151
22
9
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TD0105 |
Sulfobromophthalein disodium salt
|
Others | Others |
Sulfobromophthalein disodium salt 是一种有机阴离子染料,能够参与药物和代谢物的运输,可用于研究动物组织中表达的多种膜载体。 | |||
T40363 |
Poly-D-lysine hydrobromide (MW 30000-70000)
Poly-D-lysine HBr (MW 30000-70000) |
CaSR | GPCR/G Protein |
Poly-D-lysine hydrobromide (MW 30000-70000)(Poly-D-lysine HBr) 是一种可口服的肽类 CaSR 激动剂,可从朊病毒感染的 SN56 神经母细胞瘤细胞中去除蛋白酶 K 抗性的 PrP。 | |||
T6133 |
Remodelin hydrobromide
Remodelin,Remodelin HBR |
RAAS; Histone Acetyltransferase | Chromatin/Epigenetic; Endocrinology/Hormones |
Remodelin hydrobromide (Remodelin HBR) 是一种新型有效的选择性乙酰转移酶蛋白 NAT10 抑制剂,能改善早衰综合征细胞表型。 | |||
T3156 |
Ciliobrevin A
Hedgehog Pathway Inhibitor 4,HPI-4 |
Hedgehog/Smoothened | GPCR/G Protein; Stem Cells |
Ciliobrevin A (HPI-4) 是Hedgehog(Hh) 信号通路抑制剂,平均抑制浓度 (IC50) 值小于 10 μM。 | |||
T21788 |
BD 1008 dihydrobromide
|
Sigma receptor | GPCR/G Protein |
BD 1008 dihydrobromide 是 sigma 1 (σ1) 受体 (Ki = 2 nM) 的选择性拮抗剂。 它对 sigma1 受体具有高亲和力,对 sigma2 受体具有中等亲和力。 它通过拮抗 σ 受体减弱可卡因的毒性和刺激作用。 | |||
T4570 |
Pipobroman
Vercyte,A-8103,Amedel,哌泊溴烷 |
Others; DNA Alkylator/Crosslinker | DNA Damage/DNA Repair; Others |
Pipobroman (Vercyte) 是一种烷基化剂,是哌嗪的溴化衍生物。它通过抑制 DNA 和 RNA 聚合酶或减少嘧啶核苷酸掺入 DNA 发挥其作用。它在真性红细胞增多症和原发性血小板增多症中具有良好的临床活性,可用于癌症研究。 | |||
T13110 |
Tedatioxetine hydrobromide
Lu AA 24530 hydrobromide |
Dopamine Receptor; 5-HT Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide) 是一种血清素-去甲肾上腺素-多巴胺再摄取抑制剂 ,也是 5-HT2A、5-HT2C、5-HT3 和 α1A-肾上腺素能受体的拮抗剂,可用于治疗抑郁症和焦虑症。 | |||
T1740 |
BD-1047 dihydrobromide
BD1047.2HBr |
Sigma receptor | GPCR/G Protein |
BD-1047 dihydrobromide (BD1047.2HBr) 是一种选择性的 sigma-1 receptor 受体拮抗剂,在预测精神分裂症疗效的动物模型中具有抗精神病活性。 | |||
T2395L |
Vortioxetine hydrobromide
氢溴酸沃替西汀,Vortioxetine (Lu AA21004) HBr,Vortioxetine HBr,盐酸沃替西汀,Lu AA21004 hydrobromide |
5-HT Receptor; Serotonin Transporter | GPCR/G Protein; Neuroscience |
Vortioxetine hydrobromide (Lu AA21004 hydrobromide) 是5-HT1A、5-HT1B、5-HT3A、5-HT7受体和5-羟色胺转运体(SERT)的抑制剂,Ki 值分别为 15、33、3.7、19 和 1.6 nM。 | |||
T61151 |
Beclobrate
|
||
Beclobrate (Sgd 24774), a fibric acid derivative, exhibits potent lipid-lowering efficacy in rodent models [1]. | |||
T5351L |
PU-WS13 hydrobromide
PU-WS13 hydrobromide (1454619-14-7 Free base) |
GPR | Endocrinology/Hormones; GPCR/G Protein |
PU-WS13 hydrobromide 是一种 GRP94 抑制剂,具有抗炎活性,对小鼠 TNBC 肿瘤中的 M2 样巨噬细胞的增殖具有抑制作用。 | |||
T10813 |
Cilobradine hydrochloride
DK-AH 269 |
HCN Channel | Membrane transporter/Ion channel |
Cilobradine hydrochloride (DK-AH 269) 是一种 HCN 通道阻断剂。 | |||
T77795 |
L-DABA hydrobromide
L-2,4-Diaminobutyric acid hydrobromide |
Others; Endogenous Metabolite | Metabolism; Others |
L-DABA hydrobromide (L-2,4-Diaminobutyric acid hydrobromide) 是一种有效的 GABA 转氨酶抑制剂,具有抗肿瘤和抗惊厥活性,可用于研究神经系统疾病。 | |||
