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60

抑制剂 & 化合物

8

天然产物

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Cat. No. Product Name Target Signaling Pathways
T6822 Hydroxy-Dynasore

Dyngo-4a

Dynamin Cytoskeletal Signaling
Hydroxy-Dynasore (Dyngo-4a) 是 Dynasore 结构模拟类似物,是一种改进的,低细胞毒性的 dynamin 通用抑制剂,抑制 dynamin 依赖性转铁蛋白的内吞作用的 IC50为 5.7 μM,对大脑重组 dynamin I 和重组鼠 dynamin II 的 IC50值分别为 0.38 μM 和 2.3μM。
T23498 UNC3230

UNC 3230

Others Others
UNC3230 是一种 ATP 竞争性的磷脂酰肌醇 4 磷酸 5 激酶 1C 型 (PIP5K1C) 选择性抑制剂,其IC50约为 41 nM。它还可抑制PIP4K2C,但对其他调节磷酸肌醇水平的脂质激酶无抑制作用。它具有缓解疼痛和抗癌特性。
T14989 CMPD101

ROCK; GRK; PKC Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; GPCR/G Protein; Stem Cells
CMPD101 是膜透性的 GRK2/3高选择性小分子抑制剂,IC50分别为 18 nM 和 5.4 nM。它针对 GRK1、GRK5 ROCK-2 和 PKCα 的选择性较小,IC50值分别为 3.1 μM,2.3 μM,1.4 μM 和 8.1 μM,可研究心衰疾病。
T4993 Afloqualone

氟喹酮,HQ-495

GABA Receptor Membrane transporter/Ion channel; Neuroscience
Afloqualone (HQ-495) 是一种 GABA 受体激动剂。靶点:体外 GABA 受体:Afloqualone 是一种喹唑啉酮家族 GABA 能药物。由于其在 GABAa 受体β亚型的激动剂活性,它具有镇静和肌肉松弛作用。
T7748 Dermorphin TFA

皮啡肽三氟乙酸盐

Others; Opioid Receptor Endocrinology/Hormones; GPCR/G Protein; Neuroscience; Others
Dermorphin TFA 是在两栖类皮肤中发现的天然七肽,是 μ-阿片受体激动剂,可用于抑制神经痛。
T4641 Branaplam

LMI 070,NVS-SM1

Others; Potassium Channel; DNA/RNA Synthesis Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Others
Branaplam (LMI 070) 是一种高效、选择性和口服活性的小分子 SMN2 剪接调节剂,对 SMN 的 EC50为 20 nM。它可提高全长 SMN 蛋白并延长其生存期,也抑制 hERG,IC50为 6.3 μM。
T3217 PF-CBP1 hydrochloride

PF-CBP1 HCl

Epigenetic Reader Domain; Histone Acetyltransferase Chromatin/Epigenetic
PF-CBP1 hydrochloride (PF-CBP1 HCl) 是 CREB 结合蛋白溴结构域的一种高选择性抑制剂,抑制 CREBBP 和 EP300溴结构域的 IC50分别为 125 和 363 nM。它降低 LPS 诱导的巨噬细胞中炎症因子的表达,也可下调皮质神经元 RGS4 的表达,可用于癫痫和帕金森病等神经疾病的研究。
T2141 Mecamylamine hydrochloride

盐酸美加明,Inversine,Mevasin

AChR Neuroscience
Mecamylamine hydrochloride (Mevasin) 是一种易穿过血脑屏障的烟碱拮抗剂,用作高血压的神经节阻滞剂,具有抗神经疾病作用。
T22517 5,7-Dichlorokynurenic acid

5,7-二氯犬尿喹啉酸,5,7-dichlorokynurenic acid sodium,5,7-DCKA

NMDAR Neuroscience
5,7-Dichlorokynurenic acid (5,7-dichlorokynurenic acid sodium) 是一种专门针对于NMDA 受体甘氨酸位点的竞争性拮抗剂(KB:65 nM)。它是犬尿酸的衍生物,可降低大鼠皮质细胞培养物中 NMDA 诱导的神经元损伤程度。
T35878 N-(3-Aminopropyl)cyclohexylamine

