36
8
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0042 |
Xylometazoline hydrochloride
盐酸赛洛唑啉,Xylometazoline HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Xylometazoline hydrochloride (Xylometazoline HCl) 是一种 α- 肾上腺素受体激动剂,是一种鼻血管收缩药。 | |||
T38236 |
2′-Deoxy-2′-fluoroguanosine
|
Nucleoside Antimetabolite/Analog; Influenza Virus | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
2′-Deoxy-2′-fluoroguanosine 是一种核苷类似物,有效抑制流感病毒,抑制A 型和B 型流感病毒的EC90值 <0.35 μM。2′-Deoxy-2′-fluoroguanosine 显著抑制流感病毒在上呼吸道中的复制,从而改善鼻腔炎症和发烧。 | |||
T4563 |
Thonzylamine
neohetramine,松齐拉敏 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Thonzylamine (neohetramine) 是可口服的H1组胺受体拮抗剂,具有抗组胺和抗过敏特性,可用于鼻充血、过敏性结膜炎和其他过敏性疾病的研究。 | |||
T0397 |
Tetrahydrozoline
四氢唑林,四氢唑啉,Tetryzolin,Tetryzoline |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tetrahydrozoline (Tetryzoline) 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,广泛用于研究鼻充血、结膜充血。 | |||
T22033 |
ARC 239 dihydrochloride
|
Norepinephrine | Neuroscience |
ARC 239 dihydrochloride 是一种选择性 α2B 肾上腺素受体拮抗剂。 | |||
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。 | |||
T26009 |
Quazolast
RHC-3988,RHC 3988,RHC3988 |
Others | Others |
Quazolast (RHC 3988) 是一种有效的介质释放抑制剂,是对豚草抗原鼻腔挑战的对照。Quazolast 在防止猪笼草鼻腔挑战后的鼻塞和鼻痒方面优于安慰剂。 | |||
T71012 |
Nemazoline Free Base
|
||
Nemazoline Free Base is a nasal decongestant. It has alpha 1-agonist/alpha 2-antagonist activity and was more effective and long-acting than oxymetazoline on canine nasal mucosa, in-vitro and in-vivo. Upon intranasal administration to dogs, the compound was devoid of systemic effects up to a concentration 1000 times that needed for local decongestant effect (1.65 micrograms, atomized from a 1 microgram mL-1 solution) suggesting limited mucosal absorption. After nasal administration to rats for 1... | |||
T3612 |
Carbocisteine
Carbocysteine,羧甲司坦,Broncodeterge,Mucodyne,S-Carboxymethyl-L-cysteine |
Others | Others |
Carbocisteine (Mucodyne) 常被用作具有粘液溶解和祛痰作用的抗感染鼻喷雾剂。 | |||
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。 | |||
T21404 |
Fluticasone furoate
Veramyst,Allermist,Avamys,糠酸氟替卡松,Fluticasone furoate |
Glucocorticoid Receptor | Endocrinology/Hormones |
Fluticasone furoate (Avamys) 是一种合成的三氟化皮质类固醇,衍生自氟替卡松,Kd 为 0.3 nM。Fluticasone furoate 具有有效的抗炎、抗哮喘活性和低全身暴露。Fluticasone furoate 可用作过敏性鼻炎治疗研究的鼻喷雾剂。 | |||
T21390 |
Fexofenadine
Carboxyterfenadine,Telfast,非索非那定,MDL 16.455,Allegra |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Fexofenadine (Carboxyterfenadine) 是一种抗组胺药物,用于治疗过敏症状,如鼻塞、花粉热和荨麻疹。与第一代抗组胺药相比,它通过血脑屏障并引起镇静的能力较差。 | |||
T0900 |
Cetylpyridinium chloride monohydrate
Hexadecylpyridinium chloride monohydrate,十六烷基氯化吡啶 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cetylpyridinium chloride monohydrate (Hexadecylpyridinium chloride monohydrate) 是阳离子季铵, 是一种能杀死细菌和其他微生物的防腐剂, 用于某些类型的漱口水, 牙膏, 咽喉和鼻腔喷雾剂中, 可有效预防牙斑和减少牙龈炎。 | |||
T25199 |
Cafaminol
Cafaminolum,G1,G-1,G 1 |
||
Cafaminol (methylcoffanolamine) is a vasoconstrictor and anticatarrhal of the methylxanthine family related to caffeine which is used as a nasal decongestant. | |||