T6832 |
Fatostatin hydrobromide
Fatostatin HBr,Fatostatin A,Fatostatin A HBr,Fatostatin |
NPC1L1; Fatty Acid Synthase | Membrane transporter/Ion channel; Metabolism |
Fatostatin hydrobromide (Fatostatin A HBr) 是一种 SREBP 活化的特异性抑制剂,可抑制 SREBP-1 和 SREBP-2 的活化。它与 SCAP (SREBP 裂解激活蛋白) 结合,抑制 SREBPs 的 ER-Golgi 易位。它具有抗肿瘤作用,能抑制 ob/ob 小鼠的高血糖。它抑制了细胞中成脂基因的转录。 | |||
T3637 |
Pifithrin-β hydrobromide
Cyclic PFT-α,PFT-β,Cyclic Pifithrin-α hydrobromide,Pifithrin-β,PFT β (hydrobromide) |
Ferroptosis; p53 | Apoptosis |
Pifithrin-β hydrobromide (Cyclic PFT-α) 是一种 p53 的抑制剂,可逆地阻断 p53 依赖性转录激活和细胞凋亡。IC50值为23 μM。 | |||
T10104 |
3,4-Dihydroxybenzylamine hydrobromide
NSC 263475 hydrobromide,3,4-二羟基苄胺·氢溴酸 |
Others; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others |
3,4-Dihydroxybenzylamine hydrobromide (NSC-263475 hydrobromide) 抑制黑色素瘤细胞中的 DNA 聚合酶活性,并在具有不同程度酪氨酸酶活性的黑色素瘤细胞系中显示出生长抑制活性。 | |||
T7208 |
AMD 3465 hexahydrobromide
GENZ-644494 (hexahydrobromide) |
HIV Protease; CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
AMD 3465 hexahydrobromide (GENZ-644494 (hexahydrobromide)) 是一种 CXCR4受体拮抗剂,具有潜在的抗癌和抗 HIV 活性。 | |||
T1534 |
Darifenacin hydrobromide
氢溴酸达非那新,Darifenacin HBr,UK-88525 |
AChR | Neuroscience |
Darifenacin hydrobromide (UK-88525) 是一种选择性 M3 蕈毒碱受体拮抗剂,pKi 为 8.9。 | |||
T22864 |
Immethridine dihydrobromide
|
Others | Others |
Immethridine dihydrobromide is a histamine H3 receptor agonist. | |||
T36287 |
Pirtobrutinib
|
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
Pirtobrutinib (LOXO-305) is an advanced BTK inhibitor that displays high selectivity and operates through a non-covalent mechanism. This compound effectively inhibits various BTK C481 substitution mutations, leading to tumor regression in BTK-dependent lymphoma tumors in mouse xenograft models. Furthermore, Pirtobrutinib exhibits remarkable selectivity for BTK, with more than a 300-fold difference compared to 370 other kinases tested. Notably, at a concentration of 1 μM, Pirtobrutinib demonstrat... | |||
T8495 |
Alobresib
Vorolanib,GS-5829 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
Alobresib (Vorolanib) 是一种BET 溴结构域抑制剂,是一种抗肿瘤候选药物。 | |||
T0216 |
Eletriptan hydrobromide
Eletriptan HBr,UK-116044,依来曲普坦氢溴酸盐 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Eletriptan hydrobromide (Eletriptan HBr) 是一种口服活性激动剂,对 5-HT1B/1D 受体具有特异性亲和力,Ki 值分别为 0.92 和 3.14 nM。 | |||
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。 | |||
T1483 |
Citalopram hydrobromide
Lu 10-171,Nitalapram HBr,Bonitrile HBr,XU-62-320,Lu 10-171 HBr,氢溴酸西酞普兰,Citalopram HBr |
5-HT Receptor; Serotonin Transporter; Autophagy | Autophagy; GPCR/G Protein; Neuroscience |
Citalopram hydrobromide (XU-62-320) 是一种选择性 5-羟色胺再摄取抑制剂,可选择性地抑制 CNS 神经元对 5-羟色胺的再摄取,从而增强中枢神经系统中的 5-羟色胺能活性,也具有抗抑郁活性。它抑制兔血小板中 5-HT 的摄取,IC50为 14 nM。 | |||
