데이터를 보충하는 중입니다. 보통 1분 이내에 완료됩니다
기본 정보
- 표준 SMILES
CC(C)(C)NC[C@H](O)c1ccc(O)c(CO)c1- InChIKey
NDAUXUAQIAJITI-LBPRGKRZSA-N- 분자식
- C13H21NO3
- 평균 분자량
- 239.315 g/mol
- 단동위원소 질량
- 239.15214353
이름 및 식별자
- 우선 이름
- Levalbuterol
- IUPAC
- 4-[(1R)-2-(tert-Butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol
- 영어명
- Levalbuterol
- 분자식
- C13H21NO3
- 분자량
- 239.31
이름 및 동의어
데이터베이스 식별자
- CAS
34391-04-3- PubChem CID
- 123600
- DTXSID
DTXSID80187964- ChEMBL
CHEMBL1002- ChEBI
CHEBI:8746- UNII
- EDN2NBH5SS
- EC Number
- 608-983-3
- Nikkaji
- J428.072E
물성
물리화학적 성질
- 끓는 점
- 433.5 · 433.5±40.0 °C(Predicted)
- 밀도
- 1.152 · 1.152±0.06 g/cm3(Predicted)
- 산도 계수 (pKa)
- 9.99 · 9.99±0.31(Predicted)
- InChI
- InChI=1/C13H21NO3/c1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15/h4-6,12,14-17H,7-8H2,1-3H3/t12-/s3
- InChIKey
- NDAUXUAQIAJITI-PLAQIDKDNA-N
- SMILES
- C1(=CC=C(O)C(CO)=C1)[C@@H](O)CNC(C)(C)C |&1:9,r|
안전 및 규제
안전 데이터
- risk_code
- 22
- hazard_code
- Xn
- safety_code
- 36
화학 및 산업
응용 분야
개요Levalbuterol was launched in the US for the treatment or prevention of bronchospasm in patients with reversible obstructive airway disease. It is the single R-enantiomer version of racemic albuterol (salbutamol) marketed for more than 30 years as a mainstay in the treatment of asthma. The R-isomer can be obtained with an excellent optical purity by enantiomeric purification based on the separation of diastereomeric tartrates. This isomer retains solely the desired bronchodilating effect of the racemic mixture due to a potent agonistic effect on β2-adrenoceptors, with a lower incidence of β- mediated side effects such as pulse rate increase, tremor and decrease in blood glucose and potassium levels. A pivotal clinical trial with two doses of levalbuterol and racemic albuterol, given by nebulization, demonstrated a greater improvement in lung function for the pure enantiomer levalbuterol.
용도(R)-Salbutamol is used in composition and methods to reduce beta-agonist-mediated tachyphylaxis.
상·하류 제품 정보
상류 원료
공급사36 곳
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