NP-MRD: Showing NP-Card for [(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate (NP0212047)

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Record Information

Version

2.0

Created at

2022-09-05 10:35:02 UTC

Updated at

2022-09-05 10:35:02 UTC

NP-MRD ID

NP0212047

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate

Description

[(11R,12S,13R,16R)-12,13-dihydroxy-13,17,17-trimethyl-9-oxo-18-oxa-8-azatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]Octadeca-1(10),2,4,6-tetraen-8-yl]methyl acetate belongs to the class of organic compounds known as pyranoquinolines. These are polycyclic compounds containing a pyran ring fused to a quinoline moiety. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine. [(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate is found in Halfordia kendack. Based on a literature review very few articles have been published on [(11R,12S,13R,16R)-12,13-dihydroxy-13,17,17-trimethyl-9-oxo-18-oxa-8-azatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]Octadeca-1(10),2,4,6-tetraen-8-yl]methyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052212352D          

 29 32  0  0  1  0            999 V2000
    5.5753    3.5307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    3.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    3.9984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951    2.5952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    2.4393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0889   -1.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0867   -1.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6402    1.1667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1615    1.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  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
  6 16  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  1  0  0  0
 24 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29  9  1  1  0  0  0
 21 29  1  0  0  0  0
M  END

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
    6.0355   -2.7832    0.5093 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1729   -2.3568   -0.6254 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3661   -2.7434   -1.7960 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1162   -1.4979   -0.3676 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756   -1.0720   -1.4222 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2504   -0.1879   -0.9234 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0888   -0.7279   -0.5214 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9267   -1.9873   -0.5907 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0281    0.0239   -0.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2115    1.3882    0.0506 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4171    1.9160   -0.3700 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5985    3.2829   -0.2950 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    3.8490   -0.7023 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8007    3.0554   -1.1883 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6471    1.6901   -1.2742 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4568    1.1400   -0.8637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7862    2.2566    0.5380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7528    1.6785    1.4137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0736    1.4097    2.7146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8936    2.6625    1.5207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2525    0.4473    0.7258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3669   -0.2378    1.4836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0644   -1.1337    0.4985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2895   -1.5012   -0.7078 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7565   -2.9041   -1.1312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6283   -0.6787   -1.8082 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8149   -1.5592   -0.5767 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2596   -1.2290   -1.8310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2322   -0.5824    0.4103 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9356   -2.0488    1.3396 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1068   -2.7458    0.1741 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7747   -3.7975    0.8764 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7535   -2.0158   -1.7629 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8012   -0.7138   -2.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7806    3.9039    0.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8905    4.9233   -0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7422    3.5085   -1.5112 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4426    1.0716   -1.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0564    2.3643    3.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0085    1.1464    2.5210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5823    0.6669    3.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3914    2.7106    0.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6024    2.4195    2.3337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4443    3.6533    1.8025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6968    0.7912   -0.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0713    0.4705    1.9492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9022   -0.9141    2.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5287   -2.0274    1.0127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9688   -0.5519    0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1342   -3.3227   -1.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8362   -2.8313   -1.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7240   -3.5244   -0.2111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5977   -0.7415   -1.9988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4770   -2.5982   -0.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1626   -0.2414   -1.8509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0486   -1.1728    1.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  6
 24 27  1  0
 27 28  1  0
 27 29  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
 16  6  1  0
 29  9  1  0
 16 11  1  0
 29 21  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  0
  5 34  1  0
 19 39  1  0
 19 40  1  0
 19 41  1  0
 20 42  1  0
 20 43  1  0
 20 44  1  0
 21 45  1  6
 22 46  1  0
 22 47  1  0
 23 48  1  0
 23 49  1  0
 25 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  0
 27 54  1  1
 28 55  1  0
 29 56  1  1
 12 35  1  0
 13 36  1  0
 14 37  1  0
 15 38  1  0
M  END


  Mrv1652309052212352D          

 29 32  0  0  1  0            999 V2000
    5.5753    3.5307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    3.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    3.9984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951    2.5952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    2.4393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0889   -1.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0867   -1.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6402    1.1667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1615    1.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  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
  6 16  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  1  0  0  0
 24 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29  9  1  1  0  0  0
 21 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0212047

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCN1C(=O)C2=C(OC(C)(C)[C@@H]3CC[C@@](C)(O)[C@@H](O)[C@@H]23)C2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H27NO6/c1-12(24)28-11-23-15-8-6-5-7-13(15)18-17(20(23)26)16-14(21(2,3)29-18)9-10-22(4,27)19(16)25/h5-8,14,16,19,25,27H,9-11H2,1-4H3/t14-,16-,19+,22-/m1/s1