T69341 | Tramazoline hydrochloride | ||
Tramazoline hydrochloride is commonly used in nasal spray as a nasal decongestant by acting as an α-adrenergic receptor agonist that inhibits secretion of nasal mucus. | |||
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. | |||
T32656 |
Lerimazoline
ST-71,Trimizoline,Trimazoline,ST 71,ST71 |
||
Lerimazoline(Trimazoline, Trimizoline, ST-71) is used in the form of tramazoline hydrochloride in nasal decongestant preparations. It is used to inhibits the secretion of nasal mucus as an α-adrenergic receptor agonist. | |||
T68997 | L-Phenylephrine | ||
L-Phenylephrine is an alpha-adrenergic agonist used as a mydriatic, nasal decongestant, and cardiotonic agent. | |||
T36709 |
N’-Nitrosonornicotine
|
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N’-Nitrosonornicotine is a tobacco-specific N-nitrosamine and carcinogen that has been found in unburned tobacco and cigarette smoke.1It induces the formation of DNA adducts in isolated rat nasal mucosa and esophagus. N’-Nitrosonornicotine induces tumor formation in rat esophagus and nasal cavity, mouse lung, forestomach, and trachea, and hamster trachea and forebrain. Urinary levels of N’-nitrosonornicotine are positively correlated with the risk of esophageal cancer in smokers.2 1.Hecht, S.... | |||
T14035 |
3M-011
|
TLR | Immunology/Inflammation |
3M-011, a potent dual toll-like receptor TLR7/8 agonist and cytokine inducer, serves as a powerful adjuvant to radiotherapy, eliciting significant local and systemic immune responses. Additionally, it effectively inhibits H3N2 influenza viral replication in the nasal cavity and exhibits strong antitumor activity[1][2][3]. | |||
T38350 |
TAS 205
|
||
TAS 205 is an inhibitor of hematopoietic prostaglandin D synthase (H-PGDS; IC50= 55.8 nM).1It is selective for H-PGDS over lipocalin-type PGDS (L-PGDS) at 100 μM, as well as over enzyme and receptor panels at 10 μM. TAS 205 inhibits production of prostaglandin D2induced by A23187 in KU812 human and RBL-2H3 rat basophils with IC50values of 78.3 and 181.3 nM, respectively. It inhibits ovalbumin-induced nasal lavage fluid eosinophil infiltration and late-phase nasal obstruction in an ovalbumin-sens... | |||
T25618 |
Laninamivir trifluoroacetate
|
||
Laninamivir trifluoroacetate 是一种抗病毒化合物,用于治疗和预防甲型流感病毒和乙型流感病毒。它是一种通过鼻吸入给药的长效神经氨酸酶抑制物。 | |||
T37860 | T 26c disodium salt | ||
Highly potent and selective MMP13 inhibitor (IC50 = 6.9 pM). Exhibits >2600-fold selectivity for MMP13 over related MMPs. Inhibits degradation of bovine nasal septum cartilage explants in vitro . Orally bioavailable. Nara et al (2014) Thieno[2,3-d]pyrimidine-2-carboxamides bearing a carboxybenzene group at 5-position: highly potent, selective, and orally available MMP-13 inhibitors interacting with the S1 binding site. Bioorg.Med.Chem. 22 5487 PMID:25192810" | |||
T26770 |
Bencycloquidium Bromide
BCQB |
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Bencycloquidium Bromide is a muscarinic M3 antagonist. Bencycloquidium bromide inhibits nasal hypersecretion in a rat model of allergic rhinitis. Bencycloquidium Bromide showed high affinity toward the M(3) receptor in Chinese hamster ovary (CHO) cells (M | |||
