| |
TTD
Drug ID:
DAP000937
| Drug
Information |
| Name | Ritodrine | | Synonyms | L000737; 4-[2-[[1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]amino]ethyl]phenol; LS-187116; CID31729; CAS-23239-51-2; EINECS 247-879-9; Prestwick0_000349; Utopar; BRD-K51465424-003-03-6; KBio2_001898; AC1LEMBZ; Benzenemethanol, 4-hydroxy-alpha-(1-((2-(4-hydroxyphenyl)ethyl)amino)ethyl)-, (R*,S*)-; D02359; Prestwick3_000349; Prestwick2_000349; RITODRINE HCL; NCGC00016773-01; Spectrum4_000438; Ritodrinium; AC1LEMBT; Spectrum_001418; Ritodrinium [INN-Latin]; CID688570; KBio2_007034; NCGC00162324-02; Ritodrina [INN-Spanish]; AC1L1PV2; Lopac0_001041; AC1L1M7Q; 4-Hydroxy-alpha-(1-((2-(4-hydroxyphenyl)ethyl)amino)ethyl)benzenemethanol (R*,S*)-; Spectrum3_001458; KBio3_002455; NCGC00015887-01; BPBio1_000459; KBio2_004466; KBioGR_000796; Ritodrine [USAN:BAN:INN]; 4-[2-[[(1R,2S)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]amino]ethyl]phenol; BRD-A59174698-003-02-9; CHEMBL83063; 2-(4-Hydroxyphenethylamino)-1-(4-hydroxyphenyl)propanol; Yutopar; SPBio_001526; CHEMBL785; NCGC00179566-01; DB00867; 4-[2-[[(1S,2S)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]amino]ethyl]phenol; AC1LEMBW; Spectrum2_001423; LS-30764; Ritodrina; erythro-p-Hydroxy-alpha-(1-((p-hydroxyphenethyl)amino)ethyl)benzyl alcohol; 4-[2-[[(1S,2R)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]amino]ethyl]phenol; UNII-I0Q6O6740J; Ritodrine (USAN/INN); AC1Q59PF; BSPBio_000417; Yutopar S.R; NCGC00162324-01; Benzyl alcohol, p-hydroxy-alpha-(1-((p-hydroxyphenethyl)amino)ethyl)-, erythro-; SPBio_002338; CID688568; Prepar; Prestwick1_000349; DU-21220; Benzenemethanol, 4-hydroxy-.alpha.-[1-[[2-(4-hydroxyphenyl)ethyl]amino]ethyl]-, (R*,S*)-; AC1Q76UV; Lopac-R-0758; 4-[2-[[(1R,2R)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]amino]ethyl]phenol; Spectrum5_001225; BSPBio_002955; NCGC00015887-02; 26652-09-5; CID33572; p-Hydroxy-alpha-(1-((p-hydroxyphenethyl)amino)ethyl)benzyl alcohol; KBioSS_001898; CID688569; ritodrine; BRN 2388728; C07239 | | Trade Name | Yutopar | | Indication | Premature labour | Approved [1] | | Structure |
Click to save drug structure in 3D MOL format
Click to save drug structure in 2D MOL format | | Therapeutic Class | Sympathomimetics | | CAS Number | CAS 26652-09-5 | | Formular | C17H21NO3 | | PubChem Compound ID | CID 31729. | | PubChem Substance ID | SID 4924962. | | SuperDrug ATC ID | G02CA01; | | SuperDrug CAS ID | 026652095; | | Target | Beta adrenergic receptor |  | Agonist | [2][3] | | Ref 1 | FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (ANDA) 071438 To Reference | | Ref 2 | Acute tocolysis for uterine activity reduction in term labor: a review. Obstet Gynecol Surv. 2008 Jun;63(6):383-8; quiz 405. To Reference | | Ref 3 | Discovery of novel N-phenylglycine derivatives as potent and selective beta(3)-adrenoceptor agonists for the treatment of frequent urination and urinary incontinence. J Med Chem. 2001 Apr 26;44(9):1436-45. To Reference |
Welcome
to sign our Guestbook.
If you
find any error in data or bug in web service, please kindly report it
to Dr.
Zhu.
Dr.
Chen Yuzong
Deputy Director of Center
for Computational Science and Engineering
Professor in Department of Pharmacy
National University of Singapore, Singapore
All rights reserved.
|
|