34
12
Cat. No. | Product Name | Target | Signaling Pathways |
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T1610 |
Metaxalone
Skelaxin,Methaxalonum,美他沙酮,Zorane,NSC170959,AHR438 |
Others | Others |
Metaxalone (Methaxalonum) 具有肌肉松弛作用。 | |||
T1053 |
Mebeverine hydrochloride
盐酸麦皮凡林,Colofac Hydrochloride,Duspatalin Hydrochloride,Duspatal Hydrochloride |
Others; Sodium Channel | Membrane transporter/Ion channel; Others |
Mebeverine hydrochloride (Colofac Hydrochloride) 是 β-苯乙胺的衍生物,一种增肌剂,可有效阻止肠道蠕动。它也是电压控制的钠通道 (voltage-operated sodium channels)阻断剂,抑制细胞内钙的积累。 | |||
TP1057L |
Phe-Met-Arg-Phe Like Peptide acetate
Pqdpflrfamide acetate,Phe-Met-Arg-Phe Like Peptide acetate(98495-35-3 free base) |
Others | Others |
Phe-Met-Arg-Phe Like Peptide acetate (Pqdpflrfamide acetate)(98495-35-3 free base) 是一种来自蜗牛 Helix aspersa 的内脏和躯体肌肉的 FMRF 样肽。 FMRF (Phe-Met-Arg-Phe) 是一种由 4 个氨基酸残基组成的神经肽肽。 | |||
T21385 |
Cinitapride
西尼必利,Paxapride,Cidine,cinitapride tartrate,Blaston,Cintapro,Cinmove |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Cinitapride (Blaston) 是一种促胃药。它减缓肌肉的活动,以减轻诸如胃酸反流、胃排空延迟和溃疡性消化不良等病症的症状。 Cinitapride 作为 5-HT2 受体的拮抗剂和 5-HT1 和 5-HT4 受体的激动剂。 | |||
T7218 |
Endomorphin 2
内吗啡肽 2 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Endomorphin 2 是一种高亲和力和选择性的 μ-阿片受体激动剂,对 kappa3 结合位点具有合理的亲和力 ,Ki 为 20 到 30 nM 之间。 | |||
T14021 |
20-HETE
20-hydroxy Arachidonic Acid |
Others | Others |
20-HETE (20-hydroxy Arachidonic Acid) is a CYP450 metabolite and a potent vasoconstrictor and it is an endogenous inhibitor of the large-conductance Ca2+-activated K+ channel in renal arterioles. 20-HETE increases NADPH oxidase, ROS, and NF-κB activity, a | |||
T1115 |
Doxylamine succinate
琥珀酸多西拉敏,Decapryn |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Doxylamine succinate (Decapryn) 是一种吡啶衍生物组胺 H1 拮抗剂,具有明显的镇静特性。它竞争性阻断组胺 H1 受体并限制典型的过敏和过敏反应,可防止组胺引起的皮肤和粘膜疼痛和瘙痒。 | |||
T1050 |
Prazosin hydrochloride
Prazosin hydrochloride,哌唑嗪盐酸盐,Prazosin HCl,cp-12299-1,Peripress,Vasoflex,盐酸哌唑嗪,Minipress |
Potassium Channel; MRP; Adrenergic Receptor; ABC; Autophagy | Autophagy; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Prazosin hydrochloride (Vasoflex) 是一种选择性肾上腺素能 α-1 拮抗剂,可降低外周阻力并放松血管平滑肌。 它可用于研究高血压和酒精使用障碍。 它是一种合成哌嗪衍生物,具有降压抗肾上腺素能特性。它抑制有机阳离子转运蛋白 OCT-1 和 OCT-3,IC50分别为 1.8 和 13 μM 。 | |||
T2196 |
Fipronil
氟虫腈,Fluocyanobenpyrazole,Termidor |
P450; GluCls; GABA Receptor | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience |
Fipronil (Fluocyanobenpyrazole) 是昆虫GABA 受体的选择性拮抗剂,可抑制蟑螂神经元中谷氨酸盐引起的脱敏和非脱敏。在分离的大鼠肝微粒体中,它诱导细胞色素 P450 (CYP) 亚型CYP1A1/2、CYP2B1/2和CYP3A1/2的活性。 | |||
T0210L |
Tamsulosin
LY253351 free base,HSDB7744,(R)-(-)-YM12617 free base,Harnal-D,Flowmax,HSDB 7744,HSDB-7744 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tamsulosin ((R)-(-)-YM12617 free base) 是一种肾上腺素能受体α 1A 拮抗剂,用于良性前列腺增生(BPH)的治疗。Tansulosin 用于治疗排尿困难,这是前列腺肥大的一种常见症状。Tansulosin 和其他被称为α受体阻滞剂的药物通过放松膀胱颈部肌肉和前列腺本身的肌肉纤维来发挥作用,使其更容易排尿。 | |||
T0782 |
Benzthiazide
Aquatag,苄噻嗪,Lemazide,Dihydrex |
Carbonic Anhydrase | Metabolism |
Benzthiazide (Lemazide) 是长效利尿剂及抗高血压剂。它也是碳酸酐酶 9 的抑制剂,他对 CA9,CA2 和 CA1 的 Ki 分别为 8.0,8.8 和 10 nM。它对肿瘤细胞增殖具有抑制作用。 | |||
T68138 |
Saterinone
|
