119
22
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10674 |
Potassium Channel Activator 1
钾离子通道激活剂1,ZINC34634569 |
Potassium Channel | Membrane transporter/Ion channel |
Potassium Channel Activator 1 可用于治疗多巴胺能系统被破坏的疾病或病症的研究,例如情绪障碍 ADHD、精神分裂症和其他精神病状态。 | |||
T26645 |
Aptiganel
CNS 1102,CNS-1102,CNS1102 |
NMDAR | Neuroscience |
Aptiganel (CNS-1102) 是一种非竞争性 NMDA 拮抗剂,是一种多肽,可用于研究急性缺血性卒中。 | |||
T1641 |
Strontium ranelate
Distrontium renelate,S12911,雷尼酸锶 |
Calcium Channel; CaSR | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism |
Strontium ranelate (S12911) 是抗骨质疏松的药物,能够抑制骨吸收,促进骨形成,进而促使正骨平衡。它还能够激活非骨骼细胞中的钙敏感受体 (CaSR),进而促进肌醇 1,4,5-三磷酸的生成及丝裂原活化的蛋白激酶信号转导。 | |||
T77711 |
Calcium Channel antagonist 4
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Calcium Channel antagonist 4 是一种电压门控钙通道抑制剂(IC50 : 5-20μM)。 | |||
T31208 |
Dasolampanel
NGX-426,NGX 426,NGX426 |
GluR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Dasolampanel (NGX-426) 是一种可口服的离子型谷氨酸受体 AMPA 和 Kainate 受体拮抗剂,可用于研究慢性疼痛疾病,包括神经性疼痛和偏头痛。 | |||
T7201 |
Nelociguat
N-[4,6-二氨基-2-[1-[(2-氟苯基)甲基]-1H-吡唑并[3,4-B]吡啶-3-基]-5-嘧啶]-氨基甲酸甲酯,BAY60-4552 |
Guanylate cyclase | GPCR/G Protein |
Nelociguat (BAY60-4552) 是一种一氧化氮敏感的可溶性鸟苷酸环化酶刺激剂。 | |||
T6001 |
Nelfinavir Mesylate
Viracept,Nelfin,AG1343,AG 1343 Mesylate,甲磺酸奈非那韦 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Nelfinavir Mesylate (Viracept) 是一种口服活性的 HIV-1蛋白酶抑制剂,用于抑制 HIV 感染,是一种广谱抗癌剂。 | |||
T61535 |
Neldazosin
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Neldazosin 可作为一种有效的 α1 肾上腺素受体拮抗剂使用。 | |||
T12441 |
Phenelzine sulfate
硫酸苯乙肼,苯肼,硫酸盐 |
Monoamine Oxidase | Neuroscience |
Phenelzine sulfate 是一种非选择性的、不可逆的单胺氧化酶抑制剂 (MAOI),可用作抗抑郁药和抗焦虑药。 | |||
T7779 |
Nelfinavir
AG1341,甲磺酸萘非那韦 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Nelfinavir (AG1341) 是一种口服活性的 HIV-1 蛋白酶抑制剂,用于抑制 HIV 感染,是一种广谱抗癌剂。 | |||
T76830 |
Teneliximab
Chi220,Anti-Human CD40 Recombinant Antibody,BMS 224819 |
TNF | Apoptosis |
Teneliximab (Chi220) 是一种嵌合的单克隆抗体,也是一种肿瘤坏死因子受体超家族成员5(CD40)抑制剂,可阻断CD40-CD40L 的相互作用。Teneliximab 通过CD40 和外周B细胞损耗发挥部分激动剂活性,可用于研究器官移植排斥和类风湿关节炎。 | |||
T72170 |
NaV1.2/1.6 channel blocker-1
|
Sodium Channel | Membrane transporter/Ion channel |
NaV1.2/1.6 channel blocker-1 是一种有效的 NaV1.2/1.6 channel 阻滞剂,对 rNaV1.6 和 hNaV1.2 有抑制作用。NaV1.2/1.6 channel blocker-1 可用于研究全身性癫痫和运动障碍。 | |||
T10101 |
Calcium channel-modulator-1
|
Others; Calcium Channel | Membrane transporter/Ion channel; Metabolism; Others |
Calcium channel-modulator-1是钙离子通道调节剂(IC50:0.8 μM),具有阻塞主动脉收缩的专业化。 | |||
T16286 |
Nelonemdaz
Neu2000 |
Topoisomerase | DNA Damage/DNA Repair |
Neu2000 is an uncompetitive antagonist of N-methyl-D-aspartate (NMDA) receptor. | |||
T16977 |
Talampanel
GYKI-53773,LY-300164 |
Apoptosis; GluR | Apoptosis; Neuroscience |
Talampanel (LY-300164) 是一种口服和选择型 AMPA 受体拮抗剂,具有抗癫痫活性。在啮齿动物的中风模型中,它 具有神经保护作用。Talampanel 减弱 caspase-3 依赖性细胞凋亡。 | |||
T27828 |
Licostinel
CGP 63446,ACEA1021,ACEA 1021,ACEA-1021,CGP-63446 |
GluR | Neuroscience |
