NP-MRD: Showing NP-Card for 10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate (NP0305110)

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Record Information

Version

2.0

Created at

2022-09-10 20:39:19 UTC

Updated at

2022-09-10 20:39:19 UTC

NP-MRD ID

NP0305110

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate

Description

Triacetoxyscirpenol belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain. Triacetoxyscirpenol is an extremely weak basic (essentially neutral) compound (based on its pKa). 10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate is found in Cordyceps polyarthra and Fusarium sambucinum. Triacetoxyscirpenol is a potentially toxic compound.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241212312D          

 29 32  0  0  0  0            999 V2000
    4.3097   -1.4085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5364   -1.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9007   -1.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1275   -1.3591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9900   -0.5456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6257   -0.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3989   -0.3074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0605   -0.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7400   -1.2658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1197   -1.6427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6396   -0.9304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4999   -0.1173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2087    0.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5114    0.7076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113   -0.9304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4878   -2.2009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2749   -1.9539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8824   -2.5121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4546   -1.1487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3576   -1.8128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1928   -2.6211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8104   -3.1681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4103   -2.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8444    0.2390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7057    0.2288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2343    0.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9501    1.6367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1372    1.7778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4787    2.2701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 14  1  0  0  0  0
 11 15  1  0  0  0  0
  4 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  8 24  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
    4.6394   -1.2486    2.2913 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3430   -1.5280    1.6320 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8715   -2.6939    1.7897 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6633   -0.5799    0.8776 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4467   -0.9587    0.3025 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7663    0.0949   -0.4918 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5765    0.5914   -1.6485 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8926    1.1428   -1.2080 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6689    2.0221   -0.0275 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8467    2.8759    0.3775 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5502    2.0881    0.6465 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3223    1.2760    0.3182 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5523    2.1103   -0.2983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5769    1.5210   -1.0006 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4242    0.6053   -0.1091 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7256    1.1991    1.1169 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0396    1.4215    1.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4131    2.0484    2.7927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9893    1.0834    0.7344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5711   -0.6273    0.0013 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3018   -1.8098   -0.2729 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4069   -2.8757    0.5809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2179   -4.0476    0.1365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8267   -2.8284    1.6872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5026   -0.5335   -1.0816 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2615   -1.8306   -1.7620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0853    0.5212   -1.9955 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9396    0.6049   -3.3482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1380    0.0753   -2.8757 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7391   -0.1917    2.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4405   -1.5241    1.5747 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7857   -1.8799    3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6023   -1.8416   -0.3863 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6698   -0.1381   -2.4816 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0004    1.4559   -2.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6618    0.3685   -1.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670    1.7898   -2.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4560    3.1367   -0.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4682    2.3646    1.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4936    3.8347    0.8046 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5007    2.7671    1.4928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1050    0.9863    1.3086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2044    2.3091   -1.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3132    0.3409   -0.7183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4297    1.7227    3.0958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5083    3.1568    2.6027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6769    1.8685    3.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1310   -0.7586    1.0072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9083   -4.9014    0.7838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9746   -4.3160   -0.9250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2791   -3.8056    0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0691   -1.9866   -2.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7328   -1.9269   -2.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3277   -2.6510   -0.9973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9897    1.5881   -3.9029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3272   -0.1266   -3.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  6  5  1  1
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 15 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 20 25  1  0
 25 26  1  6
 25 27  1  0
 27 28  1  0
 28 29  1  0
 12  6  1  0
 27 14  1  0
 27 29  1  6
 25  6  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  0
  5 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
 10 39  1  0
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 11 42  1  0
 12 43  1  1
 14 44  1  6
 15 45  1  6
 18 46  1  0
 18 47  1  0
 18 48  1  0
 20 49  1  1
 23 50  1  0
 23 51  1  0
 23 52  1  0
 26 53  1  0
 26 54  1  0
 26 55  1  0
 28 56  1  0
 28 57  1  0
M  END