Adrenergic Receptor; PDE | GPCR/G Protein; Metabolism; Neuroscience |
Saterinone 是一种强效且具有选择性的磷酸二酯酶III 抑制剂,是血管α - 1-肾上腺素受体的有效拮抗剂。Saterinone 具有血管舒张作用,可用于慢性心力衰竭的急性治疗。Saterinone 对豚鼠右心室匀浆中粗cAMP 磷酸二酯酶(PDE)活性具有抑制作用,ic50值为2.3 × 10(-5) mol/l。 | |||
T26757 |
BDF 9148
BDF-9148,BDF9148 |
||
BDF 9148, a Na(+)-channel modulator, increases the contractile force of guinea-pig atria and papillary muscles. | |||
T25474 |
GW-Amide
Glycyl-tryptophanamide,GW Amide |
||
GW-Amide is a molluscan neuropeptide that exhibits potent modulatory effects on molluscan muscles. | |||
T23739 |
Antho-riamide I
|
||
Antho-Riamide I is an active peptide. It also inhibits the spontaneous contraction of sea anemone muscles. | |||
T24450 |
Mephenoxalone
Lenetran Lenetran,TAB Lenetranat |
||
Mephenoxalone is a muscle relaxant and mild anxiolytic. It inhibits neuron transmission and relaxing skeletal muscles by inhibiting the reflex arc. | |||
T32097 | Homoanserine Nitrate | ||
Homoanserine Nitrate is a dipeptide found in mammalian brains and muscles. | |||
T61174 | MT-134 | ||
MT-134 是一种 SkMII 特异性抑制剂,在肌肉中具有良好的暴露性。 | |||
T21020 |
Antazoline phosphate
|
||
Antazoline phosphate is an antihistamine with anticholinergic properties. Antazoline prevents the typical allergic symptoms on capillaries, mucous membranes, skin, and gastrointestinal and bronchial smooth muscles by antagonizing the histamine H1 receptor | |||
T40744 |
Eperisone
|
||
Eperisone is a centrally acting muscle relaxant and antispastic agent utilized in the treatment of conditions distinguished by muscle stiffness and pain. Its mechanism of action involves the relaxation of skeletal muscles and vascular smooth muscles, resulting in a range of beneficial effects including reduction of myotonia, enhancement of circulation, and suppression of the pain reflex. Additionally, Eperisone exhibits inhibitory properties on the pain reflex pathway and exerts a vasodilator ef... | |||
TP1057 |
Phe-Met-Arg-Phe Like Peptide, Snail Helix aspersa
Phe-Met-Arg-Phe Like Peptide |
||
Phe-Met-Arg-Phe-like peptide, derived from the visceral and somatic muscles of the snail Helix aspersa, is a neuropeptide known as FMRF (Phe-Met-Arg-Phe). This peptide comprises four amino acid residues[1]. | |||
T27435 |
GS 283
GS283,GS-283 |
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GS 283 is a Ca(2+) antagonist. GS 283 is also a weak histamine and muscarinic receptor blocker in rat and guinea pig tracheal smooth muscles. | |||
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. | |||
T61438 |
Propiverine
|
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Propiverine is a potent antimuscarinic agent that effectively inhibits cellular calcium influx, leading to the reduction of muscle spasm. It exhibits neurotropic and musculotropic effects specifically on the smooth muscles of the urinary bladder. Propiverine proves valuable in research concerning overactive bladder (OAB) [1] [2]. | |||
T31383 |
D-Epinephrine
L-(+)-Adrenaline,Racepinefrine, (S)-,BRN-2938799,d-Adrenaline,BRN 2938799 |
