作人类和兽医学中有效的伤口愈合促进剂和消毒剂。 | |||
T19841 |
Tribenoside
Glyvenol,Glyvenal,Ba 2140,BG-356,Glivenol,三苄糖苷,TBGF |
Others | Others |
Tribenoside (BG-356) 是血管保护剂,能够温和的镇痛、抗炎及伤口愈合,可用研究痔疮。 | |||
T40570L |
LKKTETQ acetate
LKKTETQ acetate (476014-70-7 Free base) |
Others | Others |
LKKTETQ acetate 是胸腺素 β4 蛋白中的活性位点,负责伤口愈合、肌动蛋白结合和细胞迁移。 | |||
T7116 |
Sodium gualenate
Guaiazulenesulfonate sodium,磺酸钠 |
Others | Others |
Sodium gualenate (Guaiazulenesulfonate sodium) 是一种桂皮烯的亲水性衍生物,具有良好的抗炎和愈伤活性,常用于十二指肠溃疡,胃溃疡和胃炎的研究。 | |||
T41206 |
Poly Vinyl Alcohol
Polyvinyl alcohol |
Others | Others |
Poly Vinyl Alcohol (Polyvinyl alcohol)是一种水溶性可生物降解且可用于伤口愈合的聚合物,在生物医学领域广泛使用。Poly Vinyl Alcohol 常用于制作医用辅料。 | |||
TP2319 |
Thymosin β4 acetate(75591-33-4 free base)
|
Autophagy | Autophagy |
Thymosin β4 acetate(75591-33-4 free base) 是一种胸腺激素,具有多种不同的细胞内和细胞外活性,影响伤口愈合、炎症、纤维化和组织再生。 | |||
T74048 |
PAPA NONOate
|
Endogenous Metabolite; NO Synthase | Immunology/Inflammation; Metabolism |
PAPA NONOate 是一种依赖于 pH 调节的 NO 供体。PAPA NONOate 具有潜在的抗肿瘤活性,通过增加伤口部位的胶原合成率,可用于研究糖尿病伤口愈合障碍。 | |||
T21550 |
Blebbistatin
(±)-Blebbistatin |
ATPase; Myosin | Cytoskeletal Signaling; Membrane transporter/Ion channel |
Blebbistatin ((±)-Blebbistatin) 是一种选择性的非肌肉肌球蛋白 II 抑制剂,可促进角膜内皮细胞 (CEC) 的定向迁移并加速伤口愈合,并保留了细胞连接的完整性和屏障功能。 | |||
T32613 |
LCB 03-0110 dihydrochloride
|
Src | Angiogenesis; Tyrosine Kinase/Adaptors |
LCB 03-0110 Dihydrochloride 是BTK 和SYK 家族以及DDR2家族中c-Src 激酶(IC50=1.3 nM)和酪氨酸激酶的有效抑制剂。在体外抑制LPS 诱导的巨噬细胞活化和TGF-β1诱导的成纤维细胞活化,抑制巨噬细胞和成纤维细胞的活化,并抑制伤口愈合模型中的瘢痕形成。 | |||
T4425 |
JK-P3
|
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
JK-P3 是广谱 VEGFR2抑制剂。它能够抑制 VEGF-A 刺激的 VEGFR2 激活和细胞内信号转导,也可阻碍内皮单层细胞迁移和血管生成,影响成纤维细胞生长因子受体激酶在体外的活性。它具有抗血管生成的作用。 | |||
T41231 |
GP 1a
|
Cannabinoid Receptor; PERK; Arrestin | Apoptosis; GPCR/G Protein |
GP 1a 是cannabinoid receptor 2(CB2)的强效激动剂(EC50=7.1),是在cAMP、GTPγS 和β-arrestin 招募试验中显示的。GP 1a 对CB2受体的选择性约为CB1受体的30倍,且在体外增加HL-60细胞的P-ERK1/2表达。GP 1a 对皮肤伤口愈合有益。GP 1a 可抑制炎症和纤维生成,同时促进上皮的重新形成。 | |||
T34693 |
Sphingosine phosphorylcholine
|
||
Sphingosine phosphorylcholine is a wound healing agent. | |||
T29547 |
Acemannan
Acemannanan |
||
Acemannan can produce cell proliferation and skin wound healing through AKT/mTOR signaling pathway. | |||
T28146 |
ND-336
ND336,ND-336 hydrochloride,ND 336 |
||
ND-336 is a highly selective inhibitor ofMMP-2, MMP-9 and MMP-14. ND-336 accelerates diabetic wound healing by lowering inflammation and by enhancing angiogenesis and re-epithelialization of the wound. | |||
