NP-MRD: Showing NP-Card for Debromohamigeran A (NP0081057)

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Record Information

Version

2.0

Created at

2022-04-29 02:02:29 UTC

Updated at

2022-04-29 02:02:29 UTC

NP-MRD ID

NP0081057

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Debromohamigeran A

Description

Debromohamigeran A belongs to the class of organic compounds known as naphthalenecarboxylic acids. Naphthalenecarboxylic acids are compounds containing a naphthalene moiety, which bears a carboxylic acid group one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring. Debromohamigeran A is found in Hamigera tarangaensis. Based on a literature review very few articles have been published on debromohamigeran A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
   -2.2883    4.9568   -0.1717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7957    3.6907    0.2247 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8451    2.9960   -0.5455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4863    3.5928   -1.5903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3348    1.6664   -0.1191 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9464    1.3507    1.0635 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1426    1.7426    0.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7364    2.8314    0.2436 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8027    0.4497    0.3616 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9601    0.4617    1.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5037    1.5571    1.7436 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6389   -0.7326    1.3060 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1504   -1.8727    0.7216 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8937   -3.1520    0.9195 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9940   -1.8681   -0.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3073   -0.6972   -0.2270 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0925   -0.6685   -1.0138 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0566   -1.4914   -0.6548 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0526   -2.3736    0.5175 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4540   -3.0438    0.5252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9208   -1.7637    1.8656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3015   -0.5977   -0.5613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9564    0.5140   -1.5178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4837    0.7076   -1.2344 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1189    1.3511   -2.4857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0991    5.2236    0.5273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6556    4.9155   -1.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4500    5.6706   -0.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0948    2.1460    1.6001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2288    2.4954    1.7916 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5588   -0.7426    1.9124 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2023   -3.9921    1.1452 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5708   -3.0592    1.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951   -3.3302    0.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6849   -2.8321   -0.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4241   -0.9827   -2.0630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3368   -2.1753   -1.5323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3780   -3.2528    0.4919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1305   -2.2747    0.9516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7651   -3.2027   -0.5271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4339   -3.9623    1.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8085   -1.1390    2.1264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8852   -2.5536    2.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0411   -1.0948    1.9330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5090   -0.2480    0.4444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2022   -1.1476   -0.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5186    1.4236   -1.2115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1471    0.2494   -2.5642 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4932    0.4803   -3.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0141    1.9419   -2.2647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6353    1.8359   -3.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  1
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 16  2  0
 16 15  1  0
 15 13  2  0
 13 14  1  0
 13 12  1  0
 12 10  2  0
 10 11  1  0
 16 17  1  0
 17 18  1  0
 18 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  6
 18 19  1  0
 19 20  1  0
 19 21  1  0
 24  5  1  0
 10  9  1  0
 24 17  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
 15 35  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
 12 31  1  0
 11 30  1  0
 17 36  1  6
 18 37  1  6
 22 45  1  0
 22 46  1  0
 23 47  1  0
 23 48  1  0
 25 49  1  0
 25 50  1  0
 25 51  1  0
 19 38  1  6
 20 39  1  0
 20 40  1  0
 20 41  1  0
 21 42  1  0
 21 43  1  0
 21 44  1  0
M  END


  Mrv1652304292204022D          

 25 27  0  0  1  0            999 V2000
    3.6601    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6996    1.8953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2952    2.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9074    2.1256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937   -1.7170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4628   -1.7874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1212   -1.3793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8372   -0.9695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1182   -2.2043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8312   -2.6195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1547    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0655   -1.0415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3038   -0.8892    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  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  4  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  6  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
  9 22  1  0  0  0  0
 21 23  1  0  0  0  0
 19 24  1  0  0  0  0
  3 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0081057

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]1(O)C(=O)C2=C(C=C(C)C=C2O)[C@H]2[C@H](CC[C@@]12C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O5/c1-10(2)12-6-7-19(4)16(12)13-8-11(3)9-14(21)15(13)17(22)20(19,24)18(23)25-5/h8-10,12,16,21,24H,6-7H2,1-5H3/t12-,16-,19-,20-/m1/s1

