NP-MRD: Showing NP-Card for methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate (NP0196350)

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Record Information

Version

2.0

Created at

2022-09-04 14:25:47 UTC

Updated at

2022-09-04 14:25:47 UTC

NP-MRD ID

NP0196350

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate

Description

Methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]Docosane-12,2'-oxiran]-10-ene-1-carboxylate belongs to the class of organic compounds known as furopyrans. These are organic polycyclic compounds containing a furan ring fused to a pyran ring. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate is found in Penicillium chrysogenum. Based on a literature review very few articles have been published on methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]Docosane-12,2'-oxiran]-10-ene-1-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042216252D          

 36 42  0  0  0  0            999 V2000
    2.6019   -2.6559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9988   -2.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1848   -1.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0097   -1.3040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5817   -0.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2851   -1.4960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5798   -2.2666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4701   -1.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1735   -2.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0483   -0.9822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2484   -0.2124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1252    0.5232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4589    1.1058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3308    1.9208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1935    0.7303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2377    1.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9640    1.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6045    0.5050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3226    0.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8638    1.5969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870    1.6514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0879    0.6031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6543    1.2029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4570    1.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0234    1.6122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6932    0.2219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1268   -0.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8159   -0.8316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0498   -1.1993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3241   -0.1873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6756   -0.9337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8535   -0.8649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0303   -0.9193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4744   -0.3097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5704   -1.1291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0634   -0.0844    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
 22 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 18 34  1  0  0  0  0
  5 34  1  0  0  0  0
 34 35  1  0  0  0  0
 15 36  1  0  0  0  0
 11 36  1  0  0  0  0
  5 36  1  0  0  0  0
M  END

     RDKit          3D

 66 72  0  0  0  0  0  0  0  0999 V2000
    3.2073   -1.2224    3.8148 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5199   -0.5170    2.8271 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6604   -0.7068    1.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4879   -1.6015    1.0905 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8768    0.1006    0.4574 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1722    1.4945    0.8682 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6359    1.9165    1.8722 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0781    2.4101    0.1400 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4603    3.7743   -0.1232 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5491    1.9303   -1.0524 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6149    1.1318   -1.6598 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0853    0.6011   -2.9000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2935   -0.5197   -3.1312 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9639   -0.9740   -4.2504 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8946   -1.1020   -1.7970 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4915   -2.4940   -1.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4025   -1.1852   -1.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0222   -1.3303   -0.3501 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3819   -1.8076   -0.1426 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5496   -3.3059    0.1380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6512   -2.8606   -1.1579 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6214   -1.5673   -0.2373 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0965    0.2812    0.2778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9788    1.1012   -0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8961    1.3603   -1.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2078    2.4216    0.6776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7165    0.4668    0.5318 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.4037    1.0082    0.1056 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3971   -0.1505    0.5286 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0778   -0.6808    1.9175 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4998   -0.1490   -0.8607 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6118   -0.4815    4.5484 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1045   -1.7443    3.3846 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5770   -1.9126    4.3939 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9376    2.5956    0.8438 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0616    4.2462    0.7811 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2876    4.4154   -0.5081 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6979    3.6251   -0.9149 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6808    1.6712   -1.8085 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5815   -2.4608   -1.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9565   -3.2025   -1.1274 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3712   -2.9002   -2.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1240   -0.4520   -2.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1447   -2.1829   -2.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6855   -2.1343    0.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5823   -3.8546    0.3397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5705   -2.6110   -0.5930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0490    0.4652   -2.0996 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6805    3.2599    0.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8778    2.4693    0.7789 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2489    1.9334    0.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
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  5  3  1  1
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 36 11  1  0
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 34 35  1  1
 11 10  1  0
 10  8  1  0
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 34  5  1  0
  6  5  1  0
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 34 18  1  0
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  1 37  1  0
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 35 64  1  0
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  8 40  1  1
  9 41  1  0
  9 42  1  0
  9 43  1  0
M  END


  Mrv1652309042216252D          

 36 42  0  0  0  0            999 V2000
    2.6019   -2.6559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9988   -2.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1848   -1.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0097   -1.3040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5817   -0.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2851   -1.4960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5798   -2.2666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4701   -1.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1735   -2.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0483   -0.9822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2484   -0.2124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1252    0.5232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4589    1.1058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3308    1.9208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1935    0.7303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2377    1.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9640    1.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6045    0.5050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3226    0.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8638    1.5969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870    1.6514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0879    0.6031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6543    1.2029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4570    1.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0234    1.6122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0634   -0.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
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 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
 22 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 18 34  1  0  0  0  0
  5 34  1  0  0  0  0
 34 35  1  0  0  0  0
 15 36  1  0  0  0  0
 11 36  1  0  0  0  0
  5 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0196350

