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28

抑制剂 & 化合物

3

天然产物

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Cat. No. Product Name Target Signaling Pathways
T21052 Lysidine

2-甲基咪唑啉,2-Methyl-2-iMidazoline

Nucleoside Antimetabolite/Analog Cell Cycle/Checkpoint; DNA Damage/DNA Repair
Lysidine (2-Methyl-2-iMidazoline) 是在 tRNA 之外很少见到的核苷。 Lysidine 具有更好的翻译保真度。
T22051 BU 224 hydrochloride

Imidazoline Receptor Neuroscience
BU 224 hydrochloride 是一种选择性的咪唑啉 I(2) 结合位点配体,具有镇痛和抗抑郁样活性。
T22052 BU 226 hydrochloride

Imidazoline Receptor Neuroscience
BU 226 hydrochloride 对咪唑啉受体具有亲和力,尤其是对 I2 结合位点,Ki 为 1.4 nM。 BU 226 hydrochloride 对 alpha 2-adrenoceptors 显示出低 (microM) 亲和力。
T6641 Rilmenidine Phosphate

Apoptosis; Adrenergic Receptor; Autophagy; Imidazoline Receptor Apoptosis; Autophagy; GPCR/G Protein; Neuroscience
Rilmenidine phosphate 是一种新型的抗高血压药物和口服活性选择性 I1 咪唑啉受体激动剂。它可调节白血病细胞增殖,刺激促凋亡蛋白 Bax,从而诱导人白血病 K562 细胞线粒体通路的紊乱和凋亡。它可通过减少交感神经过度活跃而发挥中枢作用,并通过抑制 Na+/H+反向转运而在肾脏中发挥作用。
T1028 Moxonidine

莫索尼定,BDF5895,莫索尼啶

Imidazoline Receptor Neuroscience
Moxonidine (BDF5895) 是咪唑啉受体亚型 1 的选择性激动剂,用作抗高血压药物。
T0115 Idazoxan hydrochloride

RX 781094,盐酸咪唑克生

Adrenergic Receptor; Imidazoline Receptor GPCR/G Protein; Neuroscience
Idazoxan hydrochloride (RX 781094) 是一种 α2-肾上腺素受体拮抗剂,改善帕金森氏病、L-DOPA 引起的运动障碍和实验性帕金森病的运动症状。它也是咪唑啉受体拮抗剂,可竞争性拮抗唑啉样药物的中枢性降压作用。
T6703 Tetrahydrozoline hydrochloride

Murine Plus,盐酸四氢萘咪唑,Tetryzoline hydrochloride,Tyzine,Tetrahydrozoline HCl,盐酸四氢唑林

Adrenergic Receptor GPCR/G Protein; Neuroscience
Tetrahydrozoline hydrochloride (Murine Plus) 是一种咪唑啉的衍生物,是一种 α-肾上腺素能 (α-adrenergic) 激动剂,能引起血管收缩,常用于研究鼻充血、结膜充血。
T22492 2-BFI hydrochloride

Imidazoline Receptor Neuroscience
2-BFI hydrochloride 是一种 I2-咪唑啉受体的高亲和力激动剂。 2-BFI hydrochloride 可用于预防中风和急性炎症性免疫疾病的研究。
T15010 CR4056

6-(1H-imidazol-1-yl)-2-phenylquinazoline

MAO; Imidazoline Receptor Metabolism; Neuroscience
CR4056 (6-(1H-imidazol-1-yl)-2-phenylquinazoline) 是一种特异性 MAO-A 抑制剂,IC50 为 202.7 nM,是 I2-咪唑啉受体的配体,IC50 为 596 nM。
T23283 2-Methoxyidazoxan monohydrochloride

RX 821002 hydrochloride

Adrenergic Receptor GPCR/G Protein; Neuroscience
L-Albizziin (2-Methoxyidazoxan monohydrochloride) 是高效的 alpha 2r 肾上腺素受体选择性拮抗剂,对 imidazoline 拮抗作用很小或没有。它对 (豚鼠) alpha 2D 肾上腺素受体 (pKd9.7) 的亲和力明显高于 (兔子) alpha 2A 肾上腺素受体 (pKd8.2)。
T28631 RX821002

RX-821002,RX 821002

RX821002 is a potent and selective antagonist of α2-adrenoceptor with low affinity for imidazoline sites. RX821002 displays selectivity for the α2D over the α2A subtypes (pKd values are 9.7 and 8.2 respectively).
T34470 S 9871

RX-801080,RX 801080,S9871,RX801080,S-9871

S 9871, also known as RX 801080, is an imidazoline derivative reported to antagonize imidazoline-stimulated insulin secretion.
T23662 Aganodine

Aganodin

Aganodine is a guanidine that activates presynaptic imidazoline receptors. Aganodine inhibits the presynaptic release of norepinephrine through its agonism at imidazoline receptors.
T68931 Tracizoline

Tracizoline is a potent I2-imidazoline receptor agonist.
T22760 Efaroxan hydrochloride