T4387 |
evobrutinib
MSC2364447C,M2951 |
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
Evobrutinib(M2951) 也称为 M-2951 和 MSC-2364447C,是布鲁顿酪氨酸激酶(BTK) 的高选择性抑制剂,BTK 对包括 B 淋巴细胞和巨噬细胞在内的各种免疫细胞的发育和功能很重要。临床前研究表明它可能对某些自身免疫性疾病有治疗作用。 | |||
T14965 |
Ciliobrevin D
|
ATPase; Hedgehog/Smoothened | GPCR/G Protein; Membrane transporter/Ion channel; Stem Cells |
Ciliobrevin D 是细胞渗透性,可逆和特异性的 AAA + ATPase 运动细胞质动力蛋白抑制剂。它在体外抑制依赖于动力蛋白的微管滑动和 ATPase 活性。它抑制Hedgehog 信号和初级纤毛形成。 | |||
T17002 |
Tazemetostat hydrobromide
E-7438 hydrobromide,氢溴酸泰泽司他,EPZ-6438 hydrobromide |
Histone Methyltransferase | Chromatin/Epigenetic |
Tazemetostat hydrobromide (E-7438 hydrobromide) 是口服的EZH2选择性抑制剂。它抑制含有 PRC2 复合体的野生型 EZH2 的活性,Ki 为 2.5 nM。它还抑制 EZH1,IC50为 392 nM。 | |||
T22534 |
8-Hydroxy-DPAT hydrobromide
7-(二丙基氨基)-5,6,7,8-四氢-1-萘酚氢溴酸盐,8-OH-DPAT hydrobromide |
5-HT Receptor | GPCR/G Protein; Neuroscience |
8-Hydroxy-DPAT hydrobromide (8-OH-DPAT hydrobromide) 是一种选择性5-HT1A 激动剂,pIC50为 8.19。它对 5-HT1结合位点的亚型有近 1000 倍的选择性。 | |||
T22761 |
EIT hydrobromide
2-Ethyl-2-thiopseudourea hydrobromide,S-Ethylisothiourea hydrobromide,S-乙基硫酸乙烯溴化氢 |
NOS | Immunology/Inflammation |
EIT hydrobromide (S-Ethylisothiourea hydrobromide) 是一种iNOS 抑制剂。 | |||
T2707 |
Pifithrin-α hydrobromide
Pifithrin hydrobromide,Pifithrin-α (PFTα) HBr,Pifithrin-α,PFTα,PFTα hydrobromide |
Ferroptosis; Aryl Hydrocarbon Receptor; p53 | Apoptosis; Immunology/Inflammation |
Pifithrin-α hydrobromide (Pifithrin-α hydrobromide) 是一种 p53 抑制剂,可抑制 p53 反应基因的 p53 依赖性反式激活。它也是芳烃受体的激动剂。 | |||
T7543 |
S-(2-aminoethyl) Isothiourea (dihydrobromide)
|
NOS | Immunology/Inflammation |
S-(2-aminoethyl) Isothiourea (dihydrobromide) 是所有 NOS 异构体的非选择性抑制剂。对于人类 nNOS、eNOS 和 iNOS,Ki 值分别为 1.8、2.1 和 0.59 µM。 | |||
T7206L |
2-Iminobiotin hydrobromide
2-亚氨基生物素,Guanidinobiotin,2-亚氨基生物素盐酸盐 |
NOS; NO Synthase | Immunology/Inflammation |
2-Iminobiotin hydrobromide (Guanidinobiotin) 是生物素 (维生素 H 或 B7) 类似物。它是一种可逆的 NO 合酶抑制剂,可作用于小鼠 iNOS(Ki:21.8 μM)和大鼠 n-cNOS(Ki:37.5 μM)。它和低温环境均可以保护人类神经细胞,使其免受缺氧诱导的细胞损伤。 | |||
T21685 |
CCT 031374 hydrobromide
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
CCT 031374 hydrobromide 是一种 TCF/β-catenin 抑制剂,具有抗肿瘤活性。 | |||
T10717 |
Inobrodib
CBP-IN-1 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
Inobrodib (CBP-IN-1) 是一种口服活性的强选择性p300/CBP 抑制剂,与 p300 和 CBP 结合,Kd 值为 1.3 和 1.7 nM。它抑制前列腺癌细胞系的细胞增殖并降低雄激素受体和 C-MYC 调节的基因表达。 | |||
T12352L |
Oxidopamine hydrobromide
6-Hydroxydopamine hydrobromide,6-羟基多巴胺氢溴酸盐,6-OHDA hydrobromide |
Mitophagy; Dopamine Receptor; Autophagy | Autophagy; GPCR/G Protein; Neuroscience |
Oxidopamine hydrobromide (6-OHDA hydrobromide) 是一种神经递质多巴胺拮抗剂,可选择性地破坏多巴胺能神经元,是一种广泛使用的神经毒素。 | |||
T8439 |
Clobenpropit dihydrobromide
|
