NP-MRD: Showing NP-Card for (2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate (NP0300569)

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Record Information

Version

2.0

Created at

2022-09-10 13:01:42 UTC

Updated at

2022-09-10 13:01:42 UTC

NP-MRD ID

NP0300569

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate

Description

Hydroperoxyacetoxycrenulide belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. (2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate is found in Dictyota dichotoma. Based on a literature review very few articles have been published on Hydroperoxyacetoxycrenulide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102215022D          

 28 30  0  0  1  0            999 V2000
    3.6204    4.5975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8448    3.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6445    3.6010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2694    3.2124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4938    2.4185    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3131    2.3219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8242    1.6743    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6181    1.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7277    0.8550    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8465    0.0386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0800    0.3439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2607    0.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7496    1.0880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758    0.8021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0086   -0.0223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8027   -0.2458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0887   -1.0196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8461    1.9074    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1261    2.3101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4173    1.8879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1149    3.1350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3949    3.5377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3836    4.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6636    4.7654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0663    5.4854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2609    4.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0564    5.1681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7652    4.7459    0.0000 O   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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 11 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
 13 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
   -0.4662    4.5426   -1.0291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1123    3.1985   -1.2167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5414    2.8329   -2.3527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2695    2.3088   -0.1830 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8703    1.0320   -0.3057 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0000    0.8445    0.6286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1049   -0.0437    0.1062 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2179   -0.0245   -1.4056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1887   -1.3906    0.7113 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3812   -1.8675    1.8344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2063   -2.4047    0.4391 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0840   -2.1316   -0.4158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0772   -1.3080   -0.5585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0465   -1.9950   -1.4194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8576   -2.7250   -2.3260 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9603   -3.0734   -1.5683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7377   -4.0477   -1.8272 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7131    0.0486   -0.1327 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0195    0.1731    1.1643 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5973    1.5576    1.4244 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0704   -0.8126    1.4450 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2870   -0.6170    0.6184 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4834   -0.3683    1.1729 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6771   -0.1787    0.3059 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2947   -1.5135   -0.0424 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2391    0.4759   -0.9885 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5952    0.6762    0.9208 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6347    0.8251    0.1368 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2764    5.2054   -0.6261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0666    4.9400   -1.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2925    4.4895   -0.2013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1572    0.9509   -1.3786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3673    1.8981    0.8513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7219    0.4618    1.6082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0480    0.5186    0.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5368   -0.6692   -1.9344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1594    1.0097   -1.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2572   -0.4044   -1.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2679   -1.7667    0.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8925   -2.5113    2.6203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4765   -1.4486    2.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -3.4872    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5483   -1.2242   -1.9732 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5507   -2.6855   -0.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0245    0.4462   -0.9024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7912    0.1171    1.9996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1319    2.2558    1.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9364    1.9367    0.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5165    1.4768    2.0450 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3824   -0.6396    2.5148 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7187   -1.8667    1.4268 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2609   -0.6616   -0.4391 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5718   -0.3071    2.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2555   -1.7270   -1.1287 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3788   -1.5236    0.2566 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7240   -2.3246    0.4687 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4148    1.2194   -0.7947 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8953   -0.3061   -1.7033 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993    0.9823   -1.4930 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1283    1.6311    0.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 24 27  1  0
 27 28  1  0
 19 18  1  0
 18  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 13 18  1  0
 11  9  1  0
 16 12  1  0
 20 47  1  0
 20 48  1  0
 20 49  1  0
 19 46  1  1
 21 50  1  0
 21 51  1  0
 22 52  1  0
 23 53  1  0
 25 54  1  0
 25 55  1  0
 25 56  1  0
 26 57  1  0
 26 58  1  0
 26 59  1  0
 28 60  1  0
 18 45  1  6
  5 32  1  6
  6 33  1  0
  6 34  1  0
  7 35  1  1
  8 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  1
 10 40  1  0
 10 41  1  0
 11 42  1  1
 14 43  1  0
 14 44  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
M  END


