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75

抑制剂 & 化合物

18

天然产物

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Cat. No. Product Name Target Signaling Pathways
T7736 2-Chloroadenosine

Adenosine Receptor GPCR/G Protein; Neuroscience
2-Chloroadenosine 是腺苷类似物,可防止大鼠海马缺血细胞长期丢失。它是尿苷内流 (Ki:33 μM) 的竞争性抑制剂,高亲和力与硝基苄基硫肌苷结合 (Ki:0.18 mM)。它是一种人红细胞核苷转运体的转运渗透剂。
T6777 Bay K 8644

(±)-BAY-K-8644,SQ 28,873

Calcium Channel Membrane transporter/Ion channel; Metabolism
Bay K 8644 (SQ 28,873)是一种二氢吡啶化合物,是一种选择性的 L 型 Ca2+ 通道激活剂,IC50 为 17.3 nM。它通过增加通道的开放时间来增加通过肌膜 Ca2+通道的 Ca2+流入。
T0370 Pheniramine maleate

Daneral,Inhiston,Trimetose,马来酸非尼拉敏

5-HT Receptor; Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Pheniramine maleate (Trimetose) 是一种具有抗组胺和血管扩张特性的烷基胺衍生物,可与组胺 H1 受体结合,从而抑制磷脂酶 A2 和内皮源性松弛因子一氧化氮的产生。
T40101 (±)-1,2-Diolein

1,2-Dioleoyl-rac-glycerol,甘油1,2-二油酸酯

PKC Chromatin/Epigenetic; Cytoskeletal Signaling
(±)-1,2-Diolein (1,2-Dioleoyl-rac-glycerol) 是一种PKC 激活剂,可以增加肌小管 Ca2+内流。
T2711 Chembridge-5861528

TCS 5861528

TRP/TRPV Channel Membrane transporter/Ion channel
Chembridge-5861528 (TCS 5861528) 是有效的 TRPA1离子通道阻断剂。
T6530 HC-030031

2-(1,3-二甲基-2,6-二氧代-2,3-二氢-1H-嘌呤-7(6H)-基)-N-(4-异丙基苯基)乙酰胺,HC030031,TOSLAB 829227

TRP/TRPV Channel Membrane transporter/Ion channel
HC-030031 (TOSLAB 829227) 是一种有效的TRPA1选择性抑制剂,拮抗福尔马林和AITC 诱发的钙流入,IC50分别为5.3±0.2和6.2±0.2μM。
T12234 NMDA-IN-1

NMDAR Neuroscience
NMDA-IN-1是一种 NR2B 选择性 NMDA 拮抗剂,对NMDA 的Ki 值为 0.85 nM,对NR2B Ca2+ influx 的IC50值为 9.7 nM。
TNU0864 HUP30

Potassium Channel; Calcium Channel Membrane transporter/Ion channel; Metabolism
HUP30是一种强效的血管舒张剂。HUP30可以刺激可溶性鸟苷酸环化酶,激活 K+离子通道,阻断细胞外 Ca2+的内流。
T16687 Pyr3

TRP/TRPV Channel Membrane transporter/Ion channel
Pyr3 是一种选择性瞬时受体电位经典通道 3 抑制剂。 Pyr3 以剂量依赖性方式抑制 TRPC3 介导的 Ca2+ 内流 (IC50 = 700 nM)。
T1425 Pemirolast potassium

BMY 26517,TWT-8152,吡嘧司特钾

Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Pemirolast potassium (TWT-8152) 是 H1组胺受体拮抗剂和肥大细胞稳定剂,是一种具有抗过敏特性的嘧啶酮衍生物。
T6645 Ropivacaine hydrochloride monohydrate

Ropivacaine HCl,Ropivacaine HCl monohydrate,LEA 103,盐酸罗哌卡因,盐酸罗哌卡因一水合物,LEA-103 HCl

Potassium Channel; Sodium Channel Membrane transporter/Ion channel
Ropivacaine hydrochloride monohydrate (LEA-103 HCl) 是钠通道阻断剂,通过可逆地抑制钠离子内流从而引起神经纤维脉冲传导阻滞。Ropivacaine HCl monohydrate 也是 K2P(双孔钾通道)TREK-1的抑制剂。在动物实验模型中,Ropivacaine HCl monohydrate 可用于神经性疼痛的缓解。
T1768 7ACC2

