78
17
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1264 |
Prolylleucine
((Benzyloxy)carbonyl)-L-prolyl-D-leucine |
Others | Others |
Prolylleucine (((Benzyloxy)carbonyl)-L-prolyl-D-leucine) 是一种二肽,含有支链氨基酸,可以影响动物的昼夜节律和行为。 | |||
T1855 |
ZCL278
ZCL 278 |
CDK; Ras | Cell Cycle/Checkpoint; GPCR/G Protein; MAPK |
ZCL278 是一种选择性 Cdc42 GTPase 抑制剂,与Cdc42结合,Kd 为 11.4 μM。 | |||
T13385 |
Zamifenacin fumarate
扎非那星富马酸盐,UK-76654 fumarate |
AChR | Neuroscience |
Zamifenacin fumarate (UK-76654 fumarate) 是肠道选择性毒蕈碱M3受体的有效拮抗剂, 可显著降低肠易激综合症的结肠蠕动。 | |||
T2319 |
Acotiamide monohydrochloride trihydrate
Acotiamide hydrochloride,YM-443 HCl,盐酸阿考替胺,Z-338 HCl |
AChE | Neuroscience |
Acotiamide monohydrochloride trihydrate (Z-338 HCl) 是一种首创的、具有口服活性的胃肠动力药。它通过促毒蕈碱受体拮抗作用和乙酰胆碱酯酶(AChE)抑制作用增强肠神经元释放的乙酰胆碱,从而增强胃排空和胃部适应性,有潜力用于功能性消化不良的研究。 | |||
TP1793 |
Nociceptin (1-13), amide
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Nociceptin (1-13), amide 是一种 ORL1 (OP4) 受体激动剂,与大鼠前脑膜结合的 Ki 为 0.75 nM,对小鼠输精管的 pEC50 为 7.9。 | |||
T7487L |
Speract TFA(76901-59-2(free base))
|
Others | Others |
Speract TFA(76901-59-2(free base)) 是一种海胆卵肽,可调节精子活力,也可刺激精子线粒体代谢。 | |||
T31597 |
Ecabapide
DQ2511,DQ 2511,DQ-2511 |
Others | Others |
Ecabapide (DQ-2511) 是一种新型促胃肠蠕动剂,能显著增强SHRSP的胃排空能力。Ecabapide 可激活的兔胃壁细胞中的环状 GMP 依赖性管家 Cl- 通道。 | |||
T33868 |
Palmitoyl glutamic acid
N-Palmitoyl-L-glutamic acid,Palmitoylglutaminic acid |
||
Palmitoyl glutamic acid (N-Palmitoyl-L-glutamic acid) 是一种酰基氨基酸,可阻断主动脉收缩,可拮抗由氟哌啶醇诱发的口腔运动障碍。Palmitoyl glutamic acid 常常添加在化妆品中。 | |||
T16518 |
PH-002
|
Others | Others |
PH-002 是一种抑制载脂蛋白 E4 神经内分子相互作用的抑制剂(IC50:116 nM)。 | |||
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。 | |||
T3638 |
Leukadherin-1
|
Integrin; Complement System | Cytoskeletal Signaling; Immunology/Inflammation |
Leukadherin-1 是 CD11b/CD18 的变构激活剂,可增加 CD11b/CD18 依赖性细胞对纤维蛋白原的粘附,减少白细胞运动和跨内皮迁移,具有抗炎作用。 | |||
T15646 |
KBU2046
|
Others | Others |
KBU2046 是口服有效的,体外细胞运动和侵袭的高选择性抑制剂。它结合伴侣异源复合物,选择性地改变调节运动性的侣伴蛋白的结合,并且缺乏经典 HSP90抑制剂的所有标志。它抑制癌症转移并延长寿命。 | |||
T0918 |
Trimebutine
曲美布汀,Mebutin |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Trimebutine (Mebutin) 是阿片受体激动剂,有抗毒蕈碱活性。它是解痉剂,可调节肠道和结肠运动,并通过抗毒蕈碱和弱μ-阿片受体激动剂作用缓解腹痛。 | |||
TP2137L |
pp60 c-src (521-533) (phosphorylated) acetate
|
Others | Others |
pp60 c-src (521-533) (phosphorylated) acetate 是粘着斑形成和细胞扩散的调节剂。它还调节细胞运动,是由促运动透明质酸受体 RHAMM 触发的信号通路中的关键成分。 | |||
T17030 |
Tegoprazan
|
ATPase; Proton pump | Membrane transporter/Ion channel |
Tegoprazan 是一种口服有效的、高选择性胃 H+/K+-ATP 酶 (H+/K+-ATPase) 抑制剂,能够控制胃酸分泌和运动,在体外检测的对猪、犬、人的 H+/K+-ATP 酶的 IC50为0.29-0.52 μM。 | |||