Apoptosis; Histamine Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Clobenpropit dihydrobromide 是一种组胺H3R 拮抗剂/反向激动剂。它与 5-HT3 受体和 α2A/α2C 肾上腺素受体结合,对组胺H4受体起部分激动剂的作用,还能促进凋亡。 | |||
T78410 |
Gly-Pro-AMC hydrobromide
Gly-Pro-AMC HCl |
||
Gly-Pro-AMC hydrobromide (Gly-Pro-AMC HCl) 为特异性荧光染料,用于细胞荧光检测,检测 Dipeptidyl peptidase IV (DPP-IV) 活性。 | |||
T5956 |
VP3.15 dihydrobromide
|
GSK-3; PDE | Metabolism; PI3K/Akt/mTOR signaling; Stem Cells |
VP3.15 dihydrobromide 是一种口服具有活力的、高效的、CNS 可渗透的PDE7-GSK3双重抑制剂,对 PDE7 和 GSK3 作用的IC50值分别为 1.59 μM 和 0.88 μM。它具有神经保护和神经修复作用,可用于研究多发性硬化症 (MS) 潜在的抗炎和促髓鞘再生联合。 | |||
T12172 |
NAN-190 hydrobromide
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
NAN-190 hydrobromide 是一种5-HT1A 选择性拮抗剂。 | |||
T70260 | AMD-3329 hydrobromide | ||
AMD-3329 hydrobromide is a biochemical in the class of potent and selective anti-HIV-1 and HIV-2 agents that inhibit virus replication by binding to the chemokine receptor CXCR4, the co-receptor for entry of X4 viruses. | |||
T24035 |
Eptazocine hydrobromide
MCV 4169,ST-2121,MCV-4169,sT 2121, l-,l-ST-2121 |
||
Eptazocine hydrobromide is an agonist of the Opioid receptor and is a kappa-Opioid receptor agonist. It is also an Opioid analgesic and an Opioid receptor antagonist. | |||
T69519 | Iroxanadine hydrobromide | ||
Iroxanadine hydrobromide is a MAPK p38 inhibitor potentially for the treatment of atherosclerosis. | |||
T71496 | Isoremoxipride hydrobromide | ||
Isoremoxipride hydrobromide is a dopamine antagonist. | |||
T15565 |
Imetit dihydrobromide
VUF 8325 dihydrobromide,SKF 91105 dihydrobromide |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Imetit dihydrobromide is a high affinity and effective agonist of histamine H3 and H4 receptors (Ki: 0.3 and 2.7 nM). Imetit mimics the histamine effect in triggering a shape change in eosinophils (EC50: 25 nM). | |||
T61999 | Quinine hydrobromide | ||
Quinidine hydrobromide 是有效的、选择性的的、具有口服活性的细胞色素 P450db (cytochrome P450db) 抑制剂。Quinidine hydrobromide 是 K+通道 (K+channel) 的有效阻断剂(IC50= 19.9 μM)。Quinidine hydrobromide 具有抗心律失常的作用。Quinidine hydrobromide 也可用作疟疾的研究。 | |||
T60530 | Mercaptoethylguanidine (MEG) (dihydrobromide) | ||
Mercaptoethylguanidine (MEG) dihydrobromide 是选择性的诱导型一氧化氮合酶抑制剂和过氧亚硝酸盐清除剂,在炎症性肠病研究中具有潜力。 | |||
T77905 |
Vobramitamab
AEX-4089 |
||
Vobramitamab为针对人源B7-H3的单克隆抗体(mAb)。该抗体通过一个可切割的连接物与前药seco-DUBA相结合,构成一种抗体-药物偶联物(ADC)名为MGC018。 | |||
T15590 |
Iodophenpropit dihydrobromide
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Iodophenpropit dihydrobromide is an effective and selective antagonist of the histamine H3 receptor. The binding of [125I]Iodophenpropit is readily reversible, selective, and of high affinity (KD: 0.32 nM). | |||
T38221 |
N,N-Dipropyldopamine (hydrobromide)
|
||
