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Search Results for " ischemia-reperfusion "

86

抑制剂 & 化合物

19

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Cat. No. Product Name Target Signaling Pathways
T9073 SRS16-86

Ferroptosis Apoptosis
SRS16-86 是一种铁死亡抑制剂,可研究肾缺血再灌注损伤和脊髓损伤。它在体内比 Ferrostatin-1 对代谢和血浆更稳定。
T22537 9-Phenanthrol

TRP/TRPV Channel Membrane transporter/Ion channel
9-Phenanthrol 是瞬时受体电位 melastatin 4 (TRPM) 通道的抑制剂,这是一种 Ca2+ 激活的非选择性阳离子通道。
T3102 NS-1619

Apoptosis; Potassium Channel Apoptosis; Membrane transporter/Ion channel
NS 1619 是 Ca2+激活的 K+(BK) 通道的激活剂,是一种高效的松弛剂,在血管和其他组织的几个平滑肌中的 EC50约为 10 – 30 μM。它抑制A2780卵巢癌细胞增殖并诱导细胞凋亡。
T9232 Mitochondrial fusion promoter M1

Mitochondrial Metabolism Metabolism
Mitochondrial fusion promoter M1 是一种线粒体动态调节剂,能够保持线粒体功能并促进细胞呼吸,减轻心肌缺血/再灌注大鼠的心脏损伤和大脑损伤。
T9714 Atpenin A5

Potassium Channel Membrane transporter/Ion channel
Atpenin A5 是高度特异性的complex II 抑制剂,IC50为 ~10 nM。Dolastatin 10也是有效的mKATP 通道激动剂,具有心脏保活的作用。
T4612 NS309

EGFR; Potassium Channel; HER Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors
NS309 是选择性钙依赖性钾离子通道 SK/IK 的激活剂,在 BK 通道上没有激活作用。
T24109 GSK329

GSK 329,GSK-329

Others Others
GSK329 是一种有效的选择性 TNNI3 相互作用激酶 (TNNI3K) 抑制剂。 GSK329 在缺血/再灌注心脏损伤模型中表现出积极的心脏保护作用。
T2058 Palosuran

ACT-058362

GPR Endocrinology/Hormones; GPCR/G Protein
Palosuran (ACT-058362) 是人类 UT 受体的新型强效特异性拮抗剂,对表达人重组受体的 CHO 细胞膜的IC50值为 3.6 nM。它可改善糖尿病大鼠的胰腺和肾脏功能。
T9765 TJ-M2010-5

MyD88 Immunology/Inflammation
TJ-M2010-5 是一种 MyD88 抑制剂,可与 TIR 结构域结合以干扰其同源二聚化并抑制 MyD88 信号传导。 TJ-M2010-5 可用于心肌缺血/再灌注损伤研究。
T1677L Montelukast sodium

MK0476,孟鲁司特钠

Leukotriene Receptor; LTR GPCR/G Protein; Immunology/Inflammation
Montelukast sodium (MK0476) 是可口服的半胱氨酸白三烯受体1 选择性拮抗剂,可用于研究预防哮喘和肝损伤。它还可减少心脏损伤,在肠缺血-再灌注损伤中也具有抗氧化作用。
T14186 17-ODYA

17-十八炔酸,Alkynyl Stearic Acid

Others; PROTAC Linker Others; PROTAC
17-ODYA (Alkynyl Stearic Acid) 是 CYP450 ω-羟化酶抑制剂。它能够抑制与花生四烯酸孵育的大鼠肾皮质微粒体形成 20-HETE 、dihydroxyeicosatrienoic acids、epoxyeicosatrienoic acids。它可以改善异丙肾上腺素诱导的培养心肌细胞凋亡和坏死。
T21334 Bucillamine

DE-019,Thiobutarit,Tiobutarit,布西拉明,SA96,DE 019,DE019

VEGFR; Antioxidant Angiogenesis; oxidation-reduction; Tyrosine Kinase/Adaptors
Bucillamine (DE019) 可防止高危器官移植中的缺血/再灌注损伤,抑制 VEGF 的产生。 Bucillamine 是一种具有抗风湿和抗血管生成特性的口服活性巯基供体和抗氧化剂。 Bucillamine 可用于脉络膜新生血管和类风湿性关节炎的研究。
T6986 Sivelestat

