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Search Results for " calcium-activated "

53

抑制剂 & 化合物

6

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T13047	Synta66	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Synta66 是一种钙池操纵钙离子通道 Orai 抑制剂，用于神经系统疾病的研究。
T10885	CRAC intermediate 2	Others; Calcium Channel	Membrane transporter/Ion channel; Metabolism; Others
	CRAC intermediate 2是CRAC 抑制剂合成的中间体化合物。
T24984	5J-4	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	5J-4 是一种有效的钙释放激活钙通道 (CRAC) 和钙池操纵性钙内流(SOCE) 阻滞剂。 5J-4 减少 IL-17 的产生并降低 RORα 和 RORγt 的表达。
T10884	CRAC intermediate 1 5-(S)-Fluorowillardiine	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	CRAC intermediate 1 (5-(S)-Fluorowillardiine)是用于CRAC 离子通道系列化合物合成的关键中间体。
T3651	YM-58483 YM 58483,BTP2	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	YM-58483 (BTP2) 是一种特异性有效的 CRAC 通道和随后的 Ca2+ 信号抑制剂，可阻断钙池操纵的阳离子内流 (SOCE)。
T8867	RO2959 Hydrochloride RO2959 HCl	IL Receptor; Calcium Channel; Interleukin	Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism
	RO2959 Hydrochloride (RO2959 HCl) 是选择性CRAC 通道抑制剂，IC50为 402 nM。它是人IL-2产生的有效抑制剂，有效阻断 T 细胞受体触发的基因表达和 T 细胞功能途径。它是由Orai1/Stim1通道介导的钙存储进入的有效阻滞剂，IC50为 25 nM。
T9522	Rimtuzalcap CAD-1883	Potassium Channel	Membrane transporter/Ion channel
	Rimtuzalcap (CAD-1883) 是首创的，选择性的小电导钙激活钾通道 (SK 通道) 正变构调节剂。Rimtuzalcap 可用于运动障碍的研究，包括脊髓小脑性共济失调 (SCA)和特发性震颤 (ET)。
TQ0033	Zegocractin CM-4620,N-(5-(6-Chloro-2,2-difluorobenzo[d][1,3]dioxol-5-yl)pyrazin-2-yl)-2-fluoro-6-methylbenzamide,CM4620	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Zegocractin (CM-4620) 是一种钙离子释放激活通道的抑制剂，对Orai1/STIM1和Orai2/STIM1的IC50值分别为 119 和 895 nM。
T0858	Flufenamic acid Arlef,Nichisedan,氟灭酸,氟芬那酸,Achless	Potassium Channel; Calcium Channel; Chloride channel; COX; AMPK; Parasite	Chromatin/Epigenetic; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; PI3K/Akt/mTOR signaling
	Flufenamic acid (Arlef) 是一种非甾体类抗炎剂，是一种邻氨基苯甲酸衍生物，具有镇痛、抗炎和解热的特性。它用于肌肉骨骼和关节疾病。
T9245	TRPM4-IN-1 CBA,4-chloro-2-(2-(2-chlorophenoxy)acetamido)benzoic acid	TRP/TRPV Channel	Membrane transporter/Ion channel
	TRPM4-IN-1 (4-chloro-2-(2-(2-chlorophenoxy)acetamido)benzoic acid) 是一种有效的阳离子通道TRPM4选择性抑制剂，IC50为 1.5 μM。TRPM4-IN-1 在心脏病和前列腺癌中具有研究价值。
T2170	SKF-96365 hydrochloride 1-[2-(4-甲氧基)-2-[3-(4-甲氧基苯基)丙氧基]乙基]咪唑,SKF96365	Apoptosis; Potassium Channel; Calcium Channel; TRP/TRPV Channel; Autophagy	Apoptosis; Autophagy; Membrane transporter/Ion channel; Metabolism
	SKF-96365 hydrochloride (SKF96365) 是store-operated Ca2+entry 抑制剂，也是TRP channel 阻滞剂。它显著抑制豚鼠离体心脏 hERG、hKCNQ1/hKCNE1、hKir2.1 和 hKv4.3 电流，延长QTc 间期。它通过诱导结直肠癌细胞的细胞周期阻滞和凋亡起抗肿瘤作用。
T7512	BMS-191011 BMS-A	Potassium Channel	Membrane transporter/Ion channel