Others Others
N-(3-Aminopropyl)cyclohexylamine, a derivative of cyclohexylamine, functions as a selective and competitive inhibitor of spermine synthase, making it suitable for research on neurological diseases[1].
TQ0157 EIPA

L593754,MH 12-43

Sodium Channel; TRP/TRPV Channel Membrane transporter/Ion channel
EIPA (L593754) 是一种有效的TRPP3 channel 抑制剂,IC50为 10.5 μM。EIPA 对Na+/H+交换 (NHE) 和巨噬细胞也有抑制作用。
TP2045 CH 275

Potent somatostatin receptor 1 (sst1) agonist; displays selectivity for sst1 (IC50 values are 30.9 nM, 345 nM, > 1 μM, > 10 μM and > 10μM for human sst1, sst3, sst4, sst2 and sst5 respectively). Attenuates somatostatin release in the rat nucleus accumbens
T7404 Dermorphin

皮啡肽

Opioid Receptor Endocrinology/Hormones; GPCR/G Protein; Neuroscience
Dermorphin 是在两栖类皮肤中发现的天然七肽,是 μ-阿片受体激动剂,可用于抑制神经痛。
TP1827L Neuronostatin-13 human acetate

Neuronostatin-13 human acetate(1096485-24-3 free base)

Others Others
Neuronostatin-13 human acetate(1096485-24-3 free base) 是一种 13 个氨基酸的肽类激素,在调节激素和心脏功能中起重要作用。
T60750 Neuronotoxicity-IN-1

Neuronotoxicity-IN-1 是一种吡啶并噻嗪衍生物。Neuronotoxicity-IN-1 具有神经保护活性,是红藻氨酸神经毒性的抑制剂。
TP1827 Neuronostatin-13 (human)

Neuronostatin-13 human

Neuronostatin-13 (Human) is a 13 amino acid residue peptide with carboxyl-terminal amidation, the primary structure is conserved in human chimpanzee and some other mammals.
TP1852L Myomodulin acetate(110570-93-9 free base)

Potassium Channel; Calcium Channel; Sodium Channel Membrane transporter/Ion channel; Metabolism
Myomodulin acetate(110570-93-9 free base) 存在于两个已识别的海兔神经元中,它们包含肌调节蛋白 A、ARC 运动神经元 B16 和腹部神经元 L10。
T23446 TCS 2210

Others Others
TCS 2210是间充质干细胞中神经元分化的诱导剂,并增加神经元标志物β-III 管蛋白的表达和神经元特异性烯醇酶的表达。
T27084 Crisdesalazine

AAD2004,AAD 2004,AAD-2004

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
Crisdesalazine (AAD 2004) 是微粒体前列腺素 E2 合酶 1 (mPGES-1) 的抑制剂。 Crisdesalazine 可减少自噬体形成、轴索病变和运动神经元变性,改善运动功能并延长寿命。
T16757 Risdiplam

RO7034067,RG7916

DNA/RNA Synthesis Cell Cycle/Checkpoint; DNA Damage/DNA Repair
Risdiplam (RO7034067) 是一种中枢和外周分布的 SMN2 前 mRNA 剪接修饰剂,可增加运动神经元存活 (SMN) 蛋白水平。
T2003 ISX-9

Isoxazole 9,Isoxazole 9 (ISX-9)

Calcium Channel; Wnt/beta-catenin Cytoskeletal Signaling; Membrane transporter/Ion channel; Metabolism; Stem Cells
ISX-9 (Isoxazole 9) 是一种神经干细胞分化的有效诱导剂,可诱导 Notch 激活的心外膜衍生细胞(NEC) 的心肌分化。它可通过电压门控的 Ca2+通道和 NMDA 受体来激活 Ca2+流入,并增加 NeuroD 表达。
T2663 GTS-21 dihydrochloride

GTS 21 dihydrochloride,DMXB-A,DMBX-anabaseine

5-HT Receptor; AChR GPCR/G Protein; Neuroscience
GTS-21 dihydrochloride (DMBX-anabaseine) 是一种选择性 α7 烟碱乙酰胆碱受体激动剂,具有抗炎和增强认知的活性。它也是一种拮抗剂,对人α4β2的 Ki 为20 nM,对5-HT3A 受体的 IC50为3.1 μM。
T5444 CLP290