T14091 |
AC-73
|
Autophagy | Autophagy |
AC-73 是一种可口服的 Cluster of Differentiation 147 (CD147) 抑制剂,具有很高的生物利用,可选择性破坏 CD147 的二聚化 (结合位点在 CD147 的 N 端 IgC2 域中包括 Glu64 和 Glu73),从而对 CD147/ERK1/2/STAT3/MMP-2 途径产生抑制,并抑制肝癌细胞的运动和侵袭。AC-73 具有抗增殖活性,诱导白血病细胞自噬。 | |||
T1052 |
Proglumide
二丙谷酰胺 |
cholecystokinin | GPCR/G Protein |
Proglumide (Binoside) 是一种非肽的、口服具有活性的胆囊收缩素(CCK)-A/B 受体拮抗剂。它能够选择性阻断 CCK 在中枢神经系统中的作用。它能够抑制胃分泌,具有保护胃十二指肠粘膜的能力,并表现出抗癫痫和抗氧化活性。 | |||
T2525 |
Alosetron hydrochloride
Lotronex,盐酸阿洛司琼,GR 68755C,GR 68755,GR 68755X |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Alosetron hydrochloride (GR 68755) 是一种高选择性的 5-HT3 受体拮抗剂,可减轻清醒或麻醉犬直肠扩张的内脏伤害性效应,具有抗炎活性,用于肠易激综合征的研究。它阻断 5HT3 介导的豚鼠肌间和粘膜下神经元的快速去极化,IC50约为 55 nM。 | |||
T4341 |
Betrixaban
贝曲西班,PRT054021 |
Factor Xa | Metabolism |
Betrixaban (PRT054021) 是一种口服具有活力的选择性factor Xa(fXa) 抑制剂,IC50=1.5 nM。 | |||
T4230 |
PF-3758309 hydrochloride
PF-03758309 hydrochloride |
Apoptosis; PAK | Apoptosis; Cytoskeletal Signaling |
PF-3758309 hydrochloride (PF-03758309 hydrochloride) 是一种口服的、可逆的 ATP 竞争性PAK4抑制剂,Kd 为 2.7 nM,Ki 为 18.7 nM。它抑制锚定独立生长、诱导凋亡、细胞骨架重塑和抑制增殖,具有 PAK4 抑制剂的预期细胞功能。 | |||
T1242 |
Alvimopan
爱维莫潘 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Alvimopan (LY 246736) 是一种选择性和竞争性 μ 阿片受体拮抗剂,IC50值为 1.7 nM。它存在于肌间和黏膜下神经元以及人体肠道固有层的免疫细胞中,可用于术后肠梗阻的研究。 | |||
T36983 |
Cyclic-di-GMP disodium
Cyclic diguanylate,5GP-5GP disodium,3',5'-Cyclic diguanylic acid,Cyclic di-GMP (sodium salt),cyclic diguanylate disodium,c-di-GMP,c-di-GMP disodium |
STING; Endogenous Metabolite | Immunology/Inflammation; Metabolism |
Cyclic-di-GMP disodium (5GP-5GP disodium) 是细菌的第二信使,也是一种 STING 激动剂,参与原核生物的多种过程,包括生物膜的形成、运动、和细胞周期的进展。Cyclic-di-GMP disodium 对癌细胞显示出抗增殖活性,可诱导 CD4 受体表达升高和细胞周期停滞。Cyclic-di-GMP disodium 可用于癌研究癌症。 | |||
T1006 |
Propantheline bromide
Neopepulsan,溴丙胺太林,Pro-Banthine,Neometantyl |
AChR | Neuroscience |
Propantheline bromide (Pro-Banthine) 是一种抗毒蕈碱剂,用于研究多汗症,遗尿,胃肠和膀胱痉挛。 | |||
T6334 |
Ridaforolimus
AP23573,Deforolimus,MK-8669 |
mTOR; Autophagy | Autophagy; PI3K/Akt/mTOR signaling |
Ridaforolimus (AP23573) 是亲脂性大环内酯类抗生素雷帕霉素的小分子非前药类似物,具有潜在的抗肿瘤活性。它是一种有效和选择性的 mTOR 抑制剂,在 HT-1080 细胞中抑制 S6 磷酸化的 IC50值为 0.2 nM。 | |||
T4980 |
Betrixaban maleate
|
Factor Xa | Metabolism |
Betrixaban maleate 是一种非维生素 K 口服抗凝剂,其作用是由 Xa 因子的竞争性和可逆抑制作用驱动的。 | |||
T24848 |
TachypleginA
Tachyplegin A,Tachyplegin-A |
||
TachypleginA is a parasite motility and invasion inhibitor. | |||
T30199 |
Atilmotin
|
||
Atilmotin is a gastrointestinal agent for treating motility disorders. | |||
