NP-MRD: Showing NP-Card for (4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one (NP0283011)

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Record Information

Version

2.0

Created at

2022-09-09 10:05:13 UTC

Updated at

2022-09-09 10:05:13 UTC

NP-MRD ID

NP0283011

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one

Description

Brevianamide P belongs to the class of organic compounds known as pyrimidones. Pyrimidones are compounds that contain a pyrimidine ring, which bears a ketone. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. Based on a literature review very few articles have been published on Brevianamide P.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092212052D          

 28 31  0  0  1  0            999 V2000
    5.2855    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8565    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8565    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5710    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2855   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8565   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8565   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2855   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2855   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4276    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7131    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7131    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4276   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4276   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0681   -0.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2638   -0.3308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0942    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2638    1.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0681    1.3394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 20 28  1  0  0  0  0
M  END

     RDKit          3D

 51 54  0  0  0  0  0  0  0  0999 V2000
   -2.7426    1.8356   -2.1622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7959    2.4626   -0.7761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4374    2.6873   -0.1947 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6232    3.2958    1.1804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4754    1.5667   -0.2604 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7858    1.9909    0.3391 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6431    1.0985    0.6534 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8341    1.5186    1.2202 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4041   -0.3477    0.4340 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9658   -0.7486   -0.9140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4195   -0.4949   -0.9885 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8732    0.7208   -1.4376 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2503    0.9629   -1.5089 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1637   -0.0122   -1.1307 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7038   -1.2209   -0.6843 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3238   -1.4558   -0.6157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0137   -0.6566    0.5987 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8959    0.2709    0.2708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2219    0.0289    0.4160 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6878   -1.1327    0.8876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7621   -2.0974    1.2291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4015   -1.8311    1.0733 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3839   -2.7608    1.4065 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0164   -3.4468    1.7660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1912   -4.0677    1.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4609   -3.5853    1.2051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8453   -2.3525    0.8716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0934   -1.1885    0.9631 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7792    1.5194   -2.4104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4188    2.5892   -2.9060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0711    0.9752   -2.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2930    3.4817   -0.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4251    1.8693   -0.1040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9979    3.5508   -0.8056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1648    4.2672    1.0092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6766    3.5627    1.6691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2678    2.6967    1.8299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2690    1.3899   -1.3614 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8901    2.3736    1.7464 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9206   -0.9417    1.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4984   -0.1600   -1.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7270   -1.8170   -1.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2423    1.5389   -1.7530 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6572    1.9021   -1.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2361    0.1605   -1.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4268   -1.9710   -0.3929 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0427   -2.4338   -0.2533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1632   -3.9418    2.2038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1503   -5.0505    2.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2076   -4.3483    1.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8705   -2.2528    0.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  9 17  1  0
 17 22  1  0
 22 23  2  0
 22 21  1  0
 21 20  2  0
 20 28  1  0
 28 27  1  0
 27 26  2  0
 26 25  1  0
 25 24  2  0
 20 19  1  0
 19 18  2  0
 18  5  1  0
 16 11  1  0
 18 17  1  0
 24 21  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  6
  4 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  6
  8 39  1  0
  9 40  1  1
 10 41  1  0
 10 42  1  0
 12 43  1  0
 13 44  1  0
 14 45  1  0
 15 46  1  0
 16 47  1  0
 27 51  1  0
 26 50  1  0
 25 49  1  0
 24 48  1  0
M  END


  Mrv1652309092212052D          

 28 31  0  0  1  0            999 V2000
    5.2855    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8565    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8565    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5710    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2855   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8565   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8565   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2855   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2855   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4276    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7131    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7131    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4276   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4276   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0681   -0.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2638   -0.3308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0942    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2638    1.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0681    1.3394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 20 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0283011

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)[C@H]1N=C(O)[C@H](CC2=CC=CC=C2)N2C(=O)C3=C(OC=CC=C3)N=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H23N3O3/c1-3-14(2)18-19-24-21-16(11-7-8-12-28-21)22(27)25(19)17(20(26)23-18)13-15-9-5-4-6-10-15/h4-12,14,17-18H,3,13H2,1-2H3,(H,23,26)/t14?,17-,18+/m0/s1