Others Others
α2 adrenoceptor antagonist and imidazoline I1 receptor ligand
T40869 Moxonidine hydrochloride

BDF5895hydrochloride,盐酸莫索尼定

Moxonidine Hydrochloride is a selective agonist at the imidazoline receptor subtype 1, used as antihypertensive agent. Target: I1-R Moxonidine Hydrochloride is a centrally acting antihypertensive agent. Mixed Nischarin (I1 imidazoline receptor) and α2-AR (adrenergic) agonist; displays 40-fold higher affinity for I1 receptors versus α2-adrenoceptors. Moxonidine reduced stimulated NE overflow (log EC50: -6.15 +/- 0.14). AGN192403, a selective ligand at I1-R, had no influence on the dose-response...
T23263 RS 45041-190 hydrochloride

Others Others
Highly selective I2 imidazoline receptor ligand
T60425 Tetrahydrozoline nitrate

Tetrahydrozoline (Tetryzoline) nitrate 是咪唑啉的衍生物。它是一种引起血管收缩的α-肾上腺素能 (α-adrenergic) 激动剂。Tetrahydrozoline 广泛用于鼻充血和结膜充血的研究。
T17113 Tolonidine

Others Others
Tolonidine is orally active and has been shown to possess hypotensive. Tolonidine is a derivative of imidazoline.
T26171 S23757

S-23757,S 23757

S23757 is an imidazoline 1 receptor (I1R) selective ligand.
T69670 Clonazoline HCl

Clonazoline HCl is the salt form of Clonazoline, a coronary vasodilator that is an imidazoline sympathomimetic, an alpha-adrenoreceptor agonist. It was used as a nasal decongestant and vasoconstrictor.
T70216 Clonazoline

Clonazoline is a coronary vasodilator that is an imidazoline sympathomimetic, an alpha-adrenoreceptor agonist. It was used as a nasal decongestant and vasoconstrictor.
T61516 PI3K/mTOR Inhibitor-3

PI3K/mTOR Inhibitor-3 (compound 12) is an imidazoline compound with potent dual inhibitory effects on PI3K and mTOR. This compound exhibits notable anti-cancer activity [1].
T27155 Dexisometheptene

TNX 201,TNX-201,(R)-Isometheptene,TNX201

Dexisometheptene is an antimigraine drug candidate. Dexisometheptene significantly increases the pain threshold of acute pain response, and potently and selectively binds to receptors in the central nervous system known as imidazoline type-1 (I1) receptor
T73214 RX 801077

2 BFI free base

RX 801077 (2 BFI free base) 为选择性咪唑啉 I2 受体 (I2R) 激动剂,其Ki值为70.1 nM,展现抗炎及神经保护效果,具备用于创伤性脑损伤 (TBI) 研究的潜力。
T21911 Rilmenidine hemifumarate

Rilmenidine (hemifumarate),S-3341 hemifumarate

Apoptosis; Imidazoline Receptor Apoptosis; Neuroscience
Rilmenidine hemifumarate (S-3341 hemifumarate) 是一种新型且具有口服活性和选择性 的 I1咪唑啉受体 (I1 imidazoline receptor) 和α2肾上腺素受体激动剂,可诱导自噬 ,调节白血病细胞增殖,刺激促凋亡蛋白 Bax,诱导人白血病 K562 细胞线粒体通路的紊乱和凋亡。
T80636 SARS-CoV-2-IN-59

SARS-CoV Microbiology/Virology
SARS-CoV-2-IN-59(compound E07)为咪唑啉衍生物,其为一种针对SARS-CoV-2的非肽类小分子抑制剂,主要作用于冠状病毒的Mpro。SARS-CoV-2-IN-59于Mpro残基(Met 165, Gln 166,Met165, His 41, Gln 189)处展现出强烈的相互作用。
T35591 Guanfacine-13C,15N3

Guanfacine-13C,15N3

Guanfacine-13C,15N3is intended for us as an internal standard for the quantification of guanfacine by GC- or LC-MS. Guanfacine is an α2-adrenergic receptor (α2-AR) agonist with Kivalues of 93, 1,380, and 3,890 nM for α2A-, α2B-, and α2C-ARs, respectively, in a radioligand binding assay.1It has EC50values of 52, 288, and 602 nM for α2A-, α2B-, and α2C-ARs, respectively, for stimulated [35S]GTPγS binding. It also binds to imidazoline receptor 1 (Ki= 19 nM in a radioligand binding assay).2Guanfacin...

