MiMeDB: Showing metabocard for 6,8-di-O-acetylmalyngamide 2 (MMDBc0023205)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 13:13:57 UTC

Update Date

2025-10-07 16:07:18 UTC

Metabolite ID

MMDBc0023205

Metabolite Identification

Common Name

6,8-di-O-acetylmalyngamide 2

Description

6,8-di-O-acetylmalyngamide 2 is a secondary metabolite belonging to the malyngamide chemical class. This compound was isolated from the marine cyanobacterium Moorea producens and is characterized by its unique acetylation pattern at the 6 and 8 positions of the malyngamide backbone. The chemical structure features an amide linkage, which is crucial for its biological activity. In biochemical pathways, 6,8-di-O-acetylmalyngamide 2 has been shown to activate adenosine monophosphate-activated protein kinase (AMPK), a key regulator of cellular energy homeostasis. The activation of AMPK is significant as it plays a role in various metabolic processes, including glucose uptake and fatty acid oxidation, thereby influencing cellular energy balance and metabolic health. The discovery of this compound and its bioactivity highlights the potential of marine-derived metabolites in influencing metabolic pathways. (PMID:29186048 )

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152115132D          

 46 46  0  0  1  0            999 V2000
   10.0813    2.9427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.8536    3.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6637   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2553   -0.2872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0223    2.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8914    3.0986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2417    2.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7818    2.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8324    0.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5919    2.1632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2923    1.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6426    0.7600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1320    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4822    1.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1827    0.1363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0435    1.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0730    1.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3430   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5835    2.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1236   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6131    0.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9421    1.6954    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   22.5034    1.6954    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   22.7734    0.2923    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.9928    0.2923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4232    0.7600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.6932    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9633    0.1363    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.3430    2.0073    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   19.5329   -0.3314    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   24.1236    2.0073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.3937    0.6041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2628    1.0718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1531    2.1632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.2575   -0.6344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2122    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.7734    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.3135   -0.3314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.5624   -0.1755    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.5624    2.0073    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   19.5329    1.8514    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.6721    0.9159    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   21.9633    2.3191    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   22.5034   -0.4873    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   20.8831    1.3836    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  2  0  0  0  0
 13 10  1  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  1  0  0  0  0
 20  2  1  0  0  0  0
 21  3  1  0  0  0  0
 22 18  2  0  0  0  0
 22 19  1  0  0  0  0
 23 14  1  0  0  0  0
 23 15  1  0  0  0  0
 24 17  1  0  0  0  0
 25 17  1  0  0  0  0
 26 16  1  0  0  0  0
 27 22  1  1  0  0  0
 28 24  1  0  0  0  0
 28 27  1  0  0  0  0
 29  4  1  6  0  0  0
 29 25  1  0  0  0  0
 29 27  1  0  0  0  0
 30 18  1  0  0  0  0
 31 19  1  4  0  0  0
 31 26  2  0  0  0  0
 32 20  2  0  0  0  0
 33 21  2  0  0  0  0
 34 26  1  0  0  0  0
 35 28  2  0  0  0  0
 29 36  1  1  0  0  0
 37  5  1  0  0  0  0
 23 37  1  1  0  0  0
 38 20  1  0  0  0  0
 24 38  1  1  0  0  0
 39 21  1  0  0  0  0
 25 39  1  6  0  0  0
 40 10  1  0  0  0  0
 41 12  1  0  0  0  0
 42 18  1  0  0  0  0
 23 43  1  1  0  0  0
 24 44  1  6  0  0  0
 25 45  1  1  0  0  0
 27 46  1  6  0  0  0
M  END


  Mrv1652305152115132D          

 46 46  0  0  1  0            999 V2000
   10.0813    2.9427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.8536    3.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6637   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2553   -0.2872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0223    2.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8914    3.0986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2417    2.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7818    2.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8324    0.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5919    2.1632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2923    1.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6426    0.7600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1320    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4822    1.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1827    0.1363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0435    1.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0730    1.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3430   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5835    2.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1236   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6131    0.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9421    1.6954    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   22.5034    1.6954    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   22.7734    0.2923    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.9928    0.2923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4232    0.7600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.6932    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9633    0.1363    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.3430    2.0073    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   19.5329   -0.3314    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   24.1236    2.0073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.3937    0.6041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2628    1.0718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1531    2.1632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.2575   -0.6344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2122    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.7734    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.3135   -0.3314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.5624   -0.1755    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.5624    2.0073    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   19.5329    1.8514    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.6721    0.9159    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   21.9633    2.3191    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   22.5034   -0.4873    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   20.8831    1.3836    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  2  0  0  0  0
 13 10  1  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  1  0  0  0  0
 20  2  1  0  0  0  0
 21  3  1  0  0  0  0
 22 18  2  0  0  0  0
 22 19  1  0  0  0  0
 23 14  1  0  0  0  0
 23 15  1  0  0  0  0
 24 17  1  0  0  0  0
 25 17  1  0  0  0  0
 26 16  1  0  0  0  0
 27 22  1  1  0  0  0
 28 24  1  0  0  0  0
 28 27  1  0  0  0  0
 29  4  1  6  0  0  0
 29 25  1  0  0  0  0
 29 27  1  0  0  0  0
 30 18  1  0  0  0  0
 31 19  1  4  0  0  0
 31 26  2  0  0  0  0
 32 20  2  0  0  0  0
 33 21  2  0  0  0  0
 34 26  1  0  0  0  0
 35 28  2  0  0  0  0
 29 36  1  1  0  0  0
 37  5  1  0  0  0  0
 23 37  1  1  0  0  0
 38 20  1  0  0  0  0
 24 38  1  1  0  0  0
 39 21  1  0  0  0  0
 25 39  1  6  0  0  0
 40 10  1  0  0  0  0
 41 12  1  0  0  0  0
 42 18  1  0  0  0  0
 23 43  1  1  0  0  0
 24 44  1  6  0  0  0
 25 45  1  1  0  0  0
 27 46  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0023205