CLP-290

Potassium Channel Membrane transporter/Ion channel
CLP-290 是一种神经特异性 K+-Cl−共转运体 KCC2的口服激活剂,在多种神经和精神疾病方面具有研究潜力。CLP290 能显著降低 STZ 大鼠的血液中 AVP 和血糖水平。
T27794 λ-Cyhalothrin

lambda-Cyhalothrin,Karate,λ-氯氟氰菊酯,Icon

Sodium Channel; Parasite Membrane transporter/Ion channel; Microbiology/Virology
λ-Cyhalothrin (Icon) 是广谱的 II 型合成除虫菊酯杀虫剂,含有 α-氰基,用于防治多种害虫。它是一种钠通道神经毒素,靶向中枢神经系统中神经元膜。
T4431 Olodanrigan

PD-126055,EMA401

RAAS Endocrinology/Hormones
Olodanrigan (EMA401) 是具有口服活性、高选择性及外周受限的血管紧张素 Ⅱ 类型 2 受体(AT2R)拮抗剂。它的缓解疼痛的机制可能是:抑制增强的 AngII/AT2R 诱导的 p38 和 p42/p44 MAPK 激活,进而阻碍 DRG 神经元的过度兴奋性及 DRG 神经元的萌发。它可用于研究神经性疼痛。
T23709 alphaSYN-IN-NAB2

alphaSYN inhibitor NAB2,alphaSYNINNAB2,alphaSYN-IN-NAB2,NAB2,alphaSYN inhibitor-NAB2

alphaSYN-IN-NAB2 是一种神经元保护剂,是一种由 NAB2基因编码的蛋白质。NAB2 高效且具有选择性地保护多种细胞免受 α-syn 毒性。NAB2 对依赖于 E3 泛素连接酶 Rsp5/Nedd4 的内体转运具有促进作用。NAB2 确定 α-syn 生物学中的一个可活性分子节点,该节点可以纠正其潜在病理学的多个方面,包括功能失调的内体和内质网到高尔基体囊泡的运输。NAB2参与细胞分化、凋亡和应激反应等细胞过程,可用来研究癌症、神经发育和神经元活动。
T33858 PACA

N-Propargyl Caffeamide

PACA, (N-propargyl Caffeamide)enhances NGF-induced neurite growth and reduces 6-hydroxydopamine neurotoxicity in neuron cultures. Parkinson's disease (PD) is associated with insufficient production of nerve growth factor (NGF).
TP1852 Myomodulin

肌调蛋白

Others; Potassium Channel; Calcium Channel; Sodium Channel Membrane transporter/Ion channel; Metabolism; Others
Myomodulin 是一种存在于软体动物、昆虫和腹足类动物中的神经肽。它存在于两个已确定的海兔神经元中,它们包含肌调节蛋白 A、ARC 运动神经元 B16 和腹部神经元 L10。
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.
T34664 SMN2-Stablizer-27

SMN2-Stablizer 27,SMN2 Stablizer-27

SMN2-Stablizer-27 is a stablizer of survival of motor neuron 2 (SMN2), and a post-translationally stablizing SMN protein for the treatment of spinal muscular atrophy (SMA).
T13071 Talsaclidine

Others Others
Talsaclidine is an agonist of muscarinic with preferential neuron-stimulating properties. Talsaclidine is a full agonist at the M1 subtype, and as a partial agonist at the M2 and M3 subtypes.
T37748 Ivermectin B1b

Ivermectin B1b is the minor component . It produces antiparasitic activity by binding to glutamate-gated chloride channels expressed on nematode neurons and pharyngeal muscle cells, inducing irreversible channel opening and very long-lasting hyperpolarization/depolarization of the neuron/muscle cell, thereby blocking further function.
T29000 Tralomethrin

