84
63
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T23498 |
UNC3230
UNC 3230 |
Others | Others |
UNC3230 是一种 ATP 竞争性的磷脂酰肌醇 4 磷酸 5 激酶 1C 型 (PIP5K1C) 选择性抑制剂,其IC50约为 41 nM。它还可抑制PIP4K2C,但对其他调节磷酸肌醇水平的脂质激酶无抑制作用。它具有缓解疼痛和抗癌特性。 | |||
T6554 |
JZL 184
JZL184 |
Lipase | Metabolism |
JZL 184 是不可逆的、选择性的MAGL 抑制剂,对MAGL 的选择性比 FAAH 高 300 倍以上。它可阻断脑膜中的 2-花生四烯酸甘油酯 (2-AG) 的水解 (IC50为 8 nM)。 | |||
T9461 |
AZ194
|
Sodium Channel | Membrane transporter/Ion channel |
CRMP2-Ubc9-NaV1.7 inhibitor 194 是一流的CRMP2-Ubc9相互作用抑制剂及NaV1.7抑制剂 (IC50=1.2 μM),口服有活性,具有抗伤害作用。AZ194 阻断 CRMP2 的 SUMOylation 以选择性地减少表面表达 NaV1.7 的量。 | |||
T1191L |
Metamizole sodium
安乃近,Analgin,安乃近钠盐(诺瓦经),Dipyron |
COX | Immunology/Inflammation; Neuroscience |
Metamizole sodium (Analgin) 是一种环氧合酶-3 (COX-3) 抑制剂,具有良好的解热作用,可用于缓解疼痛的研究。 | |||
T22733 |
DL-AP5
DL-2-氨基-5-膦酰基缬草酸 |
NMDAR | Neuroscience |
DL-AP5 是选择性 N-甲基-D-天冬氨酸 (NMDA) 受体拮抗剂的外消旋形式,具有抗惊厥作用。 | |||
T15781 |
LP-935509
|
Serine/threonin kinase; AAK1 (AP2 associated kinase 1) | Cell Cycle/Checkpoint; Metabolism; Neuroscience |
LP-935509 是一种选择性的、具有脑渗透的、小分子的衔接蛋白-2 相关激酶1 (AAK1) ATP 竞争性抑制剂,其 IC50=3.3 nM,Ki=0.9 nM。它是一种 BIKE 的有效抑制剂 (IC50=14 nM) 和中度的 GAK 抑制剂 (IC50=320 nM)。它能够逆转 SNL 手术后的疼痛。 | |||
T28118 |
MSP3
MSP-3,MSP 3 |
TRP/TRPV Channel | Membrane transporter/Ion channel |
MSP3 是瞬时受体电位香草素 1 型的激动剂 (EC50 = 0.87 μM) ,具有镇痛和神经保护作用。 | |||
T11516 |
GV-196771A
|
NMDAR | Neuroscience |
GV-196771A 一种新型的NMDA受体甘氨酸位点拮抗剂,具有强大的抗痛觉过敏活性。 | |||
T39284 |
EST73502 HCl
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
EST73502 是 μ-阿片受体激动剂 (Ki = 64 nM) 激动剂和 σ1 受体拮抗剂 (Ki = 118 nM)。 EST73502 显示出镇痛活性。 | |||
T21380 |
Pravadoline
WIN 48098-6,WIN48098-6,普拉朵林,WIN-48098-6 |
Cannabinoid Receptor | GPCR/G Protein |
Pravadoline (WIN48098-6) 是一种 cannabinoid 受体激动剂。 Pravadoline 抑制小鼠大脑中的 PGs 合成,并在受到各种热、化学和机械伤害性刺激的啮齿动物中显示出镇痛活性。 | |||
T23076L |
Nociceptin (1-7) acetate
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Nociceptin (1-7) acetate 是一种有效的阿片受体样受体 1 (ORL1) 受体激动剂。 Nociceptin (1-7) 与 nociceptin 结合可降低痛觉过敏并具有镇痛活性。 | |||
T22051 |
BU 224 hydrochloride
|
Imidazoline Receptor | Neuroscience |
BU 224 hydrochloride 是一种选择性的咪唑啉 I(2) 结合位点配体,具有镇痛和抗抑郁样活性。 | |||
TP1905 |
BW-180C
(D-丙2,D-亮5)-脑啡肽,DADLE |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
BW-180C (DADLE) 是水溶性的多肽类δ-阿片受体激动剂,也对 μ-阿片受体显示活性,在体内表现出镇痛活性。 | |||
TP2036L |
DPDPE TFA (88373-73-3 free base)
DPDPE TFA |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
DPDPE TFA 是选择性 δ-阿片受体激动剂肽,在体内具有镇痛作用。 | |||
TP1212 |
N-Boc-Phe-Leu-Phe-Leu-Phe
Boc-FLFLF |
Others | Others |
N-Boc-Phe-Leu-Phe-Leu-Phe (Boc-FLFLF) 是甲酰肽受体 1(FPR1)拮抗剂,能够增加疼痛作用,抑制膜联蛋白的抗疼痛活性。 | |||
T17309 |
(R)-(-)-Ibuprofen
levibuprofen,(R)-Ibuprofen |
NF-κB | NF-κB |