Mitochondrial Metabolism; Monocarboxylate transporter Membrane transporter/Ion channel; Metabolism
7ACC2 是单羧酸盐转运蛋白抑制剂,IC50为 11 nM。它还是线粒体丙酮酸转运的有效抑制剂,可抑制乳酸涌入,通过抑制乳酸通量来发挥抗癌作用。
T5845 7ACC1

DEAC,香豆素D1421,Coumarin D 1421,7-(二乙胺基)-2-氧代-2-苯并吡喃-3-羧酸,7-(Diethylamino)coumarin-3-carboxylic acid,D 1421

Monocarboxylate transporter Membrane transporter/Ion channel
7ACC1 (D 142) 抑制表达MCT1和MCT4肿瘤细胞的乳酸涌入,能选择性干扰肿瘤微环境乳酸通量。
T16688 Pyr6

N-[4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl]phenyl]-3-fluoro-4-pyridinecarboxamide

TRP/TRPV Channel Membrane transporter/Ion channel
Pyr6 (N-[4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl]phenyl]-3-fluoro-4-pyridinecarboxamide)是选择性的 TRPC3抑制剂,IC50值为0.49uM。
T11102 DS16570511

Calcium Channel Membrane transporter/Ion channel; Metabolism
DS16570511 是一种细胞渗透性的线粒体钙单核转运蛋白(mitochondrial calcium uniporter)小分子抑制剂,阻断了依赖于 MCU 或 MICU1 的 Ca2+流入增加。
T10782 CGP52411

DAPH

EGFR; Beta Amyloid Angiogenesis; JAK/STAT signaling; Neuroscience; Tyrosine Kinase/Adaptors
CGP52411 是一种具有口服活性的 ATP 竞争性 EGFR 抑制剂(IC50:0.3 μM)。 CGP52411 阻止 Ca2+ 离子有毒流入神经元细胞,并显着抑制和逆转 β-淀粉样蛋白 Aβ42 原纤维聚集体的形成。 CGP52411 可用于阿尔茨海默病的研究。
T0468 Lidocaine

Lignocaine,Alphacaine,Xylocaine,利多卡因

Apoptosis; ERK; NF-κB; MEK; Sodium Channel; Histamine Receptor Apoptosis; GPCR/G Protein; Immunology/Inflammation; MAPK; Membrane transporter/Ion channel; Neuroscience; NF-κB
Lidocaine (Alphacaine) 是一种酰胺衍生物,抑制涉及复杂电压和依赖性的钠通道,可用于研究室性心律失常。它通过调节 miR-145 表达和进一步抑制 MEK/ERK 和 NF-κB 信号通路来减少胃癌细胞的生长,迁移和侵袭。
T0018 Procainamide hydrochloride

Procapan,Procainamide HCl,Pronestyl,Procanbid,盐酸普鲁卡因胺

DNA Methyltransferase; Sodium Channel; AChR; Autophagy Autophagy; Chromatin/Epigenetic; Membrane transporter/Ion channel; Neuroscience
Procainamide hydrochloride (Procapan) 是一种用于研究心律失常的抗心律失常制剂。
TP1910L1 CALP1 acetate

CALP1 acetate(145224-99-3 free base)

CaMK Neuroscience
CALP1 acetate 是一种钙调蛋白 (CaM) 激动剂(Kd 为 88 µM),可与 CaM EF-hand/Ca2+ 结合位点结合。 CALP1 通过抑制钙通道的开放来阻断钙流入和细胞凋亡(IC50 为 44.78 µM)。 CALP1 阻断谷氨酸受体通道并阻断储存操作的非选择性阳离子通道。 CALP1 激活依赖于 CaM 的磷酸二酯酶活性。
T1435 Praziquantel

吡喹酮,Pyquiton,Droncit,Biltricide

Calcium Channel; Antibiotic; Parasite Membrane transporter/Ion channel; Metabolism; Microbiology/Virology
Praziquantel (Droncit) 是一种外消旋混合物,由 (R)-Praziquantel 和 (S)-Praziquantel 组成。它可研究血吸虫病。
T16686 Pyr10

TRP/TRPV Channel Membrane transporter/Ion channel
Pyr10 是吡唑衍生物,是TRPC3通道的选择性抑制剂。Pyr10抑制卡巴可刺激的TRPC3转染的 HEK293 细胞中的 Ca2+流入。它具有区分受体操纵的TRPC3和天然基质相互作用分子 1 (STIM1)/Orai1 通道的能力。
T15257 Etripamil