T25309 |
Dermabond
Liquid Bandage,2-Octyl 2-cyanoacrylate,RiteLok CON 895 |
||
Dermabond 是一种抗菌化合物,已被用于伤口愈合的基础科学研究。 | |||
T30107 | Apratyramide | ||
Apratyramide is a marine-derived peptidic stimulator of VEGF-A and other growth factors with potential application in wound healing. | |||
T40570 |
LKKTETQ
|
||
LKKTETQ, a peptide segment, is the active site within the protein thymosin β 4 responsible for actin binding, cell migration and wound healing. | |||
T21185 |
CEP03
CEP 03,CEP-03 |
||
CEP03 enhances EC/EPC proliferation, tubelike formation, and wound-healing efficiency, leading to promote angiogenesis and significantly improve blood flow perfusion recovery in the ischemic hind limbs of mice. | |||
T70826 | PF-03671148 | ||
PF-03671148 is a potent ALK inhibitor. PF-03671148 inhibits the expression of fibrotic genes and protein markers both in vitro in human fibroblasts and in vivo in a rat wound repair model. Wound healing is not inhibited by the topical application of the ALK5 inhibitor to the wound. PF-03671148 may have potential utility for the prevention of dermal scarring. | |||
T82358 |
G-{d-Arg}-GDSPASSK
|
||
G-{d-Arg}-GDSPASSK是一种抑制细胞粘附的多肽,有助于促进伤口愈合和组织修复。 | |||
T14139 |
Aganepag
AGN 210937 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Aganepag, a potent Prostanoid EP2 receptor agonist, exhibits remarkable selectivity with an EC50 of 0.19 nM, demonstrating no activity at the EP4 receptor. Its applications are primarily in the fields of wound healing, scar reduction, scar prevention, and the treatment and prevention of wrinkles. | |||
T81404 |
Prezatide copper
Bisprezatide copper,PC 1020,Iamin |
||
Prezatide Copper(亦称Iamin)具有促进伤口愈合的多重特性,且用于抑制脱发。 | |||
T34653 | SK1071 | ||
SK1071 is a novel migrastatin analogs, which demonstrated improved performance over migrastatin, with nanomolar IC50 values in chamber cell migration assays with tumor cells and human umbilical vein endothelial cells (HUVECs), and in wound healing assays. | |||
T81330 |
Q-Peptide
|
||
Q-Peptide(QHREDGS),是血管生成素-1的衍生肽。在糖尿病小鼠模型中,它通过增加角质形成细胞迁移来改善伤口愈合,并加速伤口闭合。 | |||
T41189 |
AY 254
|
||
AY 254 is a potent PAR2 biased agonist. Selectively activates ERK1/2 signaling (EC50= 2 nM for ERK1/2 phosphorylation versus 80 nM for Ca2+release). Reduces cytoKi ne-induced caspase 3/8 activation, promotes scratch-wound healing, and induces IL-8 secretion, in human colorectal cancer (HT29) cellsin vitro. | |||
T61106 | GRP78-IN-1 | ||
