NP-MRD: Showing NP-Card for (-)-17,18-Dehydroclavulone I (NP0082477)

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Record Information

Version

2.0

Created at

2022-04-29 03:31:37 UTC

Updated at

2022-04-29 03:31:37 UTC

NP-MRD ID

NP0082477

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-17,18-Dehydroclavulone I

Description

17,18-Dehydro-clavulone i belongs to the class of organic compounds known as clavulones and derivatives. These are ester derivatives of prostanoids. Thus, 17,18-dehydro-clavulone I is considered to be an eicosanoid. (-)-17,18-Dehydroclavulone I is found in Clavularia viridis. Based on a literature review very few articles have been published on 17,18-dehydro-clavulone i.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292205312D          

 32 32  0  0  1  0            999 V2000
    4.8455    1.0685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1875    0.5707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8295    1.8933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6091    2.1634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1068    1.5054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6349    0.8287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9049    0.0492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7150   -0.1067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9851   -0.8863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4450   -1.5099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6349   -1.3540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0948   -1.9777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2846   -1.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0146   -1.0422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7445   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9344   -2.2895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7150   -2.2895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5252   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0653   -1.8217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7952   -3.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8176    1.9242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8103    2.7492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0922    3.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3814    2.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6633    3.1427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9525    2.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9598    1.8989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2490    1.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8332    1.1144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5351    1.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5105    2.3726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2615    1.1569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  5 21  1  1  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
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END

     RDKit          3D

 64 64  0  0  0  0  0  0  0  0999 V2000
    3.1422    2.5952    1.5566 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7347    1.2450    1.9321 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1069    1.1544    1.4114 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5622    0.2682    0.5498 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7217   -0.7978   -0.0358 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6946   -0.6923   -1.4937 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5905   -0.4850   -2.1705 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2447   -0.3274   -1.5649 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2736   -1.3660   -1.9855 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5313   -2.6893   -1.7271 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7733   -3.5303   -0.7634 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9976   -5.0085   -0.9784 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8310   -3.1424    0.3975 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4303   -1.3754   -3.5051 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3856   -1.0321   -4.1487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6450   -0.7181   -3.1765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8384   -0.3456   -3.4556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1013   -0.8958   -1.8300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8347   -0.5841   -0.7681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2999   -0.6734    0.5611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0873   -0.3590    1.5717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4702    0.0814    1.5477 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6945    1.5064    1.1007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2085    1.7508    1.1755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5323    3.1352    0.7267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1055    3.5587   -0.4067 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2867    4.0301    1.4741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5563    5.3178    1.0041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2314   -0.7527    0.7058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3119   -1.4352    1.2046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1615   -2.3345    0.3624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6859   -1.3618    2.4274 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9156    3.3961    1.5134 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5972    2.4839    0.6198 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4016    2.9148    2.3261 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0440    0.4676    1.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7843    1.2410    3.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8048    1.9269    1.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6271    0.3335    0.2569 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3081   -1.7604    0.1750 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7483   -0.8492    0.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6310   -0.7885   -2.0281 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850   -0.4111   -3.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2667   -0.0043   -0.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8524    0.6293   -2.0990 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3435   -5.5059   -0.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7898   -5.3277   -2.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0736   -5.2064   -0.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3684   -1.6673   -3.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2034   -0.9621   -5.2379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8505   -0.2598   -0.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7208   -0.9735    0.7244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6083   -0.4461    2.5611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9396    0.0270    2.5724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3727    1.7459    0.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2661    2.2085    1.8792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5646    1.6772    2.2422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7729    1.0004    0.5894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5852    5.8960    1.0062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9178    5.3369   -0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2999    5.8469    1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1504   -2.4986    0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2348   -1.9184   -0.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5719   -3.2891    0.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
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  9 10  1  1
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 11 12  1  0
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  9 14  1  0
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 16 17  2  0
 16 18  1  0
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 20 21  2  0
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 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
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 29 30  1  0
 30 31  1  0
 30 32  2  0
 18  9  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
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 14 49  1  0
 15 50  1  0
 19 51  1  0
 20 52  1  0
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 22 54  1  1
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 28 59  1  0
 28 60  1  0
 28 61  1  0
 31 62  1  0
 31 63  1  0
 31 64  1  0
M  END


  Mrv1652304292205312D          

 32 32  0  0  1  0            999 V2000
    4.8455    1.0685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1875    0.5707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8295    1.8933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6091    2.1634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1068    1.5054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6349    0.8287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9049    0.0492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7150   -0.1067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9851   -0.8863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4450   -1.5099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6349   -1.3540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0948   -1.9777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2846   -1.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0146   -1.0422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7445   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9344   -2.2895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7150   -2.2895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5252   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0653   -1.8217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7952   -3.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8176    1.9242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8103    2.7492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0922    3.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3814    2.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6633    3.1427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9525    2.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9598    1.8989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2490    1.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8332    1.1144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5351    1.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5105    2.3726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2615    1.1569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
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 13 14  2  0  0  0  0
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 10 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  5 21  1  1  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
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
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  5 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0082477