T24849 |
TachypleginA-2
tA 2,tA-2,tA2 |
||
TachypleginA-2 is a parasite motility and invasion inhibitor. | |||
T17283 |
Zamifenacin
UK-76654 |
Others | Others |
Zamifenacin obviously decreases colonic motility in irritable bowel syndrome. Zamifenacin is an effective gut-selective muscarinic M3 receptor antagonist. | |||
T27120 |
D-AP7
|
||
D-AP7 is a specific NMDA antagonist. D-AP7 enhances motility, exhibits anxiogenic-like effect and impairs consolidation in passive avoidance. | |||
T32379 |
Kentsin
|
||
Kentsin, as a contraceptive polypeptide, has central opiate properties on gastrointestinal motility. | |||
T6597L |
Mosapride citrate dihydrate
GR-107719-B,Mosapride Citrate,GR 107719 B,AS 4370,AS-4370,TAK-370 |
||
Mosapride Citrate is a 5-HT4 receptor agonist used to stimulate gastrointestinal motility via acetylcholine. Mosapride Citrate facilitates acetylcholine release from the enteric cholinergic neurons. | |||
T11846 | LHVS | Cysteine Protease | Proteases/Proteasome |
LHVS effectively blocks T. gondii microneme protein secretion (IC50=10 μM), gliding motility, and cell invasion. LHVS is a potent, non-selective cysteine protease inhibitor. | |||
T70122 |
Acotiamide Methyl Ether
|
||
Acotiamide Methyl Ether is a metabolite of Acotiamide -- an acetylcholinesterase inhibitor which has been shown to stimulate gastric motility and improve gastric motility dysfunction in rats. Acotiamide Hydrochloride has also been shown to improve meal-related symptoms of functional dyspepsia. | |||
T70938 |
SN00799639
|
||
SN00799639, also known as SN639, is a potent inhibitor of the motility and development of parasitic larvae of Haemonchus contortus, a blood-feeding parasitic nematode of major economic importance in ruminants. SN639 displayed lower potency, with IC50 values of 8.4 μM (xL3 motility) and 0.29 μM (L4 development). | |||
T69769 |
BDP8900
|
||
BDP8900 is a potent and selective MRCK inhibitor, reducing substrate phosphorylation. BDP8900 leads to morphological changes in cancer cells along with inhibition of their motility and invasive character. | |||
T7487 |
Speract
精子活化肽 |
Others; Mitochondrial Metabolism | Metabolism; Others |
Speract 是调节精子活力的海胆蛋肽,也能够刺激精子线粒体代谢。 | |||
T35374L |
(Ala13)-Apelin-13 acetate
|
Apelin receptor | GPCR/G Protein |
(Ala13)-Apelin-13 acetate,一种 APJ 拮抗剂,可调节CRF 诱导的增强的结肠运动、内脏敏感性和肠屏障。 | |||
T68735 | Ciclotropium (free base) | ||