ONO5046,EI546,西维来司他,LY544349

Others; SARS-CoV; Serine Protease Microbiology/Virology; Others; Proteases/Proteasome
Sivelestat (ONO5046) 是一种选择性的中性粒细胞弹性蛋白酶抑制剂,其 IC50值为 44 nM,Ki 值为 200 nM。它有潜力研究 COVID-19 的急性肺损伤、急性呼吸窘迫综合征或弥散性血管内凝血。
T3230 NLRP3-IN-2

5-Chloro-N-(p-sulfamoylphenethyl)-o-anisamide,4-[2-(5-氯-2-甲氧基苯甲酰氨基)乙基]苯磺酰胺,NLRP3 Inflammasome Inhibitor I

NOD-like Receptor (NLR); NOD Immunology/Inflammation; NF-κB
NLRP3-IN-2 (5-Chloro-N-(p-sulfamoylphenethyl)-o-anisamide) 是一种能够合成格列本脲的中间物,对心肌细胞中NLRP3炎症小体的形成具有抑制作用,在小鼠心肌缺血/再灌注后限制梗死面积,且对代谢无影响。
T1677 Montelukast

孟鲁司特,Singular

Leukotriene Receptor; Lipoxygenase; LTR GPCR/G Protein; Immunology/Inflammation; Metabolism
Montelukast (Singular) 是可口服的半胱氨酸白三烯受体1 选择性拮抗剂,可用于研究预防哮喘和肝损伤。它还可减少心脏损伤,在肠缺血-再灌注损伤中也具有抗氧化作用。
T31795 FK-330

LS-192510,FR-260330,FK330,FK 330

NOS Immunology/Inflammation
FK-330(FR-260330) 是一种新型口服活性诱导型一氧化氮合酶抑制剂,具有潜在的抗癌和抗肿瘤活性,可预防大鼠肝移植缺血和再灌注损伤。
T3649 BGP-15

BGP15,BGP-15 2HCl

PARP Chromatin/Epigenetic; DNA Damage/DNA Repair
BGP-15 (BGP-15 2HCl) 是一种PARP 抑制剂,IC50和Ki 值分别为 120 和 57 μM,在缺血再灌注损伤后具有保护作用。
T13603 CDDO-3P-Im

Necroptosis Apoptosis
CDDO-3P-Im 是一种具有口服活性的坏死性凋亡抑制剂,具有化学预防作用。 CDDO-3P-Im 可用于有关缺血/再灌注的研究。
T9180 LUF6096

CF-602

Adenosine Receptor GPCR/G Protein; Neuroscience
LUF6096 (CF-602) 是一种有效的腺苷 A3 受体 (adenosine A3 receptor) 变构增强剂。LUF6096 对任何腺苷受体显示出低正构亲和力。LUF6096 在心肌缺血/再灌注损伤中显示出保护作用。
T28978 Tirilazad mesylate

U-74006 mesylate,U74006 mesylate,U 74006 mesylate,U 74006F mesylate,U-74006F mesylate,U74006F mesylate

Antiviral Immunology/Inflammation
Tirilazad mesylate (U 74006F) 是一种非糖皮质激素,是一种脂质过氧化抑制剂,具有抗病毒活性和神经保护活性。Tirilazad mesylate 能使细胞膜内病灶局限化,可减轻创伤、中风、缺血再灌注损伤引起的脊髓损伤,抑制狗体内毒素的作用,降低了内毒素诱导的肠系膜和肾脏 DO2 比容升高。Tirilazad mesylate 可用于研究神经系统疾病。
T5483 DMX-5804

DMX-5084

MAPK MAPK
DMX-5804 是一种口服有活性的MAP4K4选择性抑制剂,其对人 MAP4K4 的IC50=3 nM,pIC50=8.55。对 MINK1/MAP4K6 (pIC50=8.18) 和 TNIK/MAP4K7 (pIC50=7.96) 的作用相对较弱。它可以提高心肌细胞存活率,降低小鼠的缺血再灌注损伤。
T34268 Raxofelast