Licostinel (CGP 63446) 是一种谷氨酸受体拮抗剂。 Licostinel 可防止永久性局灶性脑缺血。 | |||
T3407L |
Rapastinel acetate
Rapastinel acetate (117928-94-6 Free base) |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Rapastinel acetate 是 N-甲基-D-天冬氨酸 (NMDA) 受体的调节剂和甘氨酸位点的部分激动剂,具有长效抗抑郁作用。 | |||
T12042 |
Minnelide
|
Others | Others |
Minnelide is a prodrug of triptolide,and shows potent antitumor activity in a number of tumor types. | |||
T34609 |
Selurampanel
BGG-492,BGG 492,BGG492 |
iGluR | Membrane transporter/Ion channel; Neuroscience |
Selurampanel (BGG492) 是一种具有口服活性和选择性的竞争性 AMPA 谷氨酸受体拮抗剂,是一种喹唑啉二酮磺酰胺。Selurampanel 可用于研究癫痫、偏头痛和耳鸣。 | |||
T28153 |
Nelivaptan
SSR149415,SR 149415,SR-149415 |
Vasopressin Receptor | GPCR/G Protein |
Nelivaptan (SR 149415) 是一种加压素 V1b 受体拮抗剂。 | |||
T77712 |
Calcium Channel antagonist 3
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Calcium Channel antagonist 3 是一种电压门控钙通道抑制剂(IC50 : 5-20μM)。 | |||
T77710 |
Calcium Channel antagonist 2
WAY-327363 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Calcium Channel antagonist 2是一种 calcium channel 拮抗剂 (IC50=5-20 μM),可用于研究像疼痛和糖尿病等由于 Ca2+ 通道造成的疾病。 | |||
T5432 |
Eganelisib
IPI-549 |
PI3K | PI3K/Akt/mTOR signaling |
Eganelisib (IPI-549) 是 PI3Kγ的选择性抑制剂,其 IC50=16 nM,选择性是其他脂类和蛋白质激酶的 100 倍以上。 | |||
T7350 |
Nelotanserin
1-[3-(4-溴-1-甲基-1H-吡唑-5-基)-4-甲氧基苯基]-3-(2,4-二氟苯基)脲,APD125 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Nelotanserin (APD125) 是5-HT2A 强完全逆向激动剂,5-HT2C 中等强度的部分反向激动剂和5-HT2B 的弱反向激动剂,IC50s 值分别为 1.7、79 和 791 nM。 | |||
T6603 |
Nelarabine
GW 506U78,Nelzarabine,奈拉滨,506U78 |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Nelarabine (GW 506U78) 是一种嘌呤核苷酸类似物,为DNA 合成抑制剂,对肿瘤细胞的IC50为0.067-2.15 μM,可作用于T 细胞急性淋巴细胞白血病。 | |||
T6999 |
Teneligliptin hydrobromide
Teneligliptin hydrobromide anhydrous,MP-513 (hydrobromide) |
Others; Proteasome; DPP-4 | Others; Proteases/Proteasome; Ubiquitination |
Teneligliptin hydrobromide (MP-513(hydrobromide)) 是β2肾上腺素能受体 (β2AR) 阻滞剂,具有抗高血压、抗氧化、清除自由基的活性。 | |||
T10659 |
Ca2+ channel agonist 1
|
Calcium Channel; CDK | Cell Cycle/Checkpoint; Membrane transporter/Ion channel; Metabolism |
Ca2+channel agonist 1 是 N-型钙离子通道激动剂和Cdk2的抑制剂,EC50分别为 14.23 μM 和 3.34 μM,可用作运动神经末梢功能障碍的潜在治疗方法。 | |||
T13312L |
Seviteronel
VT-464 |
Others | Others |
Seviteronel is an effective CYP17 lyase inhibitor (h-Lyase IC50=69 nM). In a hamster model of androgen biosynthesis inhibition, it demonstrated both exceptional in vitro lyase/hydroxylase selectivity (~10-fold) and oral activity. | |||
T22798 |
Gavestinel
GV 150526,Gavestinel sodium salt |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Gavestinel (GV 150526) 是一种非竞争性的 NMDA 受体拮抗剂,具有有效性、选择性和口服活性。Gavestinel 可与 NMDA 受体的甘氨酸位点结合,其结合亲和力(pKi 值)为 8.5。Gavestinel 可用于急性缺血性脑卒中研究。 | |||
T5819 |
Rapastinel Trifluoroacetate
Thr-Pro-Pro-Thr-NH2 Trifluoroacetate,GLYX-13 Trifluoroacetate |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Rapastinel Trifluoroacetate (GLYX-13 Trifluoroacetate) 是一种 NMDA 受体调节剂,具有甘氨酸位点部分激动剂性质,有研究抑郁症的潜力。 | |||
