NP-MRD: Showing NP-Card for (1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one (NP0249162)

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Record Information

Version

2.0

Created at

2022-09-07 11:38:49 UTC

Updated at

2022-09-07 11:38:49 UTC

NP-MRD ID

NP0249162

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one

Description

Bicycloillicinone asarone acetal belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. Based on a literature review very few articles have been published on Bicycloillicinone asarone acetal.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072213382D          

 33 37  0  0  1  0            999 V2000
    2.9869   -6.2434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9812   -5.4185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2638   -5.0110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2581   -4.1860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5407   -3.7785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5349   -2.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2465   -2.5360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9638   -2.9435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9696   -3.7685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870   -4.1760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6927   -5.0010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0693   -1.7303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2483   -1.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8308   -0.9382    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4446   -0.5308    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7491    0.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0034   -0.4201    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7594    0.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1410   -0.7276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5926    0.3797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6949    0.9102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1860   -1.2700    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7633   -1.5228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1770   -2.3354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0008   -2.3789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6219   -2.0233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3184   -2.9385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4835   -2.0495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8983   -1.2843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7223   -1.1008    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8179   -0.2764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    0.0582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9180   -2.4058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 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
 17 22  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 15 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 15 32  1  6  0  0  0
 13 33  1  0  0  0  0
  6 33  1  0  0  0  0
M  END

     RDKit          3D

 63 67  0  0  0  0  0  0  0  0999 V2000
    5.3303    0.3517    5.6255 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0848   -0.6213    4.7634 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7615   -1.2287    4.6166 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1718   -1.1060    3.2773 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1639   -0.1996    3.0377 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5920   -0.0677    1.7928 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0046   -0.8379    0.7311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0195   -1.7583    0.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5880   -1.8868    2.1972 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6014   -2.7822    2.4812 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0661   -3.6109    1.4240 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2541   -0.4851   -0.3904 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0097    0.0074    0.1521 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6840    0.9258   -0.7740 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7462    1.7373   -0.0269 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6916    2.1180   -1.1105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3792    1.2431   -2.3216 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    0.9734   -3.1179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3874    0.1327   -4.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7918    0.4487   -2.4352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9853    2.2412   -3.6354 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6022    0.1494   -1.7091 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7220   -0.6602   -2.6027 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1972    0.1663   -3.3800 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2173    0.1559   -4.7068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4382   -0.7245   -0.8307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8002   -1.8501   -1.2418 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8466   -0.3026    0.4985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3514    0.8340    0.9779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2233    1.4596    2.1856 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5712    2.6995    1.9943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2120    2.8031    0.6704 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5791    0.7413    1.2631 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4992    0.7006    6.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2841    0.8185    5.7598 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9016   -0.9709    4.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8108   -2.3058    4.9562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0400   -0.7675    5.3474 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8071    0.4301    3.8533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3531   -2.3701    0.1273 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0704   -3.9852    1.7676 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4352   -4.5167    1.3117 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2421   -3.0661    0.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5129   -0.8984    0.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0035    1.6087   -1.3238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7181    2.0024   -0.7311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147    3.2019   -1.3969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6746    1.8562   -2.9342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6115    0.5246   -5.0437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3491    0.3176   -4.9489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3946   -0.9437   -4.1973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8386   -0.6636   -2.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7386    0.8220   -2.9368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8427    0.5196   -1.3598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2128    2.7557   -2.8012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1183   -1.3396   -1.9508 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4687   -0.4855   -5.2342 H   0  0  0  0  0  0  0  0  0  0  0  0
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 10  9  1  0
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  6 33  1  0
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  6  5  1  0
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 12  7  1  0
 22 14  1  0
 29 15  1  0
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 11 41  1  0
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  8 40  1  0
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 31 63  1  0
  5 39  1  0
  3 37  1  0
  3 38  1  0
  2 36  1  0
  1 34  1  0
  1 35  1  0
M  END


  Mrv1652309072213382D          

 33 37  0  0  1  0            999 V2000
    2.9869   -6.2434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9812   -5.4185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2638   -5.0110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2581   -4.1860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5407   -3.7785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5349   -2.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2465   -2.5360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9638   -2.9435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9696   -3.7685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870   -4.1760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6927   -5.0010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0693   -1.7303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2483   -1.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8308   -0.9382    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4446   -0.5308    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7491    0.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0034   -0.4201    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7594    0.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1410   -0.7276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5926    0.3797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6949    0.9102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1860   -1.2700    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7633   -1.5228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1770   -2.3354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0008   -2.3789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6219   -2.0233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3184   -2.9385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4835   -2.0495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8983   -1.2843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7223   -1.1008    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8179   -0.2764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    0.0582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9180   -2.4058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
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 10 11  1  0  0  0  0
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 26 27  2  0  0  0  0
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 30 31  1  0  0  0  0
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 15 32  1  6  0  0  0
 13 33  1  0  0  0  0
  6 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0249162