Ciclotropium (free base) is quaternary ammonium compound with anticholinergic and parasympatholytic activity. Oral Cyclotropium bromide inhibited fasting and meal-stimulated colonic motility significantly without causing adverse side effects. After cyclotropium bromide, there was a significant correlation between antral contraction amplitude and gastric emptying. | |||
T69126 | Clofeverine (free base) | ||
Clofeverine (free base) is a highly selective relaxant for gastrointestinal smooth muscles with a beta-receptor stimulative nature. On isolated ileum, the inhibitory effect of clofeverine for spontaneous motility was comparable to that of isoproterenol and 100 times higher than that of papaverine. | |||
T61366 |
F-17
|
||
F-17 is a promising virulence factor inhibitor, displaying substantial inhibitory effects on biofilm formation, elastase activity, pyocyanin production, and swarming motility. Additionally, F-17 exhibits a strong binding affinity towards LasR and PqsR. Notably, F-17 does not exhibit any discernible cytotoxicity [1]. | |||
T78109 |
(Ala13)-Apelin-13 TFA
|
||
'(Ala13)-Apelin-13 TFA' 为高效的APJ受体拮抗剂,能够通过迷走神经胆碱能通路抑制胃动力。 | |||
T39167 |
GS-493
|
||
GS-493, a highly specific protein tyrosine phosphatase SHP2 (PTPN11) inhibitor, exhibits remarkable potency with an IC50 of 71 nM. It displays 29- and 45-fold greater affinity towards SHP2 compared to its related counterparts, SHP1 and PTP1B, respectively. In addition, GS-493 impedes both cellular motility and growth of cancer cells, portraying promising antitumor effects. | |||
T69324 | Clofeverine hydrochloride | ||
Clofeverine hydrochloride is the salt form of Clofeverine (free base), a highly selective relaxant for gastrointestinal smooth muscles with a beta-receptor stimulative nature. On isolated ileum, the inhibitory effect of clofeverine for spontaneous motility was comparable to that of isoproterenol and 100 times higher than that of papaverine. | |||
TP1948 |
PBP10
PBP 10 |
||
Selective formyl peptide receptor 2 (FPR2) antagonist; cell permeable. Selectively inhibits FPR2-mediated NADPH oxidase activity but has no effect on FPR1 signaling in neutrophils. Displays PIP2 binding activity in vitro and blocks cell motility. Also exh | |||
T15946 | MA-2029 | Others | Others |
MA-2029 is selective for the motilin receptor over various other receptors and ion channels. MA-2029 is a selective and competitive motilin receptor antagonist (IC50=4.9 nM). MA-2029 may be useful for gastrointestinal disorders associated with disturbed g | |||
T82778 |
Cardioexcitatory peptide 1
|
||