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D-Epinephrine can be used as a hormone, neurotransmitter, and medication. Epinephrine can be normally obtained from the adrenal glands and certain neurons. It involves in the fight-or-flight response by increasing blood flow to muscles, output of the hear | |||
T1120L2 |
Dacarbazine citrate
DTIC citrate |
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Dacarbazine citrate is an alkylating agent used to treat cancers of the lymphatic system and malignant melanoma (a type of skin cancer) in patients with certain conditions: islet cell carcinoma (part of the pancreas) Soft tissue sarcoma (cancer of muscles | |||
T32030 |
GYKI-16638 HCl
GYKI 16,638,GYKI16,638,GYKI-16638,GYKI-16,638,GYKI16638,GYKI 16638 |
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GYKI-16638 is a novel antiarrhythmic agent that demonstrates combined class IB and class III antiarrhythmic properties in human ventricular muscles, similar to the electrophysiological findings after chronic amiodarone treatment. In addition, GYKI 16638 h | |||
T80894 |
Uperolein
|
||
Uperolein 是由褐毛乌皮草 (Uperoleia rugosa) 和泥皮乌皮草 (Uperoleia marmorata) 产生的一种类似泡蛙肽的内十肽,具有致痉挛作用,影响胃肠道和纵向肌肉。 | |||
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. | |||
T35571 | Adenosine 3’-monophosphate (sodium salt hydrate) | ||
Adenosine 3’-monophosphate is a nucleotide and metabolite formedviahydrolysis of 2’,3’-cAMP by metal-dependent phosphodiesterases.1It reduces proliferation of rat preglomerular vascular smooth muscles cells (PGVSMCs) and glomerular mesangial cells (GMCs) in a concentration-dependent manner, an effect that is abolished by the adenosine A2Breceptor antagonist MRS1754.2Adenosine 3’-monophosphate is also a metabolic intermediate in the biosynthesis of adenosine . | |||
T37802 |
Phospho-L-Arginine (lithium salt hydrate)
|
||
Phospho-L-arginine is a phosphorylated form of L-arginine and a highly diffusible, high-energy metabolite and phosphagen involved in energy storage in invertebrates including crustaceans, insects, and Trypanosoma species. In the locust L. migratoria, phospho-L-arginine is found in the flight muscles, where it acts as both a buffer system and shuttle mechanism for high-energy phosphate. Measurement of phospho-L-arginine by 31P-NMR spectroscopy has been used to study invertebrate energy metabolism... | |||
T76049 |
Demoxytocin
|
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Demoxytocin为一种异源性环肽,属于催产素类似物。其通过影响细胞膜通透性,提升平滑肌细胞内钙离子含量,进而加强平滑肌细胞收缩力,具备刺激子宫平滑肌收缩的能力,发挥催产素功能。此外,Demoxytocin在研究早产破裂引发的分娩刺激中有应用。 | |||
T70097 | Acefylline piperazine | ||
Acefylline piperazine is a stimulant drug of the xanthine chemical class. It acts as an adenosine receptor antagonist. Acephylline piperazine is a theophylline derivative with a direct bronchodilator action. It has the advantages over theophylline in being far less toxic and producing minimal gastric irritation. It is indicated for the treatment of asthma, emphysema, acute and chronic bronchitis associated with bronchospasm.Acefylline relaxes smooth muscles, relieves bronchospasm & has a stimula... | |||
T69215 | Ambrein | ||
