NP-MRD: Showing NP-Card for goniothalaminone B (NP0041689)

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Record Information

Version

2.0

Created at

2021-06-20 23:32:48 UTC

Updated at

2021-06-30 00:16:20 UTC

NP-MRD ID

NP0041689

Secondary Accession Numbers

None

Natural Product Identification

Common Name

goniothalaminone B

Provided By

JEOL Database JEOL Logo

Description

goniothalaminone B is found in Goniothalamus scortechinii. goniothalaminone B was first documented in 2012 (Prawat, U., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212101323D          

 30 31  0  0  0  0            999 V2000
   -1.7894   -3.5481   -2.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6745   -2.1993   -2.6786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1548   -1.2892   -1.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7393   -1.5868   -0.4981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2219   -0.5813    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1157    0.7348   -0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5243    1.0457   -1.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0438    0.0331   -2.2621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4621    0.2906   -3.5472 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4059    2.4286   -1.9197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7447    2.7042   -3.0708 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1254    3.4943   -1.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1628    4.7517   -1.5603 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5152    3.1660    0.2451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117    4.2626    1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6638    4.2135    2.6046 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6726    5.2009    0.6860 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    1.7726    0.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8229    1.4662    1.8632 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -3.9726   -2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2135   -4.1281   -3.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4720   -3.6336   -1.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -2.5920   -0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0985   -0.8349    1.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3191    1.2408   -3.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0812    4.8475   -2.5442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811    5.4927   -1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4628    3.7152    3.1585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5491    5.2362    2.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    3.7014    2.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 14  1  0  0  0  0
 14 12  2  0  0  0  0
 12 10  1  0  0  0  0
  7  6  1  0  0  0  0
 10 11  2  0  0  0  0
 18 19  2  0  0  0  0
  3  4  2  0  0  0  0
 12 13  1  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  5  1  0  0  0  0
  3  2  1  0  0  0  0
  5  6  2  0  0  0  0
  2  1  1  0  0  0  0
  7  8  2  0  0  0  0
 14 15  1  0  0  0  0
  7 10  1  0  0  0  0
 15 17  2  0  0  0  0
  6 18  1  0  0  0  0
 15 16  1  0  0  0  0
  4 23  1  0  0  0  0
  5 24  1  0  0  0  0
 13 26  1  0  0  0  0
 13 27  1  0  0  0  0
  9 25  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
 16 28  1  0  0  0  0
 16 29  1  0  0  0  0
 16 30  1  0  0  0  0
M  END

     RDKit          3D

 30 31  0  0  0  0  0  0  0  0999 V2000
   -1.7894   -3.5481   -2.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6745   -2.1993   -2.6786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1548   -1.2892   -1.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7393   -1.5868   -0.4981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2219   -0.5813    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1157    0.7348   -0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5243    1.0457   -1.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0438    0.0331   -2.2621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4621    0.2906   -3.5472 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4059    2.4286   -1.9197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7447    2.7042   -3.0708 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1254    3.4943   -1.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1628    4.7517   -1.5603 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5152    3.1660    0.2451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117    4.2626    1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6638    4.2135    2.6046 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6726    5.2009    0.6860 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    1.7726    0.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8229    1.4662    1.8632 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -3.9726   -2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2135   -4.1281   -3.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4720   -3.6336   -1.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -2.5920   -0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0985   -0.8349    1.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3191    1.2408   -3.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0812    4.8475   -2.5442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811    5.4927   -1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4628    3.7152    3.1585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5491    5.2362    2.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    3.7014    2.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 14  1  0
 14 12  2  0
 12 10  1  0
  7  6  1  0
 10 11  2  0
 18 19  2  0
  3  4  2  0
 12 13  1  0
  3  8  1  0
  8  9  1  0
  4  5  1  0
  3  2  1  0
  5  6  2  0
  2  1  1  0
  7  8  2  0
 14 15  1  0
  7 10  1  0
 15 17  2  0
  6 18  1  0
 15 16  1  0
  4 23  1  0
  5 24  1  0
 13 26  1  0
 13 27  1  0
  9 25  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
 16 28  1  0
 16 29  1  0
 16 30  1  0
M  END


