Home > Compound List > Compound details
286930-03-8 molecular structure
click picture or here to close

2-[(1R)-3-[bis(propan-2-yl)amino]-1-phenylpropyl]-4-(hydroxymethyl)phenyl 2-methylpropanoate

ChemBase ID: 4440
Molecular Formular: C26H37NO3
Molecular Mass: 411.57688
Monoisotopic Mass: 411.27734405
SMILES and InChIs

SMILES:
CC(C)C(=O)Oc1c(cc(cc1)CO)[C@H](CCN(C(C)C)C(C)C)c1ccccc1
Canonical SMILES:
OCc1ccc(c(c1)[C@@H](c1ccccc1)CCN(C(C)C)C(C)C)OC(=O)C(C)C
InChI:
InChI=1S/C26H37NO3/c1-18(2)26(29)30-25-13-12-21(17-28)16-24(25)23(22-10-8-7-9-11-22)14-15-27(19(3)4)20(5)6/h7-13,16,18-20,23,28H,14-15,17H2,1-6H3/t23-/m1/s1
InChIKey:
DCCSDBARQIPTGU-HSZRJFAPSA-N

Cite this record

CBID:4440 http://www.chembase.cn/molecule-4440.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
2-[(1R)-3-[bis(propan-2-yl)amino]-1-phenylpropyl]-4-(hydroxymethyl)phenyl 2-methylpropanoate
IUPAC Traditional name
fesoterodine
Brand Name
Toviaz
Synonyms
Fesoterodine
CAS Number
286930-03-8
PubChem SID
99443256
160967872
PubChem CID
6918558

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem ALOGPS 2.1
Acid pKa 14.983366  H Acceptors
H Donor LogD (pH = 5.5) 2.2074366 
LogD (pH = 7.4) 2.650366  Log P 5.698895 
Molar Refractivity 124.0848 cm3 Polarizability 48.53328 Å3
Polar Surface Area 49.77 Å2 Rotatable Bonds 11 
Lipinski's Rule of Five false 
Log P 5.45  LOG S -5.3 
Solubility (Water) 2.05e-03 g/l 

PROPERTIES

PROPERTIES

Bioassay(PubChem)

DETAILS

DETAILS

DrugBank DrugBank
DrugBank - DB06702 external link
Item Information
Drug Groups approved
Description Fesoterodine is an antimuscarinic prodrug used for treating overactive bladder syndrome.
Indication For the treatment of overactive bladder (with symptoms of urinary frequency, urgency, or urge incontinence).
Pharmacology Fesoterodine is a prodrug. In vivo it is broken down into its active metabolite, 5-hydroxymethyl tolterodine, by plasma esterases. The 5-hydroxymethyl metabolite, which exhibits an antimuscarinic activity. Both urinary bladder contraction and salivation are mediated via cholinergic muscarinic receptors. Therefore, acting as a competitive muscarinic receptor antagonist, fesoterodine ultimately acts to decrease the detrusor pressure by its muscarinic antagonism, thereby decreasing bladder contraction and consequently, the urge to urinate.
Affected Organisms
Humans and other mammals
Half Life 7-8 hours for the active metabolite.
External Links
Wikipedia
RxList

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
    No data available
  • Searching...Please wait...

PATENTS

PATENTS

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

INTERNET

INTERNET

Baidu iconBaidu google iconGoogle