MSP-2017,(-)-MSP-2017

Calcium Channel Membrane transporter/Ion channel; Metabolism
Etripamil (MSP-2017) 是一种短效L 型钙通道拮抗剂,可用于治疗阵发性室上性心动过速的研究。它通过抑制房室结细胞中钙慢通道的钙离子流入,显示房室结传导并延长房室结不应期
T1613 Hydralazine hydrochloride

Hydralazine HCl,Apresoline,盐酸肼屈嗪

MAO; HIF/HIF Prolyl-Hydroxylase Chromatin/Epigenetic; Metabolism; Neuroscience
Hydralazine hydrochloride (Apresoline) 是一种直接作用的血管舒张剂,可抗高血压。
T1146 Nifedipine

BAY-a-1040,Procardia XL,Procardia,硝苯地平,Adalat

CaMK; Potassium Channel; Calcium Channel; Autophagy Autophagy; Membrane transporter/Ion channel; Metabolism; Neuroscience
Nifedipine (Procardia) 是一种二氢吡啶类钙通道阻滞剂,可抑制细胞外钙离子跨膜流入心肌和血管平滑肌细胞,导致主要冠状动脉和全身动脉扩张,降低心肌收缩力。它常用于心肌功能不全的相关研究。
T4996 Atosiban

阿托西班,RWJ22164,RW22164

Oxytocin Receptor; Vasopressin Receptor Endocrinology/Hormones; GPCR/G Protein
Atosiban (RW22164) 是一种脱氨基催产素类似物,是一种九肽,也是竞争性的催产素受体拮抗剂。它是一种宫缩抑制剂,可用于自发早产的研究。
T22043 BCATc Inhibitor 2

Others Others
BCATc Inhibitor 2 是选择性分支链氨基转移酶抑制剂,可用于神经退行性疾病的研究。能够抑制 rBCATc (IC50:0.2 μM),hBCATc (IC50:0.8 μM)、 rBCATm (IC50:3.0 μM)。其中BCATc 也称为 BCAT1,存在于细胞质基质中的亚型。
T3979 Emedastine

LY188695,依美斯汀,Emadine

Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Emedastine (LY188695) 是一种可口服的,选择性和高亲和力的组胺 H1受体拮抗剂,Ki 值为 1.3 nM。它是苯并咪唑衍生物,可用于过敏性鼻炎、过敏性皮肤疾病和过敏性结膜炎的研究。
T5148 Atosiban acetate

RW22164,Atosiban acetate (90779-69-4 free base),RWJ22164,醋酸阿托西班

Oxytocin Receptor; Vasopressin Receptor Endocrinology/Hormones; GPCR/G Protein
Atosiban acetate (RW22164) 是一种脱氨基催产素类似物,是一种九肽,也是竞争性的催产素受体拮抗剂。它是一种宫缩抑制剂,可用于自发早产的研究。
T4316 ML365

Potassium Channel Membrane transporter/Ion channel
ML365 是有效的,选择性的双孔结构域钾通道TASK1/KCNK3抑制剂,IC50为 4 nM。它可用于检查 TASK1 通道的特定作用。
T27639 ITH-12575

ITH-12575 is an inhibitor of Mitochondrial Na+/Ca2+ exchange (mNCX). ITH12575 reduces Ca(2+) influx through CALHM1 at low micromolar concentrations.
T26376 11-deoxy-PGF2a

11-deoxyPGF2a,11-deoxy PGF2a

11-deoxy-PGF2a, a selective activator of TREK-2 channels, stimulates DRG c-fiber nociceptor K2P currents and limits calcium influx.
T68742 Inamrinone lactate

Inamrinone lactate is a positive inotropic cardiotonic with vasodilator properties, phosphodiesterase inhibitory activity, and the ability to stimulate calcium ion influx into the cardiac cell.
T11480 GSK205

Others Others
GSK205 is a selective TRPV4 antagonist (IC50: 4.19 μM) for inhibiting TRPV4-mediated Ca2+ influx.
T37763 BTD

Selective TRPC5 activator (EC50 = 1.4 μM in a calcium influx assay, 1.3 μM in whole cell patch clamp assay). Displays >14.5-fold selectivity for TRPC5 over other TRP channels (EC50 = 20.6 μM for TRPM8). Also activates TRPC1:5 and TRPC4:5 heteromers. Beckmann et al (2017) A benzothiadiazine derivative and methylprednisolone are novel and selective activators of transient receptor potential canonical 5 (TRPC5) channels. Cell Calcium. 66 10 PMID:28807145
T71735 AAL1