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(OC(O2)[C@@H]2[C@@]34C[C@H](C(C)(C)O)[C@]2(CC=C)C(=O)C=C3OCO4)C=C1CC=C

> <INCHI_IDENTIFIER>
InChI=1S/C26H30O7/c1-6-8-15-10-17-18(11-16(15)29-5)33-23(32-17)22-25(9-7-2)19(24(3,4)28)13-26(22)21(12-20(25)27)30-14-31-26/h6-7,10-12,19,22-23,28H,1-2,8-9,13-14H2,3-5H3/t19-,22+,23?,25-,26-/m1/s1

> <INCHI_KEY>
LWEDIQNSOBIAMP-WHXOZRSJSA-N

> <FORMULA>
C26H30O7

> <MOLECULAR_WEIGHT>
454.519

> <EXACT_MASS>
454.199153306

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
48.599220377206834

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,8S,9S,11S)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0^{1,5}]undec-5-en-7-one

> <JCHEM_LOGP>
3.8300455779999982

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.027122070383122

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7869368064144213

> <JCHEM_POLAR_SURFACE_AREA>
83.45

> <JCHEM_REFRACTIVITY>
121.96620000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,8S,9S,11S)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0^{1,5}]undec-5-en-7-one

> <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       5.576 -11.654   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.565 -10.114   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.226  -9.354   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.215  -7.814   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.876  -7.053   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.865  -5.513   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.193  -4.734   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.533  -5.495   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.543  -7.035   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.882  -7.795   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.893  -9.335   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.863  -3.230   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.330  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.551  -1.751   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.697  -0.991   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.398   0.046   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.006  -0.784   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.418   0.068   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.130  -1.358   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.973   0.709   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.297   1.699   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.347  -2.371   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.425  -2.843   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.197  -4.359   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.735  -4.441   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.161  -3.777   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.594  -5.485   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.769  -3.826   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.544  -2.397   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.082  -2.055   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.260  -0.516   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.840   0.109   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       1.714  -4.491   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   33                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    7   13                                                       
CONECT   13   12   14   33                                                  
CONECT   14   13   15   22                                                  
CONECT   15   14   16   29   32                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22   17   14   23   26                                             
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   22   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   15   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   15                                                       
CONECT   33   13    6                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₀O₇

Average Mass

454.5190 Da

Monoisotopic Mass

454.19915 Da

IUPAC Name

(1S,8S,9S,11S)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0^{1,5}]undec-5-en-7-one

Traditional Name

(1S,8S,9S,11S)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0^{1,5}]undec-5-en-7-one

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(OC(O2)[C@@H]2[C@@]34C[C@H](C(C)(C)O)[C@]2(CC=C)C(=O)C=C3OCO4)C=C1CC=C

InChI Identifier

InChI=1S/C26H30O7/c1-6-8-15-10-17-18(11-16(15)29-5)33-23(32-17)22-25(9-7-2)19(24(3,4)28)13-26(22)21(12-20(25)27)30-14-31-26/h6-7,10-12,19,22-23,28H,1-2,8-9,13-14H2,3-5H3/t19-,22+,23?,25-,26-/m1/s1

InChI Key

LWEDIQNSOBIAMP-WHXOZRSJSA-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 benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxoles

Sub Class

Not Available

Direct Parent

Benzodioxoles

Alternative Parents

Substituents

Benzodioxole
Anisole
Alkyl aryl ether
Cyclohexenone
Benzenoid
Meta-dioxolane
Vinylogous ester
Tertiary alcohol
Ketone
Ether
Oxacycle
Acetal
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Aldehyde
Alcohol
Organooxygen compound
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	3.83	ChemAxon
pKa (Strongest Acidic)	15.03	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	83.45 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	121.97 m³·mol⁻¹	ChemAxon
Polarizability	48.6 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

101707022

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one (NP0249162)

MOL for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)

3D MOL for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)

3D SDF for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)

3D-SDF for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)

PDB for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)

3D PDB for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)

SMILES for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)

INCHI for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)

Structure for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)

3D Structure for NP0249162 ((1s,8s,9s,11s)-9-(2-hydroxypropan-2-yl)-11-[5-methoxy-6-(prop-2-en-1-yl)-2h-1,3-benzodioxol-2-yl]-8-(prop-2-en-1-yl)-2,4-dioxatricyclo[6.2.1.0¹,⁵]undec-5-en-7-one)