	BMS-191011 (BMS-A) 是一种大电导 Ca2+激活的钾通道 (Ca2+-activated potassium (maxi-K) channel) 激活剂，在中风模型中有研究价值。
T4330	CaCCinh-A01	Chloride channel	Membrane transporter/Ion channel
	CaCCinh-A01 是钙激活氯离子通道和TMEM16A 抑制剂，IC50值分别为 10 和 2.1 μM。
T22946	LY255283 LY 255283	Leukotriene Receptor	GPCR/G Protein
	LY255283 是白三烯 B4 (LTB4) 受体的特异性拮抗剂，抑制人外周血多形核白细胞和由钙离子载体 A23187 激活的单核细胞中 LTB(4) 的产生。
T13059	T16Ainh-A01	Chloride channel	Membrane transporter/Ion channel
	T16Ainh-A01 是氨基苯基噻唑，是有效的跨膜蛋白 16A 的抑制剂，抑制 TMEM16A 介导的氯离子电流，IC50约为1 µM。TMEM16A (ANO1)起钙激活氯离子通道(CaCC)的作用。
T24799	SKA-111 SKA 111,SKA111	Potassium Channel	Membrane transporter/Ion channel
	SKA-111 是一种选择性钙离子激活的钾离子通道 (potassium phannel ) KCa3.1 激活剂，可引起猪内皮细胞膜超极化。SKA-111结合在CaM N-瓣和S4-S5接头之间的界面中，能够改善 Bradykinin 诱导的离体大鼠心脏的冠状动脉扩张，可用于研究心血管疾病。
T4503	Talniflumate Somalgen,他尼氟酯	Chloride channel; COX; N-Acetylglucosaminyltransferase; Anion Exchanger	Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience
	Talniflumate (Somalgen) 是一种钙激活氯离子通道 (hCLCA1/mCLCA3) 阻滞剂，可减少动物模型和细胞培养中的粘蛋白合成和释放。它通过抑制环氧合酶，并抑制 Cl-/HCO3- 交换活性，具有抗炎作用。它还增加了远端肠梗阻综合征囊性纤维化小鼠模型的存活率。
T16345	NS13001 N-(4-chlorophenyl)-2-(3,5-dimethylpyrazol-1-yl)-9-methylpurin-6-amine,N-(4-Chlorophenyl)-2-(3,5-dimethyl-1H-pyrazol-1-yl)-9-methyl-9H-purin-6-amine	Potassium Channel	Membrane transporter/Ion channel
	NS13001 (N-(4-Chlorophenyl)-2-(3,5-dimethyl-1H-pyrazol-1-yl)-9-methyl-9H-purin-6-amine) 是口服有效的 SK 通道选择性正向变构调节剂。NS13001 对 SK2 和 SK3 通道的 EC50分别为 1.8 μM 和 0.14 μM。NS13001 在脊髓小脑共济失调 2 型和其他小脑共济失调方面具有研究价值。
T4674	SB297006 SB 297006	CCR	Immunology/Inflammation; Microbiology/Virology
	SB297006 是一种CCR3拮抗剂，IC50为39 nM。它能够显著抑制 CCL11 处理的神经祖细胞的增殖和神经球形成。
T5454	N-(p-amylcinnamoyl) Anthranilic Acid 2-(3-(4-戊基苯基)丙烯酰胺基)苯甲酸,ACA	Phospholipase; TRP/TRPV Channel	Membrane transporter/Ion channel; Metabolism
	N-(p-amylcinnamoyl) Anthranilic Acid (ACA) 是一种广谱磷脂酶 A2(PLA2) 抑制剂，也是TRP channel 的阻滞剂。ACA 也可逆的抑制钙离子激活氯通道 (calcium-activated chloride channels) ，在心律失常方面具有研究的潜力。
T15286	Flindokalner BMS-204352	Potassium Channel	Membrane transporter/Ion channel
	Flindokalner (BMS-204352) 是一种钾离子通道调节剂。它是大电导钙激活 K 通道正向调节剂。它是在 HEK293 细胞中表达的所有神经元 Kv7通道亚型的正调节剂。它在 Kv7.1 通道 (Ki=3.7 μM) 处显示负调节活性，并充当 GABAA 受体的负调节剂。它在体内显示出抗焦虑功效。
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。
T68583	Nco 700
	Nco 700 is a synthetic inhibitor of calcium-activated protease.
TP2329	AF2 Neuropeptide
	AF2 is the nematode neuropeptide. It also increases voltage-activated calcium currents in Ascaris suum muscle.
T24614	PF04471141 HCl PF04471141 hydrochloride,PF04471141,PF 04471141,PF-04471141
	PF-04471141 is an effective and selective inhibitor of the calcium-activated phosphodiesterase PDE1 (IC50 = 35 nM).
