54
8
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T35817 |
Photoswitchable PAD Inhibitor (technical grade)
|
||
Photoswitchable PAD inhibitor is a photoactivated protein arginine deiminase (PAD) inhibitor and a derivative of BB-Cl-amidine that contains an azobenzene photoswitch allowing optical control of PAD activity.1 Without photoactivation, it is a weak inhibitor of PAD2 (IC50 = >100 μM) and is less potent than BB-Cl-amidine in inhibiting citrulline production in vitro (kinact/KIs = 2,300, 600, 1,000, and 10,510 M-1min-1 for PAD1-4, respectively) and does not inhibit histone H3 citrullination in HEK29... | |||
T63284 |
PAD-IN-2
|
||
PAD-IN-2 是 pad4 的有效抑制剂,IC50 值 <1 μM,能够用于研究自身免疫性疾病和癌症,如类风湿性关节炎、血管炎、系统性红斑狼疮、皮肤红斑狼疮、囊性纤维化、溃疡性结肠炎、哮喘、多发性硬化和牛皮癣。 | |||
T39515 |
PAD2-IN-1
PAD2-IN-1 |
||
PAD2-IN-1, a benzimidazole-based derivative, is an efficacious and specific inhibitor of protein arginine deiminase 2 (PAD2). Demonstrating remarkable selectivity, PAD2-IN-1 exhibits a 95-fold higher affinity for PAD2 in comparison to PAD4 and a 79-fold higher affinity than PAD3. | |||
T63601 | PAD2-IN-1 hydrochloride | ||
PAD2-IN-1 hydrochloride 是有效的、选择性的蛋白精氨酸脱亚氨酶 2 (PAD2) 抑制剂,且对 PAD2 的选择性优于 PAD4 (95 倍) 和 PAD3 (79 倍),是一种基于苯并咪唑的衍生物。 | |||
T79276 | PAD4-IN-2 | ||
PAD4-IN-2(化合物5i)是一种具有IC50为1.94 μM的PAD4抑制剂。该化合物能够通过特异性抑制中性粒细胞内PAD4-H3cit-NETs途径,从而有效抑制小鼠体内肿瘤生长。 | |||
T22178L |
Spadin Acetate
Spadin Acetate(1270083-24-3 Free base) |
Others | Others |
Spadin Acetate 是一种天然肽,来源于血液中释放的前肽。 Spadin Acetate 能够阻断 TREK-1 通道活动。 Spadin Acetate 与 TREK-1 特异性结合,亲和力为 10 nM。 | |||
T26641L |
Apadenoson TFA
BAY 68-4986 TFA,Apadenoson TFA(250386-15-3 Free base),Discontinued TFA |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Apadenoson TFA 是一种有效的腺苷 A2A 受体 (A2AR) 激动剂,可用于提高SARS感染患者的存活率。 | |||
T0113 |
Mebhydrolin napadisylate
Incidal,Diazolin,Mebhydroline 1,5-naphthalenedisulfonate salt,美海屈林萘二磺酸盐,Omeril,Diazoline |
5-HT Receptor; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Mebhydrolin napadisylate (Incidal) 是一种抗组胺药,用于缓解组胺释放引起的过敏症状,如鼻过敏和过敏性皮肤病。 | |||
T16411 |
Otenzepad
AF-DX 116 |
AChR | Neuroscience |
Otenzepad (AF-DX 116) 是 M2 mAChR 的特异性拮抗剂,对大鼠心脏和兔外周肺的 IC50 分别为 386 nM 和 640 nM。 | |||
T2373 |
Vipadenant
CEB-4520,BIIB-014 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Vipadenant (CEB-4520) 是一种腺苷受体拮抗剂,抑制 A2A 和 A1 活性的 Ki 值分别为 1.3 和 68 nM。 | |||
T16564 |
PPADS tetrasodium
|
P2X Receptor; Na+/Ca2+ Exchanger | Membrane transporter/Ion channel; Neuroscience |
PPADS tetrasodiuma 是一种有效的 P2X 受体拮抗剂,也是是豚鼠气道平滑肌 Na/Ca²⁺ 交换逆模式的抑制剂,对谷氨酸/NMDA毒性有神经保护作用。PPADS tetrasodiuma 抑制 P2X1、P2X-2、P2X-3 和 P2X-5。 | |||
TQ0125 |
Capadenoson
BAY 68-4986,卡帕诺生 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Capadenoson (BAY 68-4986) 是 A1 腺苷受体的选择性激动剂。 | |||
T16999 |
Tavapadon
PF-6649751,CVL-751 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Tavapadon (CVL-751) 是一种具有口服活性,高选择性的多巴胺 D1/D5受体部分激动剂,它可有效促进运动并减少残疾,对帕金森氏病具有潜在的应用价值。 | |||
T76735 |
Mupadolimab
CPI-006 |
CD73 | Immunology/Inflammation |
Mupadolimab (CPI-006) 是一种人源化 FcγR 结合缺陷型 IgG1 抗 CD73抗体,具有潜在的抗癌活性,可激活 CD73POS B 细胞。 | |||
T16427 |
Padsevonil
UCB-0942 |
