NP-MRD: Showing NP-Card for (2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate (NP0184117)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 23:10:09 UTC

Updated at

2022-09-03 23:10:09 UTC

NP-MRD ID

NP0184117

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate

Description

(2R)-2-[(4S)-4-[(1R,2R,5S)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]Hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. (2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate is found in Siparuna pauciflora. Based on a literature review very few articles have been published on (2R)-2-[(4S)-4-[(1R,2R,5S)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]Hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042201102D          

 26 28  0  0  1  0            999 V2000
    6.4978    5.3916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6774    5.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1924    5.9729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3418    4.5517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5213    4.4655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1858    3.7118    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4321    4.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9394    3.3763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8502    2.9582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2627    2.2437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7107    1.6306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8822    0.8236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570    1.9661    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2425    1.5536    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9070    2.3073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3919    2.9748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0563    3.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2359    3.8147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5413    4.3959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7275    0.8862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425    0.2188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4579    0.4737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7434    0.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4579    1.2987    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1224    2.0524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0432    2.7866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  1  0  0  0
  6  9  1  0  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
 13 14  1  6  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 14 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 22 24  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  1  0  0  0
 13 26  1  0  0  0  0
  9 26  1  0  0  0  0
M  END

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    4.6868    2.3092    1.3513 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6213    1.2480    1.3016 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5350    1.5787    0.7942 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8116   -0.0107    1.7788 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9794   -1.1098    1.8202 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5387   -1.6774    0.5286 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9422   -3.0721    0.8634 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6720   -1.9980   -0.2517 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5516   -0.9325   -0.2498 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7698   -0.4628   -1.4896 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5656    0.2241   -1.9441 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5867    1.0802   -2.8632 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5265   -0.3139   -1.1159 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6992    0.6137   -1.0015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7429   -0.0378   -0.1253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2457   -0.2959    1.1547 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0135   -0.8895    2.1408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4804   -1.1609    3.4970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1952   -1.2022    1.8638 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3540    1.9667   -0.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3465    2.8794   -1.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7940    2.1802   -2.4328 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7892    1.2329   -2.1925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3384    0.8517   -2.3437 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2676   -0.1562   -3.4428 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1508   -0.5998    0.1789 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6335    1.9166    1.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3614    3.1240    2.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8410    2.7692    0.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0423   -0.8875    2.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5296   -1.8966    2.4204 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1578   -2.9815    1.6337 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7840   -3.6374    1.3119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6289   -3.5888   -0.0513 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0398   -2.8746   -0.0342 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7089   -0.5989   -2.0243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8834   -1.2740   -1.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0389   -1.0298   -0.5648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6743    0.5643   -0.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6542   -1.9053    3.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2997   -1.4430    4.1694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0428   -0.2201    3.9143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3340    2.3061   -0.7562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5506    2.0518    0.6049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8838    3.8545   -1.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2406    3.0602   -0.5386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8327    2.7609   -3.3815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2651    0.4229   -4.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3610   -0.7516   -3.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1928   -0.7958   -3.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2947   -1.4672    0.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2031    0.2762    0.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  6
  6  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 26  1  0
 13 14  1  0
 14 15  1  1
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 14 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  6
 26  9  1  0
 24 14  1  0
 24 22  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  5 31  1  0
  7 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
 10 36  1  0
 13 37  1  6
 26 51  1  0
 26 52  1  0
 15 38  1  0
 15 39  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
 20 43  1  0
 20 44  1  0
 21 45  1  0
 21 46  1  0
 22 47  1  6
 25 48  1  0
 25 49  1  0
 25 50  1  0
M  END