IRFI016,IRFI-016,IRFI 016

Raxofelast (IRFI-016) 具有治疗糖尿病并发症和动脉粥样硬化的潜力
T20563 PD-166793

PD-166793-0000,PD 166793,PD166793

MMP Proteases/Proteasome
PD-166793是一种具有口服活性、有效性和选择性的 MMP 抑制剂,对 MMP-2,MMP-3 和 MMP-13 具有抑制作用。PD-166793 在大鼠心力衰竭模型中改善心肌缺血和再灌注损伤。
T23356 Linsidomine hydrochloride

SIN-1 chloride

Others Others
Linsidomine hydrochloride (SIN-1 chloride) 是莫西多明的代谢产物,具有舒张血管、抑制血小板聚集和抗心绞痛的活性。在心肌缺血-再灌注模型中,Linsidomine hydrochloride 减少心肌坏死和再灌注诱导的内皮功能障碍,与海绵体的作用机制涉及一氧化氮的释放有关。
T68879 FK-330 dihydrate

FR-260330 dihydrate

NO Synthase Immunology/Inflammation
FK-330 dihydrate(FR-260330 dihydrate) 是一种新型口服活性诱导型一氧化氮合酶抑制剂,具有潜在的抗癌和抗肿瘤活性,可预防大鼠肝移植缺血和再灌注损伤。
T37379 Protectin D1

Neuroprotectin D1,NPD1

Akt; PI3K Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
Protectin D1 (Neuroprotectin D1) 是神经细胞产生的神经保护素 ,是一种潜在的心脏保护剂。Protectin D1 通过调节 PI3K/AKT 信号通路缓解心肌缺血/再灌注损伤,抑制咪喹莫特诱导的银屑病样皮肤炎症。
T36569 KR-32568

Sodium Channel Membrane transporter/Ion channel
KR-32568是一种钠/氢交换器1(NHE-1)抑制剂(IC50:230 nM)。KR-32568具有强大的心脏保护作用。当使用浓度为10μM 时,它能在离体的缺血大鼠心脏模型中恢复心脏收缩功能。KR-32568(0.3mg/kg)在缺血和再灌注损伤的大鼠模型中减少了心肌梗死的大小。
T38287 C3a Receptor Agonist

C3a receptor agonist 1,C3a受体激动剂,Complement 3a Receptor Agonist

Complement System Immunology/Inflammation
C3a Receptor Agonist (C3a receptor agonist 1) 结合免疫系统补体途径中的G 蛋白偶联C3a 受体(C3aRs)。在肠缺血再灌注损伤模型中,C3aR 的激活可防止中性粒细胞动员。C3aRs 在成年小鼠的神经祖细胞和未成熟神经元上表达。C3a 在体外刺激神经祖细胞的分化。
T50098 TIQ-A

PARP Chromatin/Epigenetic; DNA Damage/DNA Repair
TIQ-A 是一种 PARP1 抑制剂,通过碱基切除修复途径参与 DNA 单链断裂修复。 PARP1 由 DNA 损伤触发,其过度激活已被认为是许多病理状况的致病因素,包括缺血和再灌注损伤、哮喘相关炎症和动脉粥样硬化形成。
T21967 MEG hemisulfate

Mercaptoethylguanidine hemisulfate

NOS Immunology/Inflammation
MEG hemisulfate (Mercaptoethylguanidine hemisulfate) 是一种有效和选择性的诱导型 NO 合酶 (iNOS) 的抑制剂,在组织匀浆中抑制 iNOS,ecNOS 和 bNOS 的 EC50 值分别为 11.5,110 和 60 μM。MEG hemisulfate 也有效的过氧亚硝酸盐清除剂,可抑制过氧亚硝酸盐诱导的氧化过程。MEG hemisulfate 在许多炎症实验模型中具有保护作用,包括缺血/再灌注损伤,牙周炎,失血性休克,炎性肠病以及内毒素和败血性休克。
T9948 NecroX-7

LC-280126,LC28-0126,LC28 0126

NADPH-oxidase Immunology/Inflammation
NecroX-7 (LC-280126) 是一种有效的自由基清除剂和 HMGB1(高迁移率族蛋白 1) 抑制剂。NecroX-7 可以作为对乙酰氨基酚毒性的解毒剂。NecroX-7 通过抑制缺血/再灌注损伤中 HMGB1 的释放发挥保护作用。NecroX-7 抑制 HMGB1 诱导的 TNF 和 IL-6的释放,以及TLR-4和晚期糖基化终产物受体的表达,用于移植物抗宿主病 (GVHD) 研究。
T68878 L-2286