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C12C3C(OC(=O)C3(C)CC3C4(CO4)C4=CC(=O)OC(C)(C)C44OC4CC13C)OC(C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H30O10/c1-11-17(28)25(20(30)31-6)16-18(33-11)34-19(29)22(16,4)8-13-23(25,5)9-14-26(35-14)12(24(13)10-32-24)7-15(27)36-21(26,2)3/h7,11,13-14,16,18H,8-10H2,1-6H3

> <INCHI_KEY>
KXRODMCMGHNDAX-UHFFFAOYSA-N

> <FORMULA>
C26H30O10

> <MOLECULAR_WEIGHT>
502.516

> <EXACT_MASS>
502.183897166

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
49.15600171226928

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0^{2,13}.0^{4,6}.0^{6,11}.0^{18,22}]docosane-12,2'-oxiran]-10-ene-1-carboxylate

> <JCHEM_LOGP>
1.9562539809999993

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.821841352256912

> <JCHEM_POLAR_SURFACE_AREA>
130.26

> <JCHEM_REFRACTIVITY>
118.24309999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0^{2,13}.0^{4,6}.0^{6,11}.0^{18,22}]docosane-12,2'-oxiran]-10-ene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.857  -4.958   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       3.731  -3.907   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.078  -2.406   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.618  -2.434   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.953  -1.356   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.399  -2.793   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.949  -4.231   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.878  -3.032   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.324  -4.469   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.090  -1.833   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.464  -0.396   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.234   0.977   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.857   2.064   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.618   3.585   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.228   1.363   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.310   2.901   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.666   1.913   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.862   0.943   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.202   1.701   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.346   2.981   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.882   3.083   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.631   1.126   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.688   2.245   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.186   1.890   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.244   3.009   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      10.627   0.414   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.570  -0.705   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.856  -1.552   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.426  -2.239   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.072  -0.350   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.728  -1.743   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.193  -1.614   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.656  -1.716   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.619  -0.578   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.798  -2.108   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.985  -0.157   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   34   36                                             
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   36                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17   36                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   34                                                  
CONECT   19   18   20   21   22                                             
CONECT   20   19   21                                                       
CONECT   21   20   19                                                       
CONECT   22   19   23   30                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   22   31   32                                             
CONECT   31   30   32                                                       
CONECT   32   31   30   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   18    5   35                                             
CONECT   35   34                                                            
CONECT   36   15   11    5                                                  
MASTER        0    0    0    0    0    0    0    0   36    0   84    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0,.0,.0,.0,]docosane-12,2'-oxiran]-10-ene-1-carboxylic acid	Generator

Chemical Formula

C₂₆H₃₀O₁₀

Average Mass

502.5160 Da

Monoisotopic Mass

502.18390 Da

IUPAC Name

methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0^{2,13}.0^{4,6}.0^{6,11}.0^{18,22}]docosane-12,2'-oxiran]-10-ene-1-carboxylate

Traditional Name

methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0^{2,13}.0^{4,6}.0^{6,11}.0^{18,22}]docosane-12,2'-oxiran]-10-ene-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C12C3C(OC(=O)C3(C)CC3C4(CO4)C4=CC(=O)OC(C)(C)C44OC4CC13C)OC(C)C2=O

InChI Identifier

InChI=1S/C26H30O10/c1-11-17(28)25(20(30)31-6)16-18(33-11)34-19(29)22(16,4)8-13-23(25,5)9-14-26(35-14)12(24(13)10-32-24)7-15(27)36-21(26,2)3/h7,11,13-14,16,18H,8-10H2,1-6H3

InChI Key

KXRODMCMGHNDAX-UHFFFAOYSA-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
Penicillium chrysogenum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furopyrans. These are organic polycyclic compounds containing a furan ring fused to a pyran ring. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Furopyrans

Sub Class

Not Available

Direct Parent

Furopyrans

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Furopyran
Dihydropyranone
Pyran
Oxane
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tetrahydrofuran
Furan
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	1.96	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	130.26 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	118.24 m³·mol⁻¹	ChemAxon
Polarizability	49.16 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	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

162815776

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate (NP0196350)

MOL for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)

3D MOL for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)

3D SDF for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)

3D-SDF for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)

PDB for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)

3D PDB for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)

SMILES for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)

INCHI for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)

Structure for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)

3D Structure for NP0196350 (methyl 2,7,7,15,20-pentamethyl-9,16,21-trioxo-5,8,17,19-tetraoxaspiro[hexacyclo[13.6.1.0²,¹³.0⁴,⁶.0⁶,¹¹.0¹⁸,²²]docosane-12,2'-oxiran]-10-ene-1-carboxylate)