T68178 | Neltenexine HCl | ||
Neltenexine HCl is the salt form of Neltenexine free base, an elastase inhibitor that may be useful for preventing pulmonary emphysema. | |||
T77079 | Manelimab | ||
Manelimab 是一种单克隆抗体,可以抑制程序性死亡配体1 (PD-L1)。 | |||
T17276 |
Zonampanel
YM 872,唑南帕奈 |
Others | Others |
Zonampanel is a selective glutamate receptor subtype, α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor antagonist. | |||
T37522 | Teneligliptin | ||
Teneligliptin (MP-513) is a potent chemotype prolylthiazolidine-based DPP-4 inhibitor, which competitively inhibits human plasma, rat plasma, and human recombinant DPP-4 in vitro, with IC50s of approximately 1 nM. Teneligliptin (MP-513) inhibits all these DPP-4 enzymes in a concentration-dependent manner. The IC50s of Teneligliptin (MP-513) for rhDPP-4, human plasma, and rat plasma are 0.889, 1.75, and 1.35 nM, respectively. A study of enzyme inhibition kinetics is conducted for Teneligliptin (M... | |||
T38422 |
Nelonicline citrate
ABT-126 citrate |
||
Nelonicline citrate (ABT-126) is an orally active and selective α7 nicotinic receptor agonist, demonstrating a high affinity for α7 nAChRs in the human brain (Ki = 12.3 nM). This compound is utilized in the research of schizophrenia and Alzheimer's disease. | |||
T13313 |
Seviteronel racemate
VT-464 (racemate) |
Others | Others |
Seviteronel racemate is the racemate form of Seviteronel and is a potent inhibitor of CYP17 lyase. | |||
T71157 |
Neladenoson dalanate
Neladenoson bialanate ; BAY-1067197,BAY-1067197,Neladenoson bialanate |
||
Neladenoson dalanate (Neladenoson bialanate ; BAY-1067197) 是部分腺苷 A1 受体激动剂的前体,具有口服活性。Neladenoson dalanate 具有良好的药代动力学和安全性,可用于慢性心脏疾病的研究。 | |||
T34199 |
Pyrenelecithin
PPDPC,Pyrene-PC,P10PC |
||
Pyrenelecithin is a fluorescent dye used a lipid indicator. | |||
T33626 |
Nelipepimut-S
NeuVax vaccine,E75 peptide,NeuVax |
||
Nelipepimut-S, as an immunogenic peptide from the HER2 protein, is highly expressed in breast cancer. | |||
T79280 |
Nav1.3 channel inhibitor 1
|
Sodium Channel | Membrane transporter/Ion channel |
Nav1.3 channel inhibitor 1 (化合物 15b) 为状态依赖性电压门控钠通道Nav1.3的抑制剂,具有IC50值为20 nM。该化合物能穿透血脑屏障,适用于神经系统疾病研究。 | |||
T39936 |
HM Janelia Fluor® 526, SE
HM-JF526 NHS |
||
HM Janelia Fluor 526, SE (HM-JF526 NHS) is a derivative of hydroxymethyl JF526 (HM-JF526). SMLM (single-molecule localization microscopy) imaging in standard phosphate-buffered saline (pH 7.4) revealed that the HM-JF526 label showed spontaneous blinking behavior throughout the imaging session and did not require short-wavelength activation light. | |||
T38157 |
Ricinelaidic Acid
|
||
Ricinelaidic acid is a 12-hydroxy fatty acid and an antagonist of leukotriene B4 (LTB4) receptors (Ki = 2 μM in porcine neutrophil membranes). It inhibits chemotaxis and calcium flux induced by LTB4 in isolated human neutrophils (IC50s = 10 and 7 μM, respectively). Ricinelaidic acid (1 mg/kg, i.v.) inhibits bronchoconstriction induced by LTB4 in rats by 46%. | |||