TP2004	Margatoxin
	Potent KV1.3 channel blocker (IC50 = 36 pM). Displays no effect at calcium-activated channels. Reduces VEGF-induced transmembrane calcium influxes and nitric oxide production in human endothelial cells.
T80850	VU0531245 VU245
	VU0531245为SLACK通道抑制剂，其IC50值达2.1 μM。
T82723	ChTX-Lq2
	ChTX-Lq2为Ca2+激活的K+流出抑制剂，Kd值为43 nM。
T40750	12,14-Dichlorodehydroabietic acid
	12,14-Dichlorodehydroabietic acid, a chlorinated resin acid, exhibits potent calcium-activated potassium (BK) channel opening activity. It effectively inhibits GABA-dependent chloride influx in the mammalian brain, functioning as a non-competitive antagonist of GABA A receptors. Moreover, 12,14-Dichlorodehydroabietic acid induces an elevation in cytosolic free calcium levels and promotes the release of neurotransmitters.
T61818	DFBTA
	DFBTA is a highly effective and orally active inhibitor of ANO1, specifically the calcium-activated chloride channel anoctamin-1. It exhibits potent inhibitory activity, with an IC 50 of 24 nM. Notably, DFBTA demonstrates significant analgesic efficacy in treating inflammatory pain [1].
T71295	SOR-C13
	SOR-C13 is an inhibitor of transient receptor potential cation channel vanilloid family member 6 (TRPV6, CaT1 or CATL) with potential antineoplastic activity. TRPV6 calcium channel inhibitor SOR-C13 binds to TRPV6 and prevents the influx of calcium ions into TRPV6-expressing tumor cells. This inhibits the activation of nuclear factor of activated T-cell (NFAT) transcription complex which may result in an inhibition of calcium-dependent cancer cell proliferation and an induction of apoptosis in t...
T28140	NCG21 NCG-21,NCG 21
	NCG21 is a GPR120 agonist, which showed potent extracellular signal-regulated kinase (ERK) activation in a cloned GPR120 system. NCG21 potently activated ERK, intracellular calcium responses and GLP-1 secretion in murine enteroendocrine STC-1 cells that e
T80065	Calcicludine	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Calcicludine是Dendroaspis angusticeps产毒蛋白，针对高电压激活的calcium channel（特别是L型）有抑制作用，IC50为88 nM，影响兴奋性突触传递。
T64151	Mibefradil dihydrochloride hydrate
	Mibefradil dihydrochloride hydrate (Ro 40-5967 dihydrochloride hydrate) 是一种长效的钙离子通道拮抗剂。Mibefradil dihydrochloride hydrate 通过对低电压激活 (T) 钙通道的亲和力高于对高电压激活 (L) 钙通道的亲和力来发挥作用。Mibefradil dihydrochloride hydrate 能够降压药。
T80068	Slotoxin	Potassium Channel	Membrane transporter/Ion channel
	Slotoxin为Centruroides noxius霍夫曼蝎毒液中提取的多肽，能够阻断高电导钙激活钾通道(potassium channel)，其Kd值为1.5 nM[1]。
T39283	OSK-1