(R)-(-)-Ibuprofen ((R)-Ibuprofen) 是 Ibuprofen 的 R 型异构体,对 COX 无作用,可以抑制 NF-κB 的活化;(R)-(-)-Ibuprofen 具有抗炎作用,可用于缓解疼痛的研究。 | |||
T10593 |
BPR1M97
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
BPR1M97 是一种具有血脑屏障渗透性和有效性的 mu 阿片受体(MOP)和神经肽-啡肽 FQ(NOP)受体激动剂,对 MOP 的 Kis 值为1.8 nM,对 NOP 的Kis 值为 4.2 nM。BPR1M97 具有抗伤害作用和抗痛觉作用。 | |||
T22037 |
AS 1892802
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
AS 1892802是一种强效和选择性的ROCK 抑制剂。AS 1892802 用于人ROCK2、大鼠ROCK2和人ROCK1的 IC50值分别为52nM、57nM 和122nM。AS 1892802的镇痛作用起效速度与曲马多和双氯芬酸的起效速度一样快。 | |||
T0678 |
Amitriptyline hydrochloride
Amitriptyline HCl,Tryptizol,盐酸阿米替林,Domical,Annoyltin |
Trk receptor; Sigma receptor; 5-HT Receptor; Serotonin Transporter; Sodium Channel; Adrenergic Receptor; AChR; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience; Tyrosine Kinase/Adaptors |
Amitriptyline hydrochloride (Annoyltin) 是血清素再摄取转运体和去甲肾上腺素再摄取转运体抑制剂,还与多巴胺再摄取转运体结合,其Ki 为 2.58 μM。它也抑制肾上腺素能受体、毒蕈碱受体、组胺受体、5-羟色胺受体。它是TrkA 和TrkA 受体的激动剂,具有强神经营养活性和有抗抑郁作用。 | |||
TP1404L |
Hemorphin-7 acetate(152685-85-3 free base)
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Hemorphin-7 acetate(152685-85-3 free base) 是一种 hemorphin 肽,一种源自血红蛋白 β 链的内源性阿片肽。 Hemorphin 肽具有镇痛和抗高血压活性,可激活阿片受体并抑制血管紧张素转换酶 (ACE)。 | |||
T10572 |
BMT-124110
|
AAK1 (AP2 associated kinase 1) | Neuroscience |
BMT-124110是一种具有选择性的AAK1抑制剂(IC50: 0.9 nM),具有抗伤害感受活性。BMT-090605抑制BMP -2诱导蛋白激酶BIKE,其IC50为 17 nM。BMT-090605抑制细胞周期蛋白 G 相关激酶GAK,其IC50:为99 nM。 | |||
T34081 |
Piromelatine
NEU-P-11,NEU-P 11,NEU-P11 |
P2X Receptor; 5-HT Receptor; MT Receptor; Sodium Channel; TRP/TRPV Channel | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Piromelatine 是褪黑激素 MT1/MT2 受体、5-HT1A 和 5-HT1D 的激动剂,也是 5-HT2B 的拮抗剂。Piromelatine 具有抗痛觉活性,对 P2X3、TRPV1 和 Nav1.7 通道有抑制作用,可用于促进睡眠、缓解疼痛、抗神经退行性疾病和抗抑郁疾病的研究。 | |||
TP1179L |
Porcine dynorphin A(1-13) acetate
Dynorphin A Porcine Fragment 1-13 acetate,Porcine dynorphin A(1-13) acetate(72957-38-1 free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Porcine dynorphin A(1-13) acetate (Dynorphin A Porcine Fragment 1-13 acetate)(72957-38-1 free base) 是一种有效的内源性 κ opioid 受体激动剂,在生理浓度下具有镇痛作用。暴露于强啡肽 A (1-13) 会导致单个神经元中 [Ca2+]i 的急剧增加,类似于急性 NMDA 治疗所见的增加。 | |||
TP1559L |
Ziconotide Acetate (107452-89-1 free base)
醋酸齐考诺肽,Prialt,Ziconotide Acetate |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Ziconotide Acetate (107452-89-1 free base) (Prialt) 是一种镇痛剂,已用于治疗神经性和非神经性疼痛。 Ziconotide 通过与位于伤害感受通路初级传入神经元末端部分的 N 型钙通道结合起作用,因此通过有效的镇痛作用减少突触传递。 | |||
TP1901L1 |
Hemopressin (rat) acetate(568588-77-2 free base)
|
Cannabinoid Receptor | GPCR/G Protein |
Hemopressin (rat) acetate(568588-77-2 free base) 是一种衍生自血红蛋白 α1 链的九肽,起初是从大鼠脑匀浆中分离出来的。 Hemopressin 是 CB2 大麻素受体的口服活性、选择性和反向激动剂。 Hemopressin 在炎性疼痛模型中发挥镇痛作用。 | |||
