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Search Results for " cyclic adenosine monophosphate "

15

抑制剂 & 化合物

5

天然产物

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Cat. No. Product Name Target Signaling Pathways
T31931L Gizzerosine HCl

Gizzerosine HCl(89238-78-8 Free base)

Others Others
Gizzerosine 2HCl是鱼粉热处理过程中产生的一种物质,可诱导的肉鸡雏鸡组织病理学病变,可提高离体鸡原产鸡的细胞内环腺苷-3',5'-单磷酸水平。
T1433 Ritodrine hydrochloride

DU21220,盐酸利托君,Ritodrine HCl,NSC 291565

Adrenergic Receptor GPCR/G Protein; Neuroscience
Ritodrine hydrochloride (NSC 291565) 是一种 β-2肾上腺素受体激动剂。
T1024 Roflumilast

罗氟司特,B9302-107,BYK 20869,APTA 2217,BY 217

PDE; RSV Metabolism; Microbiology/Virology
Roflumilast (APTA 2217) 是一种口服的长效 4 型磷酸二酯酶抑制剂 (PDE4),具有抗炎和潜在的抗肿瘤活性,作用于PDE4A1,PDEA4,PDEB1和PDEB2,IC50分别为 0.7,0.9,0.7 和 0.2 nM。
T50023 ethyl 1-(4-aminophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate

Others Others
ethyl 1-(4-aminophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate 又称 EAPT,是一种有效的选择性 PDE4抑制剂,调节细胞内环腺苷酸(cAMP)水平。它已被用于多种科研应用,包括 cAMP 介导的信号转导通路的研究,并有潜力作为治疗炎症和免疫相关疾病的药物。
T1139 Salbutamol

Albuterol,沙丁胺醇,AH-3365

Adrenergic Receptor GPCR/G Protein; Neuroscience
Salbutamol (Albuterol) 是短效的 β2 肾上腺素受体激动剂,用于哮喘和慢性阻塞性肺疾病(COPD) 引发的支气管痉挛的研究。
T28990 Tocladesine

NSC-614491,CN 1256,CN1256,8-Cl-cAMP,NSC614491,ICN-1256

Tocladesine, a cyclic adenosine monophosphate (cAMP) receptor agonist, is used potentially for the treatment of colorectal cancer.
T25463 Griseolic acid

Griseolic acid is a cyclic adenosine 3',5'-monophosphate phosphodiesterase II inhibitor.
T24606 PDE7 inhibitor S14

PDE7 inhibitor-S14,S14

PDE7 inhibitor S14 is a cell-permeable PDE7 inhibitor that acts by targeting the cyclic adenosine monophosphate (cAMP)/cAMP-response element-binding protein (CREB) pathway.
T30955 CK 2289

CK-2289,CK2289

CK 2289 is an inhibitor of type III cyclic 3'5' -adenosine monophosphate phosphodiesterase with potential use in the treatment of congestive heart failure.
TP1283 VIP(6-28)(human, rat, porcine, bovine)

VIP(6-28)(human, rat, porcine, bovine) is a potent antagonist that effectively counteracts the effects of exogenous vasoactive intestinal peptide (VIP) on cyclic adenosine monophosphate (cAMP) signaling.
T32156 Indimilast

Indimilast is used to inhibit phosphodiesterase IV that regulates lung inflammation and causes bronchiectasis by increasing intracellular cyclic adenosine 3', 5'-monophosphate in airway smooth muscle and inflammatory cells. Potential to treat chronic obst
T76133 Phosphodiesterase II

PhosphodiesteraseII,即磷酸二酯酶 2,主要参与水解重要的第二信使环磷酸腺苷 (cAMP) 和环磷酸鸟苷 (cGMP),常用于生化研究。PhosphodiesteraseII 表达于多种组织,如肾上腺髓质、脑、心脏、血小板、巨噬细胞和内皮细胞,可参与调节许多不同的细胞内过程。
T26855 BMS-665053

BMS665053

BMS-665053 is a corticotropin-releasing factor-1 (CRF1) receptor antagonist (IC50 = 1.0 nM). BMS-665053)11 is a potent inhibitor of CRF-stimulated cyclic adenosine monophosphate (cAMP) production in human Y-79 retinoblastoma cells (IC50 = 4.9 nM). In addi
T63776 PDE1-IN-4

PDE1-IN-4 是有效的、选择性的 PDE1 (磷酸二酯酶 -1) 抑制剂,能够作用于 PDE1C (IC50: 10 nM)、PDE1A (IC50: 145 nM) 和 PDE1B (IC50: 354 nM)。PDE1-IN-4 能够调控 cAMP (3′,5′- 环磷酸腺苷) 和 cGMP (3′,5′- 环磷酸鸟苷),表现出抗纤维化效果。PDE1-IN-4 能够抑制 TGF-β1 诱导的人肺成纤维细胞分化。PDE1-IN-4 能够用于研究特发性肺纤维化 (IPF)。
T65598 Cefminox sodium

Cefminox (Sodium) is a new cephamycin antibiotic possessing a D-amino acid moiety derived from D-cysteine at the C-7B side chain. Cefminox is active against a wide range of bacteria, especially Gram-negative and anaerobic bacteria. Cefminox shows excellent in vivo efficacy (ED50) which is higher than would be expected from its in vitro activity (MIC). Moreover, cefminox possesses more potent activity in suppression of bacterial regrowth than other cephems[1]. Cefminox (Sodium) was the most activ...