EPA Pesticide Chemical Code 121501,SAGA,HAG-107,HAG 107,Scout

Tralomethrin is used as a pyrethroid insecticide. It modifies the gating kinetics of the sodium channels in neurons, increases the length of time the channel remains open after a stimulus, thereby depolarizing the neuron for a longer period of time. This leads to uncontrolled spasms, paralysis, and eventual death.
T31187 Dactylorhin B

Dactylorhin B is an active compound isolated from Coeloglossum Viride. Dactylorhin B reduces the toxic effects of β -amyloid fragments (25-35) on neuron cells and isolated rat brain mitochondria, which play an important role in neurodegenerative diseases.
T35608 16F16

16F16 is a protein disulfide isomerase (PDI) inhibitor.1It inhibits PDI reductase activity in an enzyme assay when used at concentrations ranging from 1 to 100 μg/ml.116F16 reduces PC12 cell apoptosis induced by the misfolded huntingtin protein HTTQ103. It suppresses PDI-dependent mitochondrial outer membrane permeabilization (MOMP) in isolated PC12 cell mitochondria. 16F16 (2, 3, 4, and 10 μM) reduces HTTN90Q73mutant huntingtin-induced medium spinal neuron death and MOMP in rat corticostriatal ...
T69921 BRF110

BRF110 is a brain penetrant, potent and selective agonist of nuclear receptor-related 1 (Nurr1):Retinoid X receptor α (RXRα) heterodimer. BRF110 is a neuroprotective agent that prevents dopaminergic neuron demise and striatal dopaminergic denervation in vivo against PD-causing toxins. It induced dopamine biosynthesis in vivo. BRF110 chronic dosing does not induce dyskinesia in mice model.
T38656 Nusinersen

Nusinersen is an antisense oligonucleotide drug that modifies pre–messenger RNA splicing of the SMN2 gene and thus promotes increased production of full-length SMN protein.
TP2215 Agouti-related Protein (AGRP) (25-82), human

Others Others
Agouti-related peptide (AgRP) is a neuropeptide produced in the brain by the AgRP/NPY neuron. It is only synthesized in NPY containing cell bodies located in the ventromedial part of the arcuate nucleus in the hypothalamus. The appetite-stimulating effect
T8443L MCI-225 hydrochloride hydrate

AA-10021,AA10021,MCI225,DDP-225,AA-10025,AA-10026

MCI-225 is a norepinephrine reuptake/5-HT3/5-HT reuptake inhibitor. MCI-225 could be effective in the treatment of senile dementia of the Alzheimer type, which is accompanied with both deficit in the BF-cortex cholinergic neuron and cerebral glucose hypom
T83512 [1,6-Aminosuberic acid]-arginine-Vasotocin

[1,6-Aminosuberic acid]-arginine-Vasotocin,一种类似神经垂体激素的合成肽,对黄芪周期性振荡神经元(PON)展现兴奋作用。
T76484 [Tyr8,Nle11] Substance P

[Tyr8,Nle11] Substance P 是 Substance P 的类似物。Substance P 是一种主要由神经元分泌的肽,参与许多生物学过程,包括痛觉和炎症。
T68714 Iobenguane I 131

Iobenguane I 131 is a guanidine analog with specific affinity for tissues of the sympathetic nervous system and related tumors. The radiolabeled forms are used as antineoplastic agents and radioactive imaging agents. MIBG serves as a neuron-blocking agent which has a strong affinity for, and retention in, the adrenal medulla and also inhibits ADP-ribosyltransferase.
T14693 BN201

Others Others
BN201 is able to cross the blood-brain barrier by active transport and activate pathways (IGF-1 pathway) associated with the response to stress and neuron survival. BN201 promotes neuronal differentiation, the differentiation of precursor cells to mature
T15455 RGH-5526

GYKI-11679

Others Others
RGH-5526是一种新型的抗高血压药。它引起下丘脑去甲肾上腺素(NA)周转(利用)增加,下丘脑去甲肾上腺素能神经元活性的增加可能导致外周交感神经活性的降低,从而显著降低血压。
T81974 KPZ560