L-2286 is a novel PARP inhibitor. L-2286 exerted significant protective effect against ischemia-reperfusion-induced myocardial injury in both experimental models. More importantly, L-2286 facilitated the ischemia-reperfusion-induced activation of Akt, extracellular signal-regulated kinase, and p38-MAPK in both isolated hearts and in vivo cardiac injury.
T33451 ML 7

ML7,ML-7

ML 7 is an inhibitor of myosin light chain kinase that protects cardiac function from ischemia/reperfusion (I/R) injury.
T37697 D-GsMTx4

D-GsMTx4

TRPC1/6 and Piezo2 inhibitor. Exhibits same effect as L-enantiomer, GsMTx4 (Cat. No. 4912) on TRPC channels. Inhibits mechanosensitive currents by ~70%. Protects against myocardial infarction in mouse ischemia/reperfusion model. Resistant to proteolytic digestion.
T38693 TRC160334

TRC160334

TRC160334 is a hydroxylase inhibitor of hypoxia-inducible factor (HIF). It is employed in research about ischemia/reperfusion injury.
T30512 BMS-284640

UNII-XP87V064PV,CHEMBL51879,XP87V064PV

BMS-284640 is a Na(+)/H(+) exchange agent (NHE) inhibitor that has provided substantial protection in various animal models of myocardial ischemia (MI) and reperfusion in preclinical studies.
T36509 U-74389G

U-74389G,Methylated Tirilazad

U-74389G is an antioxidant which prevents iron-dependent lipid peroxidation. It protects against ischemia-reperfusion injury in animal heart, liver, and kidney models.[1],[2],[3],[4]
T11327 FR 167653

FR 167653 sulfate

p38 MAPK MAPK
FR 167653 (FR 167653 sulfate) is effective in treating inflammation, relieving trauma and ischemia-reperfusion injury in vivo. FR 167653 , an orally active and selective p38 MAPK inhibitor, is a potent suppressor of TNF-α and IL-1β production via specific inhibition of p38 MAPK activity.
TP1373 Ac2-26

Ac2-26 TFA is an active n-terminal peptide in annexin A1 (AnxA1), which can alleviate acute lung injury caused by ischemia-reperfusion.
T39890 8-Bromo-AMP

8-Bromoadenosine 5'-monophosphate,8-Bromo-AMP,8-Bromoadenylicacid

8-Bromo-AMP, also known as 8-Bromoadenosine 5'-monophosphate, is a membrane permeable cAMP analogue. It enhances cardiac recovery from ischemia and reperfusion by elevating ATP, ADP, and total adenine nucleotide concentrations.
T39795 Tricarbonyldichlororuthenium(II) dimer

CORM-2

Tricarbonyldichlororuthenium(II) dimer, a pharmacological CO donor, prevents ischemia/reperfusion (I/R)-induced oxidative damage to the gastric mucosa by enhancing gastric blood flow (GBF) and reducing DNA oxidation and systemic inflammatory response.
T78019 Nangibotide TFA

LR12 TFA

Nangibotide TFA为TREM-1受体抑制剂,调控先天免疫反应。该化合物能降低啮齿动物心肌缺血再灌注模型的系统性及局部炎症。
T15379 GGsTop

Nahlsgen

Others Others
GGsTop is a non-toxic and irreversible inhibitor of γ glutamyl transpeptidase (GGT) (Ki: 170 μM for Human GGT). GGsTop protects hepatic ischemia-reperfusion injury in the rat model. GGsTop shows Kons of 150±10 and 51±3 /(M·s) against E.coli GGT and human GGT, respectively.
T80965 Torapsel

42-89-glycoprotein,WAY164339,pMT21:PL85

Torapsel(42-89-glycoprotein; WAY164339)为一种免疫球蛋白融合蛋白,适用于缺血再灌注损伤预防研究。
T71930 aPKC-I

aPKC-I is an inhibitor of atypical protein kinase C (aPKC ) which inhibits both PKCζ and PKCι with high specificity and prevents VEGF-induced endothelial permeability in cell culture and in vivo, thereby blocking ischemia-reperfusion (IR)-induced permeability.
T72007 COR167

