NP-MRD: Showing NP-Card for Boneratamide A (NP0078943)

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Record Information

Version

2.0

Created at

2022-04-29 00:01:38 UTC

Updated at

2022-04-29 00:01:38 UTC

NP-MRD ID

NP0078943

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Boneratamide A

Description

Boneratamide A belongs to the class of organic compounds known as proline and derivatives. Proline and derivatives are compounds containing proline or a derivative thereof resulting from reaction of proline at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Boneratamide A is found in Axinyssa aplysinoides. Based on a literature review very few articles have been published on Boneratamide A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292202012D          

 30 32  0  0  1  0            999 V2000
    2.5070   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6820    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5070    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9195    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9195    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7445    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    1.8414    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3495    3.0408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8570    3.9849    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0366    4.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5155    3.4580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1350    4.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5795    5.2906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1926    4.7385    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9996    4.9101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2545    5.6947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5516    4.2970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5551    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9840    3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674    1.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -1.0164    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
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  6  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  4 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 13 23  1  0  0  0  0
 13 24  1  0  0  0  0
  3 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
  3 28  1  0  0  0  0
 27 29  1  0  0  0  0
  2 30  1  1  0  0  0
M  END

     RDKit          3D

 68 70  0  0  0  0  0  0  0  0999 V2000
   -1.1356   -3.7381   -1.6373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4668   -2.5388   -0.7829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9201   -1.4008   -1.2182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584   -0.3947   -0.1351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9062   -1.2108    1.1060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3103   -2.5245    0.6724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6313   -0.0837   -0.1971 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3734   -1.2391   -0.8609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9641    1.1512   -0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1313    2.3457   -0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8253    2.1286   -0.0202 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8250    2.6372    1.3721 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1129    4.1522    1.3164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8424    2.0985    2.3146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2842    0.7930   -0.3122 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0176    0.5027    0.2350 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1802    0.2203   -0.4589 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1901    0.1885   -1.7174 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4591   -0.0543    0.2952 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7396    1.1391    1.1490 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1558   -1.1618    1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4931   -0.4597   -0.6039 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2297   -1.7194   -1.3565 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1143   -2.2443   -1.5734 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5188   -2.2774   -1.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4959   -1.4620   -0.9669 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7475   -0.0885   -1.0986 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5611    0.9758   -0.6338 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3412    1.7729    0.2631 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8128    1.1617   -1.2864 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2001   -4.6574   -1.0564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1879   -3.6012   -2.1889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9333   -3.8222   -2.4314 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8866   -3.4127    1.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2757   -2.6856    1.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0193   -0.0971    0.8440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1710   -1.2720   -1.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4663   -0.9946   -0.7353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2041   -2.2005   -0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9932    0.8874   -2.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0422    1.3970   -0.7126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7047    3.0945   -0.0821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0036    2.8734   -1.6853 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8475    2.5681    1.8868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8472    4.5142    0.3056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2001    4.3224    1.4475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5571    4.6866    2.1135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9232    2.8391    3.1670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4854    1.1791    2.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8685    2.0431    1.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0823    0.8031   -1.4406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0506    0.5233    1.2765 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5132    0.9802    1.9240 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7755    2.1041    0.6161 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3700   -0.8186    1.9951 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0926   -1.1842    1.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6978   -2.0983   -2.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6171   -3.3188   -1.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4951   -1.4028   -1.3818 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.6638    1.2544   -0.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 14  1  0
 12 11  1  0
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 23 24  2  0
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 28 29  2  0
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 23 22  1  0
  4  3  1  0
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 12 48  1  1
 14 52  1  0
 14 53  1  0
 14 54  1  0
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  9 43  1  0
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  7 39  1  1
  8 40  1  0
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  5 35  1  0
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  1 31  1  0
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  1 33  1  0
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 21 62  1  0
 27 67  1  6
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 25 63  1  0
 25 64  1  0
 30 68  1  0
M  END


  Mrv1652304292202012D          

 30 32  0  0  1  0            999 V2000
    2.5070   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6820    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5070    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9195    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9195    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7445    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    1.8414    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3495    3.0408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8570    3.9849    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0366    4.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5155    3.4580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1350    4.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5795    5.2906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1926    4.7385    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9996    4.9101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2545    5.6947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5516    4.2970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5551    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9840    3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674    1.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -1.0164    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
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  1  6  1  0  0  0  0
  5  7  1  6  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
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 10 11  1  0  0  0  0
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 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
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 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 13 23  1  0  0  0  0
 13 24  1  0  0  0  0
  3 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
  3 28  1  0  0  0  0
 27 29  1  0  0  0  0
  2 30  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0078943