T4436 |
RO1138452
CAY10441 |
Others; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Others |
RO1138452 (CAY10441) 是一种选择性和可口服的前列环素受体拮抗剂,pKi 为8.3。它拮抗卡前列环素诱导的人神经母细胞瘤腺苷酸环化酶的激活,以剂量依赖性方式阻断环 AMP 积累,具有镇痛活性。 | |||
T8414 |
SNC 80
Snc-80,SNC80,NIH 10815 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
SNC 80 (NIH 10815) 是有效的,高度选择性的非肽类 δ 阿片 (δ-opioid) 受体激动剂,Ki 为1.78 nM,IC50 为 2.73 nM。SNC80 还以 EC50 为 52.8 nM 来选择性激活 HEK293 细胞中的 μ-δ 异聚体。SNC80 具有抗伤害性,抗痛觉过敏和抗抑郁样作用,并可用于多种头痛症的研究。 | |||
TP1900L1 |
Hemopressin (human, mouse) acetate
Hemopressin (human, mouse) acetate(1314035-51-2 free base) |
Cannabinoid Receptor | GPCR/G Protein |
Hemopressin (human, mouse) acetate(1314035-51-2 free base) 是一种衍生自血红蛋白 α1 链的九肽,是从大鼠脑匀浆中分离出来的。 Hemopressin 是 CB1 大麻素受体的口服活性、选择性和反向激动剂。 Hemopressin 在炎性疼痛模型中发挥镇痛作用。 | |||
T27363 |
FR 64822
FR-64822,FR64822 |
||
FR64822(N-(4-pyridylcarbamoyl)amino 1,2,3,6,-tetrahydropyridine), a novel non-opioid antinociceptive compound, displays antinociceptive activities in a variety of assays with mice and rats. It has a strong antinociceptive activity in the acetic acid writh | |||
T23580 |
20681-S
20681 S |
||
20681-S has narcotic antagonistic properties and antinociceptive. | |||
T69134 | Metanicotine | ||
Metanicotine is a selective nicotinic agonist with antinociceptive properties. | |||
T69847 |
O-1057 free base
|
||
O-1057 free base is a water-soluble cannabinoid receptor agonist with antinociceptive properties. RESEARCH USE ONLY. | |||
T20912 |
DBO-83
DBO83 |
||
DBO-83, an agonist of nicotinic acetylcholine receptors (nAChRs), has anti-amnesic and antinociceptive activities. | |||
T70728 |
Vadaclidine
|
||
Vadaclidine is an orally acting antinociceptive muscarinic agonist. | |||
T69848 | O-1057 hydrochloride | ||
O-1057 hydrochloride is a water-soluble cannabinoid receptor agonist with antinociceptive properties. RESEARCH USE ONLY. | |||
T11721L | JDTic dihydrochloride | JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
JDTic is a potent antagonist of kappa-opioid receptors (KOR), blocking the κ-agonist U50, 488-induced antinociception. | |||
T25490 |
Hemorphin 4
Tyr-pro-trp-thr |
||
Hemorphin 4 is an endogenous opioid peptide of the hemorphin family which has antinociceptive properties and is derived from the β-chain of hemoglobin in the bloodstream. | |||
T27968 |
M-5011
T-3788,S-MTPPA,M 5011,M-5011C |
||
M-5011 is a non-steroidal anti-inflammatory drug and immunomodulator potentially for the treatment of inflammation and pain. M-5011 had an effective antinociceptive activity (ED50 value) of 0.63 mg/kg. M-5011 partially inhibits the generalized bone loss a | |||
