NP-MRD: Showing NP-Card for 8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one (NP0221277)

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Record Information

Version

2.0

Created at

2022-09-05 22:48:49 UTC

Updated at

2022-09-05 22:48:49 UTC

NP-MRD ID

NP0221277

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one

Description

8,17-Dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]Octadeca-6,17-dien-12-one belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. 8,17-Dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]Octadeca-6,17-dien-12-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004181500092D          

 32 37  0  0  0  0            999 V2000
   -4.1226   -1.0149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7851   -0.2621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9644   -0.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6269    0.5748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8062    0.6589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3230   -0.0097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5023    0.0744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2454    0.9209    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.5567    1.3007    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.3089    0.7939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0938    1.1621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9246    0.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1770    1.7836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7721    1.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4796    0.7113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4060   -0.1267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6136   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4780   -1.2221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9496    0.1195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2369   -0.3357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4033   -0.1151    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7999   -0.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0967   -1.5714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0798   -0.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4765   -0.1402    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5422    0.6218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0791    1.1646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6605   -0.7626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1773   -1.4312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4812   -0.8467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8187   -1.5995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6394   -1.6836    0.0000 C   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  2  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  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  2  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
  3 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END


  Mrv1533004181500092D          

 32 37  0  0  0  0            999 V2000
   -4.1226   -1.0149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7851   -0.2621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9644   -0.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6269    0.5748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8062    0.6589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3230   -0.0097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5023    0.0744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2454    0.9209    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.5567    1.3007    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.3089    0.7939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0938    1.1621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9246    0.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1770    1.7836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7721    1.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4796    0.7113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4060   -0.1267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6136   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4780   -1.2221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9496    0.1195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2369   -0.3357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4033   -0.1151    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7999   -0.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0967   -1.5714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0798   -0.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4765   -0.1402    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5422    0.6218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0791    1.1646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6605   -0.7626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1773   -1.4312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4812   -0.8467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8187   -1.5995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6394   -1.6836    0.0000 C   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  2  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  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  2  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
  3 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0221277

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C2SSC34CC56OC5C=CC(O)C6ON3C(=O)C2NC4=O)C(O)=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C20H20N2O8S2/c1-27-10-5-3-8(13(24)14(10)28-2)15-12-17(25)22-20(32-31-15,18(26)21-12)7-19-11(29-19)6-4-9(23)16(19)30-22/h3-6,9,11-12,15-16,23-24H,7H2,1-2H3,(H,21,26)

> <INCHI_KEY>
VZUFPCHAVLFFAY-UHFFFAOYSA-N

> <FORMULA>
C20H20N2O8S2

> <MOLECULAR_WEIGHT>
480.51

> <EXACT_MASS>
480.06610796

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
46.13375686369143

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8-hydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadec-6-ene-12,17-dione

> <ALOGPS_LOGP>
1.02

> <JCHEM_LOGP>
0.8785019253333335

> <ALOGPS_LOGS>
-2.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.415393002390626

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.554538598779013

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3881809378850756

> <JCHEM_POLAR_SURFACE_AREA>
130.09

> <JCHEM_REFRACTIVITY>
113.67969999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.63e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-hydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadec-6-ene-12,17-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0      -7.695  -1.895   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -7.065  -0.489   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.533  -0.332   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.903   1.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.372   1.230   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.470  -0.018   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.938   0.139   0.000  0.00  0.00           C+0
HETATM    8  S   UNK     0      -0.458   1.719   0.000  0.00  0.00           S+0
HETATM    9  S   UNK     0       1.039   2.428   0.000  0.00  0.00           S+0
HETATM   10  C   UNK     0       2.443   1.482   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.908   2.169   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.459   1.824   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.930   3.329   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.041   2.217   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.362   1.328   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.225  -0.237   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.745  -0.762   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.492  -2.281   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.506   0.223   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.176  -0.627   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0       2.619  -0.215   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       1.493  -1.496   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.047  -2.933   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.149  -1.309   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       0.889  -0.262   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       1.012   1.161   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.148   2.174   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -3.100  -1.423   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -2.198  -2.672   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -4.632  -1.580   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -5.261  -2.986   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -6.793  -3.143   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   30                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8   24                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   21   26                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   14   19                                             
CONECT   13   12   14                                                       
CONECT   14   13   12   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   12   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   10   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    7   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   10   27                                                  
CONECT   27   26                                                            
CONECT   28    6   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    3   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   74    0
END

View in JSmol

Synonyms

Value	Source
(1AS-(1aalpha,4b,4abeta,8a,9b,11aalpha,12ar*))-4,4a,8,9-tetrahydro-4-hydroxy-9-(2-hydroxy-3,4-dimethoxyphenyl)-12H-8,11-(iminomethano)-1ah,7H-(1,2,4)dithiazepino(4,3-b)oxireno(e)(1,2)benzoxa	Generator
(1AS-(1aalpha,4β,4abeta,8α,9β,11aalpha,12ar*))-4,4a,8,9-tetrahydro-4-hydroxy-9-(2-hydroxy-3,4-dimethoxyphenyl)-12H-8,11-(iminomethano)-1ah,7H-(1,2,4)dithiazepino(4,3-b)oxireno(e)(1,2)benzoxa	Generator

Chemical Formula

C₂₀H₂₀N₂O₈S₂

Average Mass

480.5100 Da

Monoisotopic Mass

480.06611 Da

IUPAC Name

8-hydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadec-6-ene-12,17-dione

Traditional Name

8-hydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadec-6-ene-12,17-dione

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C2SSC34CC56OC5C=CC(O)C6ON3C(=O)C2NC4=O)C(O)=C1OC

InChI Identifier

InChI=1S/C20H20N2O8S2/c1-27-10-5-3-8(13(24)14(10)28-2)15-12-17(25)22-20(32-31-15,18(26)21-12)7-19-11(29-19)6-4-9(23)16(19)30-22/h3-6,9,11-12,15-16,23-24H,7H2,1-2H3,(H,21,26)

InChI Key

VZUFPCHAVLFFAY-UHFFFAOYSA-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 methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Methoxyphenol
Dimethoxybenzene
O-dimethoxybenzene
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
1,2-oxazinane
Monocyclic benzene moiety
Oxazinane
Cyclic carboximidic acid
Organic disulfide
Secondary alcohol
Organic 1,3-dipolar compound
Organoheterocyclic compound
Propargyl-type 1,3-dipolar organic compound
Oxacycle
Azacycle
Carboxylic acid derivative
Ether
Oxirane
Dialkyl ether
Organooxygen compound
Alcohol
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Organonitrogen compound
Hydrocarbon derivative
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	1.02	ALOGPS
logP	0.88	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	9.55	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.09 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	113.68 m³·mol⁻¹	ChemAxon
Polarizability	46.13 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

85148368

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one (NP0221277)

MOL for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)

3D MOL for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)

3D SDF for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)

3D-SDF for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)

PDB for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)

3D PDB for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)

SMILES for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)

INCHI for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)

Structure for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)

3D Structure for NP0221277 (8,17-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-4,10-dioxa-15,16-dithia-11,18-diazapentacyclo[11.3.2.0¹,¹¹.0³,⁵.0³,⁹]octadeca-6,17-dien-12-one)