NP-MRD: Showing NP-Card for T-2 Triol (NP0137449)

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Record Information

Version

2.0

Created at

2022-05-30 16:52:48 UTC

Updated at

2022-05-30 16:52:48 UTC

NP-MRD ID

NP0137449

Secondary Accession Numbers

None

Natural Product Identification

Common Name

T-2 Triol

Description

T2 Triol, also known as T 2 triol or toxin T 3, 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. T2 Triol is a mycotoxin from Fusarium sporotrichiell. T2 Triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061308252D          

 27 30  0  0  0  0            999 V2000
    6.8525    0.6948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3543   -0.6445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3097   -1.4085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1096    0.1211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4436    0.4566    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
    2.6257   -0.0198    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
   -0.2087    0.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2168    0.1690    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
    3.3989   -0.3074    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
    4.8079   -0.0692    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
    0.7400   -1.2658    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
    1.0605   -0.5572    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
    0.4999   -0.1173    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
    4.9454   -0.8827    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
    1.3576   -1.8128    0.0000 O   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
    4.0346    0.2184    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
 10  1  1  0  0  0  0
 10  2  1  0  0  0  0
 10  5  1  0  0  0  0
 11  3  1  0  0  0  0
 11  6  2  0  0  0  0
 12  7  1  0  0  0  0
 12 11  1  0  0  0  0
 13  6  1  0  0  0  0
 14  5  1  0  0  0  0
 16 15  1  0  0  0  0
 17 15  1  0  0  0  0
 18  4  1  0  0  0  0
 18 16  1  0  0  0  0
 19  7  1  0  0  0  0
 19  8  1  0  0  0  0
 19 13  1  0  0  0  0
 19 18  1  0  0  0  0
 20  9  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21  8  1  0  0  0  0
 22 14  2  0  0  0  0
 23 15  1  0  0  0  0
 24 16  1  0  0  0  0
 25  9  1  0  0  0  0
 25 20  1  0  0  0  0
 26 12  1  0  0  0  0
 26 14  1  0  0  0  0
 27 13  1  0  0  0  0
 27 17  1  0  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
    1.1048   -1.0406    3.2841 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2569   -0.6589    2.1181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0245   -0.3978    2.3608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8713   -0.0018    1.2172 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2323   -0.0198    1.4939 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8537    0.5978    0.3970 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5984   -0.5433   -0.3154 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0988   -1.4700    0.5545 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6517   -1.0368   -1.3465 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1435   -0.5483   -2.5907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3722   -0.3674   -1.1059 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6197   -0.2631   -2.4164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8636    1.0093   -0.6679 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3420    2.2503   -0.9688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4509    1.8167   -1.6453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5207   -0.8547    0.0221 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6171   -2.2829    0.3590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2511   -3.1529   -0.6646 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0970   -0.4887   -0.3447 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8793   -0.5804    0.7898 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7814    0.4953    0.6398 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1203    0.4089    0.3827 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5924   -0.7569    0.2692 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9568    1.6267    0.2419 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8580    1.4882   -0.9535 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7357    2.6958   -1.1570 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6780    0.2451   -0.9255 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4915   -0.1116    3.8039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9827   -1.6569    2.9620 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4924   -1.5810    3.9967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4199   -0.4743    3.3643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5961    1.0670    1.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5260    1.4057    0.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5097   -0.0226   -0.7507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9268   -2.3758    0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6354   -2.1243   -1.4845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0364   -0.1556   -2.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1588   -1.2589   -2.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9437    0.5847   -2.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3999   -0.0945   -3.2103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4152    3.0814   -0.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4298    2.3706   -1.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6126   -2.5645    0.7614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9116   -2.5352    1.1751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1780   -4.0585   -0.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1499    0.5975   -0.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2959   -1.0843   -1.1963 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5394   -1.4990    0.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6316    1.6129    1.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3514    2.5328    0.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1836    1.4301   -1.8655 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4257    2.4436   -2.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3528    2.9377   -0.2968 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1309    3.5615   -1.5270 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5873    0.4067   -1.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9195   -0.0387    0.1109 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1097   -0.5662   -1.4468 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25 27  1  0
 25 24  1  0
 24 22  1  0
 22 23  2  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 16  1  0
 16 17  1  1
 17 18  1  0
 16  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 14 15  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 20  1  0
 11 16  1  0
 13 15  1  6
 13  6  1  0
 26 52  1  0
 26 53  1  0
 26 54  1  0
 25 51  1  0
 27 55  1  0
 27 56  1  0
 27 57  1  0
 24 49  1  0
 24 50  1  0
 20 48  1  6
 19 46  1  0
 19 47  1  0
 17 43  1  0
 17 44  1  0
 18 45  1  0
  4 32  1  6
  6 33  1  1
  7 34  1  6
  8 35  1  0
  9 36  1  6
 10 37  1  0
 12 38  1  0
 12 39  1  0
 12 40  1  0
 14 41  1  0
 14 42  1  0
  3 31  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
M  END