Others | Others |
Padsevonil is an effective antiepileptic compound. | |||
T5167 |
Cebranopadol
西博帕多,GRT6005 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Cebranopadol (GRT6005) 是镇痛 NOP 和阿片受体激动剂,对人 NOP、μ-阿片 (MOP)、κ-阿片 (KOP) 和 δ-阿片 (DOP) 受体的 Ki 值分别为 0.9、0.7、2.6 和 18 nM。 | |||
T19849L |
2-PADQZ hydrochloride
2-PADQZ hydrochloride (60547-97-9 Free base) |
Antiviral; Influenza Virus | Immunology/Inflammation; Microbiology/Virology |
2-PADQZ hydrochloride 显示出抗病毒活性并靶向甲型流感病毒 RNA 启动子。 | |||
T7503 |
Upadacitinib
乌帕替尼,ABT-494 |
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
Upadacitinib (ABT-494) 是高效选择性的,具有口服活性的 JAK1抑制剂,IC50为43 nM,可用于多种自身免疫性疾病的研究。它对 JAK1 的选择性约为 JAK2 的 74 倍。 | |||
T126544 | 3-O-Acetylpadmatin | ||
3-O-Acetylpadmatin 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T126544,CAS号为 100595-93-5。 | |||
T71693 | Nepadutant | ||
Nepadutant 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T71693,CAS号为 183747-35-5。 | |||
T70857 | Scopadulciol | ||
Scopadulciol is and enzyme and proton pump inhibitor. | |||
T26553 |
Aclatonium Napadisilate
Acaltonium napadisilate |
||
Aclatonium Napadisilate, a cholinergic agonist, has been shown to stimulates endocrine and exocrine pancreatic secretion. | |||
T37014 | Inupadenant | ||
Inupadenant is an orally active, highly selective A2A receptor antagonist. Inupadenant is not brain-penetrant. Inupadenant has potent anti-tumor activity[1]. [1]. Laurence Buisseret, et al. Phase 1 trial of the adenosine A2Areceptor antagonist inupadenant (EOS-850): Update on tolerability, and antitumor activity potentially associated with the expression of the A2A receptor within the tumor. Journal of Clinical Oncology. Volume 39, Issue 15_suppl. | |||
T75944 |
Spadin TFA
|
||
Spadin TFA 是一种从血液中释放的前肽衍生的天然肽,是一种有效的 TREK-1 通道阻滞剂,其 IC50值为 10 nM。Spadin TFA 增强小鼠中缝背核 5-HT 神经传递,诱导海马 CREB 激活和神经发生。Spadin TFA 可用于抗抑郁研究。 | |||
T19849 |
2-PADQZ
2PADQZ,2-PADQZ |
||
DPQ is an antiviral compound. DPQ has also been shown to bind to a widened RNA major groove at the internal loop. DPQ acts against the H1N1 and H3N2 strains of influenza A as well as influenza B. | |||
T33793 |
Olpadronic acid
Me2 APD,Me2-APD,Me2APD |
||
Olpadronic acid is a biochemical. | |||
T32076 |
Hippadine
|
||
Hippadine is isolated from Crinum bulbs and has reproductive effect. | |||
T20599 |
Padimate O
Escalol 507,Eusolex 6007,Arlatone UVB |
||
Padimate O, a UVB absorber, is a major ingredient in sunscreens. | |||
T33863 |
Padimate A
|
||
Padimate A is a sunscreen ingredient. | |||
T32722 |
Lexanopadol
GRT-13106G,GRT6006,GRT 13106G,GRT-6006,GRT 6006,GRT13106G |
||
Lexanopadol (GRT6006) is a potent ORL-1 agonist (opioid receptor-like-1), suitable for the treatment of moderate to severe chronic pain, including neuropathic pain. | |||
T24995 |
Abediterol napadisylate
LAS100977 napadisylate |
||
Abediterol napadisylate is a novel long-acting β2-agonist in persistent asthma that is efficacy, safe, and tolerable. | |||
T79638 | Lepadin E | Glutathione Peroxidase | Metabolism |
Lepadin E 是一种铁死亡(ferroptosis)诱导剂,它通过激活 p53-SLC7A11-GPX4 途径显著诱发细胞毒性。该化合物增强 p53 的表达,减少 SLC7A11 及 GPX4 的水平,进而导致活性氧 (ROS) 和脂质过氧化物的增加,并通过上调 ACSL4 来促进细胞死亡。Lepadin E 还具有显著的抗肿瘤效果。 | |||
