NP-MRD: Showing NP-Card for 1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one (NP0066443)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 10:41:50 UTC

Updated at

2022-04-28 10:41:50 UTC

NP-MRD ID

NP0066443

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one

Description

(1S,17R)-7,11-dihydroxy-17-(2-hydroxypropan-2-yl)-13-methyl-6-(3-methylbut-2-en-1-yl)-2,15-dioxatetracyclo[8.7.1.0³,⁸.0¹⁴,¹⁸]Octadeca-3(8),4,6,10,12,14(18)-hexaen-9-one belongs to the class of organic compounds known as dibenzoxepines. Dibenzoxepines are compounds containing a dibenzoxepine moiety, which consists of two benzene connected by an oxazepine ring. 1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one is found in Aspergillus rugulosus and Aspergillus rugulosus A.R.M. 325. Based on a literature review very few articles have been published on (1S,17R)-7,11-dihydroxy-17-(2-hydroxypropan-2-yl)-13-methyl-6-(3-methylbut-2-en-1-yl)-2,15-dioxatetracyclo[8.7.1.0³,⁸.0¹⁴,¹⁸]Octadeca-3(8),4,6,10,12,14(18)-hexaen-9-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282212422D          

 31 34  0  0  1  0            999 V2000
    1.5028    0.6557    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2461    1.0136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9894    0.6557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1730   -0.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6586   -0.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0166   -1.5370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8336   -0.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3192   -0.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5309   -0.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3473   -1.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9521   -1.7573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7404   -1.5141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3714   -2.0457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4410   -1.4393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0739    0.1693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1097    0.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8981    1.2168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0816    2.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2652    2.8254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8859    1.8376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2773    2.2047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9613   -0.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5661    0.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    0.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5942    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3545   -0.0738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9592    0.4873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7476    0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3523    0.8053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9312   -0.5602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1449   -1.1961    0.0000 O   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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  1  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 10 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  1 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
  4 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
  3 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 22 31  1  0  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
    6.6908   -1.1044    1.4784 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0214   -0.7127    0.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6511    0.4287   -0.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9934   -1.4162   -0.2247 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2503   -1.1341   -1.4792 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8034   -1.0896   -1.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9826   -2.1871   -1.4574 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6536   -2.0911   -1.1260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1154   -0.9845   -0.5247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9172    0.0787   -0.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2804    0.0258   -0.5547 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    1.1629   -0.2161 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5358    1.3481    0.4125 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4284    1.9117    1.0410 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8249    1.9154    0.3216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7329    3.2691    0.6623 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3714    3.9643    0.9793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9179    4.0341    0.6839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0914    3.4204    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3438    4.2725    0.4012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1555    2.0919    0.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0009    1.2810    0.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2777   -0.1167   -0.4002 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2507   -1.0379   -0.2507 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5003   -0.6227    0.3306 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7736   -2.0664    0.1420 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6564   -2.9710    0.6237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0897   -2.4679   -1.2704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8989   -2.4181    0.9211 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7107    0.2066    0.0830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3689    1.5085   -0.2705 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6129   -1.6510    1.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9616   -0.1970    2.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9917   -1.7197    2.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4730    0.3469   -1.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3240    1.4126   -0.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7622    0.3597   -0.3755 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6740   -2.2604    0.4177 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4768   -1.8783   -2.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5329   -0.1040   -1.8236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4653   -3.0213   -1.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0299   -2.9343   -1.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9594    1.2486   -0.4004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2841    3.8772    1.0661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8649    5.0999    0.9506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1387    5.2216    0.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1130    3.7416    1.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6642    4.4835   -0.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6251   -0.0322   -1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2423   -0.4930    1.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0707   -2.4483    1.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9900   -3.3101   -0.1663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0699   -3.9093    1.0855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3046   -3.5773   -1.2342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9793   -2.0110   -1.7056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2431   -2.3610   -1.9668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7118   -2.3579    0.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3116    0.2463    1.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3173   -0.2714   -0.7211 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6 11  2  0
 11 12  1  0
 11 10  1  0
 10  9  2  0
  9 24  1  0
 24 23  1  0
 23 25  1  0
 25 30  1  0
 30 31  1  0
 31 21  1  0
 21 19  1  0
 19 20  1  0
 19 18  2  0
 18 16  1  0
 16 17  1  0
 16 15  2  0
 15 22  1  0
 15 13  1  0
 13 14  2  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 26 29  1  1
  9  8  1  0
  8  7  2  0
  7  6  1  0
 13 10  1  0
 22 23  1  0
 22 21  2  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
 12 43  1  0
 23 49  1  6
 25 50  1  1
 30 58  1  0
 30 59  1  0
 20 46  1  0
 20 47  1  0
 20 48  1  0
 18 45  1  0
 17 44  1  0
 27 51  1  0
 27 52  1  0
 27 53  1  0
 28 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
  8 42  1  0
  7 41  1  0
M  END


  Mrv1652304282212422D          

 31 34  0  0  1  0            999 V2000
    1.5028    0.6557    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2461    1.0136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9894    0.6557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1730   -0.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6586   -0.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0166   -1.5370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8336   -0.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3192   -0.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5309   -0.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3473   -1.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9521   -1.7573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7404   -1.5141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3714   -2.0457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4410   -1.4393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0739    0.1693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1097    0.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8981    1.2168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0816    2.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2652    2.8254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8859    1.8376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2773    2.2047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9613   -0.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5661    0.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    0.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5942    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3545   -0.0738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9592    0.4873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7476    0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3523    0.8053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9312   -0.5602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1449   -1.1961    0.0000 O   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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  1  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 10 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  1 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
  4 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
  3 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 22 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0066443