  Mrv1652309042201102D          

 26 28  0  0  1  0            999 V2000
    6.4978    5.3916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6774    5.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1924    5.9729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3418    4.5517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5213    4.4655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1858    3.7118    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4321    4.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9394    3.3763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8502    2.9582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2627    2.2437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7107    1.6306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8822    0.8236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570    1.9661    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2425    1.5536    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9070    2.3073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3919    2.9748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0563    3.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2359    3.8147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5413    4.3959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7275    0.8862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425    0.2188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4579    0.4737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7434    0.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4579    1.2987    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1224    2.0524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0432    2.7866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  1  0  0  0
  6  9  1  0  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
 13 14  1  6  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 14 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 22 24  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  1  0  0  0
 13 26  1  0  0  0  0
  9 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0184117

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@](C)(O)C1=CC(=O)[C@@H](C1)[C@@]1(COC(C)=O)CC[C@@H]2O[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O7/c1-11(20)24-9-17(3,23)13-7-14(15(22)8-13)19(10-25-12(2)21)6-5-16-18(19,4)26-16/h8,14,16,23H,5-7,9-10H2,1-4H3/t14-,16+,17+,18+,19+/m1/s1

> <INCHI_KEY>
LTORKLXEGAHTJM-RFZNHBKKSA-N

> <FORMULA>
C19H26O7

> <MOLECULAR_WEIGHT>
366.41

> <EXACT_MASS>
366.167853177

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.62053268292008

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-2-[(4S)-4-[(1R,2R,5S)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate

> <JCHEM_LOGP>
0.39235874833333356

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.990329508608458

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.500207380079125

> <JCHEM_PKA_STRONGEST_BASIC>
-3.405042580300183

> <JCHEM_POLAR_SURFACE_AREA>
102.43

> <JCHEM_REFRACTIVITY>
91.0789

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-[(4S)-4-[(1R,2R,5S)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      12.129  10.064   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.598   9.903   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.693  11.149   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       9.971   8.497   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.440   8.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.813   6.929   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.407   7.555   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.220   6.302   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.187   5.522   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.957   4.188   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.927   3.044   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.247   1.537   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.520   3.670   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.186   2.900   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.560   4.307   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.465   5.553   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.839   6.960   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.307   7.121   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.744   8.206   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.091   1.654   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.186   0.408   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.721   0.884   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.388   1.654   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.721   2.424   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.095   3.831   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.681   5.202   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10   26                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   26                                                  
CONECT   14   13   15   20   24                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   14   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22   24                                                       
CONECT   24   23   22   14   25                                             
CONECT   25   24                                                            
CONECT   26   13    9                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
(2R)-2-[(4S)-4-[(1R,2R,5S)-2-[(Acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetic acid	Generator

Chemical Formula

C₁₉H₂₆O₇

Average Mass

366.4100 Da

Monoisotopic Mass

366.16785 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@](C)(O)C1=CC(=O)[C@@H](C1)[C@@]1(COC(C)=O)CC[C@@H]2O[C@]12C

InChI Identifier

InChI=1S/C19H26O7/c1-11(20)24-9-17(3,23)13-7-14(15(22)8-13)19(10-25-12(2)21)6-5-16-18(19,4)26-16/h8,14,16,23H,5-7,9-10H2,1-4H3/t14-,16+,17+,18+,19+/m1/s1

InChI Key

LTORKLXEGAHTJM-RFZNHBKKSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Siparuna pauciflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Bicyclic monoterpenoids

Alternative Parents

Substituents

Bicyclic monoterpenoid
Dicarboxylic acid or derivatives
Oxane
Tertiary alcohol
Carboxylic acid ester
Ketone
Cyclic ketone
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162975745

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate (NP0184117)

MOL for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)

3D MOL for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)

3D SDF for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)

3D-SDF for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)

PDB for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)

3D PDB for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)

SMILES for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)

INCHI for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)

Structure for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)

3D Structure for NP0184117 ((2r)-2-[(4s)-4-[(1r,2r,5s)-2-[(acetyloxy)methyl]-1-methyl-6-oxabicyclo[3.1.0]hexan-2-yl]-3-oxocyclopent-1-en-1-yl]-2-hydroxypropyl acetate)