N,N-Dipropyldopamine is a dopamine receptor agonist.1,2,3 It decreases dihydrophenylalanine (DOPA) levels in the limbic forebrain and striatum of reserpinized rats (ED50s = 25 and 20 μmol/kg, respectively), as well as reduces homovanillic acid levels in rat striatum when administered at a dose of 80 μmol/kg.1 N,N-Dipropyldopamine (0.5-16 mg/kg) reduces spontaneous locomotor activity in mice, an effect that can be reversed by the antipsychotic spiroperidol.2,3 | |||
T37150 |
ADTN hydrobromide
|
||
ADTN hydrobromide (6,7-ADTN) is a dopamine receptor agonist (EC50s = 3.5 and 0.65 μM in rat striatal and nucleus accumbens homogenates, respectively). ADTN hydrobromide stimulates production of cAMP in rat striatal homogenates, a process that is reduced by 70% in the presence of the dopamine antagonist fluphenazine at a concentration of 1 μM. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8304 |
Anisodamine Hydrobromide
6-Hydroxyhyoscyamine,氢溴酸山莨菪碱 |
Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Anisodamine Hydrobromide (6-Hydroxyhyoscyamine) 是来自颠茄的一种生物碱,具有抗氧化、抗炎活性。它也是一种非亚型的选择性毒蕈碱和烟碱类胆碱受体拮抗剂。 | |||
T0086 |
Galanthamine hydrobromide
Galantamine hydrobromide,Galanthamine HBr,氢溴酸加兰他敏 |
AChR; AChE | Neuroscience |
Galanthamine hydrobromide (Galantamine hydrobromide) 是一种长效的中枢活性 AChE 抑制剂,IC50为 410 nM。它是神经元烟碱型 ACh 受体的变构增强剂,IC50值为 0.35 µM,可用于阿尔茨海默症的研究。 | |||
T6560 |
Lappaconitine hydrobromide
氢溴酸高乌甲素,Lappaconite HBr,Allapinine |
Others | Others |
Lappaconitine hydrobromide (Allapinine) 是天然生物碱类化合物,具有抗心律失常作用。 | |||
T1255 |
Tobramycin
NSC 180514,妥布霉素,Nebramycin Factor 6,Deoxykanamycin B |
ribosome; Antibacterial; Antibiotic | Microbiology/Virology |
Tobramycin (NSC-180514) 是一种胃肠外给药的广谱氨基糖苷类抗生素,可研究由于敏感生物引起的中度至重度细菌感染疾病。 | |||
T0625 |
Theobromine
3, 7-Dimethylxanthine,可可碱,3,7-Dimethylxanthine |
Endogenous Metabolite; PDE; Adenosine Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Theobromine (3,7-Dimethylxanthine) 是在可可豆中发现的一种甲基黄嘌呤,抑制腺苷受体 A1 信号传导,用作支气管扩张剂和血管扩张剂。 | |||
T3524 |
Halofuginone hydrobromide
卤夫酮溴氢酸盐,Tempostatin,RU-19110 (hydrobromide),Stenorol,常山酮溴酸盐 |
Others; Calcium Channel; DNA/RNA Synthesis; Sodium Channel; Parasite; TGF-beta/Smad | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Others; Stem Cells |
Halofuginone hydrobromid 是Febrifugine 的衍生物,是竞争性脯氨酰-tRNA 合成酶抑制剂。它是 I 型胶原合成的特异性抑制剂,并通过抑制TGF-β活性可减轻骨关节炎。它具有抗疟疾、抗炎、抗癌、抗纤维化作用。 | |||
T41372 |
(22S,23S)-Homobrassinolide
油菜素内酯,SSHB |
Others | Others |
(22S,23S)-Homobrassinolide (SSHB) 在各种植物生物测定试验中均能诱导植物生长。 | |||
T2198 |
Arecoline hydrobromide
Arecoline HBr,氢溴酸槟榔碱,Arecoline bromide |
AChR | Neuroscience |
Arecoline hydrobromide (Arecoline HBr) 是从槟榔中得到的一种生物碱,具有刺激、警觉、抗焦虑和抗寄生虫作用。它是烟碱和毒蕈碱乙酰胆碱受体的部分激动剂,可诱导氧化应激。 | |||
T11041 |
Dihydro-β-erythroidine hydrobromide
DHβE hydrobromide |