GRP78-IN-1 displays interactions with specific residues on the GRP78 protein with a binding energy of -8.07 kcal/mol. This compound possesses potent cytotoxic and anti-proliferative effects on cancer cells, particularly demonstrating promising apoptosis in breast cancer cells and wound healing properties [1]. | |||
T75857 |
LL-37, human TFA
|
||
LL-37, human TFA 是一种由37个氨基酸残基组成的两亲性抗菌肽,源自组织蛋白酶,具备广谱抗菌活性。该化合物有助于防护角膜避免感染,同时调节伤口的愈合过程。 | |||
T36080 |
Rivenprost
ONO-4819 |
||
Prostaglandin E2 activates four distinct G protein-coupled receptors, EP1-4. Rivenprost is a potent and selective agonist for the EP4 receptor (Ki = 0.7, 56, 620, and >10,000 nM for EP4, EP3, EP2, and EP1, respectively). It has been used to promote EP4-mediated bone formation, prevent bone loss related to osteoporosis, drive osteoblast differentiation, and stabilize bone implants.[1][2][3][4][5] Rivenprost has also been used to support wound healing.[6] | |||
T75858 |
LL-37, human acetate
|
||
LL-37, human acetate 是一种由37个氨基酸残基组成的两亲性抗菌肽,源于组织蛋白酶的衍生物,展现出广泛的抗菌效果。该化合物不仅对角膜感染提供保护,也有助于调节伤口的愈合过程。 | |||
T74212 | BLT2 probe 1 | Leukotriene Receptor | GPCR/G Protein |
BLT2 probe 1 (化合物 13) 是一款以 CAY10583 合成激动剂为基础的荧光探针,主要靶向糖尿病伤口愈合和胃肠道病变中潜在的 BLT2。该探针适用于多种检测系统中对 BLT2 受体配体进行药理学研究。 | |||
T35408 |
(±)10(11)-EDP Ethanolamide
|
||
(±)10(11)-EDP ethanolamide is an ω-3 endocannabinoid epoxide and cannabinoid (CB) receptor agonist (EC50s = 0.43 and 22.5 nM for CB1 and CB2 receptors, respectively). It is produced though direct epoxygenation of docosahexaenoyl ethanolamide by cytochrome P450 (CYP) epoxygenases. 10,11-EDP epoxide (12.5 and 25 μM) reduces the viability of 143B metastatic osteosarcoma cells. It induces apoptosis and inhibits cell migration in a wound-healing assay in 143B, MG63, and HOS osteosarcoma cells. (±)10(... | |||
T79798 |
PHD-IN-2
|
HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism |
PHD-IN-2(Compound 91)是一种高效的PHD拮抗剂,具有IC50值小于5 nM,能在HEP3B细胞中诱导促红细胞生成素的合成,EC50值小于2.5 μM。此化合物主要用于心血管、代谢、血液、肺部、肾脏、肝脏疾病、伤口愈合以及癌症等研究领域。 | |||
T80859 |
Vitronectin
|
||
Vitronectin为一类多功能糖蛋白,广泛分布于血液及细胞外基质。该蛋白质与糖胺聚糖、胶原蛋白、纤溶酶原及尿激酶受体发生结合,并对纤溶酶原激活抑制剂1的抑制构象起稳定作用。Vitronectin常用于促进伤口愈合和肿瘤进展研究领域。 | |||
T78018 |
Plasminogen
|
||
Plasminogen是一种可由尿激酶血浆蛋白原激活剂(uPA)或组织血浆蛋白原激活剂(tPA)裂解激活的分泌性蛋白,生成血浆蛋白,该酶可以广泛裂解纤维蛋白及其他ECM成分。作为促炎调节剂,Plasminogen能促进急性及糖尿病相关伤口愈合。该蛋白在伤口愈合、炎症和低纤溶酶原血症的研究中有重要应用。 | |||
T35616 |
Migrastatin
|
||