	OSK-1 is a potent potassium channel blocker belonging to the α-KTx3 toxins. It exhibits IC50 values of 0.6 nM, 5.4 nM, and 0.014 nM for Kv1.1, Kv1.2, and Kv1.3 channels, respectively. Additionally, OSK-1 acts as a moderate blocker of the calcium-activated KCa3.1 channel, with an IC50 of 225 nM. Consequently, OSK-1 finds application as an immunosuppressive drug.
T37284	1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE
	1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE is a phospholipid that contains stearic acid at the sn-1 position and 15(S)-HETE at the sn-2 position. It is formed in human peripheral monocytes activated by the calcium ionophore A23187 by direct oxidation of 1-stearoyl-2-arachidonoyl-sn-glycero-3-PE by 15-LO. Phosphoethanolamine (PE) HETEs (PE-HETEs), including 1-stearoyl-2-15(S)-HETE-sn-glycero-3-PE, are the main source of esterified HETE in ionophore-activated monocytes.
T83740	Ziptide TFA
	Ziptide是多种丝氨酸/苏氨酸蛋白激酶的肽底物，包括MAPK激活蛋白激酶2（MAPKAPK2）、MAPKAPK3、MAPKAPK5、checkpoint kinase 1（Chk1）、AMP激活蛋白激酶（AMPK）和钙/钙调蛋白依赖型蛋白激酶II（CamKII）。它被用来评估CamKII活性以用于抑制剂的开发。
T4411	DAMGO TFA (78123-71-4(Free base))	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	DAMGO TFA (78123-71-4(Free base)) 是Mu-opioid 受体的强效选择性激动剂。它也是镇痛药。它刺激钙激活的腺苷酸环化酶相关 cAMP 的产生。通过 TGF-beta1 表达趋化因子和趋化因子受体。增加老鼠的食物摄入量。
T80050	Noxiustoxin	Potassium Channel	Membrane transporter/Ion channel
	Noxiustoxin为墨西哥蝎子Centruroides noxius毒液中的一种毒素，它能够抑制电压依赖性钾通道（Kv1.3，IC50=360 nM）及钙激活钾通道。该毒素在神经炎症疾病中具有重要作用。
T80455	ω-Conotoxin CVIB	Sodium Channel	Membrane transporter/Ion channel
	ω-Conotoxin CVIB为非选择性N型及P/Q型电压门控钙通道(VGCC)拮抗剂，能够抑制背根神经节(DRG)中神经元去极化后激活全细胞VGCC电流，其pIC50值为7.64。
T36215	17R(18S)-EpETE
	17R(18S)-EpETE is an oxylipin and a cytochrome P450 metabolite of eicosapentaenoic acid .1,217R(18S)-EpETE is an activator of large-conductance calcium-activated potassium (BKCa) channels, increasing the potassium current amplitude by 15-fold in isolated rat cerebral artery vascular smooth muscle cells (VSMCs) at +60 mV when used at a concentration of 50 nM.2It has negative chronotropic effects in isolated neonatal rat cardiomyocytes (NRCMs; EC50= ~1-2 nM) and prevents calcium-induced increases ...
T37808	Kaliotoxin
	aliotoxin是神经BK型肽基的抑制剂，对Kv通道和钙激活的钾通道能产生特异性抑制。Kaliotoxin对细胞膜电位和神经元兴奋性的调控具有研究意义。其产品编号为 T37808，CAS号为 145199-73-1
T37649	5(S),12(S)-DiHETE
	5(S),12(S)-DiHETE is a natural bioactive lipid derived from arachidonic acid . It is synthesized by glycogen-induced rabbit peritoneal polymorphonuclear leukocytes (PMNLs) incubated with AA. 5(S),12(S)-DiHETE can be produced by successive oxygenation of AA by 5-lipoxygenase (5-LO) in platelets and 12-LO in leukocytes. It can also be synthesized from 12(S)-HETE by 5-LO, in the presence of 5-LO activating protein (FLAP), activated with calcium ionophore. 5(S),12(S)-DiHETE is an epimer of leukotrie...