T28516 |
ReN-1869
NNC-05-1869,NNC 05-1869,NNC-051869,ReN 1869 |
||
ReN-1869 is a histamine H1 receptor antagonist. ReN 1869 is active against inflammation and neurogenic pain. ReN-1869 produces potent and selective antinociceptive effects on dorsal horn neurons after inflammation and neuropathy. | |||
T61708 | AZD 2066 hydrate | ||
AZD 2066 hydrate is a selective, orally active, and brain-penetrant antagonist of mGluR5. It exhibits antinociceptive effects [1]. | |||
T28495 |
R-84760 hydrochloride
R84760,R 84760,R 86436,R-86436,R86436 |
||
R-84760 is a κ-opioid receptor agonist. R-84760 produces an extremely potent antinociceptive effect against tonic pain through the kappa-opioid receptors; the sites of action of subcutaneously administered R-84760 are the supraspinal and spinal loci in th | |||
T70292 |
DDPM-2571 HCl
|
||
DDPM-2571 is a highly potent and in vivo active inhibitor of GABA transporter subtype 1 with anticonvulsant, anxiolytic, antidepressant and antinociceptive properties. DDPM-2571 was quickly distributed into the brain and was highly effective in the prevention of chemically-induced seizures (pentylenetetrazole and pilocarpine models) and 6-Hz convulsions. It demonstrated significant anxiolytic-like and antidepressant-like properties. DDPM-2571 had antinociceptive properties, both in the hot plate... | |||
TP2118 |
SNX-482
SNX 482 |
||
Potent and selective, voltage-dependent R-type CaV2.3 calcium channel blocker (IC50 = 30 nM). Antinociceptive; inhibits nociceptive C-fibre and Aδ-fibre-evoked neuronal responses. | |||
T68206 | Arbortristoside A | ||
Arbortristoside A is an anti-inflammatory and antinociceptive. This activity may be due to the inhibiting effect of prostaglandin, histamine and serotonin. Arbortristoside A has also been shown to act on ulcerations and may facilitate healing of peptic ulcers. | |||
T72151 |
(D-Met2,Pro5)-Enkephalinamide
|
||
(D-Met2,Pro5)-Enkephalinamide 是一种强效的阿片类激动剂,其具有抗痛活性。 | |||
T15165 |
DPI-3290
Org 41793 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
DPI-3290 is a specific agonist of opioid receptors (Ki: 0.18 nM, 0.46 nM, and 0.62 nM for δ-, μ-, and κ-opioid receptors, respectively) with potent antinociceptive activity. DPI-3290 is one of a series of novel centrally acting agents. | |||
TP1529 |
Galanin (1-19), human
|
||
Galanin (1-19), human, represents the fragment encompassing amino acids 1 to 19 of the human galanin neuropeptide. Galanin (GAL) is known for its extensive distribution and multifaceted biological roles, such as regulating hormone secretion, providing antinociceptive effects, and altering feeding behavior. | |||
T14691 | BMT-090605 | Others | Others |