Migrastatin is a bacterial metabolite that has been found inStreptomyceswith antimuscarinic and anticancer activities.1,2It binds to M1-5muscarinic acetylcholine receptors (Kis = >200, 200, 31, 43, and >200 μM, respectively) and inhibits calcium mobilization induced by carbamoylcholine in SK-N-SH cells (IC50= 28 μM), as well as in primary rat bladder smooth muscle cells.1Migrastatin inhibits the migration of EC17 esophageal cancer cells in a wound healing assay (IC50= 10 μg/ml) and 4T1 mouse mam... | |||
T81396 |
PRO-F
|
||
PRO-F是一种光活化H2S供体,具备ROS清除功能。该化合物通过光激活能生成荧光信号,实现H2S释放的实时追踪;其激活过程不耗费内源性成分。PRO-F在细胞内提供H2S,以防止ROS过量造成的细胞损害,并已在慢性伤口愈合和糖尿病模型中展现出促进效果。 | |||
T82151 |
Hyaluronan-binding peptide, biotin labeled
|
||
Hyaluronan-binding peptide, biotin labeled 是通过 C 端 GGGSK 残基生物素化的透明质酸结合肽,能够干预 HA 与 CD44 受体的作用,并阻碍 T 细胞增殖。 HA 在细胞外基质和细胞表面广泛表达,参与多种生物过程,包括受精、胚胎发育、伤口修复、血管新生、炎症反应和肿瘤转移。 | |||
T35671 |
Salazinic Acid
|
||
Salazinic acid is a depsidone lichen metabolite that has been found in P. sulcata.1 It is active against B. cereus, B. subtilis, S. aureus, P. aeruginosa, S. typhimurium, C. albicans, and A. niger in vitro (MICs = 3.9-30.8 mM). Salazinic acid is cytotoxic to MM98, A431, and HaCaT cells in crystal violet (EC50s = 159, 2,870, and 48 μM, respectively) and neutral red uptake assays (EC50s = 1,925, 1,913, and 907 μM, respectively).2 It increases the wound closure rate in scratch-wounded HaCaT monolay... | |||
T83874 |
S-72
|
||
S-72是一种微管聚合抑制剂,以1, 3, 10 µM的浓度在无细胞测定中抑制微管聚合,并在MCF-7和耐紫杉醇的MCF-7/T乳腺癌细胞中降低细胞活性(IC50分别为15.64和26.32 nM)。50 nM浓度的S-72能抑制MCF-7和MCF-7/T细胞的迁移和侵袭,并减少划痕实验中的伤口闭合百分比。100 nM的S-72在MCF-7/T细胞中诱导G2/M期的细胞周期阻滞以及凋亡,并在同一浓度下抑制这些细胞中干扰素基因激活剂(STING)的激活。以每天15 mg/kg的剂量,S-72抑制了耐紫杉醇的MCF-7/T和MX-1/T小鼠异种移植模型中的肿瘤生长。 | |||
T83898 |
S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine
SFN-Cys,D,L-Sulforaphane-L-cysteine |
||
S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine (SFN-Cys) 是一种异硫氰酸酯衍生物及第一类和第二类组蛋白去乙酰化酶(HDAC)抑制剂和抗癌剂硫代硫酸烯醇醚的活性代谢产物。它通过巯基乙酸途径酶从硫代硫酸烯醇醚经DL-硫代硫酸烯醇醚谷胱甘肽和硫代硫酸烯醇醚半胱氨酸甘肽中间体形成。SFN-Cys (20 µM) 通过创伤愈合和腔室分析实验,分别减少了U87MG和U373 MG胶质母细胞瘤细胞的侵袭和迁移。在45 µM的浓度下,它降低了对紫杉醇耐药的A549肺癌细胞(A549/T)中的α-微管蛋白、βIII-微管蛋白、司他敏1和X连锁抑制剂的凋亡(XIAP)的水平,并减少了细胞密度。使用30 µM浓度的SFN-Cys诱导U87MG和U373 MG细胞凋亡和G2/M期细胞周期停滞。 | |||
T64692 |
AMY-101 acetate
|
||
Complement component C3 plays a particularly versatile role in this process by keeping the cascade alert, acting as a point of convergence of activation pathways, fueling the amplification of the complement response, exerting direct effector functions, and helping to coordinate downstream immune responses[3]. In C3-/- mice alcohol-induced liver steatosis is absent or strongly reduced after chronic or acute alcohol exposure. This suggests that the complement system and its component C3 contribute... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3855 |