  Mrv1652309102215022D          

 28 30  0  0  1  0            999 V2000
    3.6204    4.5975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8448    3.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6445    3.6010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2694    3.2124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4938    2.4185    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3131    2.3219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8242    1.6743    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6181    1.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7277    0.8550    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8465    0.0386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0800    0.3439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2607    0.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7496    1.0880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758    0.8021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0086   -0.0223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8027   -0.2458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0887   -1.0196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8461    1.9074    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1261    2.3101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4173    1.8879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1149    3.1350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3949    3.5377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3836    4.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6636    4.7654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0663    5.4854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2609    4.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0564    5.1681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7652    4.7459    0.0000 O   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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 11 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
 13 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0300569

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](C\C=C\C(C)(C)OO)[C@@H]1[C@@H](C[C@@H](C)[C@@H]2C[C@@H]2C2=C1COC2=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O6/c1-12(7-6-8-22(4,5)28-25)19-17-11-26-21(24)20(17)16-10-15(16)13(2)9-18(19)27-14(3)23/h6,8,12-13,15-16,18-19,25H,7,9-11H2,1-5H3/b8-6+/t12-,13-,15+,16+,18-,19+/m1/s1

> <INCHI_KEY>
SDGDVGLXQFITGK-LSEVXLOGSA-N

> <FORMULA>
C22H32O6

> <MOLECULAR_WEIGHT>
392.492

> <EXACT_MASS>
392.21988875

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
42.61162597629901

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,4S,5R,7R,8S)-8-[(2R,4E)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0^{2,4}]dodec-1(9)-en-7-yl acetate

> <JCHEM_LOGP>
3.431306551333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.046002552247987

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.680047674401438

> <JCHEM_PKA_STRONGEST_BASIC>
-4.242182664608806

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
105.2746

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4S,5R,7R,8S)-8-[(2R,4E)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0^{2,4}]dodec-1(9)-en-7-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       6.758   8.582   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.177   7.100   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.670   6.722   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.103   5.996   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.522   4.514   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.051   4.334   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.005   3.125   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.487   3.544   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.825   1.596   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.047   0.072   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.616   0.642   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.087   0.822   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.133   2.031   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.688   1.497   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.749  -0.042   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.232  -0.459   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.766  -1.903   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.313   3.560   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.969   4.312   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.646   3.524   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.948   5.852   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.604   6.604   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.583   8.144   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.239   8.895   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.990  10.239   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.487   7.551   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.105   9.647   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -1.428   8.859   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   18                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9   11                                                       
CONECT   11   10    9   12                                                  
CONECT   12   11   13   16                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   12   17                                                  
CONECT   17   16                                                            
CONECT   18   13    5   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   24   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₂O₆

Average Mass

392.4920 Da

Monoisotopic Mass

392.21989 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H](C\C=C\C(C)(C)OO)[C@@H]1[C@@H](C[C@@H](C)[C@@H]2C[C@@H]2C2=C1COC2=O)OC(C)=O

InChI Identifier

InChI=1S/C22H32O6/c1-12(7-6-8-22(4,5)28-25)19-17-11-26-21(24)20(17)16-10-15(16)13(2)9-18(19)27-14(3)23/h6,8,12-13,15-16,18-19,25H,7,9-11H2,1-5H3/b8-6+/t12-,13-,15+,16+,18-,19+/m1/s1

InChI Key

SDGDVGLXQFITGK-LSEVXLOGSA-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
Dictyota dichotoma	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

2-furanone
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Hydroperoxide
Carboxylic acid derivative
Alkyl hydroperoxide
Oxacycle
Peroxol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organooxygen 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

27024286

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102418759

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate (NP0300569)

MOL for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)

3D MOL for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)

3D SDF for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)

3D-SDF for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)

PDB for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)

3D PDB for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)

SMILES for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)

INCHI for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)

Structure for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)

3D Structure for NP0300569 ((2s,4s,5r,7r,8s)-8-[(2r,4e)-6-hydroperoxy-6-methylhept-4-en-2-yl]-5-methyl-12-oxo-11-oxatricyclo[7.3.0.0²,⁴]dodec-1(9)-en-7-yl acetate)