BMT-090605 is a potent, selective AAK1 inhibitor, with an IC50 of 0.6 nM. BMT-090605 inhibits BMP-2-inducible protein kinase (BIKE) and Cyclin G-associated kinase (GAK) with IC50s of 45 and 60 nM, respectively[1]. BMT-090605 shows antinociceptive activity | |||
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. | |||
T73307 | TrkA-IN-4 | ||
TrkA-IN-4 是一种有效和具有口服活性的 TrkA 变构抑制剂,是TrkA-IN-3 的前药。TrkA-IN-4 显示出有效的抗伤害作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7907 |
7-Methoxyflavone
|
Others | Others |
7-Methoxyflavone 是一种分离自 Zornia brasiliensis 的化合物。它能够抑制福尔马林疼痛反应神经源期的舔爪时间 (65.6%),有外周镇痛活性,但不影响炎症期的伤害性反映。 | |||
T6S1010 |
Allomatrine
槐定碱,别苦参碱 |
Others | Others |
Allomatrine 是一种来源槐花树皮的生物碱。它能够激活 κ-阿片受体,进而产生缓解疼痛的作用。 | |||
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。 | |||
T7052 |
Gnetol
|
Tyrosinase; COX; HDAC; AChR | Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Neuroscience; Proteases/Proteasome |
Gnetol 是从买麻藤的根中分离出来的一种酚类。它是酪氨酸酶抑制剂,对鼠酪氨酸酶的 IC50为 4.5 μM,可抑制黑色素的生物合成。它有效抑制 COX-1和 HDAC,具有抗氧化、抗增殖、抗癌和保肝活性,还具有浓度依赖性的 α-淀粉酶、α-葡萄糖苷酶和脂肪形成活性。 | |||
T3254 |
PHYTOL
植醇,trans-Phytol,(E)-Phytol |
Antibacterial; PPAR; Parasite | DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
PHYTOL (trans-Phytol) 是一种从叶绿素中提取的二萜醇,广泛应用于食品添加剂和医药领域,具有很好的抗血吸虫特性。它具有抗伤害、抗氧化、抗炎、抗过敏等作用。它对结核分枝杆菌和金黄色葡萄球菌具有抗菌活性。 | |||
T6S1653 |
Albiflorin
Alibiflorin,芍药内酯苷 |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Albiflorin (Alibiflorin) 是一种牡丹根中的主要成分,是一种单萜糖苷。它具有神经保护、抗炎、抗氧化和缓解疼痛作用。 | |||
T8014 |
Epoxylinalool
氧化芳樟醇,2-(2-Hydroxy-2-Propyl)-5-Methyl-5-Vinyltetrahydrofuran |
Others | Others |
Epoxylinalool (2-(2-Hydroxy-2-Propyl)-5-Methyl-5-Vinyltetrahydrofuran) 是一种天然存在的单萜醇,广泛用于香水和调味品的生产。 | |||
T5S2360 |
Corydaline
Corydalin,紫堇碱,延胡索甲素,(+)-Corydaline |
P450; Virus Protease; Opioid Receptor; AChE | Endocrinology/Hormones; GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience |
Corydaline (Corydalin) 是从 Corydalis yanhusuo 提取的一种异喹啉生物碱,是一种新型促动力植物药的主要活性成分之一。它促进胃排空和小肠转运,促进胃的调节,具有抗乙酰胆碱酯酶、抗过敏和镇痛活性。 | |||
T0437 |
Inosine
INO 495,NSC 20262,肌苷 |
ROS; Endogenous Metabolite; Adenosine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Inosine (NSC-20262) 是由腺苷分解代谢产生的一种内源性嘌呤核苷,是腺苷受体A1R 和A2AR 的激动剂,具有抗炎免疫调节,抗伤害和神经保护作用。 | |||
T5S1882 |
Songorine
准葛尔乌头碱,Napellonine,Zongorine,Bullatine G |
Others; GABA Receptor | Membrane transporter/Ion channel; Neuroscience; Others |
Songorine (Napellonine) 是从乌头属中分离出的一种二萜生物碱,具有抗癌、抗心律不齐和抗炎活性。它是大鼠脑中的GABAA 受体拮抗剂,有用于上皮性卵巢癌的研究潜力。 | |||
T8193 |
α-Thujone
Thujone,ALPHA-(-)-THUJONE,α-侧柏酮,(-)-α-侧柏酮 |
Apoptosis; Reactive Oxygen Species; GABA Receptor; AChR; Parasite; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; NF-κB |