AAL1 is an inhibitor of dark-grown Arabidopsis thaliana seedlings, functioning through auxin receptor Transport Inhibitor Response1 (TIR1) and depending on auxin influx and efflux carriers.
T14829 Bromoenol lactone

(6E)-Bromoenol lactone

Phospholipase Metabolism
Bromoenol lactone is a suicide-based irreversible, selective, potent inhibitor of calcium-independent phospholipase A2 (iPLA2β; IC50: ~7 μM). It inhibits antigen-stimulated mast cell exocytosis without blocking Ca2+ influx.
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.
T68361 Asocainol hydrochloride

Asocainol hydrochloride ia an antiarrhythmic drug which inhibits slow Ca2+ influx. This is accompanied by alterations in normal Na+-carried action potentials. Therefore, Asocainol not only inhibits Ca2+ inflow but also interferes with the fast inward Na+ current.
T62660 MLN3126

MLN3126 是一种口服具有活力的强效 CCR9 拮抗剂。 MLN3126 抑制 CCL25 诱导的钙动员 (calcium mobilization) 和小鼠初级胸腺细胞趋化 (chemotaxis) (IC50: 6.3 nM)。
T61438 Propiverine

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].
T79618 M3/PDE4 modulator-1

M3/PDE4 modulator-1 (10f) 为多功能化合物,具备M3mAChR拮抗和PDE4抑制作用。于OVA大鼠模型中,M3/PDE4 modulator-1 (10-1000 nM/kg;iv) 能降低半胱氨酸嗜酸性粒细胞内流。
T80441 FS-2

Calcium Channel Membrane transporter/Ion channel; Metabolism
FS-2,一种特异性L型CaV通道抑制剂,能够阻断RIN beta 细胞中,高K+或葡萄糖刺激导致的L型Ca2+内流。
T37759 Fura-2 (potassium salt)

Fura-2 is a ratiometric fluorescent calcium indicator that can be used to detect calcium in cells. [1] It is a pentacarboxylate that displays excitation maxima of 340 and 380 nm at high and low calcium concentrations, respectively, when the emission is fixed at 510 nm, enabling determination of ratiometric measurements of calcium influx in live cells.
T37475 Cyclic ADP-Ribose (ammonium salt)

cADP-Ribose,cADPR,Cyclic ADP-Ribose (ammonium salt)

Cyclic ADP-ribose (cADP-ribose) is an endogenous metabolite of NAD+ that mobilizes the release of stored Ca2+ in the endoplasmic reticulum via ryanodine receptors in various cell types.[1],[2],[3],[4],[5] This second messenger is generated via the cADP-ribose synthases CD38 and CD157.[6],[5],[7] cADP-Ribose may also trigger the cell surface Ca2+ influx channel TRPM2 in a temperature-dependent manner.[8] In vitro, cADP-ribose modulates Ca2+ signaling in rat and mouse cardiomyocytes treated with i...
T26447 A 78773

A78773,A-78773

A 78773 is a potent, selective, direct, and reversible 5-lipoxygenase inhibitor. It has activity in a variety of purified cells and in more complex biological systems such as whole blood, lung fragments, and tracheal tissues. A 78773 acts against inflamma
T37760 Fura-2 (sodium salt)

Fura-2 is a ratiometric fluorescent calcium indicator that can be used to detect calcium in cells. It is a pentacarboxylate that displays excitation maxima of 340 and 380 nm at high and low calcium concentrations, respectively, when the emission is fixed at 510 nm, enabling determination of ratiometric measurements of calcium influx in live cells.
T70224 Bupivacaine tartrate

Bupivacaine is a BK/SK, Kv1, Kv3, TASK-2 K Channel and voltage-gated Na channel blocker used as an anesthetic. It maybe neurotoxic at high does, inducing apoptosis in neuroblastoma cells. It acts by binding to the intracellular portion of voltage-gated sodium channels and blocking sodium influx into nerve cells.
T23102 OBAA

Others Others
OBAA 是一种有效的磷脂酶 A2 (PLA2) 抑制剂(IC50= 70 nM),并且在布氏锥虫中阻断 Melittin 诱导的 Ca2+流入(IC50= 0.4 μM)。
T37058 D-myo-Inositol-1,3,4,5-tetraphosphate (sodium salt)