COR167 is a CB2 agonist. It displayed potent immunomodulatory activity on immune cells from healthy subjects and patients with multiple sclerosis. It also showed protective effects on rat brain tissues toward ischemia and reperfusion-induced injury. COR167 has antinociceptive properties.
T11327L FR 167653 free base

Others Others
FR 167653 free base is an orally active p38 MAPK inhibitor and is effective in treating inflammation, relieving trauma, and ischemia-reperfusion injury in vivo. It also is a potent suppressor of TNF-α and IL-1β production via specific inhibition of p38 MA
T72281 Caspase-9 Inhibitor III

Ac-LEHD-cmk

Caspase-9 Inhibitor III (Ac-LEHD-cmk) 是一种 caspase-9抑制剂。Caspase-9 Inhibitor III 对局部缺血-重新灌注诱导的心肌损伤表现出保护作用。
T63649 Ned-K

Ned-K 是一种烟酸腺嘌呤二核苷酸磷酸 (NAADP) 拮抗剂,对心肌缺血和再灌注 (sIR) 诱导的钙振荡表现出抑制作用。
TP1321 Ac2-26 TFA (151988-33-9 free base)

Ac2-26 TFA

Ac2-26 TFA, an active N-terminal peptide of annexin A1 (AnxA1), attenuates ischemia-reperfusion-induced acute lung injury. Ac2-26 also decreases AnxA1 protein expression, inhibits the activation of NF-κB and MAPK pathways in the injured lung tissue.