Others | Others |
Dihydro-β-erythroidine hydrobromide(DHβE) is a potent, oral active and competitive antagonist of neuronal nicotinic acetylcholine receptors (nAChRs). Dihydro-β-carotene hydrobromide showed selectivity to α4β4 and α4β2nAChR, with IC50 of 0.19 and 0.37 μM, | |||
T75485 | Dehydrobruceine B | ||
Dehydrobruceine B 是一种苦木素,可从鸦胆子 (Brucea javanica) 中分离得到。Dehydrobruceine B 与 Cisplatin 通过线粒体途径,协同诱导细胞凋亡 (apoptosis)。Dehydrobruceine B 还增加凋亡诱导因子 (AIF) 和 Bax 表达,抑制 Keap1-Nrf2。 | |||
TN1899L |
Lycoramine hydrobromide
石蒜胺,Lycoramine HBr |
||
Lycoramine is a natural alkaloid isolated from Lycoris chinensis. | |||
TN4636 | Neoglucobrassicin | Others | Others |
Neoglucobrassicin 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 TN4636,CAS号为 5187-84-8。 | |||
TN3796 | Dehydrobruceantinol | Others | Others |
Dehydrobruceantinol shows bitter taste and has antileukemic activity. | |||
T80014 |
Guvacine hydrobromide
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Guvacine hydrobromide为槟榔中提取的生物碱,具有作为GABA摄取抑制剂的活性。该化合物对大鼠GAT-1、GAT-2和GAT-3的GABA摄取抑制作用具有不同的IC50值,分别为39 μM、58 μM及378 μM。 | |||
TN5614 |
Dehydrobruceantin
|
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Dehydrobruceantin has anti-tuberculosis activity. | |||
TN6072 |
14-Dehydrobrowniine
|
||
14-Dehydrobrowniine是一种天然产物,属于毛茛科翠雀属,其产品编号为 TN6072,CAS号为 4829-56-5。14-Dehydrobrowniine可用作对照参考。 | |||
T82304 |
Glucobrassicanapin potassium
4-Pentenylglucosinolate potassium |
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Glucobrassicanapin (4-Pentenylglucosinolate) potassium 是脂肪族硫代葡萄糖苷类化合物,主要存在于白菜等蔬菜作物中。 | |||
TN3797 | Dehydrobruceine A | Antifection | Microbiology/Virology |
Dehydrobruceine A shows strong antitrypanosomal activities with IC(50) values in the range of 2.9-17.8nM. | |||
T1255L |
Tobramycin Sulfate
Dartobcin,Nebcine,Tobraneg,Tobrasix |
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Tobramycin Sulfate is a broad-spectrum antibiotic. It is effective against gram-negative bacteria. It especially potent against the Pseudomonas species. | |||
TN3051 | 4-Methoxyglucobrassicin | Others | Others |
4-Methoxyglucobrassicin 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 TN3051,CAS号为 83327-21-3。 | |||
T80013 |
Arecaidine hydrobromide
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GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Arecaidine hydrobromide,一种吡啶生物碱,有效抑制GABA吸收。作为H+偶联的氨基酸转运蛋白1(PAT1,SLC36A1)的底物,它竞争性地抑制L-脯氨酸的摄取。 | |||
TN4237 |
Hydrocotarnine hydrobromide
|
Others | Others |
Hydrocotarnine hydrobromide 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 TN4237,CAS号为 5985-00-2。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-01725 |
Leptin Receptor Protein, Human, Recombinant (His)
LEPRD,OB-R,OBR,LEP-R,CD295,leptin receptor |