T79639 | Lepadin H | Ferroptosis | Apoptosis |
Lepadin H 是一种具有显著细胞毒性的海洋生物碱,能够诱导铁死亡。它通过增加 p53 表达、提升 ROS 生成和脂质过氧化来展开作用,同时抑制 SLC7A11 和 GPX4,上调 ACSL4。Lepadin H 主要通过 p53-SLC7A11-GPX4 路径实现其诱导铁死亡的功能。 | |||
T7503L |
Upadacitinib tartrate
ABT 494,ABT-494,ABT494 |
||
Upadacitinib is a potent and selective JAK inhibitor. Upadacitinib is approximately 74 fold selective for Jak1 over Jak2 in cellular assays dependent on specific, relevant cytokines. Upadacitinib demonstrates efficacy in rat arthritis models. | |||
T34058 |
Phyllospadine
|
||
Phyllospadine is a natural flavonoidal alkaloid from the sea-grass Phyllosphadix iwatensis. | |||
T69648 | Inupadenant HCl | ||
Inupadenant, also known as EOS-850, is a highly selective small molecule antagonist of the adenosine A2a receptor, in the adenosine triphosphate adenosine pathway, a key driver of immunosuppression in the tumor microenvironment across a broad range of tumors. | |||
T81604 | Opadotina | ||
Opadotina为anvatabart opadotin的小分子衍生物,具备抗肿瘤(antineoplastic)活性。 | |||
T10749 |
Cebranopadol ((1α,4α)stereoisomer)
GRT6005 (1α,4α)stereoisomer |
Others | Others |
Cebranopadol ((1α,4α)stereoisomer) is a stereoisomer of cebranopadol which is a potent ORL-1 agonist. | |||
T40572 |
Lesogaberan napadisylate
AZD-3355 napadisylate |
||
Lesogaberan (AZD-3355) napadisylate is a potent and selective agonist of GABA B receptors, with an EC 50 of 8.6 nM for human recombinant GABA B receptors. It demonstrates an affinity (Ki) of 5.1 nM for rat GABA B receptors and 1.4 μM for GABA A receptors, as determined by its displacement of [3H]GABA binding in brain membranes. Notably, Lesogaberan napadisylate exerts a peripheral mode of action, inhibiting transient lower esophageal sphincter relaxation. | |||
T26641 |
Apadenoson
ATL 146e,BMS 068645,ATL146e,BMS-068645,ATL-146e,BMS068645 |
||
Apadenoson 是一种有效的腺苷A2受体激动剂,对Adenosine A3 receptors 有抑制作用,IC 为45 nM。Apadenoson 具有抗炎活性,可用来研究神经系统疾病。 | |||
T35906 |
Padanamide A
|
||
Padanamide A is a bacterial metabolite originally isolated from a marine Streptomyces species. It is active against five strains of P. falciparum (EC50s = 160-340 nM), is not cytotoxic to HEK293 or HepG2 human cell lines, but is cytotoxic to Jurkat T lymphocytes with an IC50 value of approximately 60 μg/ml. | |||
T19356 |
HTBA
|
Others | Others |
HTBA 是一种用于测定尿肌酐的低成本酶促纸基分析试剂 (enz-PAD)。 | |||
T9828 | N-[1-(Aminocarbonyl)-4-[(2-chloro-1-iminoethyl)amino]butyl]benzamide | PAD | Chromatin/Epigenetic |
N-[1-(Aminocarbonyl)-4-[(2-chloro-1-iminoethyl)amino]butyl]benzamide 是Cl-amidine (S 构型)的消旋形式。Cl-amidine 口服有效的 PAD 抑制剂。 | |||
T20982 |
Sodium 3-nitrobenzenesulfonate
|
Others | Others |
Sodium 3-nitrobenzenesulfonate 是一种温和的氧化剂。 Sodium 3-nitrobenzenesulfonate 在轧染印花或蒸汽印花时可以保护色光,并抵消还原物质的作用。 | |||
T10831L |
Cl-amidine hydrochloride
|
Apoptosis; PAD | Apoptosis; Chromatin/Epigenetic |
Cl-amidine hydrochloride 是一种口服有效的PAD 抑制剂,可阻断组蛋白 3 瓜氨酸化和中性粒细胞胞外陷阱的形成,并提高败血症小鼠的存活率。它可诱导癌细胞凋亡,还可诱导 miR-16 引起细胞周期阻滞。 | |||
T4978 |
Sarpogrelate hydrochloride
