NP-MRD: Showing NP-Card for [(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate (NP0267525)

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Record Information

Version

2.0

Created at

2022-09-08 12:19:56 UTC

Updated at

2022-09-08 12:19:56 UTC

NP-MRD ID

NP0267525

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate

Description

Hydroxyoligosporon belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. [(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate was first documented in 1995 (PMID: 7797441). Based on a literature review very few articles have been published on Hydroxyoligosporon.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082214192D          

 31 32  0  0  1  0            999 V2000
    4.2868    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0164    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914    0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914   -4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.8908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -5.6052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.3197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -7.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914   -7.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.7487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -7.7487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 10 28  1  0  0  0  0
 29 28  1  1  0  0  0
 10 29  1  0  0  0  0
 29 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  2  0  0  0  0
M  END

     RDKit          3D

 63 64  0  0  0  0  0  0  0  0999 V2000
    8.9569    0.2525    3.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2919   -0.1210    2.2845 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5343   -1.1198    2.2255 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4860    0.6189    1.1328 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8461    0.2470   -0.0545 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3622    0.2724    0.1344 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6192   -0.8202   -0.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1519   -0.8456    0.1429 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6431   -1.8321   -0.7034 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5003    0.4765   -0.0727 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4045    0.5063   -1.1176 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8753   -0.2636   -2.1860 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1117    0.0617   -0.5990 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0474    0.0834   -1.3817 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1032    0.5468   -2.7892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2437   -0.3750   -0.8196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3197   -0.3658   -1.5738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6372   -0.8118   -1.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6632   -0.7789   -1.8637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4612   -0.2934   -3.2624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0095   -1.1569   -1.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0970   -1.4818    0.0161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8531   -0.3654    0.9290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8585   -0.0803    1.8019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1098   -0.8696    1.8031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6951    1.0404    2.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4549    1.6514    2.6036 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2684    1.1920    1.1247 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007    1.6585    0.2380 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6507    1.4882    0.5095 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3080    2.4112    1.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6569   -0.5684    3.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5009    1.2074    3.4541 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1642    0.3753    4.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1165    1.0262   -0.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1394   -0.7212   -0.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1236   -1.7222   -0.3069 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9279   -1.2194    1.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8290   -2.7438   -0.3650 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3090    1.5485   -1.4816 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2513   -1.0158   -2.3865 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9727   -0.2981    0.4300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1403   -0.2921   -3.4976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7280    1.2948   -2.9562 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0781    0.9856   -2.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3349   -0.7200    0.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2320   -0.0224   -2.5892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6657   -1.1744   -0.0562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6647   -0.9089   -3.7346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3759   -0.4804   -3.8489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2354    0.7900   -3.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6791   -0.2702   -1.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3811   -2.0072   -2.0644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0667   -1.9945    0.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3319   -2.2813    0.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9866    0.2567    0.9831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5836   -0.7811    0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9272   -1.9590    2.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7789   -0.4638    2.5875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5212    1.7758    2.6447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7645    0.6129    3.7965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6029    2.6318    2.6931 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9720    2.6097   -0.2851 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  2  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 28  1  1
 28 29  1  0
 29 30  1  0
 30 31  2  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 30  6  1  0
 29 10  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  5 35  1  0
  5 36  1  0
  7 37  1  0
  8 38  1  1
  9 39  1  0
 29 63  1  6
 11 40  1  6
 12 41  1  0
 13 42  1  0
 15 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 17 47  1  0
 18 48  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  0
 22 55  1  0
 23 56  1  0
 25 57  1  0
 25 58  1  0
 25 59  1  0
 26 60  1  0
 26 61  1  0
 27 62  1  0
M  END


  Mrv1652309082214192D          

 31 32  0  0  1  0            999 V2000
    4.2868    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0164    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914    0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914   -4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.8908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -5.6052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.3197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -7.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914   -7.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.7487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -7.7487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 10 28  1  0  0  0  0
 29 28  1  1  0  0  0
 10 29  1  0  0  0  0
 29 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0267525