T60263 |
Povafonidine
|
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Povafonidine (PGE-6201204) 是一种有效的 α-2 肾上腺素受体激动剂。Povafonidine 可以收缩血管,减轻粘膜充血,可用于鼻塞研究。 | |||
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。 | |||
T64314 |
OxyMetazoline
|
||
OxyMetazoline 是一种 α-肾上腺素受体 (α-adrenoceptor) 激动剂,能够作用于 α1A (IC50: 0.02 μM)、α1B (IC50: 0.25 μM)、α2A (IC50: 0.58 μM) 和 α2C (IC50: 0.13 μM)。OxyMetazoline 能够用于研究缓解鼻黏膜充血。 | |||
T78112 |
Voxvoganan trihydrochloride
LTX-109 trihydrochloride |
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Voxvoganan (LTX-109) trihydrochloride为有效的局部抗菌剂,特别是针对S. aureus,其MIC为2-4 μg/mL。该化合物主要用于研究细菌性皮肤感染和真菌感染。 | |||
T14359 |
AVX 13616
|
Others | Others |
AVX 13616 shows the potent in vivo antibacterial activity of Avexa’s lead antibacterial candidate; particularly against drug-resistant Staphylococcus pathogens. IC50 value: 2-4 ug/ml (MICs) Target: antibacterial agent AVX13616 was as active as mupirocin i | |||
T83840 |
Uridine-5'-O-(3-thiotriphosphate) sodium
UTP-γ-S |
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Uridine-5'-O-(3-thiotriphosphate) (UTP-γ-S) 是UTP的一种抗水解衍生物,是嘌呤P2Y2受体的激动剂。在表达人类P2Y2受体的1321N1星形胶质瘤细胞中,其可诱导肌醇磷酸盐的形成(EC50 = 240 nM),并且在来自囊性纤维化患者的原代鼻上皮细胞中以浓度依赖的方式诱导氯离子分泌。UTP-γ-S在分离的人类冠状动脉中诱导血管收缩(EC50 = 25.1 µM)。 | |||
T37262 |
14,15-Leukotriene E4
14,15-Leukotriene E4 |
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Leukotrienes (LTs) are a group of acute inflammatory mediators derived from arachidonic acid in leukocytes. The majority of these metabolites are formed through the 5-lipoxygenase (5-LO) pathway. 14,15-LTE4 is a metabolite of 14,15-LTC4 and 14,15-LTD4, an alternate class of LTs synthesized by a pathway involving the dual actions of 15- and 12-LOs on arachidonic acid via 15-HpETE and 14,15-LTA4 intermediates. These metabolites are classified as eoxins because they are formed mostly by eosinophils... | |||
T80090 |
Lugdunin
|
Antibiotic | Microbiology/Virology |
Lugdunin是一种具有抗菌活性的肽类抗生素。该化合物能够通过破坏细菌细胞膜的电位来抑制革兰氏阳性菌的生长,特别是对金黄色葡萄球菌(Staphylococcus aureus)表现出高效能,有效降低其在皮肤和鼻腔的定植能力。此外,Lugdunin还能在人类角质形成细胞和小鼠皮肤中促进LL-37和CXCL8/MIP-2的表达。 | |||
T37261 |
14,15-Leukotriene D4
14,15-Leukotriene D4 |
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14,15-Leukotriene D4 (14,15-LTD4) is a member of an alternate class of LTs synthesized by a pathway involving the dual actions of 15- and 12-lipoxygenases (15- and 12-LOs) on arachidonic acid via 15-HpETE and 14,15-LTA4 intermediates. 14,15-LTD4 is classified as an eoxin (EXD4), because it is formed mostly by eosinophils. However, mast cells and nasal polyps can synthesize 14,15-LTD4 as well. Little is known about the physiological actions of 14,15-LTD4. It has weak contractile activity on both ... | |||
T68525 | Nafarelin acetate hydrate | ||