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC\C=C/C\C=C/C[C@]1(OC(C)=O)C=CC(=O)\C1=C\C=C/[C@@H](CCC(=O)OC)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O7/c1-5-6-7-8-9-10-17-25(32-20(3)27)18-16-23(28)22(25)13-11-12-21(31-19(2)26)14-15-24(29)30-4/h6-7,9-13,16,18,21H,5,8,14-15,17H2,1-4H3/b7-6-,10-9-,12-11-,22-13-/t21-,25-/m0/s1

> <INCHI_KEY>
VNMUCAJMMSZIGB-PMPMEWTASA-N

> <FORMULA>
C25H32O7

> <MOLECULAR_WEIGHT>
444.524

> <EXACT_MASS>
444.21480337

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
47.52818168970391

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (4R,5Z)-4-(acetyloxy)-7-[(1E,2S)-2-(acetyloxy)-2-[(2Z,5Z)-octa-2,5-dien-1-yl]-5-oxocyclopent-3-en-1-ylidene]hept-5-enoate

> <ALOGPS_LOGP>
4.47

> <JCHEM_LOGP>
3.8891695793333323

> <ALOGPS_LOGS>
-5.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.500636249562725

> <JCHEM_POLAR_SURFACE_AREA>
95.97000000000003

> <JCHEM_REFRACTIVITY>
125.52860000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.39e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
17,18-dehydro-clavulone I

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       9.045   1.994   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.817   1.065   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.015   3.534   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.470   4.038   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.399   2.810   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.518   1.547   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.022   0.092   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.535  -0.199   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.039  -1.654   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.031  -2.819   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.518  -2.527   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.510  -3.692   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.998  -3.401   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.494  -1.945   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       6.990  -4.565   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.478  -4.274   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      12.535  -4.274   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      14.047  -4.565   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      15.055  -3.401   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      14.551  -6.020   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.726   3.592   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.713   5.132   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.372   5.890   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.045   5.108   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.705   5.866   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.378   5.085   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.392   3.545   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.065   2.763   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      12.755   2.080   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      14.066   2.890   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      14.020   4.429   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      15.422   2.160   0.000  0.00  0.00           C+0
CONECT    1    2    3    6                                                  
CONECT    2    1                                                            
CONECT    3    1    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   21   29                                             
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15                                                            
CONECT   17   10   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21    5   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29    5   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₂O₇

Average Mass

444.5240 Da

Monoisotopic Mass

444.21480 Da

IUPAC Name

methyl (4R,5Z)-4-(acetyloxy)-7-[(1E,2S)-2-(acetyloxy)-2-[(2Z,5Z)-octa-2,5-dien-1-yl]-5-oxocyclopent-3-en-1-ylidene]hept-5-enoate

Traditional Name

17,18-dehydro-clavulone I

CAS Registry Number

Not Available

SMILES

CC\C=C/C\C=C/C[C@]1(OC(C)=O)C=CC(=O)\C1=C\C=C/[C@@H](CCC(=O)OC)OC(C)=O

InChI Identifier

InChI=1S/C25H32O7/c1-5-6-7-8-9-10-17-25(32-20(3)27)18-16-23(28)22(25)13-11-12-21(31-19(2)26)14-15-24(29)30-4/h6-7,9-13,16,18,21H,5,8,14-15,17H2,1-4H3/b7-6-,10-9-,12-11-,22-13-/t21-,25-/m0/s1

InChI Key

VNMUCAJMMSZIGB-PMPMEWTASA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Clavularia viridis	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as clavulones and derivatives. These are ester derivatives of prostanoids.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Clavulones and derivatives

Alternative Parents

Substituents

Clavulone
Fatty alcohol ester
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acid methyl ester
Methyl ester
Carboxylic acid ester
Ketone
Cyclic ketone
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Clavulones and derivatives (LMFA03120018 )

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	4.47	ALOGPS
logP	3.89	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	95.97 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	125.53 m³·mol⁻¹	ChemAxon
Polarizability	47.53 Å³	ChemAxon
Number of Rings	1	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

4446353

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5283232

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (-)-17,18-Dehydroclavulone I (NP0082477)

MOL for NP0082477 ((-)-17,18-Dehydroclavulone I)

3D MOL for NP0082477 ((-)-17,18-Dehydroclavulone I)

3D SDF for NP0082477 ((-)-17,18-Dehydroclavulone I)

3D-SDF for NP0082477 ((-)-17,18-Dehydroclavulone I)

PDB for NP0082477 ((-)-17,18-Dehydroclavulone I)

3D PDB for NP0082477 ((-)-17,18-Dehydroclavulone I)

SMILES for NP0082477 ((-)-17,18-Dehydroclavulone I)

INCHI for NP0082477 ((-)-17,18-Dehydroclavulone I)

Structure for NP0082477 ((-)-17,18-Dehydroclavulone I)

3D Structure for NP0082477 ((-)-17,18-Dehydroclavulone I)