α-Thujone 是一种从西方金钟柏精油中分离出来的单萜,可穿透血脑屏障。它是 GABAA 受体的可逆调节剂,在抑制 GABA 诱导的电流时,它的 IC50为 21 μM。它诱导 ROS 依赖性细胞毒性,还诱导细胞凋亡和自噬。它具有抗伤害,抗肿瘤、杀虫和驱虫活性。 | |||
T5S1131 |
Ganoderic acid C6
灵芝酸C6 |
Others | Others |
Ganoderic acid C6 是醛糖还原酶活性的抑制剂。 | |||
T6S0743 |
Sesamoside
|
Others | Others |
Sesamoside 是分离自鸢尾叶的茎中的萜类,具有抗氧化和抗糖基化活性。 | |||
T20225 |
Dicentrine, (-)-
L-Dicentrine,荷包牡丹碱,NSC 251699,NSC251699,NSC-251699 |
Others | Others |
Dicentrine, (-)- (NSC-251699) 是一种在几种植物物种中发现的非卟啉生物碱,在小鼠内脏痛的急性模型中显示出显著的镇痛活性。 | |||
TN2540 |
1-Hydroxybaccatin I
|
Others | Others |
1-Hydroxybaccatin I 对对苯醌诱导的腹部收缩具有显着的镇痛活性。 | |||
T5783 |
Rosamultin
野蔷薇苷,罗莎白素 |
Antioxidant; HIV Protease | Microbiology/Virology; oxidation-reduction; Proteases/Proteasome |
Rosamultin 是从Potentilla anserina L 分离的 19 α-羟基型三萜。它抑制 HIV-1 蛋白酶,具有抗氧化、抗炎和镇痛作用。 | |||
TN1027 |
β-Amyrin
β-香树脂醇,beta-Amyrin |
Beta Amyloid | Neuroscience |
β-Amyrin (beta-Amyrin) 是一种番茄果实的表面蜡和蒲公英咖啡中的成分,能抑制淀粉样 β 诱导的增强效应损害。它可用于研究 AD。 | |||
T7035 |
ANTHRAQUINONE-2-CARBOXYLIC ACID
|
IRAK; Syk | Angiogenesis; Immunology/Inflammation; NF-κB; Tyrosine Kinase/Adaptors |
Anthraquinone-2-carboxylic acid 从 Brazilian taheebo 中分离得到,具有抗炎、缓解疼痛的作用。 | |||
TN1823 |
Kaempferol 3-O-β-D-galactopyranoside
Kaempferol 3-O-beta-D-galactoside,Kaempferol-3-O-galactoside,三叶豆苷 |
Immunology/Inflammation related | Immunology/Inflammation |
Kaempferol 3-O-β-D-galactopyranoside 是黄酮类化合物的衍生物,分离自木樨状菌 (Consolida oliverana) 的地上部分。 | |||
T4833 |
Ac-DL-Trp-OH
N-乙酰-DL-色氨酸,N-Acetyl-DL-tryptophan |
Others; Endogenous Metabolite | Metabolism; Others |
Ac-DL-Trp-OH (N-Acetyl-DL-tryptophan) 是内源性代谢产物的一种。 | |||
T8169 |
Decursinol
|
Others | Others |
Decursinol 是一种分离自Angelica gigas 的根中的、口服具有活性的抗伤害药物。它具有抗肿瘤和抗转移作用。 | |||
T2757 |
Myricitrin
杨梅苷,Myricetrin,Myricitrine |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
Myricitrin (Myricitrine) 是从杨梅根皮中分离出来的类黄酮化合物,具有镇痛作用。它是主要的抗氧化剂。 | |||
T6S0627 |
Mesaconitine
新乌碱,新乌头碱;中乌头碱 |
TNF | Apoptosis |
Mesaconitine 是乌头属植物的一种主要活性成分,通过循环 AMP 和刺激中枢 β-肾上腺素能系统具有镇痛活性,还有抗炎活性。 | |||
T3409 |
Plantamajoside
Y0160,C10485,大车前苷,车前子甙 |
Others | Others |
Plantamajoside (Y0160) 是一种苯丙烷类糖苷,从车前Plantago asiaticaL.中分离出来得到。它对 LPS 诱导的急性肺损伤小鼠模型具有保护作用。它对肺部炎症具有潜在的研究价值。 | |||
T5S0662 |
Gelsemine
钩吻碱,Gelsemin |
Antioxidant | oxidation-reduction |
Gelsemine (Gelsemin) 是一种从中草药 Gelsemium elegans 中获得的生物碱,具有抗伤害和促进睡眠活性,可有效缓解慢性疼痛。 | |||
T3981 |
Acacetin
4'-Methoxyapigenin,金合欢素,5,7-Dihydroxy-4'-methoxyflavone,Linarigenin |
Apoptosis; IAP; COX; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Neuroscience |
Acacetin (5,7-Dihydroxy-4'-methoxyflavone) 是一种来自狗舌草的口服有效类黄酮。它停在 PI3Kγ 的 ATP 结合口袋中,可导致癌细胞周期停滞,并诱导细胞凋亡和自噬。它有抗癌和抗炎活性,有潜力研究疼痛相关疾病。 | |||
TN1403 |
Arjunolic acid
|