Ambrein is a triterpene alcohol that is the chief constituent of ambergris, a secretion from the digestive system of the sperm whale, and has been suggested as the possible active component producing the supposed aphrodisiac effects of ambergris. It serves as the biological precursor for a number of aromatic derivatives such as ambroxan and is thought to possess fixative properties for other odorants. It has been shown to act as an analgesic and it has been proven to increase sexual behavior in ... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T8198 |
Visnagin
|
Others | Others |
Visnagin 是一种抗氧化剂呋喃香豆素衍生物。它具有预防Cerulein 诱导的急性胰腺炎的潜力。它在血管平滑肌中具有良好的血管扩张作用。它具有抗炎作用,可用于缓解疼痛的研究。 | |||
T19493 |
Octadecanal
十八烷醛,stearaldehyde |
Endogenous Metabolite | Metabolism |
Octadecanal (stearaldehyde) 是存在于大腿和胸部肌肉中的一种长链醛。 | |||
TN3243 |
7-O-Methyleriodictyol
|
AChR | Neuroscience |
7-O-Methyleriodictyol 是一种从单乳蒿中分离出的黄烷酮,对大鼠分离的平滑肌有生物学作用。 | |||
T4739 |
Sodium creatine phosphate dibasic tetrahydrate
磷酸肌酸二钠盐,Creatine phosphate disodium salt tetrahydrate |
Others; Endogenous Metabolite | Metabolism; Others |
Sodium creatine phosphate dibasic tetrahydrate (Creatine phosphate disodium salt tetrahydrate) 主要存在于脊椎动物的骨骼肌中,是测定肌酸激酶的底物,能够用于骨骼肌收缩过程中 ATP 的再生。 | |||
T6805 |
Choline bitartrate
2,3,4-trihydroxy-4-oxobutanoate,2-hydroxyethyl(trimethyl)azanium,酒石酸氢胆碱 |
Others; AChR | Neuroscience; Others |
Choline bitartrate (2-hydroxyethyl(trimethyl)azanium) 是一种存在于食物中的营养胆碱,可影响肝脏疾病、动脉粥样硬化和神经系统疾病等疾病。它是神经递质乙酰胆碱的前体,作为甲基供体参与各种代谢过程和脂质代谢。 | |||
T5543 |
TriacetonaMine
四甲基哌啶酮,Odoratine,tempidon,tmpone,Vincubine,2,2,6,6-Tetramethyl-4-piperidinone |
Others | Others |
TriacetonaMine (Vincubine) 是一种合成医药产品、农药和聚合物光稳定剂的中间体。它是热解油的主要组分。它是植物和真菌提取物的人工制品,使用丙酮和氢氧化铵,或在分离过程的不同步骤中天然出现铵盐。 | |||
T0266 |
Quinidine hydrochloride monohydrate
奎宁树,奎尼丁盐酸盐一水合物,奎尼丁盐酸盐,Quinidine hydrochloride |
Potassium Channel; Sodium Channel; Parasite | Membrane transporter/Ion channel; Microbiology/Virology |
Quinidine hydrochloride monohydrate 是一种抗心律失常剂,也是 K+通道 (K+channel) 的有效阻断剂,其IC50值为 19.9 μM。它是一种有效且选择性的细胞色素 P450db (cytochrome P450db) 抑制剂,也可用作疟疾的研究。 | |||
T0892 |
Diphylline
二羟丙茶碱,Dyphylline,Diprophylline |
PDE; Adenosine Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Diphylline (Diprophylline) 是一种A1/A2腺苷受体拮抗剂,也是环状核苷酸磷酸二酯酶抑制剂。它是一种黄嘌呤衍生物,具有支气管扩张和血管扩张作用,有用于治疗慢性支气管炎和肺气肿的潜力。 | |||
T19515 |
Phosphocreatine dipotassium
Creatinephosphoric acid (dipotassium),Creatine phosphate (dipotassium) |
Others | Others |
Phosphocreatine dipotassium, primarily found in the skeletal muscles of vertebrates and one of organic compounds known as alpha amino acids and derivatives. | |||
TN5234 |
Vindorosine
|
Calcium Channel; Sodium Channel | Membrane transporter/Ion channel; Metabolism |
Vindorosine has blood vessel relaxation effect, possible underlying mechanisms involving the inhibition of Ca(2+) entry via L-type Ca(2+) channels in vascular smooth muscles. | |||
T2O2683 |
L-Proline
L-(-)-Proline,proline,脯氨酸,L-脯氨酸 |
Endogenous Metabolite | Metabolism |
L-Proline (proline) 是人体非必需氨基酸。它是胶原蛋白的重要组成部分,对关节和肌腱的正常运作很重要。它还有助于维持和加强心脏肌肉。 | |||
T4883 |
Creatine
Methylguanidoacetic acid,肌酸 |
Endogenous Metabolite | Metabolism |
Creatine (Methylguanidoacetic acid) 是一种内源性氨基酸代谢物,在细胞能量中发挥重要作用,尤其是在肌肉和大脑中。 |