D-myo-Inositol-1,3,4,5-tetraphosphate (Ins(1,3,4,5)-P4) is formed by the phosphorylation of Ins(1,4,5)P3 by inositol 1,4,5-triphosphate 3-kinase. Ins(1,3,4,5)-P4 increases intracellular calcium levels by two distinct mechanisms: opening calcium channels on both the endoplasmic reticulum to release calcium from internal stores and on the plasma membrane to allow the influx of calcium from outside the cell.
T61475 Ropivacaine mesylate

Ropivacaine mesylate 是一种高效的钠通道 (sodium channel) 阻断剂,通过可逆性抑制钠离子内流 (sodium ion influx),引致神经纤维脉冲传导阻滞。此外,Ropivacaine 还能抑制 K2P(双孔钾通道)TREK-1,其在 COS-7 细胞膜上的 IC50 值为 402.7 μM。

化合物

2-Chloroadenosine
Cat.No: T7736
Synonym:
Target: Adenosine Receptor
Bay K 8644
Cat.No: T6777
Synonym: (±)-BAY-K-8644,SQ 28,873
Target: Calcium Channel
Pheniramine maleate
Cat.No: T0370
Synonym: Daneral,Inhiston,Trimetose,马来酸非尼拉敏
Target: 5-HT Receptor, Histamine Receptor
(±)-1,2-Diolein
Cat.No: T40101
Synonym: 1,2-Dioleoyl-rac-glycerol,甘油1,2-二油酸酯
Target: PKC
Chembridge-5861528
Cat.No: T2711
Synonym: TCS 5861528
Target: TRP/TRPV Channel
HC-030031
Cat.No: T6530
Synonym: 2-(1,3-二甲基-2,6-二氧代-2,3-二氢-1H-嘌呤-7(6H)-基)-N-(4-异丙基苯基)乙酰胺,HC030031,TOSLAB 829227
Target: TRP/TRPV Channel
NMDA-IN-1
Cat.No: T12234
Synonym:
Target: NMDAR
HUP30
Cat.No: TNU0864
Synonym:
Target: Potassium Channel, Calcium Channel
Pyr3
Cat.No: T16687
Synonym:
Target: TRP/TRPV Channel
Pemirolast potassium
Cat.No: T1425
Synonym: BMY 26517,TWT-8152,吡嘧司特钾
Target: Histamine Receptor
Ropivacaine hydrochloride monohydrate
Cat.No: T6645
Synonym: Ropivacaine HCl,Ropivacaine HCl monohydrate,LEA 103,盐酸罗哌卡因,盐酸罗哌卡因一水合物,LEA-103 HCl
Target: Potassium Channel, Sodium Channel
7ACC2
Cat.No: T1768
Synonym:
Target: Mitochondrial Metabolism, Monocarboxylate transporter
7ACC1
Cat.No: T5845
Synonym: DEAC,香豆素D1421,Coumarin D 1421,7-(二乙胺基)-2-氧代-2-苯并吡喃-3-羧酸,7-(Diethylamino)coumarin-3-carboxylic acid,D 1421
Target: Monocarboxylate transporter
Pyr6
Cat.No: T16688
Synonym: N-[4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl]phenyl]-3-fluoro-4-pyridinecarboxamide
Target: TRP/TRPV Channel
DS16570511
Cat.No: T11102
Synonym:
Target: Calcium Channel
CGP52411
Cat.No: T10782
Synonym: DAPH
Target: EGFR, Beta Amyloid
Lidocaine
Cat.No: T0468
Synonym: Lignocaine,Alphacaine,Xylocaine,利多卡因
Target: Apoptosis, ERK, NF-κB, MEK, Sodium Channel, Histamine Receptor
Procainamide hydrochloride
Cat.No: T0018
Synonym: Procapan,Procainamide HCl,Pronestyl,Procanbid,盐酸普鲁卡因胺
Target: DNA Methyltransferase, Sodium Channel, AChR, Autophagy
CALP1 acetate
Cat.No: TP1910L1
Synonym: CALP1 acetate(145224-99-3 free base)
Target: CaMK
Praziquantel
Cat.No: T1435
Synonym: 吡喹酮,Pyquiton,Droncit,Biltricide
Target: Calcium Channel, Antibiotic, Parasite
Pyr10
Cat.No: T16686
Synonym:
Target: TRP/TRPV Channel
Etripamil
Cat.No: T15257
Synonym: MSP-2017,(-)-MSP-2017
Target: Calcium Channel
Hydralazine hydrochloride
Cat.No: T1613
Synonym: Hydralazine HCl,Apresoline,盐酸肼屈嗪
Target: MAO, HIF/HIF Prolyl-Hydroxylase
Nifedipine
Cat.No: T1146
Synonym: BAY-a-1040,Procardia XL,Procardia,硝苯地平,Adalat
Target: CaMK, Potassium Channel, Calcium Channel, Autophagy
Atosiban
Cat.No: T4996
Synonym: 阿托西班,RWJ22164,RW22164
Target: Oxytocin Receptor, Vasopressin Receptor
BCATc Inhibitor 2
Cat.No: T22043
Synonym:
Target: Others
Emedastine
Cat.No: T3979
Synonym: LY188695,依美斯汀,Emadine
Target: Histamine Receptor
Atosiban acetate
Cat.No: T5148
Synonym: RW22164,Atosiban acetate (90779-69-4 free base),RWJ22164,醋酸阿托西班
Target: Oxytocin Receptor, Vasopressin Receptor
ML365
Cat.No: T4316
Synonym:
Target: Potassium Channel
ITH-12575
Cat.No: T27639
Synonym:
Target:
11-deoxy-PGF2a
Cat.No: T26376
Synonym: 11-deoxyPGF2a,11-deoxy PGF2a
Target:
Inamrinone lactate
Cat.No: T68742
Synonym:
Target:
GSK205
Cat.No: T11480
Synonym:
Target: Others
BTD
Cat.No: T37763
Synonym:
Target:
AAL1
Cat.No: T71735
Synonym:
Target:
Bromoenol lactone
Cat.No: T14829
Synonym: (6E)-Bromoenol lactone
Target: Phospholipase
12,14-Dichlorodehydroabietic acid
Cat.No: T40750
Synonym:
Target:
Asocainol hydrochloride
Cat.No: T68361
Synonym:
Target:
MLN3126
Cat.No: T62660
Synonym:
Target:
Propiverine
Cat.No: T61438
Synonym:
Target:
M3/PDE4 modulator-1
Cat.No: T79618
Synonym:
Target:
FS-2
Cat.No: T80441
Synonym:
Target: Calcium Channel
Fura-2 (potassium salt)
Cat.No: T37759
Synonym:
Target:
Cyclic ADP-Ribose (ammonium salt)
Cat.No: T37475
Synonym: cADP-Ribose,cADPR,Cyclic ADP-Ribose (ammonium salt)
Target:
A 78773
Cat.No: T26447
Synonym: A78773,A-78773
Target:
Fura-2 (sodium salt)
Cat.No: T37760
Synonym:
Target:
Bupivacaine tartrate
Cat.No: T70224
Synonym:
Target:
OBAA
Cat.No: T23102
Synonym:
Target: Others
D-myo-Inositol-1,3,4,5-tetraphosphate (sodium salt)
Cat.No: T37058
Synonym:
Target:
Ropivacaine mesylate
Cat.No: T61475
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
TN1121 Evocarpine