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C(O)C2=C(O[C@H]3[C@@H](COC4=C(C)C=C(O)C(=C34)C2=O)C(C)(C)O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O6/c1-12(2)6-7-14-8-9-17-19(21(14)27)22(28)18-16(26)10-13(3)23-20(18)24(31-17)15(11-30-23)25(4,5)29/h6,8-10,15,24,26-27,29H,7,11H2,1-5H3/t15-,24+/m1/s1

> <INCHI_KEY>
MYJGUMZTENHAAQ-MYYSRTQBSA-N

> <FORMULA>
C25H28O6

> <MOLECULAR_WEIGHT>
424.493

> <EXACT_MASS>
424.188588622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
45.8501376468263

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,17R)-7,11-dihydroxy-17-(2-hydroxypropan-2-yl)-13-methyl-6-(3-methylbut-2-en-1-yl)-2,15-dioxatetracyclo[8.7.1.0^{3,8}.0^{14,18}]octadeca-3(8),4,6,10(18),11,13-hexaen-9-one

> <ALOGPS_LOGP>
3.75

> <JCHEM_LOGP>
5.752419021

> <ALOGPS_LOGS>
-4.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.552005891866758

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.765805138631583

> <JCHEM_PKA_STRONGEST_BASIC>
-2.842394839787014

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
118.9682

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.06e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,17R)-7,11-dihydroxy-17-(2-hydroxypropan-2-yl)-13-methyl-6-(3-methylbut-2-en-1-yl)-2,15-dioxatetracyclo[8.7.1.0^{3,8}.0^{14,18}]octadeca-3(8),4,6,10(18),11,13-hexaen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       2.805   1.224   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.193   1.892   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.580   1.224   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.923  -0.277   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.963  -1.481   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.631  -2.869   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.423  -1.481   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.463  -0.277   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.991  -0.731   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.648  -2.233   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.777  -3.280   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.249  -2.826   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.427  -3.819   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.823  -2.687   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.138   0.316   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.205   1.817   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.676   2.271   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.019   3.773   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.362   5.274   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.520   3.430   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.518   4.115   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.395  -0.731   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.523   0.316   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.181   1.817   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.709   2.271   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.995  -0.138   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.124   0.910   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.595   0.456   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.724   1.503   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.938  -1.046   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.737  -2.233   0.000  0.00  0.00           O+0
CONECT    1    2    8   17                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5   22                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   12                                                  
CONECT    8    7    1    9                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11   14                                                  
CONECT   11   10   12                                                       
CONECT   12   11    7   13                                                  
CONECT   13   12                                                            
CONECT   14   10                                                            
CONECT   15    9   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    1   18                                                  
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22    4   23   31                                                  
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24    3                                                       
CONECT   26   23   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   22                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₈O₆

Average Mass

424.4930 Da

Monoisotopic Mass

424.18859 Da

IUPAC Name

(1S,17R)-7,11-dihydroxy-17-(2-hydroxypropan-2-yl)-13-methyl-6-(3-methylbut-2-en-1-yl)-2,15-dioxatetracyclo[8.7.1.0^{3,8}.0^{14,18}]octadeca-3(8),4,6,10(18),11,13-hexaen-9-one

Traditional Name

(1S,17R)-7,11-dihydroxy-17-(2-hydroxypropan-2-yl)-13-methyl-6-(3-methylbut-2-en-1-yl)-2,15-dioxatetracyclo[8.7.1.0^{3,8}.0^{14,18}]octadeca-3(8),4,6,10(18),11,13-hexaen-9-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(O)C2=C(O[C@H]3[C@@H](COC4=C(C)C=C(O)C(=C34)C2=O)C(C)(C)O)C=C1

InChI Identifier

InChI=1S/C25H28O6/c1-12(2)6-7-14-8-9-17-19(21(14)27)22(28)18-16(26)10-13(3)23-20(18)24(31-17)15(11-30-23)25(4,5)29/h6,8-10,15,24,26-27,29H,7,11H2,1-5H3/t15-,24+/m1/s1

InChI Key

MYJGUMZTENHAAQ-MYYSRTQBSA-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
Aspergillus rugulosus	LOTUS Database	35616633
Aspergillus rugulosus A.R.M. 325	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzoxepines. Dibenzoxepines are compounds containing a dibenzoxepine moiety, which consists of two benzene connected by an oxazepine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzoxepines

Sub Class

Dibenzoxepines

Direct Parent

Dibenzoxepines

Alternative Parents

Substituents

Dibenzoxepine
1-benzopyran
Benzopyran
Chromane
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Vinylogous acid
Tertiary alcohol
Ketone
Oxacycle
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.75	ALOGPS
logP	5.75	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	8.77	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	118.97 m³·mol⁻¹	ChemAxon
Polarizability	45.85 Å³	ChemAxon
Number of Rings	4	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

162854067

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one (NP0066443)

MOL for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)

3D MOL for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)

3D SDF for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)

3D-SDF for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)

PDB for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)

3D PDB for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)

SMILES for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)

INCHI for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)

Structure for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)

3D Structure for NP0066443 (1,12a-Dihydro-6,8-dihydroxy-1-(1-hydroxy-1-methylethyl)-4-methyl-9-(3-methylbut-2-enyl[1]benzopyrano[4,5-bc][1]benzoxepin-7(2H)-one)