Cardioexcitatory peptide 1为从非洲大蜗牛(Achatina)心房分离的心兴奋性神经肽。该化合物对心脏具有显著的兴奋效应,并能影响肌肉组织的运动及神经活动。 | |||
T25912 |
Oxypyrronium bromide
L.D. 3055,Immetropan,LD 3055,LD3055,LD-3055 |
||
Oxypyrronium bromide 一种含有季铵的抗胆碱能和解痉剂。在动物模型中,它抑制胃运动、迷走神经刺激或乙酰胆碱静脉注射引起的低血压;鼓索神经刺激引起的流涎和节前颈交感神经刺激引起收缩。 | |||
T63237 | Acotiamide hydrochloride | ||
Acotiamide hydrochloride 是选择性的、口服具有活力的、可逆的乙酰胆酶碱酯 (AChE) 抑制剂 (IC50: 1.79 μM),能够提高胃收缩性,加速胃排空延迟,能够用于研究胃动力障碍的功能性消化不良及肠道炎症。 | |||
T78949 | AM841 | Cannabinoid Receptor | GPCR/G Protein |
AM841是一种高亲和力的亲电子配体,能与CB1大麻素受体中第六螺旋的半胱氨酸发生共价作用并激活该受体。此外,AM841能减少Forskolin刺激下的cAMP积累,并且减缓胃肠蠕动。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3603 |
Sodium lauryl sulfoacetate
月桂醇磺基乙酸酯钠,鱼腥草,新鱼腥草素钠,Sodium houttuyfonate |
NF-κB; MAPK | MAPK; NF-κB |
Sodium lauryl sulfoacetate (Sodium houttuyfonate) 是一种植物来源的固体阴离子表面活性剂,也是一种具有抗免疫抑制作用的免疫佐剂。 | |||
T7283 |
sodium lauroyl-α-hydroxyethyl sulfonate
鱼腥草 |
NF-κB; MAPK | MAPK; NF-κB |
sodium lauroyl-α-hydroxyethyl sulfonate 是抗假单胞菌药物,抑制假单胞菌的毒力相关运动。 | |||
TN6791 |
Palvanil
Hexadecanamide |
TRP/TRPV Channel | Membrane transporter/Ion channel |
Palvanil (Hexadecanamide) 是一种快速脱敏的 TRPV1 激动剂。它可能是治疗 IBS 的有前途的药物,因为它可以调节肠道蠕动并减轻内脏疼痛。 | |||
T5S1331 |
Herbacetin
|
c-Met/HGFR; Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
Herbacetin 是一种亚麻籽中的天然类黄酮,具有多种药理活性,如抗氧化、抗炎、抗癌作用。 它是鸟氨酸脱羧酶Ornithine decarboxylase (ODC)变构抑制剂,能够直接与 ODC 上的 Asp44,Asp243 和 Glu384 结合。其中鸟氨酸脱羧酶是多胺生物合成中的限速酶。 | |||
T4S1619 |
L-Hyoscyamine sulfate
Hyoscyamine sulfate hydrate,Levsin Sulfate,Hyoscyamine Sulphate,硫酸天仙子胺水合物,L-莨菪碱硫酸盐 |
AChR | Neuroscience |
L-Hyoscyamine sulfate (Levsin Sulfate) 是来自山莨菪的一种托烷生物碱,是竞争性的毒蕈碱受体拮抗剂。它是 Atropine 的左旋异构体。 | |||
T0962 |
L-Hyoscyamine
Daturine,Hyoscyamine,L-莨菪碱,L-天仙子胺 |
AChR | Neuroscience |
L-Hyoscyamine (Daturine) 是从山莨菪中提取的一种托烷生物碱,是竞争性的毒蕈碱受体拮抗剂。它是 Atropine 的左旋异构体。 | |||
T1437 |
D-Panthenol
D-泛醇,D-Pantothenyl alcohol,Ilopan,Dexpanthenol,Pantothenol |
Endogenous Metabolite | Metabolism |
D-Panthenol (D-Pantothenyl alcohol) 是 D-pantothenic acid 和胆碱能剂的酒精类似物。D-Panthenol 作为乙酰化反应所必需的辅酶A的前体,参与乙酰胆碱的合成。虽然 D-Panthenol 作用的确切机制尚不清楚,但它可能增强乙酰胆碱的作用。D-Panthenol 作用于胃肠道,增加下肠蠕动。它也适用于局部皮肤,以缓解瘙痒和促进愈合。 | |||
T6S1684 |
8-Gingerol
|
Antioxidant; Antibacterial; TRP/TRPV Channel | Membrane transporter/Ion channel; Microbiology/Virology; oxidation-reduction |
8-Gingerol 分离自姜的根状茎,是口服有效的 TRPV1激活剂,EC50值为5.0 µM。8-Gingerol 抑制 COX-2,还能抑制体外 H. pylori 的生长。 | |||
T10909 |
Cyclic-di-GMP
c-di-GMP,cyclic diguanylate,5GP-5GP |
Others | Others |
Cyclic-di-GMP is a STING agonist and ubiquitous second messenger, which regulates the formation, motility and virulence of biofilms in various bacterial species. | |||