Apoptosis; cAMP; Anti-infection; Calcium Channel; Antibacterial Apoptosis; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology
Evocarpine 是从 Evodiae fructus 分离得到的一种喹诺酮类生物碱,有抗细菌活性。它可通过电压依赖性钙通道抑制 Ca2+内流。
T8118 Bekanamycin

Kanamycin B,卡那霉素,卡那霉素 B

Antibacterial; Antibiotic Microbiology/Virology
Bekanamycin (Kanamycin B) 是一种提取自 Streptomyces kanamyceticus 的氨基糖苷类抗生素,抑制一系列革兰氏阳性和阴性细菌。
T23735 Jamaicin

An-Co-A4,AnCoA-4,An Co A4,AnCoA4

Calcium Channel Membrane transporter/Ion channel; Metabolism
Jamaicin (AnCoA4) 是一种从鸡血藤植物中提取的异黄酮,是一种 STIM1-Orai1 通道的抑制剂,可阻断钙离子流入,减少其与 STIM1 的相互作用,抑制 T 细胞的活化。
TN1154 Nepetin

6-Methoxyluteolin,泽兰黄酮,6-甲氧基藤黄菌素

Calcium Channel; Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience
Nepetin (6-Methoxyluteolin) 是一种分离自Eupatorium ballotaefoliumHBK 中的天然类黄酮,具有有效的抗炎作用。它在 ARPE-19 细胞中能够抑制IL-6(IC50:4.43 μM) 、IL-8 (IC50:43.42 μM) 、MCP-1 (IC50:4.17 μM) 的分泌。
TN1136 Procyanidin A1