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1=C[C@H](O)[C@]2(O[C@H]2C1=O)C(O)\C=C(/C)\C=C\C=C(/C)CC\C=C(/C)CO

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O7/c1-15(8-6-10-17(3)13-25)7-5-9-16(2)11-20(27)24-21(28)12-19(14-30-18(4)26)22(29)23(24)31-24/h5,7,9-12,20-21,23,25,27-28H,6,8,13-14H2,1-4H3/b9-5+,15-7+,16-11+,17-10+/t20?,21-,23-,24+/m0/s1

> <INCHI_KEY>
LHMNMGQVKTZDNX-RXBIHYLLSA-N

> <FORMULA>
C24H32O7

> <MOLECULAR_WEIGHT>
432.513

> <EXACT_MASS>
432.21480337

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
47.309787377038965

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,5S,6R)-6-[(2E,4E,6E,10E)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate

> <JCHEM_LOGP>
1.670075992999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.78938152136406

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.023252255189181

> <JCHEM_PKA_STRONGEST_BASIC>
-2.079706816326345

> <JCHEM_POLAR_SURFACE_AREA>
116.59

> <JCHEM_REFRACTIVITY>
120.64189999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,5S,6R)-6-[(2E,4E,6E,10E)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       8.002   7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.336   5.390   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.668   5.390   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001   0.770   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.897   0.206   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.357   0.206   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.667  -1.127   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.897  -2.461   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.357  -2.461   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667  -3.795   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.897  -5.128   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -6.462   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.897  -7.796   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.357  -7.796   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667  -9.129   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.897 -10.463   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667 -11.797   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.897 -13.130   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.357 -13.130   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667 -14.464   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.207 -14.464   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.001   5.390   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                                                       
CONECT    6    5    7   30                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   28   29                                             
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   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                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26                                                            
CONECT   28   10   29                                                       
CONECT   29   28   10   30                                                  
CONECT   30   29    6   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₇

Average Mass

432.5130 Da

Monoisotopic Mass

432.21480 Da

IUPAC Name

[(1R,5S,6R)-6-[(2E,4E,6E,10E)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate

Traditional Name

[(1R,5S,6R)-6-[(2E,4E,6E,10E)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1=C[C@H](O)[C@]2(O[C@H]2C1=O)C(O)\C=C(/C)\C=C\C=C(/C)CC\C=C(/C)CO

InChI Identifier

InChI=1S/C24H32O7/c1-15(8-6-10-17(3)13-25)7-5-9-16(2)11-20(27)24-21(28)12-19(14-30-18(4)26)22(29)23(24)31-24/h5,7,9-12,20-21,23,25,27-28H,6,8,13-14H2,1-4H3/b9-5+,15-7+,16-11+,17-10+/t20?,21-,23-,24+/m0/s1

InChI Key

LHMNMGQVKTZDNX-RXBIHYLLSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Farsesane sesquiterpenoid
Sesquiterpenoid
Long chain fatty alcohol
Fatty alcohol
Cyclohexenone
Fatty acyl
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
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	1.67	ChemAxon
pKa (Strongest Acidic)	13.02	ChemAxon
pKa (Strongest Basic)	-2.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	116.59 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	120.64 m³·mol⁻¹	ChemAxon
Polarizability	47.31 Å³	ChemAxon
Number of Rings	2	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

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

101921797

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Anderson MG, Jarman TB, Rickards RW: Structures and absolute configurations of antibiotics of the oligosporon group from the nematode-trapping fungus Arthrobotrys oligospora. J Antibiot (Tokyo). 1995 May;48(5):391-8. doi: 10.7164/antibiotics.48.391. [PubMed:7797441 ]
LOTUS database [Link]

Showing NP-Card for [(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate (NP0267525)

MOL for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)

3D MOL for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)

3D SDF for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)

3D-SDF for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)

PDB for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)

3D PDB for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)

SMILES for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)

INCHI for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)

Structure for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)

3D Structure for NP0267525 ([(1r,5s,6r)-6-[(2e,4e,6e,10e)-1,12-dihydroxy-3,7,11-trimethyldodeca-2,4,6,10-tetraen-1-yl]-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate)