NP-MRD: Showing NP-Card for (4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione (NP0246616)

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Record Information

Version

2.0

Created at

2022-09-07 08:09:07 UTC

Updated at

2022-09-07 08:09:07 UTC

NP-MRD ID

NP0246616

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione

Description

Ushikulide B belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. Based on a literature review very few articles have been published on Ushikulide B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072210092D          

 50 52  0  0  0  0            999 V2000
   10.2694   -1.4120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4805   -1.6532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8771   -1.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0628   -0.2866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0882   -1.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4848   -0.7689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6959   -1.0101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0925   -0.4474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2782    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0671    0.5976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6705    0.0349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4594    0.2761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9069   -1.2512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1179   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9323   -2.2962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1433   -2.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5400   -1.9747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9577   -3.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1687   -3.5824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5654   -3.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7764   -3.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7510   -2.2159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2476   -1.5570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1477   -1.6532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3587   -1.8943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3333   -0.8493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1223   -0.6082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7300   -0.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9156    0.5172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1267    0.2761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3123    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8629    0.3880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5529    1.4023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4980    1.8837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2869    2.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4726    2.9287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2615    3.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8649    2.6072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6792    1.8034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4682    2.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6538    2.8484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0505    3.4110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4428    3.0895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2825    1.2407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0715    1.4818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0969    0.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7002   -0.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4892    0.1153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5146   -0.9297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7256   -1.1709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 13  1  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
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  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
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 38 37  1  4  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 39 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
  8 48  1  0  0  0  0
 47 49  1  0  0  0  0
 14 49  1  0  0  0  0
 49 50  1  0  0  0  0
M  END

     RDKit          3D

118120  0  0  0  0  0  0  0  0999 V2000
    7.2499   -3.5405   -0.2349 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7440   -3.4880   -0.0488 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0572   -3.0983   -1.3278 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3583   -4.0304   -2.2961 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4690   -1.7309   -1.8084 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1345   -0.6583   -0.7874 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7786   -0.6115   -0.5291 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4154    0.1623    0.5656 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6195    0.9965    0.9703 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2776    1.6783   -0.2080 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5013    0.7243   -1.3441 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8864    0.7413   -1.8991 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0412   -0.7991    1.6604 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5605   -1.1000    1.5448 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3015   -1.6004    0.2848 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2718   -1.3527   -0.5738 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.1301   -1.1641   -0.2657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7418   -1.9868    0.5751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7090   -3.4346    0.4286 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3744   -4.0689    0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6966   -3.9332   -0.6366 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1266   -5.1049   -1.1549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0269   -4.3050   -0.0778 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7294   -5.2277   -1.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9178   -3.1799    0.3153 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9497   -3.7574    1.0977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5658   -2.4466   -0.8056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0027   -1.1016   -1.1130 C   0  0  1  0  0  0  0  0  0  0  0  0
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    1.2735    3.5107   -0.7660 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.5334   -4.3769   -0.8916 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4535    2.5877    2.2139 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4836    1.2031    0.0181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2077    0.0951    1.8594 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4853   -0.2228    3.8706 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4328    1.1928    3.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1393    1.3599    3.2528 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
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 37100  1  0
 37101  1  0
 38102  1  0
 40103  1  0
 40104  1  0
 41105  1  0
 42106  1  0
 42107  1  0
 42108  1  0
 43109  1  0
 43110  1  0
 43111  1  0
 46112  1  0
 46113  1  0
 47114  1  6
 49115  1  1
 50116  1  0
 50117  1  0
 50118  1  0
M  END


  Mrv1652309072210092D          

 50 52  0  0  0  0            999 V2000
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    4.9323   -2.2962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1433   -2.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5400   -1.9747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9577   -3.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1687   -3.5824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7764   -3.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7510   -2.2159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2476   -1.5570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1477   -1.6532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3587   -1.8943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3333   -0.8493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1223   -0.6082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7300   -0.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9156    0.5172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1267    0.2761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3123    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8629    0.3880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5529    1.4023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4980    1.8837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2869    2.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4726    2.9287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2615    3.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8649    2.6072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6792    1.8034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4682    2.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6538    2.8484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0505    3.4110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4428    3.0895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2825    1.2407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0715    1.4818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0969    0.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7002   -0.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4892    0.1153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5146   -0.9297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7256   -1.1709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 13  1  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
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  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
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 38 37  1  4  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 39 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
  8 48  1  0  0  0  0
 47 49  1  0  0  0  0
 14 49  1  0  0  0  0
 49 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0246616