  Mrv0541 02241212312D          

 29 32  0  0  0  0            999 V2000
    4.3097   -1.4085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5364   -1.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9007   -1.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1275   -1.3591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9900   -0.5456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6257   -0.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3989   -0.3074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0605   -0.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7400   -1.2658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1197   -1.6427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6396   -0.9304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4999   -0.1173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2087    0.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5114    0.7076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113   -0.9304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4878   -2.2009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2749   -1.9539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8824   -2.5121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4546   -1.1487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3576   -1.8128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1928   -2.6211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8104   -3.1681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4103   -2.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8444    0.2390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7057    0.2288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2343    0.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9501    1.6367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1372    1.7778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4787    2.2701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 14  1  0  0  0  0
 11 15  1  0  0  0  0
  4 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  8 24  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0305110

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC12CCC(C)=CC1OC1C(OC(C)=O)C(OC(C)=O)C2(C)C11CO1

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O8/c1-11-6-7-20(9-25-12(2)22)15(8-11)29-18-16(27-13(3)23)17(28-14(4)24)19(20,5)21(18)10-26-21/h8,15-18H,6-7,9-10H2,1-5H3

> <INCHI_KEY>
YWQOKOBRSAAKTG-UHFFFAOYSA-N

> <FORMULA>
C21H28O8

> <MOLECULAR_WEIGHT>
408.4422

> <EXACT_MASS>
408.178417872

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
41.70799618160409

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate

> <ALOGPS_LOGP>
1.63

> <JCHEM_LOGP>
0.8181250156666671

> <ALOGPS_LOGS>
-3.04

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.930786787117016

> <JCHEM_POLAR_SURFACE_AREA>
100.66000000000003

> <JCHEM_REFRACTIVITY>
98.2512

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.73e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0       8.045  -2.629   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.601  -2.092   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.415  -3.074   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.971  -2.537   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.715  -1.018   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.901  -0.037   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.345  -0.574   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.980  -1.040   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.381  -2.363   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.223  -3.066   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.194  -1.737   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.933  -0.219   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.390   0.570   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.955   1.321   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       3.008  -1.737   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -0.911  -4.108   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.380  -3.647   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.514  -4.689   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.715  -2.144   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.534  -3.384   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.227  -4.893   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.379  -5.914   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.766  -5.381   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.576   0.446   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.184   0.427   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.171   1.610   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.640   3.055   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.123   3.319   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.627   4.238   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   15                                                  
CONECT    5    4    6    8   25                                             
CONECT    6    5    7                                                       
CONECT    7    6    2                                                       
CONECT    8    5    9   12   24                                             
CONECT    9    8   10   20                                                  
CONECT   10    9   11   16                                                  
CONECT   11   10   12   15                                                  
CONECT   12   11    8   13   14                                             
CONECT   13   12   14                                                       
CONECT   14   13   12                                                       
CONECT   15   11    4                                                       
CONECT   16   10   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    9   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24    8                                                            
CONECT   25    5   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₈O₈

Average Mass

408.4422 Da

Monoisotopic Mass

408.17842 Da

IUPAC Name

10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate

Traditional Name

10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC12CCC(C)=CC1OC1C(OC(C)=O)C(OC(C)=O)C2(C)C11CO1

InChI Identifier

InChI=1S/C21H28O8/c1-11-6-7-20(9-25-12(2)22)15(8-11)29-18-16(27-13(3)23)17(28-14(4)24)19(20,5)21(18)10-26-21/h8,15-18H,6-7,9-10H2,1-5H3

InChI Key

YWQOKOBRSAAKTG-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
Cordyceps polyarthra	LOTUS Database	35616633
Fusarium sambucinum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Trichothecenes

Alternative Parents

Substituents

Trichothecene skeleton
Tricarboxylic acid or derivatives
Oxepane
Oxane
Carboxylic acid ester
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
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	1.63	ALOGPS
logP	0.82	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	100.66 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	98.25 m³·mol⁻¹	ChemAxon
Polarizability	41.71 Å³	ChemAxon
Number of Rings	4	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

4212745

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate (NP0305110)

MOL for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)

3D MOL for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)

3D SDF for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)

3D-SDF for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)

PDB for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)

3D PDB for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)

SMILES for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)

INCHI for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)

Structure for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)

3D Structure for NP0305110 (10',11'-bis(acetyloxy)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2'-ylmethyl acetate)