化合物

SRS16-86
Cat.No: T9073
Synonym:
Target: Ferroptosis
9-Phenanthrol
Cat.No: T22537
Synonym:
Target: TRP/TRPV Channel
NS-1619
Cat.No: T3102
Synonym:
Target: Apoptosis, Potassium Channel
Mitochondrial fusion promoter M1
Cat.No: T9232
Synonym:
Target: Mitochondrial Metabolism
Atpenin A5
Cat.No: T9714
Synonym:
Target: Potassium Channel
NS309
Cat.No: T4612
Synonym:
Target: EGFR, Potassium Channel, HER
GSK329
Cat.No: T24109
Synonym: GSK 329,GSK-329
Target: Others
Palosuran
Cat.No: T2058
Synonym: ACT-058362
Target: GPR
TJ-M2010-5
Cat.No: T9765
Synonym:
Target: MyD88
Montelukast sodium
Cat.No: T1677L
Synonym: MK0476,孟鲁司特钠
Target: Leukotriene Receptor, LTR
17-ODYA
Cat.No: T14186
Synonym: 17-十八炔酸,Alkynyl Stearic Acid
Target: Others, PROTAC Linker
Bucillamine
Cat.No: T21334
Synonym: DE-019,Thiobutarit,Tiobutarit,布西拉明,SA96,DE 019,DE019
Target: VEGFR, Antioxidant
Sivelestat
Cat.No: T6986
Synonym: ONO5046,EI546,西维来司他,LY544349
Target: Others, SARS-CoV, Serine Protease
NLRP3-IN-2
Cat.No: T3230
Synonym: 5-Chloro-N-(p-sulfamoylphenethyl)-o-anisamide,4-[2-(5-氯-2-甲氧基苯甲酰氨基)乙基]苯磺酰胺,NLRP3 Inflammasome Inhibitor I
Target: NOD-like Receptor (NLR), NOD
Montelukast
Cat.No: T1677
Synonym: 孟鲁司特,Singular
Target: Leukotriene Receptor, Lipoxygenase, LTR
FK-330
Cat.No: T31795
Synonym: LS-192510,FR-260330,FK330,FK 330
Target: NOS
BGP-15
Cat.No: T3649
Synonym: BGP15,BGP-15 2HCl
Target: PARP
CDDO-3P-Im
Cat.No: T13603
Synonym:
Target: Necroptosis
LUF6096
Cat.No: T9180
Synonym: CF-602
Target: Adenosine Receptor
Tirilazad mesylate
Cat.No: T28978
Synonym: U-74006 mesylate,U74006 mesylate,U 74006 mesylate,U 74006F mesylate,U-74006F mesylate,U74006F mesylate
Target: Antiviral
DMX-5804
Cat.No: T5483
Synonym: DMX-5084
Target: MAPK
Raxofelast
Cat.No: T34268
Synonym: IRFI016,IRFI-016,IRFI 016
Target:
PD-166793
Cat.No: T20563
Synonym: PD-166793-0000,PD 166793,PD166793
Target: MMP
Linsidomine hydrochloride
Cat.No: T23356
Synonym: SIN-1 chloride
Target: Others
FK-330 dihydrate
Cat.No: T68879
Synonym: FR-260330 dihydrate
Target: NO Synthase
Protectin D1
Cat.No: T37379
Synonym: Neuroprotectin D1,NPD1
Target: Akt, PI3K
KR-32568
Cat.No: T36569
Synonym:
Target: Sodium Channel
C3a Receptor Agonist
Cat.No: T38287
Synonym: C3a receptor agonist 1,C3a受体激动剂,Complement 3a Receptor Agonist
Target: Complement System
TIQ-A
Cat.No: T50098
Synonym:
Target: PARP
MEG hemisulfate
Cat.No: T21967
Synonym: Mercaptoethylguanidine hemisulfate
Target: NOS
NecroX-7
Cat.No: T9948
Synonym: LC-280126,LC28-0126,LC28 0126
Target: NADPH-oxidase
L-2286
Cat.No: T68878
Synonym:
Target:
ML 7
Cat.No: T33451
Synonym: ML7,ML-7
Target:
D-GsMTx4
Cat.No: T37697
Synonym: D-GsMTx4
Target:
TRC160334
Cat.No: T38693
Synonym: TRC160334
Target:
BMS-284640
Cat.No: T30512
Synonym: UNII-XP87V064PV,CHEMBL51879,XP87V064PV
Target:
U-74389G
Cat.No: T36509
Synonym: U-74389G,Methylated Tirilazad
Target:
FR 167653
Cat.No: T11327
Synonym: FR 167653 sulfate
Target: p38 MAPK
Ac2-26
Cat.No: TP1373
Synonym:
Target:
8-Bromo-AMP
Cat.No: T39890
Synonym: 8-Bromoadenosine 5'-monophosphate,8-Bromo-AMP,8-Bromoadenylicacid
Target:
Tricarbonyldichlororuthenium(II) dimer
Cat.No: T39795
Synonym: CORM-2
Target:
Nangibotide TFA
Cat.No: T78019
Synonym: LR12 TFA
Target:
GGsTop
Cat.No: T15379
Synonym: Nahlsgen
Target: Others
Torapsel
Cat.No: T80965
Synonym: 42-89-glycoprotein,WAY164339,pMT21:PL85
Target:
aPKC-I
Cat.No: T71930
Synonym:
Target:
COR167
Cat.No: T72007
Synonym:
Target:
FR 167653 free base
Cat.No: T11327L
Synonym:
Target: Others
Caspase-9 Inhibitor III
Cat.No: T72281
Synonym: Ac-LEHD-cmk
Target:
Ned-K
Cat.No: T63649
Synonym:
Target:
Ac2-26 TFA (151988-33-9 free base)
Cat.No: TP1321
Synonym: Ac2-26 TFA
Target:
Cat. No. Product Name Target Signaling Pathways
T3672 Nomilin

MAPK MAPK
Nomilin 是一种柠檬苦素类化合物,从柑桔类提取物中获得,是抗肥胖症和降糖药。
TN1895 Luteolinidin chloride

CD38 Immunology/Inflammation
Luteolinidin chloride 是天然的脱氧花青素,分离自苔藓和蕨类植物中。它是一种有效的 CD38 抑制剂,可以保留 eNOS 功能并预防体内内皮功能障碍,同时可以保护心脏免受 I/R 损伤。
TN6490 Regaloside C

Others Others
Regaloside C 是一种从百合属的中分离出来的甘油葡糖苷,具有抗炎作用。
T3890 Verbenalin

Verbenalol β-D-glucopyranoside,马鞭草苷,Verbenaloside,Verbenalol glucoside,Cornin

Others Others
Verbenalin (Verbenaloside) 是马鞭草苷,具有抗炎、抗真菌、抗病毒等活性。它能减轻脑缺血再灌注损伤。它可用于前列腺炎的研究。
T2163 Dihydrocapsaicin