化合物

Lysidine
Cat.No: T21052
Synonym: 2-甲基咪唑啉,2-Methyl-2-iMidazoline
Target: Nucleoside Antimetabolite/Analog
BU 224 hydrochloride
Cat.No: T22051
Synonym:
Target: Imidazoline Receptor
BU 226 hydrochloride
Cat.No: T22052
Synonym:
Target: Imidazoline Receptor
Rilmenidine Phosphate
Cat.No: T6641
Synonym:
Target: Apoptosis, Adrenergic Receptor, Autophagy, Imidazoline Receptor
Moxonidine
Cat.No: T1028
Synonym: 莫索尼定,BDF5895,莫索尼啶
Target: Imidazoline Receptor
Idazoxan hydrochloride
Cat.No: T0115
Synonym: RX 781094,盐酸咪唑克生
Target: Adrenergic Receptor, Imidazoline Receptor
Tetrahydrozoline hydrochloride
Cat.No: T6703
Synonym: Murine Plus,盐酸四氢萘咪唑,Tetryzoline hydrochloride,Tyzine,Tetrahydrozoline HCl,盐酸四氢唑林
Target: Adrenergic Receptor
2-BFI hydrochloride
Cat.No: T22492
Synonym:
Target: Imidazoline Receptor
CR4056
Cat.No: T15010
Synonym: 6-(1H-imidazol-1-yl)-2-phenylquinazoline
Target: MAO, Imidazoline Receptor
2-Methoxyidazoxan monohydrochloride
Cat.No: T23283
Synonym: RX 821002 hydrochloride
Target: Adrenergic Receptor
RX821002
Cat.No: T28631
Synonym: RX-821002,RX 821002
Target:
S 9871
Cat.No: T34470
Synonym: RX-801080,RX 801080,S9871,RX801080,S-9871
Target:
Aganodine
Cat.No: T23662
Synonym: Aganodin
Target:
Tracizoline
Cat.No: T68931
Synonym:
Target:
Efaroxan hydrochloride
Cat.No: T22760
Synonym:
Target: Others
Moxonidine hydrochloride
Cat.No: T40869
Synonym: BDF5895hydrochloride,盐酸莫索尼定
Target:
RS 45041-190 hydrochloride
Cat.No: T23263
Synonym:
Target: Others
Tetrahydrozoline nitrate
Cat.No: T60425
Synonym:
Target:
Tolonidine
Cat.No: T17113
Synonym:
Target: Others
S23757
Cat.No: T26171
Synonym: S-23757,S 23757
Target:
Clonazoline HCl
Cat.No: T69670
Synonym:
Target:
Clonazoline
Cat.No: T70216
Synonym:
Target:
PI3K/mTOR Inhibitor-3
Cat.No: T61516
Synonym:
Target:
Dexisometheptene
Cat.No: T27155
Synonym: TNX 201,TNX-201,(R)-Isometheptene,TNX201
Target:
RX 801077
Cat.No: T73214
Synonym: 2 BFI free base
Target:
Rilmenidine hemifumarate
Cat.No: T21911
Synonym: Rilmenidine (hemifumarate),S-3341 hemifumarate
Target: Apoptosis, Imidazoline Receptor
SARS-CoV-2-IN-59
Cat.No: T80636
Synonym:
Target: SARS-CoV
Guanfacine-13C,15N3
Cat.No: T35591
Synonym: Guanfacine-13C,15N3
Target:
Cat. No. Product Name Target Signaling Pathways
T0925 Allantoin

Glyoxyldiureide,尿囊素,5-Ureidohydantoin

Endogenous Metabolite; Imidazoline Receptor Metabolism; Neuroscience
Allantoin (Glyoxyldiureide) 是一种存在于尿液和植物中的尿素乙内酰脲,用于皮肤病制剂。
T3158 Harmane

Loturine,Harman,Aribine,哈尔满碱

Adrenergic Receptor; Monoamine Oxidase; Imidazoline Receptor GPCR/G Protein; Neuroscience
Harmane (Loturine) 是一种在咖啡和烟草烟雾中发现的 β-咔啉生物碱,是有效的神经毒素,可引起严重的动作震颤和精神病学表现。它还是选择性的单胺氧化酶抑制剂,具有致突变作用,对 MAO A/B 的 IC50值分别为 0.5 和 5 μM。
T4808 Agmatine sulfate

Agmatine sulfate salt,硫酸胍基丁胺

Endogenous Metabolite; NO Synthase; Imidazoline Receptor Immunology/Inflammation; Metabolism; Neuroscience
Agmatine sulfate (Agmatine sulfate salt) 是咪唑啉受体的内源性激动剂和一氧化氮合酶抑制剂。它靶向神经递质系统,离子通道和一氧化氮合成。

天然产物

Allantoin
Cat.No: T0925
Synonym: Glyoxyldiureide,尿囊素,5-Ureidohydantoin
Target: Endogenous Metabolite, Imidazoline Receptor
Harmane
Cat.No: T3158
Synonym: Loturine,Harman,Aribine,哈尔满碱
Target: Adrenergic Receptor, Monoamine Oxidase, Imidazoline Receptor
Agmatine sulfate
Cat.No: T4808
Synonym: Agmatine sulfate salt,硫酸胍基丁胺
Target: Endogenous Metabolite, NO Synthase, Imidazoline Receptor
TargetMol Loading
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