T62543	JNc-440
	JNc-440 是一种有效的抗高血压剂。JNc-440 能够提高内皮细胞瞬时受体电位香草酸亚型 4 (TRPV4) 和钙离子激活钾通道 3 (KCa2.3) 的相互作用。JNc-440 也可以提高小鼠血管扩张，具有降压活性。
T22014	8-CPT-2Me-cAMP, sodium salt
	8-CPT-2Me-cAMP sodium is a sodium salt compound that selectively activates exchange proteins activated by cAMP (Epac). These Epac proteins are cAMP-sensitive guanine nucleotide exchange factors (GEFs) responsible for activating small GTPases Rap1 and Rap2. 8-CPT-2Me-cAMP sodium specifically activates Epac1 with an EC50 value of 2.2 μM, while showing no activation of PKA with an EC50 value greater than 10 μM [1]. Additionally, 8-CPT-2Me-cAMP sodium stimulates the Epac-mediated release of calcium ...
T35955	PAR2 (1-6) amide (human) (trifluoroacetate salt) PAR2 (1-6) amide (human) (trifluoroacetate salt)
	PAR2 (1-6) amide is a synthetic peptide agonist of proteinase-activated receptor 2 (PAR2) that corresponds to residues 1-6 of the amino terminal tethered ligand sequence of human PAR2 and residues 37-42 of the full-length sequence.1It binds to NCTC 2544 cells expressing human PAR2 (Ki= 9.64 μM in a radioligand binding assay) and induces calcium mobilization in the same cells (EC50= 0.075 μM).2PAR2 (1-6) amide (100 μM) reduces colony formation of A549 lung cancer cells.1It induces superoxide prod...
T71303	Flufenamic Acid-d4
	Flufenamic acid-d4 is intended for use as an internal standard for the quantification of flufenamic acid by GC- or LC-MS. Flufenamic acid is a non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor (IC50s = 3 and 9.3 µM for human COX-1 and COX-2, respectively). Flufenamic acid inhibits TNF-α-induced increases in COX-2 levels and NF-κB activation in HT-29 colon cancer cells in a concentration-dependent manner. It inhibits calcium influx induced by fMLP or A23187 in human polymorphonuclear...
T37821	AP 14145 hydrochloride
	KCa2 (small conductance Ca2+-activated potassium) channel negative allosteric modulator (IC50 = 1.1 μM). Increases the EC50 of Ca2+ on KCa2.3 channels by ~3-fold. Prolongs atrial effective refractory period (AERP) in rats. Reduces atrial fibrillation (AF) duration and prolongs atrial refractoriness without affecting ventricular refractory period in an animal AF model. Diness et al (2017) Termination of vernakalant-resistant atrial fibrillation by inhibition of small-conductance Ca2+-activated K+...
T83868	(±)13,14-EDT (±)13,14-Epoxydocosatrienoic Acid,(±)13,14-EpDoTrE,(±)-Dihomo-13,14-EET
	(±)13,14-EDT是一种氧脂和腎上腺酸的代谢产物，通过细胞色素P450（CYP）途径形成。在50 nM的浓度下，它能激活分离的大鼠冠状小动脉平滑肌细胞中的大导电钙激活钾通道（KCa1.1/BK），并导致分离的猪小动脉扩张（EC50 = 12 pM）。(±)13,14-EDT还能使用TP受体激动剂U-46619预收缩的分离牛冠状动脉放松。

