ChemicalBook--->CAS DataBase List--->62929-91-3

62929-91-3

62929-91-3 Structure

62929-91-3 Structure
IdentificationBack Directory
[Name]

PROCATEROL HYDROCHLORIDE
[CAS]

62929-91-3
[Synonyms]

meptin
opc2009
Epcalol
Cateptin
Astoprotin
PROCATEROL HCL
Einecs 263-763-0
Procaterol hydrochlorid
Procaterol HCl,Procaterol hydrochloride
Procaterol hydrochloride Solution, 100ppm
Procaterol hydrochloride Solution, 1000ppm
8-HYDROXY-5-(1-HYDROXY-2-PROPAN-2-YLAMINO-BUTYL)-1H-QUINOLIN-2-ONE
5-(1-hydroxy-2-isopropylamino)butyl-8-hydroxycarbostyrilhydrochloride
erythro-8-hydroxy-5-[1-hydroxy-2-(isopropylamino)butyl]-2(1h)-quinolinone
8-hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1h)-quinolinonmono
(+/-)-ERYTHRO-8-HYDROXY-5-[1-HYDROXY-2-(ISOPROPYLAMINO)BUTYL]CARBOSTYRIL HYDROCHLORIDE
8-hydroxy-5-[1-hydroxy-2-(propan-2-ylamino)butyl]-1H-quinolin-2-one hydrate hydrochloride
(R*,S*)-(1)-8-Hydroxy-5-(1-hydroxy-2-(isopropylamino)butyl)quinolin-2(1H)-one monohydrochloride
(R*,S*)-(±)-8-hydroxy-5-[1-hydroxy-2-(isopropylamino)butyl]quinolin-2(1H)-one monohydrochloride
rel-8-Hydroxy-5-[(1R,2S)-1-hydroxy-2-[(1-methylethyl)amino]butyl]-2(1H)quinolinone hydrochloride
2(1H)-Quinolinone, 8-hydroxy-5-[1-hydroxy-2-[(1-methylethyl)amino]butyl]-, monohydrochloride, (R*,S*)-
2(1H)-Quinolinone, 8-hydroxy-5-[1-hydroxy-2-[(1-methylethyl)amino]butyl]-, monohydrochloride, (R*,S*)-(+-)-
2(1H)-Quinolinone, 8-hydroxy-5-[(1R,2S)-1-hydroxy-2-[(1-methylethyl)amino]butyl]-, monohydrochloride, rel- (9CI)
[EINECS(EC#)]

263-763-0
[Molecular Formula]

C16H23ClN2O3
[MDL Number]

MFCD04221378
[MOL File]

62929-91-3.mol
[Molecular Weight]

326.82
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

Soluble to 100 mM in water and to 100 mM in DMSO
[form ]

Powder
[color ]

White to off-white
[Stability:]

Hygroscopic
[InChI]

1S/C16H22N2O3.ClH/c1-4-12(17-9(2)3)16(21)11-5-7-13(19)15-10(11)6-8-14(20)18-15;/h5-9,12,16-17,19,21H,4H2,1-3H3,(H,18,20);1H/t12-,16+;/m0./s1
[InChIKey]

AEQDBKHAAWUCMT-CVHDTDHSSA-N
[SMILES]

Cl.CC[C@H](NC(C)C)[C@H](O)c1ccc(O)c2NC(=O)C=Cc12
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Warning
[Hazard statements ]

H361
[Precautionary statements ]

P201-P202-P281-P308+P313-P405-P501
[WGK Germany ]

2
[RTECS ]

VC8296000
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Description]

Procaterol is an agonist of β2-adrenergic receptors (β2-ARs). It binds to (Kd = 46 pM), and is selective for, β2-ARs over β1-ARs (Kd = 4,000 pM). Procaterol binds more potently to β2-ARs in isolated guinea pig lung than to β1-ARs in isolated guinea pig cardiac ventricle in the presence (IC50s = 175 and 1,660 nM, respectively) and absence of GTP (Item No. 16060; IC50s = 55.1 and 1,660 nM, respectively). It inhibits contractions induced by acetylcholine (Item No. 23829) in isolated guinea pig trachea (EC50 = 10.5 nM). In vivo, procaterol inhibits histamine-induced airflow obstruction in a guinea pig model of ovalbumin-sensitized asthma when administered via inhalation at a dose of 10 μg/ml.
[Uses]

adrenergic agonists
[General Description]

Procaterol is used to prevent lung fibroblast migration. It has anti-inflammatory properties. It can block type 2 T helper (Th2)-related chemokine production in human monocytes and bronchial epithelial cells.
[Biological Activity]

Specific and very potent β 2 agonist.
[Biochem/physiol Actions]

β2-adrenoceptor agonist; bronchodilator.
[storage]

Store at RT
[References]

[1] S MARULLO. Selective binding of ligands to beta 1, beta 2 or chimeric beta 1/beta 2-adrenergic receptors involves multiple subsites.[J]. EMBO Journal, 1990, 9 5: 1471-1476. DOI: 10.1002/j.1460-2075.1990.tb08264.x
[2] HIDEO KIKKAWA  Katsuo I  Kazuaki Naito. Tracheal Relaxing Effects and β2-Selectivity of TA-2005, a Newly Developed Bronchodilating Agent, in Isolated Guinea Pig Tissues[J]. Japanese journal of pharmacology, 1991, 57 2: Pages 175-185. DOI: 10.1254/jjp.57.175
[3] SHIRO YOSHIZAKI. Sympathomimetic amines having a carbostyril nucleus[J]. Journal of Medicinal Chemistry, 1976, 19 9: 1138-1142. DOI: 10.1021/jm00231a011
[4] MIRZA. Inhaled procaterol inhibits histamine-induced airflow obstruction and microvascular leakage in guinea-pig airways with allergic inflammation[J]. Clinical and Experimental Allergy, 2008, 28 5: 644-652. DOI: 10.1046/j.1365-2222.1998.00263.x
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