  Mrv0541 05061308252D          

 27 30  0  0  0  0            999 V2000
    6.8525    0.6948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3543   -0.6445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3097   -1.4085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1096    0.1211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4436    0.4566    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
    2.6257   -0.0198    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
   -0.2087    0.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2168    0.1690    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
    3.3989   -0.3074    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
    4.8079   -0.0692    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
    0.7400   -1.2658    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
    1.0605   -0.5572    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
    0.4999   -0.1173    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
    4.9454   -0.8827    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
    1.3576   -1.8128    0.0000 O   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
    4.0346    0.2184    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
 10  1  1  0  0  0  0
 10  2  1  0  0  0  0
 10  5  1  0  0  0  0
 11  3  1  0  0  0  0
 11  6  2  0  0  0  0
 12  7  1  0  0  0  0
 12 11  1  0  0  0  0
 13  6  1  0  0  0  0
 14  5  1  0  0  0  0
 16 15  1  0  0  0  0
 17 15  1  0  0  0  0
 18  4  1  0  0  0  0
 18 16  1  0  0  0  0
 19  7  1  0  0  0  0
 19  8  1  0  0  0  0
 19 13  1  0  0  0  0
 19 18  1  0  0  0  0
 20  9  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21  8  1  0  0  0  0
 22 14  2  0  0  0  0
 23 15  1  0  0  0  0
 24 16  1  0  0  0  0
 25  9  1  0  0  0  0
 25 20  1  0  0  0  0
 26 12  1  0  0  0  0
 26 14  1  0  0  0  0
 27 13  1  0  0  0  0
 27 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0137449

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC(=O)OC1CC2(CO)C(OC3C(O)C(O)C2(C)C32CO2)C=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O7/c1-10(2)5-14(22)26-12-7-19(8-21)13(6-11(12)3)27-17-15(23)16(24)18(19,4)20(17)9-25-20/h6,10,12-13,15-17,21,23-24H,5,7-9H2,1-4H3

> <INCHI_KEY>
DDAUKBBLCGQHIP-UHFFFAOYSA-N

> <FORMULA>
C20H30O7

> <MOLECULAR_WEIGHT>
382.448

> <EXACT_MASS>
382.199153314

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
39.97793675367593

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10',11'-dihydroxy-2'-(hydroxymethyl)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 3-methylbutanoate

> <ALOGPS_LOGP>
0.55

> <JCHEM_LOGP>
0.13718673633333262

> <ALOGPS_LOGS>
-2.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.386503966093859