化合物

Cat.No: T13047

Target: Calcium Channel

CRAC intermediate 2

Cat.No: T10885

Target: Others, Calcium Channel

Cat.No: T24984

Target: Calcium Channel

CRAC intermediate 1

Cat.No: T10884

Synonym: 5-(S)-Fluorowillardiine

Target: Calcium Channel

Cat.No: T3651

Synonym: YM 58483,BTP2

Target: Calcium Channel

RO2959 Hydrochloride

Cat.No: T8867

Synonym: RO2959 HCl

Target: IL Receptor, Calcium Channel, Interleukin

Cat.No: T9522

Synonym: CAD-1883

Target: Potassium Channel

Cat.No: TQ0033

Synonym: CM-4620,N-(5-(6-Chloro-2,2-difluorobenzo[d][1,3]dioxol-5-yl)pyrazin-2-yl)-2-fluoro-6-methylbenzamide,CM4620

Target: Calcium Channel

Flufenamic acid

Cat.No: T0858

Synonym: Arlef,Nichisedan,氟灭酸,氟芬那酸,Achless

Target: Potassium Channel, Calcium Channel, Chloride channel, COX, AMPK, Parasite

Cat.No: T9245

Synonym: CBA,4-chloro-2-(2-(2-chlorophenoxy)acetamido)benzoic acid

Target: TRP/TRPV Channel

SKF-96365 hydrochloride

Cat.No: T2170

Synonym: 1-[2-(4-甲氧基)-2-[3-(4-甲氧基苯基)丙氧基]乙基]咪唑,SKF96365

Target: Apoptosis, Potassium Channel, Calcium Channel, TRP/TRPV Channel, Autophagy

Cat.No: T7512

Synonym: BMS-A

Target: Potassium Channel

Cat.No: T4330

Target: Chloride channel

Cat.No: T22946

Synonym: LY 255283

Target: Leukotriene Receptor

Cat.No: T13059

Target: Chloride channel

Cat.No: T24799

Synonym: SKA 111,SKA111

Target: Potassium Channel

Cat.No: T4503

Synonym: Somalgen,他尼氟酯

Target: Chloride channel, COX, N-Acetylglucosaminyltransferase, Anion Exchanger

Cat.No: T16345

Synonym: N-(4-chlorophenyl)-2-(3,5-dimethylpyrazol-1-yl)-9-methylpurin-6-amine,N-(4-Chlorophenyl)-2-(3,5-dimethyl-1H-pyrazol-1-yl)-9-methyl-9H-purin-6-amine

Target: Potassium Channel

Cat.No: T4674

Synonym: SB 297006

Target: CCR

N-(p-amylcinnamoyl) Anthranilic Acid

Cat.No: T5454

Synonym: 2-(3-(4-戊基苯基)丙烯酰胺基)苯甲酸,ACA

Target: Phospholipase, TRP/TRPV Channel

Cat.No: T15286

Synonym: BMS-204352

Target: Potassium Channel

Cat.No: T0782

Synonym: Aquatag,苄噻嗪,Lemazide,Dihydrex

Target: Carbonic Anhydrase

Cat.No: T68583

AF2 Neuropeptide

Cat.No: TP2329

Cat.No: T24614

Synonym: PF04471141 hydrochloride,PF04471141,PF 04471141,PF-04471141

Cat.No: TP2004

Cat.No: T80850

Synonym: VU245

Cat.No: T82723

12,14-Dichlorodehydroabietic acid

Cat.No: T40750

Cat.No: T61818

Cat.No: T71295

Cat.No: T28140

Synonym: NCG-21,NCG 21

Cat.No: T80065

Target: Calcium Channel

Mibefradil dihydrochloride hydrate

Cat.No: T64151

Cat.No: T80068

Target: Potassium Channel

Cat.No: T39283

1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE

Cat.No: T37284

Cat.No: T83740

DAMGO TFA (78123-71-4(Free base))