> <INCHI_KEY>
WSNJPVCNURDQDC-NBHJVPQVSA-N

> <FORMULA>
C22H27NO6

> <MOLECULAR_WEIGHT>
401.459

> <EXACT_MASS>
401.183837593

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.68439691059806

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(11R,12S,13R,16R)-12,13-dihydroxy-13,17,17-trimethyl-9-oxo-18-oxa-8-azatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-1(10),2,4,6-tetraen-8-yl]methyl acetate

> <JCHEM_LOGP>
0.7196628200000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.012607183383732

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.535511704706433

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3909387063533344

> <JCHEM_POLAR_SURFACE_AREA>
96.30000000000001

> <JCHEM_REFRACTIVITY>
105.58760000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(11R,12S,13R,16R)-12,13-dihydroxy-13,17,17-trimethyl-9-oxo-18-oxa-8-azatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-1(10),2,4,6-tetraen-8-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      10.407   6.591   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.895   6.300   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.887   7.464   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.391   4.844   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.879   4.553   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       6.375   3.098   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       4.862   2.807   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.854   3.971   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.358   1.352   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.366   0.188   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.879   0.479   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.887  -0.685   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.399  -0.394   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.903   1.061   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.895   2.225   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.383   1.934   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.862  -1.267   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.350  -1.558   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.899  -2.997   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.029  -2.349   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.342  -0.394   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.830  -0.685   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.179   0.479   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.326   1.934   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.195   2.178   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.302   3.474   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.838   2.225   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.342   3.680   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.846   1.061   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   16                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   29                                                  
CONECT   10    9   11   17                                                  
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    6                                                  
CONECT   17   10   18                                                       
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   24   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27    9   21                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Value	Source
[(11R,12S,13R,16R)-12,13-Dihydroxy-13,17,17-trimethyl-9-oxo-18-oxa-8-azatetracyclo[8.8.0.0,.0,]octadeca-1(10),2,4,6-tetraen-8-yl]methyl acetic acid	Generator

Chemical Formula

C₂₂H₂₇NO₆

Average Mass

401.4590 Da

Monoisotopic Mass

401.18384 Da

IUPAC Name

[(11R,12S,13R,16R)-12,13-dihydroxy-13,17,17-trimethyl-9-oxo-18-oxa-8-azatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-1(10),2,4,6-tetraen-8-yl]methyl acetate

Traditional Name

[(11R,12S,13R,16R)-12,13-dihydroxy-13,17,17-trimethyl-9-oxo-18-oxa-8-azatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-1(10),2,4,6-tetraen-8-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCN1C(=O)C2=C(OC(C)(C)[C@@H]3CC[C@@](C)(O)[C@@H](O)[C@@H]23)C2=CC=CC=C12

InChI Identifier

InChI=1S/C22H27NO6/c1-12(24)28-11-23-15-8-6-5-7-13(15)18-17(20(23)26)16-14(21(2,3)29-18)9-10-22(4,27)19(16)25/h5-8,14,16,19,25,27H,9-11H2,1-4H3/t14-,16-,19+,22-/m1/s1

InChI Key

WSNJPVCNURDQDC-NBHJVPQVSA-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

Species Name	Source	Reference
Halfordia kendack	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoquinolines. These are polycyclic compounds containing a pyran ring fused to a quinoline moiety. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Quinolones and derivatives

Direct Parent

Pyranoquinolines

Alternative Parents

Substituents

Pyranoquinoline
Dihydroquinolone
Pyranopyridine
Dihydroquinoline
Alkyl aryl ether
Pyridinone
Benzenoid
Pyridine
Pyran
Vinylogous ester
Tertiary alcohol
Heteroaromatic compound
Cyclic alcohol
Carboxylic acid ester
Lactam
Secondary alcohol
1,2-diol
Carboxylic acid derivative
Ether
Oxacycle
Azacycle
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Alcohol
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
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	0.72	ChemAxon
pKa (Strongest Acidic)	13.54	ChemAxon
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	96.3 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	105.59 m³·mol⁻¹	ChemAxon
Polarizability	42.68 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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162864844

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate (NP0212047)

MOL for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)

3D MOL for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)

3D SDF for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)

3D-SDF for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)

PDB for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)

3D PDB for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)

SMILES for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)

INCHI for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)

Structure for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)

3D Structure for NP0212047 ([(6ar,9r,10s,10ar)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-6ah,7h,8h,10h,10ah-isochromeno[4,3-c]quinolin-12-yl]methyl acetate)