化合物

Gizzerosine HCl
Cat.No: T31931L
Synonym: Gizzerosine HCl(89238-78-8 Free base)
Target: Others
Ritodrine hydrochloride
Cat.No: T1433
Synonym: DU21220,盐酸利托君,Ritodrine HCl,NSC 291565
Target: Adrenergic Receptor
Roflumilast
Cat.No: T1024
Synonym: 罗氟司特,B9302-107,BYK 20869,APTA 2217,BY 217
Target: PDE, RSV
ethyl 1-(4-aminophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate
Cat.No: T50023
Synonym:
Target: Others
Salbutamol
Cat.No: T1139
Synonym: Albuterol,沙丁胺醇,AH-3365
Target: Adrenergic Receptor
Tocladesine
Cat.No: T28990
Synonym: NSC-614491,CN 1256,CN1256,8-Cl-cAMP,NSC614491,ICN-1256
Target:
Griseolic acid
Cat.No: T25463
Synonym:
Target:
PDE7 inhibitor S14
Cat.No: T24606
Synonym: PDE7 inhibitor-S14,S14
Target:
CK 2289
Cat.No: T30955
Synonym: CK-2289,CK2289
Target:
VIP(6-28)(human, rat, porcine, bovine)
Cat.No: TP1283
Synonym:
Target:
Indimilast
Cat.No: T32156
Synonym:
Target:
Phosphodiesterase II
Cat.No: T76133
Synonym:
Target:
BMS-665053
Cat.No: T26855
Synonym: BMS665053
Target:
PDE1-IN-4
Cat.No: T63776
Synonym:
Target:
Cefminox sodium
Cat.No: T65598
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
TCO2745 Cyclic AMP

Adenosine 3',5'-cyclophosphate,cAMP,腺苷环磷酸酯,环磷腺苷,Cyclic 3',5'-monophosphate adenosine,3',5'-AMP,Adenosine Cyclophosphate

Others; Endogenous Metabolite Metabolism; Others
Cyclic AMP (cAMP)(Adenosine 3',5'-cyclophosphate) 是有丝分裂信使,可以促进 G1期到 S 期的细胞周期进程。
T4S0792 Pinoresinol 4-O-β-D-glucopyranoside

(+)-pinor,(+)-pinoresinol-β-D-glucoside; (+)-pinor,(+)-pinoresinol-β-D-glucoside

Others Others
(+)-pinoresinol-β-D-glucoside; (+)-pinor 是连翘中主要的活性呋喃类木脂素。它显示出抗氧化、降血压和环磷酸腺苷 (cAMP) 磷酸二酯酶抑制活性。
TN3013 4,5-Dimethoxycanthin-6-one

Methylnigakinone

P450; Antibacterial; PDE Metabolism; Microbiology/Virology
4,5-Dimethoxycanthin-6-one 从 Picrasma quassioides BENNET (Simaroubaceae)是一种从 Picrasma quassioides BENNET (Simaroubaceae) 中分离得到生物碱。4,5-Dimethoxycanthin-6-one 是一种有效的、非竞争性的 CYP1A2 介导的 phenacetin O-deethylation 抑制剂(IC50 : 1.7 μM, Ki : 2.6 μM),对环磷酸腺苷(cAMP)磷酸二酯酶有很强的抑制作用。4,5-Dimethoxycanthin-6-one 具有抗菌活性,对金黄色葡萄球菌及其耐药菌株有抑制作用。4,5-Dimethoxycanthin-6-one 对肿瘤细胞株 U937 和 HepG2 具有细胞毒性。
TN1841 Kushenol A

苦参新醇 A,Leachianone E

cAMP GPCR/G Protein
Kushenol A is a kind of Adenosine 3', 5'-cyclic monophosphate(cAMP)phosphodiesterase inhibitiors, it shows selective alpha-glucosidase inhibitory activity. Kushenol A and kushenol C exhibit inhibitory activity against Sodium-dependent glucose cotransporter 2(SGLT2).
TN4433 Licoarylcoumarin

cAMP; HIV Protease; Antifection GPCR/G Protein; Microbiology/Virology; Proteases/Proteasome
Licoarylcoumarin is a strong inhibitor of adenosine 3',5'-cyclic monophosphate (cAMP) phosphodiesterase. Licoarylcoumarin has antibacterial effects on the VRE strains; it has anti-HIV activity, and it has inhibitory effects on xanthine oxidase.

天然产物

Cyclic AMP
Cat.No: TCO2745
Synonym: Adenosine 3',5'-cyclophosphate,cAMP,腺苷环磷酸酯,环磷腺苷,Cyclic 3',5'-monophosphate adenosine,3',5'-AMP,Adenosine Cyclophosphate
Target: Others, Endogenous Metabolite
Pinoresinol 4-O-β-D-glucopyranoside
Cat.No: T4S0792
Synonym: (+)-pinor,(+)-pinoresinol-β-D-glucoside; (+)-pinor,(+)-pinoresinol-β-D-glucoside
Target: Others
4,5-Dimethoxycanthin-6-one
Cat.No: TN3013
Synonym: Methylnigakinone
Target: P450, Antibacterial, PDE
Kushenol A
Cat.No: TN1841
Synonym: 苦参新醇 A,Leachianone E
Target: cAMP
Licoarylcoumarin
Cat.No: TN4433
Synonym:
Target: cAMP, HIV Protease, Antifection
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