NP-MRD: Showing NP-Card for trichothecinol b (NP0304507)

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Record Information

Version

2.0

Created at

2022-09-10 19:38:52 UTC

Updated at

2022-09-10 19:38:53 UTC

NP-MRD ID

NP0304507

Secondary Accession Numbers

None

Natural Product Identification

Common Name

trichothecinol b

Description

Trichothecinol B 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. trichothecinol b is found in Trichothecium roseum. trichothecinol b was first documented in 2015 (PMID: 25633363). Based on a literature review very few articles have been published on Trichothecinol B.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 53  0  0  0  0  0  0  0  0999 V2000
   -4.8690    1.1017    3.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1509   -0.2736    2.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4251   -0.8833    1.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2833   -0.2177    1.0257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0062    0.9710    1.3872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5001   -0.8348    0.0640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4110   -0.1287   -0.4930 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5819    0.0600   -1.9817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2324   -0.3585   -2.5227 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7159    0.6386   -2.4364 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9523    1.1127   -1.1729 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2342    1.8829   -1.2300 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3685    1.4906   -0.7142 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5682    2.3599   -0.8458 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5072    0.2050   -0.0001 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8888    0.3570    1.3316 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2990   -0.6546   -0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0007    0.0765   -0.1001 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7855    0.7225    1.2580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1242   -0.9161   -0.2861 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2596   -1.8987    0.8143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0672   -1.5412   -1.6516 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6905   -2.7224   -1.9623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6947   -2.6731   -1.9332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8969    1.1982    3.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6401    1.3604    3.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0092    1.8507    2.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9887   -0.8625    2.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6382   -1.9039    1.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3687    0.8613   -0.0346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3116   -0.6937   -2.3278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8490    1.0946   -2.2547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2826   -0.6926   -3.5701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1638    1.8782   -0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1652    2.8521   -1.7617 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3714    3.2656   -1.4412 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4137    1.8355   -1.3482 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9214    2.6589    0.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3791   -0.3230   -0.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8462    0.5788    1.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3615   -1.0699   -1.2302 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3882   -1.5225    0.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0838    1.5845    1.1997 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3130   -0.0266    1.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7015    1.0647    1.7340 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6551   -2.1819    1.3299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0142   -1.5981    1.5737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6737   -2.8505    0.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2094   -2.8725   -2.9540 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1599   -3.3613   -1.1820 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  1
 18 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  1  0
 23 24  1  0
 20  7  1  0
 22 24  1  6
 22  9  1  0
 18 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  0
  7 30  1  1
  8 31  1  0
  8 32  1  0
  9 33  1  6
 11 34  1  1
 12 35  1  0
 14 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  6
 16 40  1  0
 17 41  1  0
 17 42  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 21 46  1  0
 21 47  1  0
 21 48  1  0
 23 49  1  0
 23 50  1  0
M  END


  Mrv1652309102221382D          

 24 27  0  0  1  0            999 V2000
   -0.5871    2.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3878    2.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6160    1.6082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0434    1.0142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2716    0.2214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2428    1.2130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3298    0.6190    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0430   -0.1545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4690   -0.8610    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2869   -0.9685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8809   -0.3960    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6309   -0.7398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3036   -0.2622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0536   -0.6059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2264    0.5592    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8991    1.0368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4764    0.9030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8037    0.4254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7880    1.2503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1133    0.8771    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2208    1.6951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0084   -0.0725    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8217    0.0659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5350   -0.7076    0.0000 O   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  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0304507

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C/C(=O)O[C@@H]1C[C@H]2O[C@@H]3C=C(C)[C@@H](O)C[C@]3(C)[C@]1(C)[C@]21CO1

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O5/c1-5-6-16(21)24-14-8-15-19(10-22-19)18(14,4)17(3)9-12(20)11(2)7-13(17)23-15/h5-7,12-15,20H,8-10H2,1-4H3/b6-5-/t12-,13+,14+,15+,17-,18+,19-/m0/s1