原花青素 A1,Proanthocyanidin A1,原花色素A1

LDL; Calcium Channel; PKC Chromatin/Epigenetic; Cytoskeletal Signaling; Membrane transporter/Ion channel; Metabolism
Procyanidin A1 (Proanthocyanidin A1) 是一种原花青素二聚体,具有抗过敏作用,可抑制蛋白激酶 C 激活下游脱粒或 RBL-213 细胞内部储存的 Ca2+流入。
TN2322 Yangambin

Calcium Channel; PAFR GPCR/G Protein; Membrane transporter/Ion channel; Metabolism
Yangambin 是从诸如番荔枝科植物中分离出来的呋喃木脂素,是选择性PAF 受体拮抗剂,通过调控Ca2+通道抑制 Ca2+流入,导致 [Ca2+]i 在血管平滑肌细胞和随后的外周血管舒张中减少,具有降压作用。
T5S0890 Oleandrin

Neriostene,Folinerin,Foliandrin,欧夹竹桃苷

Apoptosis; ATPase; Potassium Channel; Sodium Channel Apoptosis; Membrane transporter/Ion channel
Oleandrin (Folinerin) 是夹竹桃属中的一种类固醇,可抑制Na+/K+-ATPase 活性,IC50为 620 nM。
T5120 Rhamnose

6-Deoxyhexopyranose,L-鼠李糖,6-Deoxy-L-mannose,alpha-L-Rhamnose

Calcium Channel; Endogenous Metabolite Membrane transporter/Ion channel; Metabolism
alpha-L-Rhamnose (6-Deoxy-L-mannose) 是存在植物和细菌中的一种单糖。Rhamnose- 免疫原连接物能被用于免疫疗法。Rhamnose 能通过胞外途径穿过上皮细胞,能够作为肠吸收的标志。
TN1065 Hirsutine

Apoptosis Apoptosis
Hirsutine 是一种来自钩藤的吲哚生物碱,可诱导细胞凋亡,是一种登革热病毒抑制剂,且毒性低。它具有抗癌、心脏保护、抗高血压、抗心律失常和血管舒张活性。
T4S1422 Praeruptorin E

白花前胡素 E,白花前胡素E

Others; Calcium Channel Membrane transporter/Ion channel; Metabolism; Others
Praeruptorin E 是白花前胡中的一种主要成分,是钙拮抗剂,pD2′值为 5.2。
T6S2140 β-Anhydroicaritin

Anhydroicaritin,Beta-Anhydroicaritin,脱水淫羊藿素

MMP; Others; TNF; Interleukin Apoptosis; Immunology/Inflammation; Others; Proteases/Proteasome
β-Anhydroicaritin 是从乳香提取的一种天然产物,具有重要的生物学和药理学作用,如抗骨质疏松症,雌激素调节和抗肿瘤特性。它改善牙周组织的降解,抑制糖尿病大鼠 TNF-α 和 MMP-3 的合成和分泌。它抑制细胞内 Ca2+的升高,并显著降低 iNOS 蛋白的表达。
T37687 Cyclic ADP-ribose ammonium

Cyclic ADP-ribose ammonium (cADPR ammonium) is a powerful calcium mobilization second messenger synthesized from NAD+ by an ADP-ribosyl cyclase. It primarily raises cytosolic calcium levels through Ryanodine receptor-mediated release from the endoplasmic reticulum, while also facilitating extracellular influx through the opening of TRPM2 channels [1][2][3].
T19253 Cyclic ADP-​ribose

cADPR

Calcium Channel Membrane transporter/Ion channel; Metabolism
Cyclic ADP-ribose (cADPR) is an effective calcium mobilization second messenger, which is synthesized from NAD + by ADP-ribosyl cyclase. Cyclic ADP-ribose mainly increases cytosolic calcium through Ryanodine receptor-mediated endoplasmic reticulum release
T82753 Celangulin

Celangulin是一种从Celastrus angulatus中提取的天然杀虫成分,该化合物通过激活细胞质膜上的钙通道来增加细胞内Ca2+浓度,并能激活内质网钙通道。
TN2511 Britannilactone diacetate