  Mrv1652306212101323D          

 30 31  0  0  0  0            999 V2000
   -1.7894   -3.5481   -2.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6745   -2.1993   -2.6786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1548   -1.2892   -1.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7393   -1.5868   -0.4981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2219   -0.5813    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1157    0.7348   -0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5243    1.0457   -1.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0438    0.0331   -2.2621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4621    0.2906   -3.5472 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4059    2.4286   -1.9197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7447    2.7042   -3.0708 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1254    3.4943   -1.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1628    4.7517   -1.5603 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5152    3.1660    0.2451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117    4.2626    1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6638    4.2135    2.6046 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6726    5.2009    0.6860 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    1.7726    0.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8229    1.4662    1.8632 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -3.9726   -2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2135   -4.1281   -3.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4720   -3.6336   -1.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -2.5920   -0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0985   -0.8349    1.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3191    1.2408   -3.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0812    4.8475   -2.5442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811    5.4927   -1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4628    3.7152    3.1585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5491    5.2362    2.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    3.7014    2.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 14  1  0  0  0  0
 14 12  2  0  0  0  0
 12 10  1  0  0  0  0
  7  6  1  0  0  0  0
 10 11  2  0  0  0  0
 18 19  2  0  0  0  0
  3  4  2  0  0  0  0
 12 13  1  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  5  1  0  0  0  0
  3  2  1  0  0  0  0
  5  6  2  0  0  0  0
  2  1  1  0  0  0  0
  7  8  2  0  0  0  0
 14 15  1  0  0  0  0
  7 10  1  0  0  0  0
 15 17  2  0  0  0  0
  6 18  1  0  0  0  0
 15 16  1  0  0  0  0
  4 23  1  0  0  0  0
  5 24  1  0  0  0  0
 13 26  1  0  0  0  0
 13 27  1  0  0  0  0
  9 25  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
 16 28  1  0  0  0  0
 16 29  1  0  0  0  0
 16 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0041689

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)C(N([H])[H])=C(C(=O)C([H])([H])[H])C(=O)C2=C([H])C([H])=C1OC([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H11NO5/c1-5(15)8-10(14)13(18)9-6(11(8)16)3-4-7(19-2)12(9)17/h3-4,17H,14H2,1-2H3

> <INCHI_KEY>
CPHSHRAZAZSFMD-UHFFFAOYSA-N

> <FORMULA>
C13H11NO5

> <MOLECULAR_WEIGHT>
261.233

> <EXACT_MASS>
261.063722458

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
25.442296564809865

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-acetyl-3-amino-5-hydroxy-6-methoxy-1,4-dihydronaphthalene-1,4-dione

> <ALOGPS_LOGP>
1.47

> <JCHEM_LOGP>
0.4441113819999999

> <ALOGPS_LOGS>
-2.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.264065871868723

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.703228745354718

> <JCHEM_PKA_STRONGEST_BASIC>
-4.791175240215828

> <JCHEM_POLAR_SURFACE_AREA>
106.69

> <JCHEM_REFRACTIVITY>
67.8776

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.70e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-acetyl-3-amino-5-hydroxy-6-methoxynaphthalene-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 30 31  0  0  0  0  0  0  0  0999 V2000
   -1.7894   -3.5481   -2.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6745   -2.1993   -2.6786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1548   -1.2892   -1.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7393   -1.5868   -0.4981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2219   -0.5813    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1157    0.7348   -0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5243    1.0457   -1.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0438    0.0331   -2.2621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4621    0.2906   -3.5472 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4059    2.4286   -1.9197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7447    2.7042   -3.0708 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1254    3.4943   -1.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1628    4.7517   -1.5603 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5152    3.1660    0.2451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117    4.2626    1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6638    4.2135    2.6046 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6726    5.2009    0.6860 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    1.7726    0.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8229    1.4662    1.8632 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -3.9726   -2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2135   -4.1281   -3.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4720   -3.6336   -1.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -2.5920   -0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0985   -0.8349    1.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3191    1.2408   -3.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0812    4.8475   -2.5442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811    5.4927   -1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4628    3.7152    3.1585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5491    5.2362    2.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    3.7014    2.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 14  1  0
 14 12  2  0
 12 10  1  0
  7  6  1  0
 10 11  2  0
 18 19  2  0
  3  4  2  0
 12 13  1  0
  3  8  1  0
  8  9  1  0
  4  5  1  0
  3  2  1  0
  5  6  2  0
  2  1  1  0
  7  8  2  0
 14 15  1  0
  7 10  1  0
 15 17  2  0
  6 18  1  0
 15 16  1  0
  4 23  1  0
  5 24  1  0
 13 26  1  0
 13 27  1  0
  9 25  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
 16 28  1  0
 16 29  1  0
 16 30  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.789  -3.548  -2.248  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.675  -2.199  -2.679  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.155  -1.289  -1.797  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.739  -1.587  -0.498  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.222  -0.581   0.323  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.116   0.735  -0.146  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.524   1.046  -1.436  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.044   0.033  -2.262  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.462   0.291  -3.547  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.406   2.429  -1.920  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.745   2.704  -3.071  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.125   3.494  -1.001  0.00  0.00           C+0
HETATM   13  N   UNK     0       0.163   4.752  -1.560  0.00  0.00           N+0
HETATM   14  C   UNK     0       0.515   3.166   0.245  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.012   4.263   1.139  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.664   4.213   2.605  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.673   5.201   0.686  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.435   1.773   0.742  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.823   1.466   1.863  0.00  0.00           O+0
HETATM   20  H   UNK     0      -0.808  -3.973  -2.013  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.213  -4.128  -3.074  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.472  -3.634  -1.396  0.00  0.00           H+0
HETATM   23  H   UNK     0      -0.804  -2.592  -0.093  0.00  0.00           H+0
HETATM   24  H   UNK     0       0.099  -0.835   1.334  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.319   1.241  -3.751  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.081   4.848  -2.544  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.681   5.493  -1.086  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.463   3.715   3.159  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.549   5.236   2.977  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.289   3.701   2.765  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    3    1                                                       
CONECT    3    4    8    2                                                  
CONECT    4    3    5   23                                                  
CONECT    5    4    6   24                                                  
CONECT    6    7    5   18                                                  
CONECT    7    6    8   10                                                  
CONECT    8    3    9    7                                                  
CONECT    9    8   25                                                       
CONECT   10   12   11    7                                                  
CONECT   11   10                                                            
CONECT   12   14   10   13                                                  
CONECT   13   12   26   27                                                  
CONECT   14   18   12   15                                                  
CONECT   15   14   17   16                                                  
CONECT   16   15   28   29   30                                             
CONECT   17   15                                                            
CONECT   18   14   19    6                                                  
CONECT   19   18                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    4                                                            
CONECT   24    5                                                            
CONECT   25    9                                                            
CONECT   26   13                                                            
CONECT   27   13                                                            
CONECT   28   16                                                            
CONECT   29   16                                                            
CONECT   30   16                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