CCRIS1589,二氢辣椒素,6,7-Dihydrocapsaicin,8-Methyl-N-vanillylnonanamide

Others; TRP/TRPV Channel Membrane transporter/Ion channel; Others
Dihydrocapsaicin (CCRIS1589) 是一种天然来源的辣椒素,是TRPV1的选择性激动剂,同时可以增加 p-Akt 水平。它可以增强低温诱导的神经保护。
TN4661 Nodosin

IL Receptor; Autophagy Autophagy; Immunology/Inflammation
Nodosin 是一种二萜化合物,从Isodon trichocarpusKudo 和I. JaponicusHARA 中提取得到。
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。
T5S2178 Fargesin

辛夷脂素,(+/-)-Fargesin

Adrenergic Receptor GPCR/G Protein; Neuroscience
Fargesin ((+/-)-Fargesin) 是一种活性新木脂素,从木兰植物中分离得到,具有抗高血压和抗炎活性。
T2S0500 Ilexsaponin A

毛冬青皂苷A,毛冬青皂苷甲,Ilexsaponin A1

Others Others
Ilexsaponin A (Ilexsaponin A1)1 是分离自冬凌草的根中,利用抗凋亡途径减轻缺血再灌注引起的心肌损伤。它能够减少心肌梗塞的大小,减少 LDH,AST 和 CK-MB 的血清水平,促进细胞活力并抑制缺氧/复氧心肌细胞的凋亡。
T3900 Emodin-8-glucoside

大黄素-8-β-D-吡喃葡萄糖苷,Emodin glucoside B,Anthraglycoside B

Others Others
Emodin-8-glucoside (Anthraglycoside B) 是从芦荟中分离出的蒽醌衍生物,与 DNA 的小沟结合。它具有保护缺血和再灌注引起的局灶性脑损伤的作用。它直接刺激成骨细胞的细胞增殖和分化。
T3388 Calycosin-7-O-β-D-glucoside

毛蕊异黄酮苷,calycosin-7-O-beta-D-glucopyranoside,Calycosin-7-O-beta-D-glucoside

MMP; Reactive Oxygen Species Immunology/Inflammation; Metabolism; NF-κB; Proteases/Proteasome
Calycosin-7-O-β-D-glucoside (calycosin-7-O-beta-D-glucopyranoside) 是一种异黄酮,从黄芪中分离得到。它具有多种生物活性,包括心脏保护、神经保护、抗炎和抗氧化作用。
T4518 Licochalcone D

ERK; NF-κB MAPK; NF-κB
Licochalcone D 是一种 NF-κB p65的有效抑制剂,是一种存在于 Glycyrrhiza inflate 中的黄酮类化合物,具有抗氧化、抗炎、抗癌等作用。
T3893 Forsythoside B

连翘酯苷 B,连翘脂苷B

TNF; NF-κB Apoptosis; NF-κB
Forsythoside B 是传统中药植物独一味叶子中分离的一种苯乙醇苷。它可抑制 TNF-alpha,IL-6,IκB, 调节 NF-κB。它抑制炎症反应,具有抗氧化和神经保护作用。
T3779 Crocin II

Crocin 2,西红花苷II,Crocetin gentiobiosylglucosyl ester,藏红花,Tricrocin,Crocin B

Caspase; COX; NO Synthase Apoptosis; Immunology/Inflammation; Neuroscience; Proteases/Proteasome
Crocin II (Crocetin gentiobiosylglucosyl ester) 是从栀子果实中分离出来的一种天然产物,具有抗氧化、抗癌和抗抑郁活性。它抑制 iNOS 和 COX-2的蛋白质和 m-RNA 的表达,还抑制NO 产生,IC50值为 31.1 μM。
TN1618 Erigeroside

Others Others
Erigeroside has the protective effects on cerebral ischemia-reperfusion injury in rat, its ability of anti-oxidation and scavenging oxidation free radical may be one of its protective mechanisms.
TN1431 Baohuoside VII

宝藿苷,宝藿苷VII

Others Others
Baohuoside aglycone possesses cardioprotective effect in prevention of ischemia/ reperfusion injury and reduce the myocardial infraction, the mechnism is due to the reduction of the injury of free radicals. Baohuoside VII in vivo exhibits significant anti
T1208 Citicoline sodium

