NP-MRD: Showing NP-Card for (1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione (NP0293790)

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Record Information

Version

2.0

Created at

2022-09-10 01:59:53 UTC

Updated at

2022-09-10 01:59:53 UTC

NP-MRD ID

NP0293790

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione

Description

Shearinine H belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Based on a literature review very few articles have been published on Shearinine H.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309102203592D          

 45 52  0  0  1  0            999 V2000
    9.5658    2.3497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9097    1.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5885    2.0687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1115    1.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8930    0.5958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4727    0.0087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0935   -0.7240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2795   -0.5898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6351   -1.1049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8668   -0.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7428    0.0112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3872    0.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1556    0.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0785    0.5003    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2628    0.3764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8362    1.0825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7737   -0.2880    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5444    0.5045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8976   -1.1036    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2533   -1.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4849   -1.3183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3610   -0.5026    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7162   -1.0173    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5847   -0.1975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9696   -0.8116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1612   -0.5323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5408   -1.0761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9879    0.3177    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7161    0.4561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4092    0.6668    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1163    1.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8914    0.8355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0054    0.0125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2292    0.8066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8876    1.3992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0411    1.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7449    1.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2290    1.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5620   -1.5927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3777   -1.4688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8043   -2.1749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2709    0.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3376   -0.6050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0923    0.1402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4894    1.0128    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
  5 13  1  0  0  0  0
 14 11  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 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
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 30 29  1  6  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 22 33  1  0  0  0  0
 17 33  1  0  0  0  0
 33 34  1  1  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 28 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 19 39  1  0  0  0  0
 39 40  1  0  0  0  0
 10 40  1  0  0  0  0
 40 41  2  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 42 45  1  0  0  0  0
  2 45  1  0  0  0  0
M  END


  Mrv1652309102203592D          

 45 52  0  0  1  0            999 V2000
    9.5658    2.3497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9097    1.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5885    2.0687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1115    1.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8930    0.5958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4727    0.0087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0935   -0.7240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2795   -0.5898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6351   -1.1049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8668   -0.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7428    0.0112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3872    0.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1556    0.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0785    0.5003    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2628    0.3764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8362    1.0825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7737   -0.2880    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5444    0.5045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8976   -1.1036    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2533   -1.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4849   -1.3183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3610   -0.5026    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7162   -1.0173    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5847   -0.1975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9696   -0.8116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1612   -0.5323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5408   -1.0761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9879    0.3177    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7161    0.4561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4092    0.6668    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1163    1.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8914    0.8355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0054    0.0125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2292    0.8066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8876    1.3992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0411    1.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7449    1.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2290    1.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5620   -1.5927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3777   -1.4688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8043   -2.1749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2709    0.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3376   -0.6050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0923    0.1402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4894    1.0128    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
  5 13  1  0  0  0  0
 14 11  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 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
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 30 29  1  6  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 22 33  1  0  0  0  0
 17 33  1  0  0  0  0
 33 34  1  1  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 28 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 19 39  1  0  0  0  0
 39 40  1  0  0  0  0
 10 40  1  0  0  0  0
 40 41  2  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 42 45  1  0  0  0  0
  2 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0293790

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)O[C@@]23CC[C@@]4(C)[C@@](O)(CC[C@H]5CC(=O)C6=C(C=C7C(CC8=C7CC(C)(C)OC8(C)C)=C6)N=C(O)[C@]45C)C2=CC(=O)[C@@H]1O3

> <INCHI_IDENTIFIER>
InChI=1S/C37H45NO7/c1-31(2)18-23-21-16-25-22(13-19(21)14-24(23)32(3,4)44-31)26(39)15-20-9-10-36(42)28-17-27(40)29-33(5,6)45-37(28,43-29)12-11-34(36,7)35(20,8)30(41)38-25/h13,16-17,20,29,42H,9-12,14-15,18H2,1-8H3,(H,38,41)/t20-,29-,34+,35+,36+,37-/m0/s1

> <INCHI_KEY>
HKZWWQIFBARFIO-DLFOISLCSA-N

> <FORMULA>
C37H45NO7

> <MOLECULAR_WEIGHT>
615.767

> <EXACT_MASS>
615.319602793

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
69.34577006881604

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4R,5S,23S,26S,30R)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0^{1,27}.0^{4,26}.0^{5,23}.0^{8,20}.0^{10,18}.0^{11,16}]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione

> <JCHEM_LOGP>
5.421824325333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.63664208386771

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.943548862463383

> <JCHEM_PKA_STRONGEST_BASIC>
1.0163346442096937

> <JCHEM_POLAR_SURFACE_AREA>
114.65000000000002

> <JCHEM_REFRACTIVITY>
171.8323

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,5S,23S,26S,30R)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0^{1,27}.0^{4,26}.0^{5,23}.0^{8,20}.0^{10,18}.0^{11,16}]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      17.856   4.386   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.498   2.986   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      19.765   3.862   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.008   2.597   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.600   1.112   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      17.682   0.016   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.975  -1.351   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.455  -1.101   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.252  -2.063   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.818  -1.502   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.587   0.021   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.790   0.983   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.224   0.422   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      11.346   0.934   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       9.824   0.703   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.028   2.021   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.911  -0.538   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.483   0.942   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.142  -2.060   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.939  -3.022   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.505  -2.461   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.274  -0.938   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.070  -1.899   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.825  -0.369   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.677  -1.515   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.168  -0.994   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.009  -2.009   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.844   0.593   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.203   0.851   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.497   1.245   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.817   2.135   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.264   1.560   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.477   0.023   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.894   1.506   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.523   2.612   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       1.943   2.206   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.390   3.643   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.427   2.477   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.382  -2.973   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      11.905  -2.742   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      12.701  -4.060   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      19.172   0.406   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      19.297  -1.129   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      20.706   0.262   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      19.580   1.891   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   45                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    7   42                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   40                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12    8    5                                                  
CONECT   14   11   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   33                                             
CONECT   18   17                                                            
CONECT   19   17   20   39                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   33                                             
CONECT   23   22                                                            
CONECT   24   22   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   36                                                  
CONECT   29   28   30                                                       
CONECT   30   29   24   31   35                                             
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   22   17   34                                             
CONECT   34   33                                                            
CONECT   35   30   36                                                       
CONECT   36   35   28   37   38                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   19   40                                                       
CONECT   40   39   10   41                                                  
CONECT   41   40                                                            
CONECT   42    6   43   44   45                                             
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45   42    2                                                       
MASTER        0    0    0    0    0    0    0    0   45    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₅NO₇

Average Mass

615.7670 Da

Monoisotopic Mass

615.31960 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1(C)O[C@@]23CC[C@@]4(C)[C@@](O)(CC[C@H]5CC(=O)C6=C(C=C7C(CC8=C7CC(C)(C)OC8(C)C)=C6)N=C(O)[C@]45C)C2=CC(=O)[C@@H]1O3

InChI Identifier

InChI=1S/C37H45NO7/c1-31(2)18-23-21-16-25-22(13-19(21)14-24(23)32(3,4)44-31)26(39)15-20-9-10-36(42)28-17-27(40)29-33(5,6)45-37(28,43-29)12-11-34(36,7)35(20,8)30(41)38-25/h13,16-17,20,29,42H,9-12,14-15,18H2,1-8H3,(H,38,41)/t20-,29-,34+,35+,36+,37-/m0/s1

InChI Key

HKZWWQIFBARFIO-DLFOISLCSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Indene
Aryl ketone
Aryl alkyl ketone
Ketal
Dihydropyranone
Pyran
Benzenoid
Meta-dioxolane
Cyclic alcohol
Tertiary alcohol
Vinylogous amide
Carboxamide group
Ketone
Lactam
Secondary carboxylic acid amide
Acetal
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Azacycle
Organic oxide
Alcohol
Organopnictogen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organooxygen compound
Organonitrogen 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

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

17262461

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16104608

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione (NP0293790)

MOL for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)

3D MOL for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)

3D SDF for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)

3D-SDF for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)

PDB for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)

3D PDB for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)

SMILES for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)

INCHI for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)

Structure for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)

3D Structure for NP0293790 ((1s,4r,5s,23s,26s,30r)-6,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azaoctacyclo[28.2.1.0¹,²⁷.0⁴,²⁶.0⁵,²³.0⁸,²⁰.0¹⁰,¹⁸.0¹¹,¹⁶]tritriaconta-6,8(20),9,11(16),18,27-hexaene-21,29-dione)