RDKit          3D

30 31  0  0  0  0  0  0  0  0999 V2000
   -1.7894   -3.5481   -2.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6745   -2.1993   -2.6786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1548   -1.2892   -1.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7393   -1.5868   -0.4981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2219   -0.5813    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1157    0.7348   -0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5243    1.0457   -1.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0438    0.0331   -2.2621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4621    0.2906   -3.5472 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4059    2.4286   -1.9197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7447    2.7042   -3.0708 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1254    3.4943   -1.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1628    4.7517   -1.5603 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5152    3.1660    0.2451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117    4.2626    1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6638    4.2135    2.6046 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6726    5.2009    0.6860 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    1.7726    0.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8229    1.4662    1.8632 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -3.9726   -2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2135   -4.1281   -3.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4720   -3.6336   -1.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -2.5920   -0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0985   -0.8349    1.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3191    1.2408   -3.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0812    4.8475   -2.5442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811    5.4927   -1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4628    3.7152    3.1585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5491    5.2362    2.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    3.7014    2.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 14  1  0
 14 12  2  0
 12 10  1  0
  7  6  1  0
 10 11  2  0
 18 19  2  0
  3  4  2  0
 12 13  1  0
  3  8  1  0
  8  9  1  0
  4  5  1  0
  3  2  1  0
  5  6  2  0
  2  1  1  0
  7  8  2  0
 14 15  1  0
  7 10  1  0
 15 17  2  0
  6 18  1  0
 15 16  1  0
  4 23  1  0
  5 24  1  0
 13 26  1  0
 13 27  1  0
  9 25  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
 16 28  1  0
 16 29  1  0
 16 30  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₃H₁₁NO₅

Average Mass

261.2330 Da

Monoisotopic Mass

261.06372 Da

IUPAC Name

2-acetyl-3-amino-5-hydroxy-6-methoxy-1,4-dihydronaphthalene-1,4-dione

Traditional Name

2-acetyl-3-amino-5-hydroxy-6-methoxynaphthalene-1,4-dione

CAS Registry Number

Not Available

SMILES

[H]OC1=C2C(=O)C(N([H])[H])=C(C(=O)C([H])([H])[H])C(=O)C2=C([H])C([H])=C1OC([H])([H])[H]

InChI Identifier

InChI=1S/C13H11NO5/c1-5(15)8-10(14)13(18)9-6(11(8)16)3-4-7(19-2)12(9)17/h3-4,17H,14H2,1-2H3

InChI Key

CPHSHRAZAZSFMD-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Goniothalamus scortechinii	JEOL database	Prawat, U., et al, Phytochem. Lett. 5, 529 (2012)

Chemical Taxonomy

Classification

Not classified

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	1.47	ALOGPS
logP	0.44	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	8.7	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	106.69 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	67.88 m³·mol⁻¹	ChemAxon
Polarizability	25.44 Å³	ChemAxon
Number of Rings	2	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

Not Available

References

General References

Prawat, U., et al. (2012). Prawat, U., et al, Phytochem. Lett. 5, 529 (2012). Phytochem..

Showing NP-Card for goniothalaminone B (NP0041689)

MOL for NP0041689 (goniothalaminone B)

3D MOL for NP0041689 (goniothalaminone B)

3D SDF for NP0041689 (goniothalaminone B)

3D-SDF for NP0041689 (goniothalaminone B)

PDB for NP0041689 (goniothalaminone B)

3D PDB for NP0041689 (goniothalaminone B)

SMILES for NP0041689 (goniothalaminone B)

INCHI for NP0041689 (goniothalaminone B)

Structure for NP0041689 (goniothalaminone B)

3D Structure for NP0041689 (goniothalaminone B)