> <DATABASE_NAME>
MIME

> <SMILES>
[H]C(Cl)=C(CN=C(O)CC\C([H])=C(/[H])C[C@]([H])(CCCCCCC)OC)[C@@]1([H])C(=O)[C@]([H])(C[C@]([H])(OC(C)=O)[C@@]1(C)O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C29H46ClNO8/c1-6-7-8-9-11-14-23(37-5)15-12-10-13-16-26(34)31-19-22(18-30)27-28(35)24(38-20(2)32)17-25(29(27,4)36)39-21(3)33/h10,12,18,23-25,27,36H,6-9,11,13-17,19H2,1-5H3,(H,31,34)/b12-10+,22-18-/t23-,24-,25-,27-,29+/m0/s1

> <INCHI_KEY>
VCYLDGFZBOWHOI-XZALHDRTSA-N

> <FORMULA>
C29H46ClNO8

> <MOLECULAR_WEIGHT>
572.14

> <EXACT_MASS>
571.2911951

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
60.602377062579436

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4E,7S)-N-[(2E)-2-[(1R,2S,3S,5S)-3,5-bis(acetyloxy)-2-hydroxy-2-methyl-6-oxocyclohexyl]-3-chloroprop-2-en-1-yl]-7-methoxytetradec-4-enimidic acid

> <ALOGPS_LOGP>
4.94

> <JCHEM_LOGP>
4.381648167333332

> <ALOGPS_LOGS>
-5.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.3464962622761

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.599249465976876

> <JCHEM_PKA_STRONGEST_BASIC>
3.5191989317698273

> <JCHEM_POLAR_SURFACE_AREA>
131.72000000000003

> <JCHEM_REFRACTIVITY>
149.99030000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.11e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4E,7S)-N-[(2E)-2-[(1R,2S,3S,5S)-3,5-bis(acetyloxy)-2-hydroxy-2-methyl-6-oxocyclohexyl]-3-chloroprop-2-en-1-yl]-7-methoxytetradec-4-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0      18.818   5.493   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      44.527   6.366   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      46.039  -1.492   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      39.677  -0.536   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      29.908   4.911   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      20.331   5.784   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.339   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.851   4.911   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      23.859   3.747   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      31.421   1.128   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      25.372   4.038   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      30.412   2.292   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      32.933   1.419   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.380   2.874   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      28.900   2.001   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      33.941   0.255   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      43.014   2.001   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      37.470   2.292   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      37.974  -0.328   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      44.023   4.911   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      45.031  -0.328   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      38.478   1.128   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      27.892   3.165   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      42.006   3.165   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      42.510   0.546   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      35.453   0.546   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      39.990   1.419   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      40.494   2.874   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      40.998   0.255   0.000  0.00  0.00           C+0
HETATM   30 Cl   UNK     0      37.974   3.747   0.000  0.00  0.00          Cl+0
HETATM   31  N   UNK     0      36.461  -0.619   0.000  0.00  0.00           N+0
HETATM   32  O   UNK     0      45.031   3.747   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      45.535   1.128   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      35.957   2.001   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      39.486   4.038   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      41.547  -1.184   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      28.396   4.620   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      42.510   4.620   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      43.519  -0.619   0.000  0.00  0.00           O+0
HETATM   40  H   UNK     0      30.916  -0.328   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0      30.916   3.747   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0      36.461   3.456   0.000  0.00  0.00           H+0
HETATM   43  H   UNK     0      27.388   1.710   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0      40.998   4.329   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0      42.006  -0.910   0.000  0.00  0.00           H+0
HETATM   46  H   UNK     0      38.982   2.583   0.000  0.00  0.00           H+0
CONECT    1    6                                                            
CONECT    2   20                                                            
CONECT    3   21                                                            
CONECT    4   29                                                            
CONECT    5   37                                                            
CONECT    6    1    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   11                                                       
CONECT   10   12   13   40                                                  
CONECT   11    9   14                                                       
CONECT   12   10   15   41                                                  
CONECT   13   10   16                                                       
CONECT   14   11   23                                                       
CONECT   15   12   23                                                       
CONECT   16   13   26                                                       
CONECT   17   24   25                                                       
CONECT   18   22   30   42                                                  
CONECT   19   22   31                                                       
CONECT   20    2   32   38                                                  
CONECT   21    3   33   39                                                  
CONECT   22   18   19   27                                                  
CONECT   23   14   15   37   43                                             
CONECT   24   17   28   38   44                                             
CONECT   25   17   29   39   45                                             
CONECT   26   16   31   34                                                  
CONECT   27   22   28   29   46                                             
CONECT   28   24   27   35                                                  
CONECT   29    4   25   27   36                                             
CONECT   30   18                                                            
CONECT   31   19   26                                                       
CONECT   32   20                                                            
CONECT   33   21                                                            
CONECT   34   26                                                            
CONECT   35   28                                                            
CONECT   36   29                                                            
CONECT   37    5   23                                                       
CONECT   38   20   24                                                       
CONECT   39   21   25                                                       
CONECT   40   10                                                            
CONECT   41   12                                                            
CONECT   42   18                                                            
CONECT   43   23                                                            
CONECT   44   24                                                            
CONECT   45   25                                                            
CONECT   46   27                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   92    0
END