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.971460619409964

> <JCHEM_PKA_STRONGEST_BASIC>
-2.80362619935356

> <JCHEM_POLAR_SURFACE_AREA>
108.75000000000001

> <JCHEM_REFRACTIVITY>
95.24019999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.58e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10',11'-dihydroxy-2'-(hydroxymethyl)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 3-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      12.791   1.297   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.861  -1.203   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.045  -2.629   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.071   0.226   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.161   0.852   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.415  -3.074   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.901  -0.037   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.184   0.427   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.390   0.570   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.605   0.315   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.601  -2.092   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.345  -0.574   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.971  -2.537   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.975  -0.129   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.223  -3.066   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.381  -2.363   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.194  -1.737   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.980  -1.040   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.715  -1.018   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.933  -0.219   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.171   1.610   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       9.231  -1.648   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -0.911  -4.108   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       2.534  -3.384   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.955   1.321   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       7.531   0.408   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       3.008  -1.737   0.000  0.00  0.00           O+0
CONECT    1   10                                                            
CONECT    2   10                                                            
CONECT    3   11                                                            
CONECT    4   18                                                            
CONECT    5   10   14                                                       
CONECT    6   11   13                                                       
CONECT    7   12   19                                                       
CONECT    8   19   21                                                       
CONECT    9   20   25                                                       
CONECT   10    1    2    5                                                  
CONECT   11    3    6   12                                                  
CONECT   12    7   11   26                                                  
CONECT   13    6   19   27                                                  
CONECT   14    5   22   26                                                  
CONECT   15   16   17   23                                                  
CONECT   16   15   18   24                                                  
CONECT   17   15   20   27                                                  
CONECT   18    4   16   19   20                                             
CONECT   19    7    8   13   18                                             
CONECT   20    9   17   18   25                                             
CONECT   21    8                                                            
CONECT   22   14                                                            
CONECT   23   15                                                            
CONECT   24   16                                                            
CONECT   25    9   20                                                       
CONECT   26   12   14                                                       
CONECT   27   13   17                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
12,13-Epoxy-trichothec-9-ene-3alpha,4beta,8alpha,15-tetrol 8-isovalerate	HMDB
Deacetyl HT 2 toxin	HMDB
Deacetyl-HT-2 toxin	HMDB
T 2 Triol	HMDB
T-2 Triol	HMDB
Toxin T 2 triol	HMDB
Toxin T 3	HMDB
Toxin T-2 triol	HMDB
10',11'-Dihydroxy-2'-(hydroxymethyl)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 3-methylbutanoic acid	Generator
Scirpentriol	MeSH
3,4,15-Trihydroxy-8-(3-methylbutyryloxy)-1,2,3-epoxytrichothec--9-ene	MeSH

Chemical Formula

C₂₀H₃₀O₇

Average Mass

382.4480 Da

Monoisotopic Mass

382.19915 Da

IUPAC Name

10',11'-dihydroxy-2'-(hydroxymethyl)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 3-methylbutanoate

Traditional Name

10',11'-dihydroxy-2'-(hydroxymethyl)-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 3-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)OC1CC2(CO)C(OC3C(O)C(O)C2(C)C32CO2)C=C1C

InChI Identifier

InChI=1S/C20H30O7/c1-10(2)5-14(22)26-12-7-19(8-21)13(6-11(12)3)27-17-15(23)16(24)18(19,4)20(17)9-25-20/h6,10,12-13,15-17,21,23-24H,5,7-9H2,1-4H3

InChI Key

DDAUKBBLCGQHIP-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

Not Available

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
Fatty acid ester
Oxepane
Oxane
Fatty acyl
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Alcohol
Organic oxygen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
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	0.55	ALOGPS
logP	0.14	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	12.97	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	108.75 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	95.24 m³·mol⁻¹	ChemAxon
Polarizability	39.98 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	No	ChemAxon

External Links

HMDB ID

HMDB0035396

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB014071

KNApSAcK ID

C00012640

Chemspider ID

529359

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

608974

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for T-2 Triol (NP0137449)

MOL for NP0137449 (T-2 Triol)

3D MOL for NP0137449 (T-2 Triol)

3D SDF for NP0137449 (T-2 Triol)

3D-SDF for NP0137449 (T-2 Triol)

PDB for NP0137449 (T-2 Triol)

3D PDB for NP0137449 (T-2 Triol)

SMILES for NP0137449 (T-2 Triol)

INCHI for NP0137449 (T-2 Triol)

Structure for NP0137449 (T-2 Triol)

3D Structure for NP0137449 (T-2 Triol)