> <INCHI_KEY>
VRHZKNFFKJZHFD-DPEWJACVSA-N

> <FORMULA>
C19H26O5

> <MOLECULAR_WEIGHT>
334.412

> <EXACT_MASS>
334.178023937

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
35.286878575417354

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,2S,2'R,4'S,7'R,9'R,11'R)-4'-hydroxy-1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-en-11'-yl (2Z)-but-2-enoate

> <JCHEM_LOGP>
2.0523903006666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.590462255210799

> <JCHEM_PKA_STRONGEST_BASIC>
-2.977931809570797

> <JCHEM_POLAR_SURFACE_AREA>
68.29

> <JCHEM_REFRACTIVITY>
88.91310000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2S,2'R,4'S,7'R,9'R,11'R)-4'-hydroxy-1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-en-11'-yl (2Z)-but-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.096   4.853   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.591   4.482   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.016   3.002   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.948   1.893   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.374   0.413   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      -0.453   2.264   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.616   1.156   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.080  -0.288   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.875  -1.607   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.402  -1.808   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.511  -0.739   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.911  -1.381   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.167  -0.489   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.567  -1.131   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.023   1.044   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.278   1.935   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.623   1.686   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.367   0.794   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.338   2.334   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.078   1.637   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.279   3.164   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.882  -0.135   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.401   0.123   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.865  -1.321   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   20                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   11   19   20                                             
CONECT   19   18                                                            
CONECT   20   18    7   21   22                                             
CONECT   21   20                                                            
CONECT   22   20    9   23   24                                             
CONECT   23   22   24                                                       
CONECT   24   23   22                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₅

Average Mass

334.4120 Da

Monoisotopic Mass

334.17802 Da

IUPAC Name

(1'S,2S,2'R,4'S,7'R,9'R,11'R)-4'-hydroxy-1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-en-11'-yl (2Z)-but-2-enoate

Traditional Name

(1'S,2S,2'R,4'S,7'R,9'R,11'R)-4'-hydroxy-1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-en-11'-yl (2Z)-but-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C/C(=O)O[C@@H]1C[C@H]2O[C@@H]3C=C(C)[C@@H](O)C[C@]3(C)[C@]1(C)[C@]21CO1

InChI Identifier

InChI=1S/C19H26O5/c1-5-6-16(21)24-14-8-15-19(10-22-19)18(14,4)17(3)9-12(20)11(2)7-13(17)23-15/h5-7,12-15,20H,8-10H2,1-4H3/b6-5-/t12-,13+,14+,15+,17-,18+,19-/m0/s1

InChI Key

VRHZKNFFKJZHFD-DPEWJACVSA-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
Trichothecium roseum	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
Fatty acid ester
Oxepane
Oxane
Fatty acyl
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

trichothecene (CHEBI:69620 )

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	2.05	ChemAxon
pKa (Strongest Acidic)	14.59	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	68.29 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	88.91 m³·mol⁻¹	ChemAxon
Polarizability	35.29 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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8421767

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10246280

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wang Y, Zhang L, Li GT, Li ZH, Dong ZJ, Li Y, Liu JK: Identification and Cytotoxic Activities of Two New Trichothecenes and a New Cuparane-Type Sesquiterpenoid from the Cultures of the Mushroom Engleromyces goetzii. Nat Prod Bioprospect. 2015 Jan 30. doi: 10.1007/s13659-014-0051-1. [PubMed:25633363 ]
LOTUS database [Link]

Showing NP-Card for trichothecinol b (NP0304507)

MOL for NP0304507 (trichothecinol b)

3D MOL for NP0304507 (trichothecinol b)

3D SDF for NP0304507 (trichothecinol b)

3D-SDF for NP0304507 (trichothecinol b)

PDB for NP0304507 (trichothecinol b)

3D PDB for NP0304507 (trichothecinol b)

SMILES for NP0304507 (trichothecinol b)

INCHI for NP0304507 (trichothecinol b)

Structure for NP0304507 (trichothecinol b)

3D Structure for NP0304507 (trichothecinol b)