HDAC Chromatin/Epigenetic; DNA Damage/DNA Repair
KPZ560作为HDAC1和HDAC2的有效抑制剂,在IC50数值上分别达到12 nM 和68 nM 。此化合物能提升小鼠颗粒神经元树突的棘密度,同时也能抑制MCF乳腺癌细胞系的生长。
T35538 HPI-1 (hydrate)

HPI-1 hydrate

HPI-1 (hydrate) is a Hedgehog (Hh) pathway inhibitor that suppresses signaling through Sonic Hh (IC50= 1.5 μM) without significantly affecting Wnt signaling (IC50≥ 30 μM).1HPI-1 suppresses Hh activation induced by loss of Suppressor of Fused or by Gli overexpression, suggesting action at posttranslational modification of Gli protein or at the interaction of Gli with a co-factor.1HPI-1 (hydrate) also inhibits signaling through the oncogenic Smoothened (Smo) mutant SmoM2 in neuron precursors, prev...
T64082 ABC44

ABC44 是丝氨酸水解酶 (serine hydrolase) 的有效抑制剂,对棕榈酰蛋白硫酯酶 1 (PPT1) 原位和体外的 IC50 分别为 0.1 μM 和 6.5 μM。ABC44 能够用于研究婴儿晚期神经元样脂褐质沉积症。
T81575 PA22-2 free acid

Cys-Laminin A chain 2091-2108

PA22-2 (free acid) (Cys-Laminin A chain 2091-2108) 为促进神经突生长和神经元样过程形成的多肽。该化合物适用于人腺样囊性癌细胞培养和肽功能化磷脂双层制备<sup>[3]。
T76392 β-Bag cell peptide

β-Bag cell peptide是一种提高袋细胞神经元(bag cell neuron)中cAMP水平、并能降低电压依赖性钾电流的神经活性肽。
T70186 Methazolamide-d6

Methazolamide-d6 is intended for use as an internal standard for the quantification of methazolamide by GC- or LC-MS. Methazolamide is a carbonic anhydrase inhibitor. It reduces intraocular pressure and cerebrospinal fluid flow in a rat model of glaucoma. Methazolamide reduces electroshock-induced seizures in rats with an ED50 value of 19.2 mg/kg. It also inhibits production of reactive oxygen species (ROS) in a primary cortical neuron (PCN) cellular model of subarachnoid hemorrhage (SAH) and re...

