Mrv1533005111514022D          

 26 27  0  0  0  0            999 V2000
   -2.1434    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7144   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2539    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7144    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7144   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  2  0  0  0  0
 16  2  1  0  0  0  0
 16 12  1  0  0  0  0
 16 13  1  0  0  0  0
 17  3  1  1  0  0  0
 17 14  1  0  0  0  0
 18  4  1  1  0  0  0
 18 15  1  0  0  0  0
 19  8  2  0  0  0  0
 19  9  1  0  0  0  0
 19 12  1  0  0  0  0
 20 10  2  0  0  0  0
 20 11  1  0  0  0  0
 21  5  1  0  0  0  0
 21  6  1  0  0  0  0
 21  7  1  0  0  0  0
 21 20  1  0  0  0  0
 22 13  1  0  0  0  0
 22 14  1  0  0  0  0
 22 15  1  0  0  0  0
 23 17  1  0  0  0  0
 23 18  1  0  0  0  0
 24 16  1  0  0  0  0
 17 25  1  6  0  0  0
 18 26  1  6  0  0  0
M  END
> <DATABASE_ID>
DB09056

> <DATABASE_NAME>
drugbank

> <SMILES>
[H]C(C)(CN1C[C@]([H])(C)O[C@]([H])(C)C1)CC1=CC=C(C=C1)C(C)(C)CC

> <INCHI_IDENTIFIER>
InChI=1S/C21H35NO/c1-7-21(5,6)20-10-8-19(9-11-20)12-16(2)13-22-14-17(3)23-18(4)15-22/h8-11,16-18H,7,12-15H2,1-6H3/t16?,17-,18+

> <INCHI_KEY>
MQHLMHIZUIDKOO-AYHJJNSGSA-N

> <FORMULA>
C21H35NO

> <MOLECULAR_WEIGHT>
317.517

> <EXACT_MASS>
317.271864751

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.22982056877301

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,6S)-2,6-dimethyl-4-(2-{[4-(2-methylbutan-2-yl)phenyl]methyl}propyl)morpholine

> <ALOGPS_LOGP>
5.44

> <JCHEM_LOGP>
5.617119812666667

> <ALOGPS_LOGS>
-5.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
8.490758527201018

> <JCHEM_POLAR_SURFACE_AREA>
12.47

> <JCHEM_REFRACTIVITY>
99.60729999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.85e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,6S)-2,6-dimethyl-4-(2-{[4-(2-methylbutan-2-yl)phenyl]methyl}propyl)morpholine

> <JCHEM_VEBER_RULE>
1

> <DRUGBANK_ID>
DB09056

> <DRUG_GROUPS>
approved; investigational

> <GENERIC_NAME>
Amorolfine

> <SYNONYMS>
Amorolfin; Amorolfina; Amorolfine

> <INTERNATIONAL_BRANDS>
Curanail; Loceryl; Locetar; Odenil

> <SALTS>
Amorolfine hydrochloride

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