Tracheloside
|
Estrogen Receptor/ERR; Phosphorylase | Endocrinology/Hormones; Metabolism |
Tracheloside 是抗雌激素木质素,利用 ERK1/2 刺激促进角质形成细胞增殖,是一种良好的促进伤口愈合的药物。 | |||
T3881 |
Vaccarin
|
Integrin; Akt; PERK; AMPK | Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
Vaccarin 是从王不留行中提取的一种黄酮糖苷,可显著促进伤口愈合以及伤口部位的内皮和成纤维细胞增殖。它通过激活 AMPK 信号通路改善胰岛素抵抗和脂肪变性。 | |||
T5S1982 |
Periplocin
Periplocoside,杠柳毒苷 |
Apoptosis; Others | Apoptosis; Others |
Periplocin (Periplocoside) 是从黑龙骨中分离出的一种强心类固醇。它可促进肿瘤细胞凋亡并抑制肿瘤生长。它通过激活 Na/K-ATPase 介导的 Src/ERK 和 PI3K/Akt 途径,具有促进伤口愈合的潜力。 | |||
TN1686 |
Ginsenoside Rg4
人参皂苷 RG4 |
Antibacterial | Microbiology/Virology |
Ginsenoside Rg4 是分离自Panax ginsengC. A. Meyer 叶子中的一种人参三醇型人参皂苷。人参三醇型人参皂苷具有多种生物活性,包括防腐,抗糖尿病,伤口愈合,免疫刺激和抗氧化活性等。 | |||
TN3016 |
4',6,7-Trimethoxyisoflavone
|
MMP | Proteases/Proteasome |
4',6,7-Trimethoxyisoflavone 通过 NOX2 诱导促进伤口愈合,从而导致集体迁移和 MMP 活化。 | |||
T2827 |
Asiatic acid
Asiantic acid,Dammarolic acid,积雪草酸 |
Apoptosis; p38 MAPK; Parasite | Apoptosis; MAPK; Microbiology/Virology |
Asiatic acid (Dammarolic acid) 是在Centella asiatica 中发现的一种五环三萜,有抗炎活性,可诱导黑色素瘤细胞的凋亡,有可能治疗皮肤癌。 | |||
TN1079 |
Deoxyelephantopin
|
NF-κB | NF-κB |
Deoxyelephantopin 是来自Elephantopus scaber 的,具有生物活性的天然倍半萜烯内酯,能够抑制NF-κB,MAPK,PI3K/Akt 和β-catenin 信号传导。它可广泛用于癌症方面的研究。 | |||
T1125 |
Shikonin
NSC 252844,Isoarnebin 4,(+)-Shikonin,紫草素,Alkanna Red,C.I. 75535,Anchusa acid |
TNF; NF-κB; Chloride channel; HIV Protease; PKM | Apoptosis; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
Shikonin (Anchusa acid) 属于天然产物,是一种 TMEM16A 氯离子通道抑制剂 (IC50=6.5 μM) 和选择性 PKM2 抑制剂。Shikonin 具有抗肿瘤、抗炎和伤口愈合活性。 | |||
TN2077 |
(+/-)-Pinocembrin
NSC 43318,(±)-5,7-Dihydroxyflavanone |
GPR; Others | Endocrinology/Hormones; GPCR/G Protein; Others |
(+/-)-Pinocembrin (NSC-43318) 是一种来自腋松的天然产物,它是一种 GPR120 配体,能促进 HaCaT 细胞系的伤口愈合。 | |||
TN7082 |
demethyldaphnoretin-7-O-glucoside
|
Others | Others |
demethyldaphnoretin-7-O-glucoside 是从 Daphne oleoides Schreber subsp. 中分离出来的天然产物。在土耳其传统医学中,它的地上部分已被用于治疗疟疾、风湿病和伤口愈合。 | |||
TN1132 |
Procyanidin A2
原花青素 A2,原花青素A2 |
IL Receptor; TNF; transporter; Antibacterial | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology |
Procyanidin A2 是一种具有抗癌、抗氧化、抗菌和抗炎活性的黄酮类天然产物,存在于蔓越莓和越橘中。 | |||
TN1641 | (-)-Fenchone | Others; Antioxidant; Antifungal | Microbiology/Virology; Others; oxidation-reduction |