> <INCHI_KEY>
UOBOWSHNMYJJFQ-CXRLMVSZSA-N

> <FORMULA>
C22H23N3O3

> <MOLECULAR_WEIGHT>
377.444

> <EXACT_MASS>
377.173941613

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
39.388203320945294

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,7S)-7-benzyl-4-(butan-2-yl)-6-hydroxy-15-oxa-2,5,8-triazatricyclo[8.5.0.0^{3,8}]pentadeca-1(10),2,5,11,13-pentaen-9-one

> <JCHEM_LOGP>
3.9661820426666656

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.500328327951685

> <JCHEM_PKA_STRONGEST_BASIC>
1.9500363737539428

> <JCHEM_POLAR_SURFACE_AREA>
74.49000000000001

> <JCHEM_REFRACTIVITY>
117.28280000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4R,7S)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0^{3,8}]pentadeca-1(10),2,5,11,13-pentaen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       9.866   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.533   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.199   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.865   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.199   2.310   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       8.533   1.540   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       8.533  -0.000   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.866  -0.770   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.199  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.199  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.533  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.866  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.200  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.200  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.866  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.533  -4.620   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       5.865   0.000   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       5.865   1.540   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       4.532   2.310   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       3.198   1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.198   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.532  -0.770   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.532  -2.310   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.994  -0.960   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.492  -0.617   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.176   0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.492   2.157   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.994   2.500   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   18                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17    9   18   22                                                  
CONECT   18   17    5   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   28                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   17   23                                                  
CONECT   23   22                                                            
CONECT   24   21   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   20                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₃N₃O₃

Average Mass

377.4440 Da

Monoisotopic Mass

377.17394 Da

IUPAC Name

(4R,7S)-7-benzyl-4-(butan-2-yl)-6-hydroxy-15-oxa-2,5,8-triazatricyclo[8.5.0.0^{3,8}]pentadeca-1(10),2,5,11,13-pentaen-9-one

Traditional Name

(4R,7S)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0^{3,8}]pentadeca-1(10),2,5,11,13-pentaen-9-one

CAS Registry Number

Not Available

SMILES

CCC(C)[C@H]1N=C(O)[C@H](CC2=CC=CC=C2)N2C(=O)C3=C(OC=CC=C3)N=C12

InChI Identifier

InChI=1S/C22H23N3O3/c1-3-14(2)18-19-24-21-16(11-7-8-12-28-21)22(27)25(19)17(20(26)23-18)13-15-9-5-4-6-10-15/h4-12,14,17-18H,3,13H2,1-2H3,(H,23,26)/t14?,17-,18+/m0/s1

InChI Key

UOBOWSHNMYJJFQ-CXRLMVSZSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrimidones. Pyrimidones are compounds that contain a pyrimidine ring, which bears a ketone. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazines

Sub Class

Pyrimidines and pyrimidine derivatives

Direct Parent

Pyrimidones

Alternative Parents

Substituents

Pyrimidone
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Vinylogous ester
Carboxamide group
Lactam
Secondary carboxylic acid amide
Carboxylic acid derivative
Oxacycle
Azacycle
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.97	ChemAxon
pKa (Strongest Acidic)	4.5	ChemAxon
pKa (Strongest Basic)	1.95	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	74.49 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	117.28 m³·mol⁻¹	ChemAxon
Polarizability	39.39 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78441111

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

49831333

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one (NP0283011)

MOL for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)

3D MOL for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)

3D SDF for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)

3D-SDF for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)

PDB for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)

3D PDB for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)

SMILES for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)

INCHI for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)

Structure for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)

3D Structure for NP0283011 ((4r,7s)-7-benzyl-6-hydroxy-4-(sec-butyl)-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]pentadeca-1(10),2,5,11,13-pentaen-9-one)