T40442 |
Propylparaben sodium
Propyl4-hydroxybenzoatesodium,羟苯丙酯钠,Propylparahydroxybenzoatesodium |
||
Propylparaben sodium (propyl parahydroxybenzoate) is a naturally occurring antimicrobial preservative found in plants and bacteria. Widely utilized in cosmetics, pharmaceuticals, and foods, this compound impairs antral follicle growth and steroidogenic function by modifying the cell-cycle, apoptosis, and steroidogenesis pathways. Additionally, propylparaben sodium reduces sperm count and motility in rats. | |||
T72243 |
Cyclic-di-GMP diammonium
5GP-5GP diammonium,c-di-GMP diammonium ; cyclic diguanylate diammonium ; 5GP-5GP diammonium,c-di-GMP diammonium,cyclic diguanylate diammonium |
||
Cyclic di-GMP (c-di-GMP) diammonium 是一种STING 激活剂和无处不在的第二信使,调节生物膜的形成、运动和各种细菌的毒力。 | |||
TN4639 |
Neolitsine
|
Others | Others |
Neolitsine has anthelmintic activity, it exhibits EC90 values (concentration at which 90% loss of larval motility is observed) of 6.4 microg/mL.Neolitsine and dicentrine have potent vasorelaxing effects on precontracted rat aortic preparations with mean IC 50 values between 0.08 and 2.48 microM. | |||
T64248 | Cyclic-di-GMP sodium | ||
Cyclic di-GMP sodium (c-di-GMP sodium) 是一种 STING 激活剂,也是一种无处不在的第二信使,具有调节生物膜的形成、运动和各种细菌的毒力的作用。 | |||
TN1550 |
Danshenxinkun A
丹参新醌甲,丹参新醌A |
Others | Others |
Danshenxinkun A, Danshenxinkun B and Neocryptotanshinone may intervene thrombotic diseases by adjusting the targets mainly involved in pathways of endocrine system, signal transduction, signaling molecules and interaction, cell motility, environmental ada | |||
T75556 | 8β,9α-Dihydroxylindan-4(5),7(11)-dien-8alpha,12-olide | ||
8β,9α-Dihydroxylindan-4(5),7(11)-dien-8alpha,12-olide (compound 3) 是一种抗LIMK1活性的倍半萜类化合物,能够抑制细胞运动。 | |||
T75520 | Aplyronine A | ||
Aplyronine A是具有特异性肌动蛋白解聚活性、抗肿瘤及促凋亡功能的化合物,适用于癌症、肌肉收缩、细胞运动和细胞分裂等研究领域。 | |||
TN1834 |
Kobusin
去甲槟郎碱,自旋七叶素 |
Others; NOS; NF-κB | Immunology/Inflammation; NF-κB; Others |
Kobusin, a Calmodulin inhibitor, shows mild antiplasmodial,anti-inflammatory, and cytotoxic activities; it may be beneficial for the treatment of neuro-inflammatory diseases through the inhibition of iNOS expression and peroxynitrite scavenging potential. Kobusin can mildly reduce gastrointestinal motility in mice, it activates CFTR and CaCCgie chloride channel activities in mouse colonic epithelia and shows inhibitory effects toward ANO1/CaCC-mediated short-circuit currents in ANO1/CaCC-express... |