T27123 |
Dasolampanel etibutil
|
||
Dasolampanel etibutil is a novel selective antagonist of ionotropic glutamate receptor 5 (iGluR5). | |||
T39698 |
Gemnelatinib
|
||
Gemnelatinib (WO2018077227, implementation example 1) is a tyrosine kinase inhibitor with potential applications in cancer research. | |||
T38259 |
Phenelfamycin E
|
||
Phenelfamycin E is an antibiotic originally isolated from Streptomyces. It is active against β-hemolytic Streptoccus, S. pneumoniae, C. difficile, C. perfringens, and P. magnus128 μg/ml). Phenelfamycin E (4-64 mg/kg) increases survival in a mouse model of lethal S. pyogenes infection in a dose-dependent manner. Dietary administration of phenelfamycin E increases body weight in chickens. | |||
T123944 |
Canellin E
|
||
T60923 |
Zelquistinel
|
||
Zelquistinel 用于研究抑郁、焦虑和其他相关精神疾病的研究。它是一种 N-甲基-D-天冬氨酸(NMDA)受体的部分激动剂。 | |||
T41197 |
Phalloidin-Janelia Fluor®646
Phalloidin-Janelia Fluor®646,Phalloidin-JF646 |
||
Phalloidin-Janelia Fluor®646 is a red fluorescent F-actin probe. Phalloidin-Janelia Fluor®646 is composed of the F-actin probe, Phalloidin, conjugated to Janelia Fluor®646. It is suitable for use in confocal and super-resolution microscopy techniques such as dSTORM. Excitation/emission maximum λ = 646/664 nm. | |||
T25663 | Lentinellic acid | ||
Lentinellic acid, derived from Lentinellus species (Basidiomycetes), is an antimicrobial and cytotoxic sesquiterpenoid and biologically active protoilludane. | |||
T34226 | Quinelorane | ||
Quinelorane is dextrorotary isomer. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5645 |
Nerol
Cis-Geraniol,橙花醇,Neryl alcohol |
Apoptosis; Reactive Oxygen Species; Mitochondrial Metabolism; Endogenous Metabolite; Antifungal | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Nerol (Neryl alcohol) 是橙花油的一种单萜, 它通过增强 Ca2+和ROS 来触发线粒体功能障碍并诱导凋亡,具有抗真菌活性。它可减轻哺乳动物心脏中哇巴因引发的心律失常的严重程度。 | |||
T5776 |
pimpinellin
|
Apoptosis; Anti-infection | Apoptosis; Microbiology/Virology |
Pimpinellin 是贯众的一种成分,可通过诱导肿瘤细胞凋亡抑制肿瘤细胞的生长,可作为具有 GABA 受体活性的蛋白质的拮抗剂。 | |||
T8061 |
Citronellal
(±)-Citronellal,香茅醛 |
Others | Others |
Citronellal ((±)-Citronellal) 是多种芳香植物精油的单萜烯,具有促进睡眠、安定和抗伤害的作用。它可以降低机械伤害感受,且部分通过 NO-cGMP-ATP 敏感型 K⁺渠道通道介导的。 | |||
T6S0071 |
Fraxinellone
|
HIF/HIF Prolyl-Hydroxylase; STAT; PD-1/PD-L1 | Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Metabolism; Stem Cells |
Fraxinellone 是从白鲜的根皮中分离出来的一种天然产物,是PD-L1抑制剂,可抑制HIF-1α蛋白质合成。它通过靶向 PD-L1,有用于癌症免疫的潜力。 | |||
T8057 |
Citronellyl acetate
|
Apoptosis; Others | Apoptosis; Others |
Citronellyl acetate 是一种植物次生代谢产物,具有杀菌、杀幼虫、杀菌和驱虫杀虫作用,以及抗伤害活性。它在人肝癌细胞中具有促凋亡活性。 | |||
T8013 |
(S)-(-)-Citronellal
(S)-(-)-3,7-Dimethyl-6-Octenal,(-)-香茅醛,(-)-Citronellal |
Others; Endogenous Metabolite | Metabolism; Others |
(S)-(-)-Citronellal ((S)-(-)-3,7-Dimethyl-6-Octenal) 是存在于Corymbia citriodora 和Cymbopogon nardus 中的一种单萜类化合物。 | |||
T4593 |
ISOPIMPINELLIN
5,8-Dimethoxypsoralen,异茴芹内酯,4,9-Dimethoxypsoralen |