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1CC[C@@H](C)[C@]2(CCC(C)=C2)[C@@H]1NC(=O)C(C)(C)N1[C@H](CCC1=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H38N2O4/c1-14(2)17-8-7-16(4)24(12-11-15(3)13-24)20(17)25-22(30)23(5,6)26-18(21(28)29)9-10-19(26)27/h13-14,16-18,20H,7-12H2,1-6H3,(H,25,30)(H,28,29)/t16-,17+,18-,20-,24-/m1/s1

> <INCHI_KEY>
CIYFWEZTKZBJJG-DGPQGTHCSA-N

> <FORMULA>
C24H38N2O4

> <MOLECULAR_WEIGHT>
418.578

> <EXACT_MASS>
418.283157712

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
46.842022094483525

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-1-(1-{[(5S,6R,7S,10R)-2,10-dimethyl-7-(propan-2-yl)spiro[4.5]dec-1-en-6-yl]carbamoyl}-1-methylethyl)-5-oxopyrrolidine-2-carboxylic acid

> <ALOGPS_LOGP>
3.05

> <JCHEM_LOGP>
3.462928186333334

> <ALOGPS_LOGS>
-4.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
15.479537013536593

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6764221108968065

> <JCHEM_PKA_STRONGEST_BASIC>
-1.367767186884691

> <JCHEM_POLAR_SURFACE_AREA>
86.71000000000001

> <JCHEM_REFRACTIVITY>
115.84729999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.08e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-1-(1-{[(5S,6R,7S,10R)-7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl]carbamoyl}-1-methylethyl)-5-oxopyrrolidine-2-carboxylic acid

> <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       4.680  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.140  -0.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.140   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.680   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.450   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.450   3.437   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.990   3.437   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.680   4.771   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       2.370   3.437   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       3.140   4.771   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.386   5.676   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.370   6.105   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       1.600   7.438   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       0.068   7.599   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.962   6.455   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.252   9.106   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.082   9.876   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.226   8.845   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.733   9.165   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.208  10.630   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.763   8.021   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.036   5.335   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.703   6.875   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.465   2.016   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.246   2.445   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.370  -1.897   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   30                                                  
CONECT    3    2    4   25   28                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    4   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   23   24                                             
CONECT   14   13   15   19                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   13                                                            
CONECT   24   13                                                            
CONECT   25    3   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27    3                                                       
CONECT   29   27                                                            
CONECT   30    2                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₈N₂O₄

Average Mass

418.5780 Da

Monoisotopic Mass

418.28316 Da

IUPAC Name

(2R)-1-(1-{[(5S,6R,7S,10R)-2,10-dimethyl-7-(propan-2-yl)spiro[4.5]dec-1-en-6-yl]carbamoyl}-1-methylethyl)-5-oxopyrrolidine-2-carboxylic acid

Traditional Name

(2R)-1-(1-{[(5S,6R,7S,10R)-7-isopropyl-2,10-dimethylspiro[4.5]dec-1-en-6-yl]carbamoyl}-1-methylethyl)-5-oxopyrrolidine-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1CC[C@@H](C)[C@]2(CCC(C)=C2)[C@@H]1NC(=O)C(C)(C)N1[C@H](CCC1=O)C(O)=O

InChI Identifier

InChI=1S/C24H38N2O4/c1-14(2)17-8-7-16(4)24(12-11-15(3)13-24)20(17)25-22(30)23(5,6)26-18(21(28)29)9-10-19(26)27/h13-14,16-18,20H,7-12H2,1-6H3,(H,25,30)(H,28,29)/t16-,17+,18-,20-,24-/m1/s1

InChI Key

CIYFWEZTKZBJJG-DGPQGTHCSA-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
Axinyssa aplysinoides	Animalia	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as proline and derivatives. Proline and derivatives are compounds containing proline or a derivative thereof resulting from reaction of proline at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Proline and derivatives

Alternative Parents

Substituents

Proline or derivatives
Monoterpenoid
P-menthane monoterpenoid
Oxoproline
Pyrrolidine carboxylic acid
Pyrrolidine carboxylic acid or derivatives
Pyrrolidone
2-pyrrolidone
N-alkylpyrrolidine
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Lactam
Secondary carboxylic acid amide
Monocarboxylic acid or derivatives
Azacycle
Carboxylic acid
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.05	ALOGPS
logP	3.46	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	3.68	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	86.71 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	115.85 m³·mol⁻¹	ChemAxon
Polarizability	46.84 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

C00043318

Chemspider ID

9548387

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11373470

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Boneratamide A (NP0078943)

MOL for NP0078943 (Boneratamide A)

3D MOL for NP0078943 (Boneratamide A)

3D SDF for NP0078943 (Boneratamide A)

3D-SDF for NP0078943 (Boneratamide A)

PDB for NP0078943 (Boneratamide A)

3D PDB for NP0078943 (Boneratamide A)

SMILES for NP0078943 (Boneratamide A)

INCHI for NP0078943 (Boneratamide A)

Structure for NP0078943 (Boneratamide A)

3D Structure for NP0078943 (Boneratamide A)