Cat.No: T4411

Target: Opioid Receptor

Cat.No: T80050

Target: Potassium Channel

ω-Conotoxin CVIB

Cat.No: T80455

Target: Sodium Channel

Cat.No: T36215

Cat.No: T37808

5(S),12(S)-DiHETE

Cat.No: T37649

Cat.No: T62543

8-CPT-2Me-cAMP, sodium salt

Cat.No: T22014

PAR2 (1-6) amide (human) (trifluoroacetate salt)

Cat.No: T35955

Synonym: PAR2 (1-6) amide (human) (trifluoroacetate salt)

Flufenamic Acid-d4

Cat.No: T71303

AP 14145 hydrochloride

Cat.No: T37821

Cat.No: T83868

Synonym: (±)13,14-Epoxydocosatrienoic Acid,(±)13,14-EpDoTrE,(±)-Dihomo-13,14-EET

Cat. No.	Product Name	Target	Signaling Pathways
T3904	Gomisin J	Calcium Channel; AMPK	Chromatin/Epigenetic; Membrane transporter/Ion channel; Metabolism; PI3K/Akt/mTOR signaling
	Gomisin J 是在五味子中发现的小分子量木脂素，具有血管舒张活性，在非酒精性脂肪性肝病方面有研究潜力。它通过激活 AMPK、LKB1 和 Ca2+/钙调蛋白依赖性蛋白激酶 II 以及抑制 HepG2 细胞中的胎球蛋白 A 来调节脂肪生成酶和脂肪分解酶以及炎症分子的表达，从而抑制脂质积累。
T5701	OPHIOPOGONIN D 麦冬皂苷 D,麦冬皂苷D	RAAS; Calcium Channel; NF-κB; PPAR	DNA Damage/DNA Repair; Endocrinology/Hormones; Membrane transporter/Ion channel; Metabolism; NF-κB
	Ophiopogonin D 是从麦冬的块茎中分离的一种天然产物，是罕见的天然存在的 C29甾体糖苷。它是一种 CYP2J3 诱导剂，用于炎症和心血管疾病的相关研究。
T2946	Tanshinone IIA sulfonate sodium 丹参酮IIA磺酸盐,丹参酮IIA-磺酸钠,Tanshinone IIA sulfonate,Sodium Tanshinone IIA sulfonate,Tanshinone IIA sodium sulfonate,sodium	CaMK; P450; Calcium Channel	Membrane transporter/Ion channel; Metabolism; Neuroscience
	Tanshinone IIA sulfonate sodium (Tanshinone IIA sodium sulfonate) 是从丹参中提取的丹参酮IIA 的水溶性衍生物，是SOCE 抑制剂，用于心血管疾病的研究。
T0728	Ethosuximide Zarontin,乙琥胺	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Ethosuximide (Zarontin) 是一种抗癫痫药物，可改善多种神经退行性疾病模型的表型，且阻断低电压激活的 T 型钙通道。
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。
TN4051	Fargesone B	cAMP; Calcium Channel	GPCR/G Protein; Membrane transporter/Ion channel; Metabolism
	Fargesone B inhibits the vascular smooth muscle contraction by suppressing the voltage- and receptor-activated calcium influxes in a nonselective manner.

天然产物

Cat.No: T3904

Target: Calcium Channel, AMPK

Cat.No: T5701

Synonym: 麦冬皂苷 D,麦冬皂苷D

Target: RAAS, Calcium Channel, NF-κB, PPAR

Tanshinone IIA sulfonate sodium

Cat.No: T2946

Synonym: 丹参酮IIA磺酸盐,丹参酮IIA-磺酸钠,Tanshinone IIA sulfonate,Sodium Tanshinone IIA sulfonate,Tanshinone IIA sodium sulfonate,sodium

Target: CaMK, P450, Calcium Channel

Cat.No: T0728

Synonym: Zarontin,乙琥胺

Target: Calcium Channel

Dihydrocapsaicin

Cat.No: T2163

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

Target: Others, TRP/TRPV Channel

Cat.No: TN4051

Target: cAMP, Calcium Channel

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