Human | HEK293 |
Leptin Receptor or CD295 belongs to the gp130 family of cytokine receptors that are known to stimulate gene transcription via activation of cytosolic STAT proteins. This protein is a receptor for leptin (an adipocyte-specific hormone that regulates body weight) and is involved in the regulation of fat metabolism, as well as in a novel hematopoietic pathway that is required for normal lymphopoiesis. Leptin Receptor/CD295 is transmembrane catalytic receptors found on NPY/AgRP and alpha-MSH/CART ne... | |||
TMPY-00874 |
Leptin Receptor Protein, Human, Recombinant (His & hFc)
LEP-R,OBR,CD295,OB-R,LEPRD,leptin receptor |
Human | HEK293 |
Leptin Receptor or CD295 belongs to the gp130 family of cytokine receptors that are known to stimulate gene transcription via activation of cytosolic STAT proteins. This protein is a receptor for leptin (an adipocyte-specific hormone that regulates body weight) and is involved in the regulation of fat metabolism, as well as in a novel hematopoietic pathway that is required for normal lymphopoiesis. Leptin Receptor/CD295 is transmembrane catalytic receptors found on NPY/AgRP and alpha-MSH/CART ne... | |||
TMPJ-00977 |
LEPR Protein, Mouse, Recombinant (mFc)
LEPR,CD295,OB-R,LEP-R,HuB219,Leptin receptor,OBR,DB... |
Mouse | Human Cells |
The Leptin receptor is a member of the Class I cytokine receptor family. It mediates the activities of Leptin, a multi-functional hormone produced primarily by adipose tissues that plays roles in food intake, energy metabolism, angiogenesis, reproduction, hematopoiesis, bone metabolism, and immune function. The human Leptin R gene encodes 1165 amino acids (aa) including a signal peptide, an extracellular region with cytokine receptor homology (CRH), multiple fibronectin type III domains and a WS... | |||
TMPJ-00975 |
LEPR Protein, Mouse, Recombinant (hFc)
CD295,DB,HuB219,OB receptor,LEP-R,Leptin receptor,OBR |
Mouse | Human Cells |
The Leptin receptor is a member of the Class I cytokine receptor family. It mediates the activities of Leptin, a multi-functional hormone produced primarily by adipose tissues that plays roles in food intake, energy metabolism, angiogenesis, reproduction, hematopoiesis, bone metabolism, and immune function. The human Leptin R gene encodes 1165 amino acids (aa) including a signal peptide, an extracellular region with cytokine receptor homology (CRH), multiple fibronectin type III domains and a WS... | |||
TMPJ-00411 |
LEPR Protein, Human, Recombinant (hFc)
LEPR,Leptin receptor,OB-R,OB receptor,OBR,CD295,DB,... |
Human | Human Cells |