盐酸沙格雷酯,MCI-9042 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Sarpogrelate hydrochloride (MCI-9042) 是一种选择性5-HT2R 拮抗剂,可用于研究与血栓形成有关的血管疾病,对 5-HT2A、5-HT2B 和 5-HT2C 受体的pKi 值分别为 8.52、6.57 和 7.43。 | |||
T10831L2 | Cl-amidine TFA | Others | Others |
Cl-amidine TFA is an orally active inhibitor of peptidyl arginine deminase (PAD) (IC50s: 0.8 μM, 6.2 μM, and 5.9 μM for PAD1, PAD3, and PAD4). Cl-amidine induces apoptosis in cancer cells. | |||
T10482L |
BB-Cl-Amidine hydrochloride
BB-Cl-Amidine hydrochloride (1802637-39-3 free base) |
Others | Others |
BB-Cl-Amidine hydrochloride 是一种肽基精氨酸脱胺酶(PAD)的抑制剂。 | |||
T10831 | Cl-amidine | Others | Others |
Cl-amidine is an orally active inhibitor of peptidyl arginine deminase (PAD) (IC50s: 0.8 μM, 6.2 μM, and 5.9 μM for PAD1, PAD3, and PAD4). Cl-amidine induces apoptosis in cancer cells. | |||
T36107 |
YW3-56
YW3-56 |
||
YW3-56 is a potent peptidylarginine deiminase (PAD) inhibitor, with an IC50 of 1-5 μM for PAD4. Compared with Cl-amidine, YW3-56 shows >60-fold increase in cell growth inhibition efficacy (IC50 about 2.5 μM) but only 5-fold increase in PAD4 inhibition (IC sub>50 about 1-5 μM). At 2-4 μM concentrations, YW3-56 displays mainly cytostatic effects by slowing cell division, whereas at higher concentrations, it exerts cytotoxic effects by altering cell morphology and killing cells[1]. [1]. Wang Y, et ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN2033 |
Padmatin
李属素,Blumeatin C |
Others | Others |
Padmatin (Blumeatin C) 是一种从 Prunus puddum 中分离出来的二氢黄酮醇。 | |||
TN4850 |
Pterocarpadiol D
|
Others | Others |
Pterocarpadiols A-D are a kind of very rare 6a,11b-dihydroxypterocarpans, and their presence as markers may be helpful in chemotaxonomical classification. | |||
TN4847 |
Pterocarpadiol A
|
Others | Others |
Pterocarpadiols A-D are a kind of very rare 6a,11b-dihydroxypterocarpans, and their presence as markers may be helpful in chemotaxonomical classification. | |||
TN4849 |
Pterocarpadiol C
|
Others | Others |
Pterocarpadiols A-D are a kind of very rare 6a,11b-dihydroxypterocarpans, and their presence as markers may be helpful in chemotaxonomical classification. | |||
T83360 |
3-epi-Padmatin
|
||
3-epi-Padmatin是从Inula graveolens中提取的一种天然产物。 | |||
TN4848 |
Pterocarpadiol B
|
Others | Others |
Pterocarpadiols A-D are a kind of very rare 6a,11b-dihydroxypterocarpans, and their presence as markers may be helpful in chemotaxonomical classification. | |||
T2205 |
Acefylline
Theophylline-7-acetic acid,茶碱乙酸,Carboxymethyltheophylline,acetyloxytheophylline,Theophyllineacetic acid |
TNF; PAD; PKA; HDAC; PDE; Adenosine Receptor | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; GPCR/G Protein; Metabolism; Neuroscience; Tyrosine Kinase/Adaptors |
Acefylline (Theophylline-7-acetic acid) 是黄嘌呤衍生物,是一种腺苷受体拮抗剂。它是蛋白质精氨酸脱亚氨酶 (PAD) 激活剂,也是一种支气管扩张剂,可抑制大鼠肺 cAMP 磷酸二酯酶同工酶。 | |||
T16946 |
Streptonigrin
Bruneomycin |
Others | Others |
Streptonigrin is a natural product produced by Streptomyces flocculus, has both anti-tumor and anti-bacterial activity. Streptonigrin acts as a pan-PAD inhibitor (IC50s: 48.3±34.2 µM, 26.1±0.3 µM, 0.43±0.03 µM, and 2.5±0.4 µM for PAD1, PAD2, PAD3, and PAD |