Antiviral; DNA/RNA Synthesis; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology |
Isopimpinellin (4,9-Dimethoxypsoralen) 是从 Pimpinella saxifrage 根部分离得到的一种天然产物,具有抗病毒和抗利什曼病活性。 | |||
T3240 |
Citronellol
dihydrogeraniol,香茅醇,β-香茅醇,(±)-β-Citronellol |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Citronellol ((±)-β-Citronellol) 是一种单萜类化合物,从头状天竺葵中分离到。它可通过上调 TNF-α,RIP1/RIP3 的活性,下调 caspase-3/caspase-8 的活性,以及增加活性氧 (ROS) 的聚集来诱导肿瘤细胞的坏死性凋亡。 | |||
T8266 |
(R)-Citronellol
D-Citronellol,(R)-(+)-β-Citronellol,(R)-3,7-二甲基-6-辛烯醇 |
Others; Endogenous Metabolite | Metabolism; Others |
(R)-Citronellol ((R)-(+)-β-Citronellol) 是一种存在于天竺葵精油中的醇单萜。它抑制肥大细胞的脱颗粒,并且不影响咖啡因的苦味感。它能够用于装饰性化妆品,盥洗用品以及非化妆品中。 | |||
T2927 |
Trigonelline chloride
Gynesine Hydrochloride,盐酸葫芦巴碱,Coffearine Hydrochloride,Nicotinic acid N-methylbetaine Hydrochloride,Trigonelline hydrochloride |
Others; Antibacterial; Antifungal; HSV | Microbiology/Virology; Others |
Trigonelline chloride (Coffearine Hydrochloride) 是一种大量存在于咖啡中的生物碱,具有潜在抗糖尿病活性。它还具有抗HSV-1,抗菌和抗真菌活性。 | |||
T2887 |
Trigonelline
Trigenolline,葫芦巴碱 |
Apoptosis; Others; Ferroptosis; Endogenous Metabolite | Apoptosis; Metabolism; Others |
Trigonelline (Trigenolline) 是一种大量存在于咖啡中的生物碱,具有潜在抗糖尿病活性。它是Nrf2抑制剂,可阻断 Nrf2 依赖的蛋白酶体活性,从而增强胰腺癌细胞凋亡。 | |||
TN4931 |
(S)-(-)-beta-Citronellol
|
Others | Others |
(S)-(-)-beta-Citronellol 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4931,CAS号为 7540-51-4。 | |||
TN4077 | Fortunellin | Others | Others |
Fortunellin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4077,CAS号为 20633-93-6。 | |||
T13449 |
(R)-(+)-Citronellal
(+)-Citronellal,(R)-(+)-香茅醛 |
Others | Others |
(R)-(+)-Citronellal is a natural product isolated from citrus,used for insect repellent and antifungal properties. | |||
TN6516 |
Selaginellin F
|
||
Selaginellin F is a natural product from Selaginella pulvinata. | |||
TN6515 |
Selaginellin
|
||
Selaginellin has a neuroprotective effect against L-glutamate-induced neurotoxicity through mechanisms related to anti-oxidation and anti-apoptosis via scavenging reactive oxygen species and up-regulating the expression of klotho gene. Selaginellin shows | |||
T29795 |
Akagerinelactone
|
||
Akagerinelactone is a biochemical. | |||
T30951 |
Citronellol acetate, (R)-
AI300205,AI3-00205,AI3 00205 |
||
Citronellol acetate, (R)- is a biochemical. | |||
T72802 |
Spongionellol A
|
||
Spongionellol A 是一种 MDR1(p-糖蛋白) 抑制剂。Spongionellol A 通过诱导 caspase 依赖性的凋亡 (apoptosis) 而对前列腺癌细胞具有较强的细胞毒活性和选择性。Spongionellol A 可用于癌症的研究,如前列腺癌。 | |||
TN4628 |
Nelumol A
|
FXR | Metabolism |
Nelumol A, and nelumal A show a potency comparable to the endogenous ligand, they may as a valuable potential novel lead compound in the search for FXR agonists. | |||
T75625 | Axinelline A | ||
Axinelline A 是一种有效的 COX 抑制剂,对 COX-2和 COX-1的IC50分别为 2.22 μΜ 和 8.89 μM。Axinelline A 显示抗炎活性。 | |||
TN6105 |
Thalmineline
|
||
Thalmineline 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6105,CAS号为 28328-00-9。 |