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(O)CC1OC2(CCC1C)CC1OC(=O)\C=C/C(C)C(O)C(C)C(O)CC(O)C(C)(O)CCCCC=C(CC(C)C)C(=O)CC(O2)C1C

> <INCHI_IDENTIFIER>
InChI=1S/C40H68O10/c1-9-30(41)20-33-25(4)16-18-40(49-33)23-35-28(7)34(50-40)21-32(43)29(19-24(2)3)13-11-10-12-17-39(8,47)36(44)22-31(42)27(6)38(46)26(5)14-15-37(45)48-35/h13-15,24-28,30-31,33-36,38,41-42,44,46-47H,9-12,16-23H2,1-8H3/b15-14-,29-13?

> <INCHI_KEY>
SDCSOFPQBXHXPZ-ZWHAKWGUSA-N

> <FORMULA>
C40H68O10

> <MOLECULAR_WEIGHT>
708.974

> <EXACT_MASS>
708.48124839

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
118

> <JCHEM_AVERAGE_POLARIZABILITY>
80.71996254178956

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4Z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione

> <JCHEM_LOGP>
5.918873446000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.328287667602304

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.59508459569065

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7174031331997375

> <JCHEM_POLAR_SURFACE_AREA>
162.98

> <JCHEM_REFRACTIVITY>
194.44570000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4Z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      19.170  -2.636   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.697  -3.086   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.571  -2.036   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      16.917  -0.535   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      15.098  -2.486   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.972  -1.435   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      12.499  -1.886   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      11.373  -0.835   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.719   0.665   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.192   1.116   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.318   0.065   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.791   0.515   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.026  -2.336   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.553  -2.786   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.207  -4.286   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.734  -4.736   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.608  -3.686   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.388  -6.237   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.915  -6.687   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.789  -5.637   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.316  -6.087   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.135  -4.136   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.062  -2.906   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.009  -3.086   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.536  -3.536   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.356  -1.585   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.828  -1.135   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.229  -0.535   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.576   0.965   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.103   0.515   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.450   2.016   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.611   0.724   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       1.032   2.618   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       2.796   3.516   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.269   3.966   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.615   5.467   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.088   5.917   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.214   4.867   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.868   3.366   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.341   3.816   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       8.687   5.317   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       7.561   6.367   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      10.160   5.767   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.994   2.316   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       9.467   2.766   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       7.648   0.815   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.774  -0.235   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      10.247   0.215   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       8.427  -1.735   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       6.955  -2.186   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13   48                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    6   12                                                  
CONECT   12   11                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15   49                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44   39   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47    8                                                       
CONECT   49   47   14   50                                                  
CONECT   50   49                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₆₈O₁₀

Average Mass

708.9740 Da

Monoisotopic Mass

708.48125 Da

IUPAC Name

(4Z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione

Traditional Name

(4Z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione

CAS Registry Number

Not Available

SMILES

CCC(O)CC1OC2(CCC1C)CC1OC(=O)\C=C/C(C)C(O)C(C)C(O)CC(O)C(C)(O)CCCCC=C(CC(C)C)C(=O)CC(O2)C1C

InChI Identifier

InChI=1S/C40H68O10/c1-9-30(41)20-33-25(4)16-18-40(49-33)23-35-28(7)34(50-40)21-32(43)29(19-24(2)3)13-11-10-12-17-39(8,47)36(44)22-31(42)27(6)38(46)26(5)14-15-37(45)48-35/h13-15,24-28,30-31,33-36,38,41-42,44,46-47H,9-12,16-23H2,1-8H3/b15-14-,29-13?

InChI Key

SDCSOFPQBXHXPZ-ZWHAKWGUSA-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 macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Ketal
Oxane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Cyclic ketone
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	5.92	ChemAxon
pKa (Strongest Acidic)	13.6	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	162.98 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	194.45 m³·mol⁻¹	ChemAxon
Polarizability	80.72 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

139587397

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione (NP0246616)

MOL for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)

3D MOL for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)

3D SDF for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)

3D-SDF for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)

PDB for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)

3D PDB for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)

SMILES for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)

INCHI for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)

Structure for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)

3D Structure for NP0246616 ((4z)-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,25-pentamethyl-18-(2-methylpropyl)-2,22-dioxaspiro[bicyclo[19.3.1]pentacosane-23,2'-oxane]-4,17-diene-3,19-dione)