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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4351 |
DAMGO
Dagol,DAGO,RX-783006 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
DAMGO (DAGO) 是一种阿片受体激动剂,Kd 值为 3.46 nM。它能够影响啮齿动物的运动活动,可作为镇痛剂。 | |||
T7416 |
WS-12
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
WS-12 是有效的TRPM8激动剂,EC50为 39 nM。 | |||
T8410 |
ASP7663
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
ASP7663 是口服有效的TRPA1选择性激动剂。ASP7663具有抗便秘和抗腹痛的功效。 | |||
T30824 |
Cgp 29030A
Cgp29030A,Cgp-29030A |
Others | Others |
CGP 29030A 是一种新的哌嗪衍生物,具有镇痛活性,对潜在的痛觉背角神经元有显著的抑制作用,可用于研究疼痛性疾病。 | |||
T40045 |
Sivopixant
S-600918,Sivopixant |
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
Sivopixant (S-600918) 是P2X3受体选择性拮抗剂 (P2X3IC50=4.2 nM; P2X2/3IC50=1100 nM)。Sivopixant 可用于缓解疼痛的研究。 | |||
T50030 |
1-(2,4-difluorophenyl)guanidine hydrochloride
|
Others | Others |
1-(2,4-difluorophenyl)guanidine hydrochloride 是一种化合物,是电压门控钠通道Nav1.7的强效选择性抑制剂,Nav1.7是疼痛信号传输的关键参与者,因此它能够减少疼痛信号的传递,从而产生镇痛作用。 | |||
T15360 |
Furobufen
|
Others | Others |
Furobufen is an anti-inflammatory agent. It produces antiarthritic and has antipyretic effects. Furobufen also has an analgesic effect in inflamed tissue. | |||
T23944 |
DA 5018
DA-5018,DA5018 |
||
DA 5018 is a capsaicin derivative and is also a new non-narcotic analgesic. It has an antipruritic effect. | |||
T73339 |
Anrikefon
HSK21542 |
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Anrikefon (HSK21542) 为 kappa 阿片受体(kappa opioid receptor)激动剂,具缓解疼痛作用。 | |||
TP1331 |
Super-TDU (1-31) TFA
|
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Super-tdu (1-31) TFA is an endogenous ligand of heptapeptide receptor and has a strong anti-analgesic effect. | |||
T21843 |
GEMSA
|
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GEMSA 是一种有效的脑啡肽转化酶抑制剂 (enkephalin convertase,Ki=8.8 nM),具有镇痛作用。 | |||
T25959 |
Pipebuzone
LD-4644,LD 4644,LD4644,Pipebuzonum |
||
Pipebuzone 是一种抗炎、解热、镇痛药,用于治疗各种风湿性疾病。它在临床和病理上都具有良好的耐受性,并具有可靠的抗炎作用。 | |||
T11010 | Detomidine carboxylic acid | Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Detomidine carboxylic acid is the main urine metabolite of detomidine. Detomidine is a synthetic α2-adrenergic agonist and an animal analgesic. Detomidine also has heart and breathing effects, and has a diuretic effect. | |||
T60526 | N-Salicyloyltryptamine | ||
N-Salicyloyltryptamine(STP) 是一种色胺类似物,具有抗惊厥、抗炎、镇痛和血管舒张的作用。N-Salicyloyltryptamine 作为电压依赖性离子通道(包括Na+、Ca2+、K+离子通道)抑制剂,可抑制 K+电流,IC50值为 34.6 μM ( /to)。 | |||
T24692 |
QAQ dichloride
|
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QAQ dichloride is a photoswitchable compound that blocks voltage-gated Na v and K v channels. Its channel-blocking activity is observed in the trans form of the azobenzene photoswitch, while the cis form does not exhibit this effect. This compound is membrane-impermeant and selectively enters pain-sensing neurons expressing endogenous import channels. QAQ dichloride functions as a light-sensitive analgesic and provides a valuable tool for investigating signaling mechanisms involved in acute and ... | |||
T71491 | Enadoline (Free Base) | ||
Enadoline (Free Base) is a kappa-opioid receptor agonist; PD 129290 (CAM 570; CI 977) is the S,S(-)-enantiomer; PD 129289 (CAM 569) is the corresponding R,R(+)-enantiomer. In human studies, it produced visual distortions and feelings of dissociation, reminiscent of the effects of salvinorin A. It was studied as a potential analgesic, but abandoned because of the dose-limiting effects of dysphoria, which could be expected from a κ-opioid agonist. There was mention of its potential in treating com... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN6989 |
Isotoosendanin
异川楝素,(1S,2S,4R,5S,6R,9S,10S,11R,13R,18S,20R)-20-(acetyloxy)-6-(furan-3-yl)-11,15,18-trihydroxy-5,10,14-trimethyl-3,8-dioxo-16-oxapentacyclo[12.3.3.01,13.02,1?.0?,?]icosan-4-yl acetate |
Others | Others |
Isotoosendanin ((1S,2S,4R,5S,6R,9S,10S,11R,13R,18S,20R)-20-(acetyloxy)-6-(furan-3-yl)-11,15,18-trihydroxy-5,10,14-trimethyl-3,8-dioxo-16-oxapentacyclo[12.3.3.01,13.02,1?.0?,?]icosan-4-yl acetate) 是一种从楝树 Melia toosendan 果实中分离出的柠檬苦素类天然产物,具有抗炎和镇痛作用。 | |||
TN1517L |
Cochinchinenin A
|
Others | Others |
Cochinchinenin A 是龙血镇痛作用的物质基础。 | |||
TN1517 |
1-(2,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)propan-1-one
剑叶龙血素A,Cochinchinenin A |
Others | Others |
1-(2,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)propan-1-one (Cochinchinenin A) 是龙血镇痛作用的物质基础。 | |||
T8209 |
Saikosaponin b3
柴胡皂苷b3 |
Others | Others |
Saikosaponin b3 是从 Bupleurum falcatum L. 的根中分离得到的。Saikosaponin b3 抑制 ACTH 诱导的脂肪细胞中的脂肪分解并具有镇痛作用。 | |||
T3S0509 |
Gaultherin
|
COX | Immunology/Inflammation; Neuroscience |
Gaultherin 是一种分离自 Gaultheria yunnanensis 中的天然水杨酸酯衍生物。它是一种非甾体类抗炎药,具有止痛和抗炎作用,与 Aspirin 相比没有胃溃疡作用。 | |||
T1407 |
(-)-Menthol
L-Menthol,Levomenthol,(-)-薄荷醇,薄荷冰,Menthomenthol,Menthacamphor |
Opioid Receptor; Endogenous Metabolite; TRP/TRPV Channel | Endocrinology/Hormones; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
(-)-Menthol (Levomenthol) 分离自薄荷油,L-Menthol 是瞬时受体电位 M8 (TRPM8)的激活剂,TRPM8 是 Ca2+-可渗透的非选择性阳离子通道,并增加 [Ca2+]i。L-Menthol 具有抗肿瘤活性。 | |||
T5S1889 |
Yunaconitine
Guayewuanine B,滇乌头碱 |
Others | Others |
Yunaconitine (Guayewuanine B) 是一种乌头类生物碱,具有剧毒。 | |||
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。 | |||
T5S0661 |
Koumine
|
Others | Others |
Koumine 是一种从钩吻中得到的生物碱,具有高效抗肿瘤活性,在肿瘤细胞中能够提高 Bax/Bcl-2 的蛋白比例和 caspase-3 的表达。在类风湿性关节炎动物模型中,它能够预防关节炎的发展。它具有抗焦虑、抗应激、抗银屑病作用,也可用于缓解疼痛的研究。 | |||
T5S0045 |
Isofraxidin
6,8-Dimethoxyumbelliferone,异秦皮啶,Phytodolor,异嗪皮啶 |
MMP; ERK; p38 MAPK; TLR; COX | Immunology/Inflammation; MAPK; Neuroscience; Proteases/Proteasome |
Isofraxidin (Phytodolor) 是来自刺五加的香豆素成分,抑制MMP-7表达和人肝癌细胞侵袭。它作用于肝癌细胞,抑制ERK1/2磷酸化。它减弱iNOS 和COX-2表达,还抑制TLR4/髓样分化蛋白 2 复合物的形成。 | |||
T3929 |
Kaurenoic acid
Kauren-19-Oic Acid,异贝壳杉烯酸,kaurenoate,kaur-16-en-18-oic acid |
Others | Others |
Kaurenoic acid (kaurenoate) 是一种二萜,来源于 Sphagneticola trilobata 中,可以抑制细胞因子的产生和激活 NO–cyclic GMP–PKG–ATP- 敏感型钾通道信号通路,并抑制炎症疼痛。 | |||
TN4379 |
Kansuinine A
|
IL Receptor; STAT; Interleukin | Immunology/Inflammation; JAK/STAT signaling; Stem Cells |
Kansuinine A 对IL-6 诱导的 Stat3激活有作用。Kansuinine A 显示出抗病毒和抗肿瘤活性。 | |||
T6S1699 |
Shogaol
[6]-Shogaol,姜烯酚,6-姜烯酚,6-Shogaol |
Lipoxygenase; Autophagy | Autophagy; Metabolism |
6-Shogaol (6-Shogaol) 是从生姜中分离的一种天然产物,具有抗癌、抗炎和抗氧化的多种生物活性。 | |||
TN2248 |
Sylvestroside I
林生续断苷I,匙羹藤皂苷 I |
Others | Others |
Sylvestroside I may have analgesic effect. | |||
TMA0805 |
Lupanine
|
ATPase; Potassium Channel; Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Lupanine has a weak sedative effect on the central nervous system, interaction with specific drugs used for treatment of the CNS and for analgesic activity. Lupanine improves glucose homeostasis by influencing KATP-channels of pancreatic beta cells. |