化合物

Hydroxy-Dynasore
Cat.No: T6822
Synonym: Dyngo-4a
Target: Dynamin
UNC3230
Cat.No: T23498
Synonym: UNC 3230
Target: Others
CMPD101
Cat.No: T14989
Synonym:
Target: ROCK, GRK, PKC
Afloqualone
Cat.No: T4993
Synonym: 氟喹酮,HQ-495
Target: GABA Receptor
Dermorphin TFA
Cat.No: T7748
Synonym: 皮啡肽三氟乙酸盐
Target: Others, Opioid Receptor
Branaplam
Cat.No: T4641
Synonym: LMI 070,NVS-SM1
Target: Others, Potassium Channel, DNA/RNA Synthesis
PF-CBP1 hydrochloride
Cat.No: T3217
Synonym: PF-CBP1 HCl
Target: Epigenetic Reader Domain, Histone Acetyltransferase
Mecamylamine hydrochloride
Cat.No: T2141
Synonym: 盐酸美加明,Inversine,Mevasin
Target: AChR
5,7-Dichlorokynurenic acid
Cat.No: T22517
Synonym: 5,7-二氯犬尿喹啉酸,5,7-dichlorokynurenic acid sodium,5,7-DCKA
Target: NMDAR
N-(3-Aminopropyl)cyclohexylamine
Cat.No: T35878
Synonym:
Target: Others
EIPA
Cat.No: TQ0157
Synonym: L593754,MH 12-43
Target: Sodium Channel, TRP/TRPV Channel
CH 275
Cat.No: TP2045
Synonym:
Target:
Dermorphin
Cat.No: T7404
Synonym: 皮啡肽
Target: Opioid Receptor
Neuronostatin-13 human acetate
Cat.No: TP1827L
Synonym: Neuronostatin-13 human acetate(1096485-24-3 free base)
Target: Others
Neuronotoxicity-IN-1
Cat.No: T60750
Synonym:
Target:
Neuronostatin-13 (human)
Cat.No: TP1827
Synonym: Neuronostatin-13 human
Target:
Myomodulin acetate(110570-93-9 free base)
Cat.No: TP1852L
Synonym:
Target: Potassium Channel, Calcium Channel, Sodium Channel
TCS 2210
Cat.No: T23446
Synonym:
Target: Others
Crisdesalazine
Cat.No: T27084
Synonym: AAD2004,AAD 2004,AAD-2004
Target: Prostaglandin Receptor
Risdiplam
Cat.No: T16757
Synonym: RO7034067,RG7916
Target: DNA/RNA Synthesis
ISX-9
Cat.No: T2003
Synonym: Isoxazole 9,Isoxazole 9 (ISX-9)
Target: Calcium Channel, Wnt/beta-catenin
GTS-21 dihydrochloride
Cat.No: T2663
Synonym: GTS 21 dihydrochloride,DMXB-A,DMBX-anabaseine
Target: 5-HT Receptor, AChR
CLP290
Cat.No: T5444
Synonym: CLP-290
Target: Potassium Channel
λ-Cyhalothrin
Cat.No: T27794
Synonym: lambda-Cyhalothrin,Karate,λ-氯氟氰菊酯,Icon
Target: Sodium Channel, Parasite
Olodanrigan
Cat.No: T4431
Synonym: PD-126055,EMA401
Target: RAAS
alphaSYN-IN-NAB2
Cat.No: T23709
Synonym: alphaSYN inhibitor NAB2,alphaSYNINNAB2,alphaSYN-IN-NAB2,NAB2,alphaSYN inhibitor-NAB2
Target:
PACA
Cat.No: T33858
Synonym: N-Propargyl Caffeamide
Target:
Myomodulin
Cat.No: TP1852
Synonym: 肌调蛋白
Target: Others, Potassium Channel, Calcium Channel, Sodium Channel
Mephenoxalone
Cat.No: T24450
Synonym: Lenetran Lenetran,TAB Lenetranat
Target:
SMN2-Stablizer-27
Cat.No: T34664
Synonym: SMN2-Stablizer 27,SMN2 Stablizer-27
Target:
Talsaclidine
Cat.No: T13071
Synonym:
Target: Others
Ivermectin B1b
Cat.No: T37748
Synonym:
Target:
Tralomethrin
Cat.No: T29000
Synonym: EPA Pesticide Chemical Code 121501,SAGA,HAG-107,HAG 107,Scout
Target:
Dactylorhin B
Cat.No: T31187
Synonym:
Target:
16F16
Cat.No: T35608
Synonym:
Target:
BRF110
Cat.No: T69921
Synonym:
Target:
Nusinersen
Cat.No: T38656
Synonym:
Target:
Agouti-related Protein (AGRP) (25-82), human
Cat.No: TP2215
Synonym:
Target: Others
MCI-225 hydrochloride hydrate
Cat.No: T8443L
Synonym: AA-10021,AA10021,MCI225,DDP-225,AA-10025,AA-10026
Target:
[1,6-Aminosuberic acid]-arginine-Vasotocin
Cat.No: T83512
Synonym:
Target:
[Tyr8,Nle11] Substance P
Cat.No: T76484
Synonym:
Target:
Iobenguane I 131
Cat.No: T68714
Synonym:
Target:
BN201
Cat.No: T14693
Synonym:
Target: Others
RGH-5526
Cat.No: T15455
Synonym: GYKI-11679
Target: Others
KPZ560
Cat.No: T81974
Synonym:
Target: HDAC
HPI-1 (hydrate)
Cat.No: T35538
Synonym: HPI-1 hydrate
Target:
ABC44
Cat.No: T64082
Synonym:
Target:
PA22-2 free acid
Cat.No: T81575
Synonym: Cys-Laminin A chain 2091-2108
Target:
β-Bag cell peptide
Cat.No: T76392
Synonym:
Target:
Methazolamide-d6
Cat.No: T70186
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T0508 γ-Aminobutyric acid