Citicoline sodium salt,CDP-choline,胞磷胆碱钠

Apoptosis; Others; Endogenous Metabolite Apoptosis; Metabolism; Others
Citicoline sodium (CDP-choline) 是一种合成细胞膜组分磷脂酰胆碱的中间体,有神经保护作用。
TN3914 Echinatine

ATPase; IL Receptor; TNF Apoptosis; Immunology/Inflammation; Membrane transporter/Ion channel
Echinatin exerts a protective effect against ischemia/reperfusion (I/R)-induced myocardial injury on hearts, this effect may be attributed to the antioxidant and anti-inflammatory activities of this compound. Echinatin can inhibit DNP-ATPase activity whil
T36448 (E)-Ajoene

(E)-Ajoene is a disulfide that has been found inA. sativumand has diverse biological activities.1,2,3,4It is active against Gram-positive and Gram-negative bacteria (MICs = 10-250 and 150->500 μg/ml, respectively) and fungi (MICs = 15-50 μg/ml).1(E)-Ajoene inhibits proliferation of a variety of cancer cells, including MDA-MB-231 breast, HeLa cervical, and WHCO1 esophageal cancer cells (IC50s = 18.6, 61, and 39.2 μM, respectively).2It also inhibits human glutathione reductase andT. cruzitrypanoth...

天然产物

Nomilin
Cat.No: T3672
Synonym:
Target: MAPK
Luteolinidin chloride
Cat.No: TN1895
Synonym:
Target: CD38
Regaloside C
Cat.No: TN6490
Synonym:
Target: Others
Verbenalin
Cat.No: T3890
Synonym: Verbenalol β-D-glucopyranoside,马鞭草苷,Verbenaloside,Verbenalol glucoside,Cornin
Target: Others
Dihydrocapsaicin
Cat.No: T2163
Synonym: CCRIS1589,二氢辣椒素,6,7-Dihydrocapsaicin,8-Methyl-N-vanillylnonanamide
Target: Others, TRP/TRPV Channel
Nodosin
Cat.No: TN4661
Synonym:
Target: IL Receptor, Autophagy
3'-Methoxypuerarin
Cat.No: T4S2084
Synonym: 3'-甲氧基葛根素,3’- Methoxy Puerarin
Target: Antioxidant
Fargesin
Cat.No: T5S2178
Synonym: 辛夷脂素,(+/-)-Fargesin
Target: Adrenergic Receptor
Ilexsaponin A
Cat.No: T2S0500
Synonym: 毛冬青皂苷A,毛冬青皂苷甲,Ilexsaponin A1
Target: Others
Emodin-8-glucoside
Cat.No: T3900
Synonym: 大黄素-8-β-D-吡喃葡萄糖苷,Emodin glucoside B,Anthraglycoside B
Target: Others
Calycosin-7-O-β-D-glucoside
Cat.No: T3388
Synonym: 毛蕊异黄酮苷,calycosin-7-O-beta-D-glucopyranoside,Calycosin-7-O-beta-D-glucoside
Target: MMP, Reactive Oxygen Species
Licochalcone D
Cat.No: T4518
Synonym:
Target: ERK, NF-κB
Forsythoside B
Cat.No: T3893
Synonym: 连翘酯苷 B,连翘脂苷B
Target: TNF, NF-κB
Crocin II
Cat.No: T3779
Synonym: Crocin 2,西红花苷II,Crocetin gentiobiosylglucosyl ester,藏红花,Tricrocin,Crocin B
Target: Caspase, COX, NO Synthase
Erigeroside
Cat.No: TN1618
Synonym:
Target: Others
Baohuoside VII
Cat.No: TN1431
Synonym: 宝藿苷,宝藿苷VII
Target: Others
Citicoline sodium
Cat.No: T1208
Synonym: Citicoline sodium salt,CDP-choline,胞磷胆碱钠
Target: Apoptosis, Others, Endogenous Metabolite
Echinatine
Cat.No: TN3914
Synonym:
Target: ATPase, IL Receptor, TNF
(E)-Ajoene
Cat.No: T36448
Synonym:
Target:
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