IL Receptor; TNF; Reactive Oxygen Species; JNK; AChE | Apoptosis; Immunology/Inflammation; MAPK; Metabolism; Neuroscience; NF-κB |
Arjunolic acid 是分离自蓝莓的皂苷,具有抗氧化、抗菌和抗炎症等多种生物活性,在保护细胞和组织免受活性氧的有害作用中发挥重要作用。 | |||
TN2031 |
γ-Terpinene
Moslene,p-Mentha-1,4-diene,Crithmene |
Antioxidant | oxidation-reduction |
γ-Terpinene (p-Mentha-1,4-diene) 是一种单萜化合物,具有高抗氧化属性,适合口服。它展示了直接的自由基清除能力,并且已知是一种有效的抗痛剂。 | |||
T4S1990 |
Carvacrol
香荆芥酚,Karvakrol,O-Thymol,cymophenol,香芹酚 |
Apoptosis; Others; Gamma-secretase; Endogenous Metabolite; Antifungal | Apoptosis; Metabolism; Microbiology/Virology; Neuroscience; Others; Proteases/Proteasome; Stem Cells |
Carvacrol (O-Thymol) 是唇形科植物中的一种单萜酚类天然产物,具有镇痛、抗焦虑、抗抑郁、抗氧化、抗炎和抗癌作用。 | |||
TN1377 |
α-Spinasterol
Α-波菜甾醇,alpha-Spinasterol,菠甾醇 |
COX; Antibacterial; TRP/TRPV Channel | Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
α-Spinasterol 是一种从Spinacia oleracea 分离的瞬时受体电位香草酸 1 拮抗剂,具有抗菌、抗炎、抗抑郁、抗氧化和抗伤害作用。它抑制COX-1和COX-2活性,IC50值分别为 16.17 μM 和 7.76 μM。 | |||
TN1413 |
Atranorin
荔枝素,巴美灵,荔枝素 |
Endogenous Metabolite; NO Synthase; Ras | GPCR/G Protein; Immunology/Inflammation; MAPK; Metabolism |
Atranorin 是地衣的次生代谢产物,具有显着的抗伤害、抗炎和氧化还原活性,对 H(2)O(2) 诱导的氧化应激下的细胞具有细胞保护作用。 | |||
T5814 |
Aurantiamide
TMC-58B,橙黄胡椒酰胺 |
p38 MAPK; NF-κB | MAPK; NF-κB |
Aurantiamide 是马齿苋的活性成分,具有多种生物活性(如抗氧化、抗血小板、抗炎、抗肿瘤活性等),具有口服活性。 | |||
TN1712 |
Gossypin
|
NF-κB; S6 Kinase | MAPK; NF-κB; PI3K/Akt/mTOR signaling |
Gossypin 是一种从Hibiscus vitifolius 中分离得到的黄酮,能够抑制NF-κB 和 NF-κB 的调节基因表达。在小鼠原代骨髓细胞和 RAW264.7 细胞中,它也可抑制 RANKL 诱导的破骨细胞形成。它具有抗氧化、抗炎、抗癌、抗衰老、抗糖尿病和保护肝脏的活性。 | |||
T5S0581 |
Sec-O-Glucosylhamaudol
亥茅酚苷,Hamaudol 3-glucoside |
Others; Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience; Others |
Sec-O-Glucosylhamaudol (Hamaudol 3-glucoside) 是从滨海前胡中分离得到的一种天然产物,能够降低 μ 阿片受体的蛋白水平,可用于缓解疼痛的研究。它通过调节脂多糖刺激的 RAW264.7 细胞系中的 p38 丝裂原活化蛋白激酶具有抗炎作用。 | |||
T6S1369 |
Vitexin
牡荆素,Apigenin-8-C-glucoside |
Antioxidant | oxidation-reduction |
Vitexin 是一种存在于多种药用植物(如榕树、螺旋藻)中的 c-糖基化的黄酮。 它具有广泛的药理作用,包括抗氧化,抗癌,抗炎,抗痛觉过敏和神经保护作用。 | |||
T6S1579 |
Monotropein
水晶兰苷,Monotropeine |
Others | Others |
Monotropein (Monotropeine) 是从Morinda officinalis 中获得,能够抑制硫酸葡聚糖硫酸钠诱导的结肠炎小鼠模型中炎性因子的表达。 | |||
T10191L |
7-Chlorokynurenic acid
7-chloro-4-hydroxy-2-carboxyquinoline,7-氯犬尿酸,7-CKA |
GluR; NMDAR | Neuroscience |
7-Chlorokynurenic acid (7-chloro-4-hydroxy-2-carboxyquinoline) 是一种有效的选择性 NMDA 受体拮抗剂,对甘氨酸 B 激动剂位点的 IC50 为 0.56 μM。 7-Chlorokynurenic acid 抑制谷氨酸再摄取到突触小泡中,Ki 为 0.59 μM,并在神经轴输送后显示出镇痛作用。 | |||
T2S2362 |
Dehydrocorydaline nitrate
去氢延胡索甲素硝酸盐,硝酸脱氢紫堇碱 |
BCL; Others; PARP; p38 MAPK; Caspase; Parasite; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; MAPK; Microbiology/Virology; Others; Proteases/Proteasome |