Synonyms

Not Available

Molecular Formula

C₂₉H₄₆ClNO₈

Average Mass

572.14

Monoisotopic Mass

571.2911951

IUPAC Name

(4E,7S)-N-[(2E)-2-[(1R,2S,3S,5S)-3,5-bis(acetyloxy)-2-hydroxy-2-methyl-6-oxocyclohexyl]-3-chloroprop-2-en-1-yl]-7-methoxytetradec-4-enimidic acid

Traditional Name

(4E,7S)-N-[(2E)-2-[(1R,2S,3S,5S)-3,5-bis(acetyloxy)-2-hydroxy-2-methyl-6-oxocyclohexyl]-3-chloroprop-2-en-1-yl]-7-methoxytetradec-4-enimidic acid

CAS Registry Number

Not Available

SMILES

[H]C(Cl)=C(CN=C(O)CC\C([H])=C(/[H])C[C@]([H])(CCCCCCC)OC)[C@@]1([H])C(=O)[C@]([H])(C[C@]([H])(OC(C)=O)[C@@]1(C)O)OC(C)=O

InChI Identifier

InChI=1S/C29H46ClNO8/c1-6-7-8-9-11-14-23(37-5)15-12-10-13-16-26(34)31-19-22(18-30)27-28(35)24(38-20(2)32)17-25(29(27,4)36)39-21(3)33/h10,12,18,23-25,27,36H,6-9,11,13-17,19H2,1-5H3,(H,31,34)/b12-10+,22-18-/t23-,24-,25-,27-,29+/m0/s1

InChI Key

VCYLDGFZBOWHOI-XZALHDRTSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monocyclic monoterpenoids. These are monoterpenoids containing 1 ring in the isoprene chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Monocyclic monoterpenoids

Alternative Parents

Substituents

Monocyclic monoterpenoid
Alpha-acyloxy ketone
Fatty acyl
N-acyl-amine
Fatty amide
Dicarboxylic acid or derivatives
Cyclitol or derivatives
Tertiary alcohol
Cyclic alcohol
Cyclic ketone
Secondary carboxylic acid amide
Ketone
Carboxylic acid ester
Carboxamide group
Chloroalkene
Haloalkene
Vinyl halide
Vinyl chloride
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Carbonyl group
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0011 g/L	ALOGPS
logP	4.94	ALOGPS
logP	4.38	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	5.6	ChemAxon
pKa (Strongest Basic)	3.52	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	131.72 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	149.99 m³·mol⁻¹	ChemAxon
Polarizability	60.6 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Cyanobacteria	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

63002542

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139590546

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for 6,8-di-O-acetylmalyngamide 2 (MMDBc0023205)

MOL for #<Metabolite:0x00007f8dd043d590>

3D MOL for #<Metabolite:0x00007f8dd043d590>

3D SDF for #<Metabolite:0x00007f8dd043d590>

3D-SDF for #<Metabolite:0x00007f8dd043d590>

PDB for #<Metabolite:0x00007f8dd043d590>

3D PDB for #<Metabolite:0x00007f8dd043d590>

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Structure for #<Metabolite:0x00007f8dd043d590>

3D Structure for #<Metabolite:0x00007f8dd043d590>