(-)-Fenchone 是一种双环单萜类化合物,广泛分布于植物中,可从Foeniculum vulgare 和Peumus boldus 中提取。(-)-Fenchone 具有广泛的生物活性,包括抗氧化,伤口愈合,止泻,抗真菌,抗伤害感受和支气管扩张剂活性。(-)-Fenchone 是一种潜在的抗肿瘤化合物。 | |||
TN6926 |
Paeonoside
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Others | Others |
Paeonoside 发现与P. suffruticosa 中,具有生物活性,可以促进成骨细胞分化过程中的伤口愈合和迁移。Paeonoside 具有一定的抗糖尿病活性,可防止脓毒症和败血症引起的死亡。Paeonoside 对 MC3T3-E1细胞的前成骨细胞没有细胞毒性作用,以剂量依赖性的方式显著恢复伤口区域并促进细胞迁移和促进碱性磷酸酶(ALP)染色及其活性。 | |||
T3O2749 |
L-Leucine
(S)-Leucine,Leu,L-亮氨酸,亮氨酸 |
mTOR | PI3K/Akt/mTOR signaling |
L-Leucine ((S)-Leucine) 是必需的支链氨基酸,能够激活 mTOR 信号通路。 | |||
T5S2347 |
Deoxyshikonin
去氧紫草素,Arnebin 7 |
Others; HIF/HIF Prolyl-Hydroxylase; Antibacterial | Chromatin/Epigenetic; Metabolism; Microbiology/Virology; Others |
Deoxyshikonin (Arnebin 7) 是从紫草中分离的天然产物,具有抗肿瘤活性,在体外具有促血管生成作用。它和没食子酸十二烷基酯在体内外均与青霉素有显着的协同抗菌活性。 | |||
TN6872 |
Trypsin
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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。 | |||
T13559 | Astragaloside VI | EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Astragaloside VI could improve wound healing by activating the EGFR/ERK signaling pathway. | |||
TN6495 | 3,4-O-dimethylcedrusin | ||
3′,4-O-Dimethylcedrusin can improve wound healing in vivo by stimulating the formation of fibroblasts and collagen. | |||
T4454 |
Traumatic Acid
Dodec-2-Enedioic Acid,2E-Dodecenedioic Acid,愈伤酸,Trans-2-Dodecenedioic Acid |
Antioxidant | oxidation-reduction |
Traumatic Acid (Dodec-2-Enedioic Acid) 是一种单不饱和二元羧酸,从菜豆中分离得到。它可减少膜磷脂的过氧化,并表现出抗氧化和对胶原生物合成的刺激作用。它可用于许多与胶原蛋白生物合成障碍和氧化应激有关的皮肤疾病的研究。 | |||
TN5044 |
Specioside
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Others | Others |
Specioside has antioxidant, analgesic, anti-dyspeptic, astringent, liver stimulating and wound healing activities. It ameliorates oxidative stress and promotes longevity in Caenorhabditis elegans. | |||
T81322 |
Quercetin-3-O-[(6-caffeoyl)-β-glucopyranosyl (1→3) α-rhamnopyranoside]-7-O-α-rhamnopyranoside
|
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Quercetin-3-O-[(6-caffeoyl)-β-glucopyranosyl (1→3) α-rhamnopyranoside]-7-O-α-rhamnopyranoside,一种具备伤口愈合活性的化合物,可从Ophioglossum vulgatumL地上部分分离得到。 | |||
T78490 |
Polygalacturonic acid
Galacturonic acid polymer |
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Polygalacturonic acid(Galacturonic acid polymer)为透明胶状物,构成细胞壁关键组分。该酸应用于制备银纳米颗粒(AgNPs),充当抗氧化剂与抗炎剂,防护细胞遭受ROS增高引起的损伤,并促进伤口愈合。Polygalacturonic acid纳米颗粒亦显示抗菌性能。 |