Nafarelin is a gonadotropin-releasing hormone agonist (GnRH agonist) which acts as an analog of GnRH. Nafarelin increases the release of FSH and LH by the anterior pituitary, which in turn leads to an increase of estrogen/progesterone. When administered, Nafarelin has the purpose of causing increase estrogen that will negatively feed back upon hypothalamus to decrease GnRH ( negative feedback loop ) Through negative feedback, Nafarelin causes a decrease in pituitary secretion of gonadotropins lu... | |||
T65252 | Pepsin | ||
Pepsin is an endopeptidase that breaks down proteins into smaller peptides and amino acids that can be easily absorbed in the small intestine[1]. Pepsin is stable at pH ranges as high as pH 6. Above this pH, pepsin is rapidly irreversibly inactivated and elevation of pH of the reaction mixture to pH 8 results in complete inactivation of pepsin[2]. Pepsin has been posited to be a reliable biological marker of EER. An immunologic pepsin assay of combined sputum and saliva was determined to be 100%... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T4S0878 |
Prunetin
樱黄素,Prunusetin |
ERK; Dehydrogenase; NF-κB | MAPK; Metabolism; NF-κB |
Prunetin (Prunusetin) 是一种O-甲基化异黄酮,具有抗炎的作用。它是人醛脱氢酶的有效抑制剂。 | |||
T0335 |
Sodium salicylate
水杨酸钠,Salicylic acid sodium salt,2-Hydroxybenzoic acid sodium salt |
Apoptosis; NF-κB; COX; S6 Kinase; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; MAPK; Neuroscience; NF-κB; PI3K/Akt/mTOR signaling |
Sodium salicylate (2-Hydroxybenzoic acid sodium salt) 是一种S6K 的抑制剂,可抑制COX-2活性。它还是一种NF-κB 抑制剂,可降低炎症基因的表达,促进老化肌肉的修复。 | |||
T1287 |
Synephrine
辛弗林,Oxedrine |
Endogenous Metabolite; Adrenergic Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Synephrine (Oxedrine) 是来自 Citrus aurantium 的α-adrenergic 和β-adrenergic 激动剂,是一种生物碱。它也是一种拟交感神经化合物,能够用于减肥。 | |||
TN1610 |
Epimagnolin A
|
Parasite | Microbiology/Virology |
Epimagnolin A 是一种糠醛木脂素,具有中等的抗疟原虫活性,IC50值为5.7 μg/mL。 | |||
T4764 |
5-Methoxy-5-oxopentanoic acid
戊二酸单乙酯,mono-Methyl glutarate,METHYL HYDROGEN GLUTARATE |
Others; Endogenous Metabolite | Metabolism; Others |
5-Methoxy-5-oxopentanoic acid (mono-Methyl glutarate) 是内源性代谢产物的一种。 | |||
T35455 |
N-Nitrosodiethylamine
Diethylnitrosamine,NDEA |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
N-Nitrosodiethylamine (NDEA) 是致癌物质二烷基硝胺。它主要存在于水、烟草烟雾、腌制食品、油炸食品以及许多酒精饮料中。它与 DNA 修复/复制相关的核酶的变化相关。 | |||
TN6646 |
Fargesol
|
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(-)-Fargesol is a nartural product from the flowers buds of Magnolia fargesii,the dried flower buds of M. fargesii, has been used as therapy for nasal empyema and headache. | |||
T37272 |
9(S),12(S),13(S)-TriHOME
|
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9(S),12(S),13(S)-TriHOME is a linoleic acid-derived oxylipin that has diverse biological activities.1,2,3,4It has been found in various plants and is produced in human eosinophils in a 15-lipoxygenase-dependent, soluble epoxide hydrolase-independent manner.1,59(S),12(S)13(S)-TriHOME inhibits antigen-induced β-hexosaminidase release from RBL-2H3 mast cells (IC50= 28.7 μg/ml).2It inhibits LPS-induced nitric oxide (NO) production in BV-2 microglia (IC50= 40.95 μM).3In vivo, 9(S),12(S),13(S)-TriHOME... |