> <INCHI_KEY>
NIVOQQYVGQDRLU-DJGFWBNSSA-N

> <FORMULA>
C20H26O5

> <MOLECULAR_WEIGHT>
346.423

> <EXACT_MASS>
346.178023937

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
37.242895700735936

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,3aR,4R,9bR)-4,6-dihydroxy-3a,8-dimethyl-5-oxo-1-(propan-2-yl)-1H,2H,3H,3aH,4H,5H,9bH-cyclopenta[a]naphthalene-4-carboxylate

> <ALOGPS_LOGP>
2.67

> <JCHEM_LOGP>
4.303570939

> <ALOGPS_LOGS>
-4.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.37375626508422

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.589839895650714

> <JCHEM_PKA_STRONGEST_BASIC>
-4.855118274632102

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
93.72489999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,3aR,4R,9bR)-4,6-dihydroxy-1-isopropyl-3a,8-dimethyl-5-oxo-1H,2H,3H,9bH-cyclopenta[a]naphthalene-4-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       6.832   1.460   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.719  -0.076   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.223  -0.443   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.412   0.866   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.406   2.042   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.039   3.538   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.151   4.604   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.561   3.968   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.873   0.818   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.145  -0.539   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.956  -1.848   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.228  -3.205   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.495  -1.800   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.597  -3.337   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.826  -2.575   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.163  -1.810   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       5.821  -4.115   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.151  -4.890   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.606  -0.587   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.206   0.722   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.522   2.079   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.062   2.127   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.289   3.388   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.122  -1.944   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.167  -1.660   0.000  0.00  0.00           C+0
CONECT    1    2    5                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   13   25                                             
CONECT    4    3    5    9                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10   22                                                  
CONECT   10    9   11   19                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    3   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   10   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21    9                                                       
CONECT   23   21                                                            
CONECT   24   19                                                            
CONECT   25    3                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₆O₅

Average Mass

346.4230 Da

Monoisotopic Mass

346.17802 Da

IUPAC Name

methyl (1R,3aR,4R,9bR)-4,6-dihydroxy-3a,8-dimethyl-5-oxo-1-(propan-2-yl)-1H,2H,3H,3aH,4H,5H,9bH-cyclopenta[a]naphthalene-4-carboxylate

Traditional Name

methyl (1R,3aR,4R,9bR)-4,6-dihydroxy-1-isopropyl-3a,8-dimethyl-5-oxo-1H,2H,3H,9bH-cyclopenta[a]naphthalene-4-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]1(O)C(=O)C2=C(C=C(C)C=C2O)[C@H]2[C@H](CC[C@@]12C)C(C)C

InChI Identifier

InChI=1S/C20H26O5/c1-10(2)12-6-7-19(4)16(12)13-8-11(3)9-14(21)15(13)17(22)20(19,24)18(23)25-5/h8-10,12,16,21,24H,6-7H2,1-5H3/t12-,16-,19-,20-/m1/s1

InChI Key

NIVOQQYVGQDRLU-DJGFWBNSSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Hamigera tarangaensis	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthalenecarboxylic acids. Naphthalenecarboxylic acids are compounds containing a naphthalene moiety, which bears a carboxylic acid group one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Naphthalenes

Sub Class

Naphthalenecarboxylic acids and derivatives

Direct Parent

Naphthalenecarboxylic acids

Alternative Parents

Substituents

2-naphthalenecarboxylic acid
Tetralin
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Acyloin
Tertiary alcohol
Vinylogous acid
Methyl ester
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Carbonyl group
Organic oxygen compound
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	2.67	ALOGPS
logP	4.3	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	8.59	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	93.72 m³·mol⁻¹	ChemAxon
Polarizability	37.24 Å³	ChemAxon
Number of Rings	3	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

C00046714

Chemspider ID

8982847

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10807542

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Debromohamigeran A (NP0081057)

MOL for NP0081057 (Debromohamigeran A)

3D MOL for NP0081057 (Debromohamigeran A)

3D SDF for NP0081057 (Debromohamigeran A)

3D-SDF for NP0081057 (Debromohamigeran A)

PDB for NP0081057 (Debromohamigeran A)

3D PDB for NP0081057 (Debromohamigeran A)

SMILES for NP0081057 (Debromohamigeran A)

INCHI for NP0081057 (Debromohamigeran A)

Structure for NP0081057 (Debromohamigeran A)

3D Structure for NP0081057 (Debromohamigeran A)