Dehydrocorydaline nitrate 是生物碱。Dehydrocorydaline 调节 Bax,Bcl-2蛋白表达,激活 caspase-7,caspase-8,并使 PARP 失活。它能增强 p38 MAPK 活化,具有抗炎、抗癌、抗疟疾等功效。 | |||
T5S2358 |
Dehydrocorydaline
Dehydrocorydalin,脱氢紫堇碱,13-Methylpalmatine |
BCL; PARP; p38 MAPK; Caspase; Parasite; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; MAPK; Microbiology/Virology; Proteases/Proteasome |
Dehydrocorydaline (13-Methylpalmatine) 是一种生物碱。它调节Bax,Bcl-2蛋白表达,激活caspase-7,caspase-8,并使PARP 失活。它能增强p38 MAPK 活化,具有抗炎、抗癌等功效。它具有强大的抗疟疾作用,并具低细胞毒性。 | |||
T2S2264 |
Linalool
Linalol,(±)-Linalool,Phantol,沉香醇 |
Apoptosis; IL Receptor; TNF; Endogenous Metabolite; iGluR | Apoptosis; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Linalool (Linalol) 是存在芫荽等植物中的单萜类天然产物,是竞争性NMDA 受体拮抗剂,具有抗肿瘤和抗心脏毒性的作用。它通过激活 Nrf2 诱导抗氧化防御和通过抑制 NF-κB 减少炎症反应来保护其免受 LPS/GalN 诱导的肝损伤,具有镇痛、抗菌和抗炎的特性。 | |||
T4S0969 |
Obtusifolin
决明蒽醌,决明蒽醌;美决明子素 |
Antioxidant; NF-κB | NF-κB; oxidation-reduction |
Obtusifolin 是分离自决明子的种子中,能够抑制NF-kB 通路,调节气道上皮细胞中 MUC5AC 粘蛋白的基因表达和产生。它通过靶向甲状旁腺激素相关蛋白来抑制邻苯二甲酸酯诱导的乳腺癌骨转移。 | |||
T3S2259 |
Methyl eugenol
4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Methyl eugenol (4-allylveratrole) 是一种苯丙类化合物,存在于植物叶子、果实、根茎中,当植物相应的部位因食草动物进食而受损时,就会释放。它可用于消灭雄性东方果蝇。 | |||
TN1059 |
Ganoderic acid B
|
IL Receptor; HIV Protease; JAK; STAT | Angiogenesis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Microbiology/Virology; Proteases/Proteasome; Stem Cells |
Ganoderic acid B 是从灵芝中分离的一种三萜类天然产物。它是端粒酶抑制剂,抑制 Epstein-Barr 病毒抗原的活化。它是 HIV-1 蛋白酶抑制剂。 | |||
TN1989 |
Niga-ichigoside F1
苦莓苷F1 |
Others; Nrf2 | Immunology/Inflammation; Others |
Niga-ichigoside F1(NI) has anti-inflammatory, gastroprotective ,antinociceptive, and cytotoxic effects. | |||
TN4141 | Glochidone | Others | Others |
Glochidone shows pronounced antinociceptive properties in mice. | |||
TCS2336 |
Evodine
|
P-gp | Membrane transporter/Ion channel; Neuroscience |
Evodine 是吴茱萸中的主要柠檬苦素,是P-gp 有效抑制剂,可通过保留抗氧化剂防御系统,针对谷氨酸诱导的毒性具有保护作用。 | |||
TN4777 |
Physalin G
|
Others | Others |
Physalin G has antinociceptive property. | |||
TN4440 |
Limonexic acid
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Limonexic acid shows antinociceptive actions , it produces dose-related inhibition of glutamate- and capsaicin-induced pain. Limonexic acid can effectively protect hepatocyte against CCl4-induced injury. | |||
TN3476 |
Baccatin VI
|
Others | Others |
Baccatin VI 对对苯并醌诱发的腹部收缩具有显著的抗伤害活性。 | |||
TN4048 | Exoticin | Others | Others |
Exoticin shows antinociceptive and neuropharmacological activities, it could be considered as a suitable candidate for the development of analgesic and anxiolytic agents. | |||
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