The Leptin receptor is a member of the Class I cytokine receptor family. It mediates the activities of Leptin, a multi-functional hormone produced primarily by adipose tissues that plays roles in food intake, energy metabolism, angiogenesis, reproduction, hematopoiesis, bone metabolism, and immune function. The human Leptin R gene encodes 1165 amino acids (aa) including a signal peptide, an extracellular region with cytokine receptor homology (CRH), multiple fibronectin type III domains and a WS... | |||
TMPJ-00976 |
LEPR Protein, Mouse, Recombinant (His)
OBR,DB,Leptin receptor,OB receptor,CD295,OB-R,LEPR,... |
Mouse | Human Cells |
The Leptin receptor is a member of the Class I cytokine receptor family. It mediates the activities of Leptin, a multi-functional hormone produced primarily by adipose tissues that plays roles in food intake, energy metabolism, angiogenesis, reproduction, hematopoiesis, bone metabolism, and immune function. The human Leptin R gene encodes 1165 amino acids (aa) including a signal peptide, an extracellular region with cytokine receptor homology (CRH), multiple fibronectin type III domains and a WS... | |||
TMPH-03038 |
Cobra venom factor Protein, Naja kaouthia, Recombinant (His & SUMO)
Cobra venom factor,Complement C3 homolog,CVFk,CVF |
Naja kaouthia | E. coli |
Complement-activating protein in cobra venom. It is a structural and functional analog of complement component C3b, the activated form of C3. It binds factor B (CFB), which is subsequently cleaved by factor D (CFD) to form the bimolecular complex CVF/Bb. CVF/Bb is a C3/C5 convertase that cleaves both complement components C3 and C5. Structurally, it resembles the C3b degradation product C3c, which is not able to form a C3/C5 convertase. Unlike C3b/Bb, CVF/Bb is a stable complex and completely re... | |||
TMPH-03037 |
Alpha-cobratoxin Protein, Naja kaouthia, Recombinant (GST & His & Myc)
Alpha-CT,Alpha-Ctx,Alpha-EPTX-Nk2a,Long neurotoxin 1,Alpha-C... |
Naja kaouthia | E. coli |
Monomer: binds with high affinity to muscular (alpha-1-beta-1-gamma-delta/CHRNA1-CHRNB1-CHRNG-CHRND) nAChR (tested on Torpedo californica, Kd=0.2-4.5 nM) and neuronal alpha-7/CHRNA7 nicotinic acetylcholine receptors (Kd=13-105 nM). Also inhibits GABA(A) channels. Heteropentamer targets studied are composed of alpha-1-beta-3-gamma-2 (GABRA1-GABRB3-GABRG2) subunits (IC(50)=236 nM), alpha-1-beta-2-gamma-2 (GABRA1-GABRB2-GABRG2) subunits (IC(50)=469 nM), alpha-2-beta-2-gamma-2 (GABRA2-GABRB2-GABRG2)... | |||
TMPH-00031 |
Aerolysin Protein, Aeromonas sobria, Recombinant (His & Myc)
Hemolysin |
Aeromonas sobria | E. coli |
Secreted, cytolytic toxin that forms pores in host membranes after proteolytic removal of a C-terminal propeptide, leading to destruction of the membrane permeability barrier and cell death. The pores are formed by transmembrane beta-strands and are approximately 3 nm in diameter. |