Gamma-aminobutyric acid,4-Aminobutyric acid,4-氨基丁酸,γ-氨基丁酸,GABA,4-Aminobutanoic acid,Piperidic acid

GABA Receptor; Endogenous Metabolite Membrane transporter/Ion channel; Metabolism; Neuroscience
γ-Aminobutyric acid (4-Aminobutyric acid) 是成年哺乳动物大脑中主要的抑制性神经递质,能够与离子移变 GABA 受体(GABAA) 受体和促代谢受体 (GABAB) 受体结合发挥作用。
TN1494 Cimicifugoside H-1

黑升麻苷H-1

Others Others
Cimicifugoside H1 是C. foetidaL.C 提取物的主要成分,是一种环甾烷醇木糖苷。它对骨吸收及卵巢切除术引起的骨质流失具有抑制作用。
T6S1010 Allomatrine

槐定碱,别苦参碱

Others Others
Allomatrine 是一种来源槐花树皮的生物碱。它能够激活 κ-阿片受体,进而产生缓解疼痛的作用。
T4S2084 3'-Methoxypuerarin

3'-甲氧基葛根素,3’- Methoxy Puerarin

Antioxidant oxidation-reduction
3'-Methoxypuerarin 是一种提取自葛根中的异黄酮,具有神经元保护作用。
T3836 Eudesmin

MAPK; S6 Kinase MAPK; PI3K/Akt/mTOR signaling
Eudesmin 通过抑制S6K1信号通路来干扰成脂分化,具有抗肿瘤、抗炎和抗菌活性。
T5S2357 Acetylcorynoline

(+)-Corynoline Acetate,O-Acetylcorynoline,乙酰紫堇灵

Antifungal Microbiology/Virology
Acetylcorynoline (O-Acetylcorynoline) 是提取自 Corydalis bungeana 中的一种主要生物碱成分,具有抗炎活性。
T8270 Deserpidine

地舍平,Harmonyl

RAAS Endocrinology/Hormones
Deserpidine (Harmonyl) 是从 Rauwolfia canescens 的根中分离的生物碱。Deserpidine 与 Reserpine 相关。Deserpidine 是竞争性血管紧张素转化酶抑制剂,可以被用作抗高血压药以及镇定剂。Deserpidine 还减少了肾上腺皮质血管紧张素 II 诱导的醛固酮分泌。
T4752 1-Aminocyclopropane-1-carboxylic acid

1-Aminocyclopropanecarboxylic acid,1-氨基环丙烷羧酸,1-Amino-1-carboxycyclopropane,ACC

Endogenous Metabolite; NMDAR Metabolism; Neuroscience
1-Aminocyclopropane-1-carboxylic acid (ACC) 是内源性代谢产物的一种。

天然产物

γ-Aminobutyric acid
Cat.No: T0508
Synonym: Gamma-aminobutyric acid,4-Aminobutyric acid,4-氨基丁酸,γ-氨基丁酸,GABA,4-Aminobutanoic acid,Piperidic acid
Target: GABA Receptor, Endogenous Metabolite
Cimicifugoside H-1
Cat.No: TN1494
Synonym: 黑升麻苷H-1
Target: Others
Allomatrine
Cat.No: T6S1010
Synonym: 槐定碱,别苦参碱
Target: Others
3'-Methoxypuerarin
Cat.No: T4S2084
Synonym: 3'-甲氧基葛根素,3’- Methoxy Puerarin
Target: Antioxidant
Eudesmin
Cat.No: T3836
Synonym:
Target: MAPK, S6 Kinase
Acetylcorynoline
Cat.No: T5S2357
Synonym: (+)-Corynoline Acetate,O-Acetylcorynoline,乙酰紫堇灵
Target: Antifungal
Deserpidine
Cat.No: T8270
Synonym: 地舍平,Harmonyl
Target: RAAS
1-Aminocyclopropane-1-carboxylic acid
Cat.No: T4752
Synonym: 1-Aminocyclopropanecarboxylic acid,1-氨基环丙烷羧酸,1-Amino-1-carboxycyclopropane,ACC
Target: Endogenous Metabolite, NMDAR
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