1,6-O,O-Diacetylbritannilactone

IL Receptor; PARP; ROS; MAPK; Caspase; JAK; JNK; STAT Angiogenesis; Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; JAK/STAT signaling; MAPK; Proteases/Proteasome; Stem Cells
1,6-O,O-Diacetylbritannilactone(OODBL) has anti-inflammatory activity, it has a potential therapeutic efficacy on inflammatory diseases especially allergic airway disease as a lead compound. OODBL has anti-asthmatic activity, it reduces leukotriene C4 pro
TN4624 Nantenine

Others Others
Nantenine is an acetylcholinesterase inhibitor, it functions as an effective antagonist against a wide range of MDMA-induced effects in mice. Nantenine has anticonvulsant effect, which seems attributable to its stimulation and the resultant decrease of Ca
TN2534 1-Hydroxy-2,3,5-trimethoxyxanthone

IκB/IKK; Calcium Channel; NOS; 5-HT Receptor; COX GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB
1-Hydroxy-2,3,5-trimethoxyxanthone (HM-1) has vasodilator action ,which involves both an endothelium-dependent mechanism involving NO and an endothelium-independent mechanism by inhibiting Ca(2+) influx through L-type voltage-operated Ca(2+) channels; a minor contribution to the effects of HM-1 may be related to inhibition of the protein kinase C-mediated release of intracellular Ca(2+) stores. HM-1,at the concentration of 1 ug/mL, can effectively inhibit the osteoclast differentiation in a co-c...
T37219 N-Palmitoyl Glycine

The acyl amides are a family of endogenous lipids that act as potent modulators of pain and inflammation. The best characterized members of this family are the arachidonoyl amides, which includes N-arachidonoyl ethanolamide (AEA; anandamide). N-palmitoyl glycine (PalGly) contains an 18-carbon saturated fatty acid that is amide-linked to glycine and is structurally similar to the phospholipid-derived N-acyl ethanolamines. Endogenously produced in rat skin and spinal cord, PalGly is present in 100...

天然产物

Evocarpine
Cat.No: TN1121
Synonym:
Target: Apoptosis, cAMP, Anti-infection, Calcium Channel, Antibacterial
Bekanamycin
Cat.No: T8118
Synonym: Kanamycin B,卡那霉素,卡那霉素 B
Target: Antibacterial, Antibiotic
Jamaicin
Cat.No: T23735
Synonym: An-Co-A4,AnCoA-4,An Co A4,AnCoA4
Target: Calcium Channel
Nepetin
Cat.No: TN1154
Synonym: 6-Methoxyluteolin,泽兰黄酮,6-甲氧基藤黄菌素
Target: Calcium Channel, Histamine Receptor
Procyanidin A1
Cat.No: TN1136
Synonym: 原花青素 A1,Proanthocyanidin A1,原花色素A1
Target: LDL, Calcium Channel, PKC
Yangambin
Cat.No: TN2322
Synonym:
Target: Calcium Channel, PAFR
Oleandrin
Cat.No: T5S0890
Synonym: Neriostene,Folinerin,Foliandrin,欧夹竹桃苷
Target: Apoptosis, ATPase, Potassium Channel, Sodium Channel
Rhamnose
Cat.No: T5120
Synonym: 6-Deoxyhexopyranose,L-鼠李糖,6-Deoxy-L-mannose,alpha-L-Rhamnose
Target: Calcium Channel, Endogenous Metabolite
Hirsutine
Cat.No: TN1065
Synonym:
Target: Apoptosis
Praeruptorin E
Cat.No: T4S1422
Synonym: 白花前胡素 E,白花前胡素E
Target: Others, Calcium Channel
β-Anhydroicaritin
Cat.No: T6S2140
Synonym: Anhydroicaritin,Beta-Anhydroicaritin,脱水淫羊藿素
Target: MMP, Others, TNF, Interleukin
Cyclic ADP-ribose ammonium
Cat.No: T37687
Synonym:
Target:
Cyclic ADP-​ribose
Cat.No: T19253
Synonym: cADPR
Target: Calcium Channel
Celangulin
Cat.No: T82753
Synonym:
Target:
Britannilactone diacetate
Cat.No: TN2511
Synonym: 1,6-O,O-Diacetylbritannilactone
Target: IL Receptor, PARP, ROS, MAPK, Caspase, JAK, JNK, STAT
Nantenine
Cat.No: TN4624
Synonym:
Target: Others
1-Hydroxy-2,3,5-trimethoxyxanthone
Cat.No: TN2534
Synonym:
Target: IκB/IKK, Calcium Channel, NOS, 5-HT Receptor, COX
N-Palmitoyl Glycine
Cat.No: T37219
Synonym:
Target:
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