Mrv0541 11221315272D          

 25 26  0  0  0  0            999 V2000
   11.9276   -8.3862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9276   -9.2112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6439   -9.6237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3559   -9.2112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3559   -8.3862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6439   -7.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0652   -7.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7777   -8.3820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.4903   -7.9695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2053   -8.3812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4893   -7.1445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7795   -9.2070    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.4950   -9.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4968  -10.4431    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.2086   -9.2038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7843  -10.8534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7862  -11.6785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5016  -12.0894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2152  -11.6753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2134  -10.8503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5016  -12.9144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2161  -13.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7871  -13.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0726  -12.9143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5016  -13.7394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  2  0  0  0  0
  8 12  1  6  0  0  0
  6  1  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
  5  7  1  0  0  0  0
 13 15  2  0  0  0  0
  1  2  2  0  0  0  0
  7  8  1  0  0  0  0
  2  3  1  0  0  0  0
  8  9  1  0  0  0  0
  3  4  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 14  1  0  0  0  0
  9 10  1  0  0  0  0
  4  5  1  0  0  0  0
  9 11  2  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 21 25  1  0  0  0  0
M  END
> <DATABASE_ID>
DBMET01322

> <DATABASE_NAME>
drugbank

> <SMILES>
CC(O)(CO)C1CC[C@@H](CC1)C(=O)N[C@H](CC1=CC=CC=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H27NO5/c1-19(25,12-21)15-9-7-14(8-10-15)17(22)20-16(18(23)24)11-13-5-3-2-4-6-13/h2-6,14-16,21,25H,7-12H2,1H3,(H,20,22)(H,23,24)/t14-,15?,16-,19?/m1/s1

> <INCHI_KEY>
IQRZZFUXRZWAPZ-XZZQLLPFSA-N

> <FORMULA>
C19H27NO5

> <MOLECULAR_WEIGHT>
349.4214

> <EXACT_MASS>
349.188922979

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_NEUTRAL_MICROSPECIES_CHARGE>
-0.9993040243517041

> <JCHEM_AVERAGE_POLARIZABILITY>
38.15222883222668

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-2-{[4-(1,2-dihydroxypropan-2-yl)cyclohexyl]formamido}-3-phenylpropanoic acid

> <ALOGPS_LOGP>
1.27

> <JCHEM_LOGP>
1.5884998096666672

> <ALOGPS_LOGS>
-2.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NEUTRAL_CHARGE>
-1

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.650010175749676

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8430717354513138

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0542754786718378

> <JCHEM_POLAR_SURFACE_AREA>
106.86000000000001

> <JCHEM_REFRACTIVITY>
92.76329999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.81e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
tetrahydrofolic acid

> <JCHEM_VEBER_RULE>
0

> <DRUGBANK_ID>
DBMET01322

> <NAME>
Nateglinide metabolite M11/M12

$$$$