NP-MRD: Showing NP-Card for trichotriol (NP0326314)

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Record Information

Version

1.0

Created at

2022-09-12 07:45:38 UTC

Updated at

2022-09-12 07:45:38 UTC

NP-MRD ID

NP0326314

Secondary Accession Numbers

None

Natural Product Identification

Common Name

trichotriol

Description

Trichotriol belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). trichotriol is found in Fusarium sporotrichioides. It was first documented in 1990 (PMID: 2317042). Based on a literature review a small amount of articles have been published on Trichotriol (PMID: 9430709) (PMID: 2034260).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 45  0  0  0  0  0  0  0  0999 V2000
    4.1571    1.2697    0.3252 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9916    0.3068    0.1900 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4247   -1.0015    0.1586 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9936    0.5919    1.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7582    0.1415    1.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3395   -0.6388   -0.0089 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6498   -2.1105    0.3236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1645   -0.6125   -0.2223 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4842   -1.5354   -1.3562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8618   -1.1140    1.0093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0870   -0.2228    1.2034 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8083    0.6698    2.2160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2075    0.5171   -0.1028 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8240    1.7681    0.0521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7283    0.7268   -0.4560 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1652    1.9958   -0.2341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4314    1.4883   -1.5665 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0794   -0.3070   -1.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2682    0.6011   -1.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2953    1.5631    1.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1038    0.8149   -0.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9346    2.2138   -0.2317 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7780   -1.1689   -0.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3182    1.1841    2.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0671    0.3960    1.9830 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2291   -2.1987    1.2709 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2674   -2.5762   -0.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2763   -2.6962    0.5080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4888   -1.0213   -2.3440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7834   -2.3868   -1.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4962   -1.9550   -1.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2379   -1.1670    1.9016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2645   -2.1500    0.8475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9858   -0.8211    1.4428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1414    1.3411    1.9320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7264   -0.0484   -0.8891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3238    2.0252   -0.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8474    2.8739   -0.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1145    2.2512   -0.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4852   -1.2367   -1.7601 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3919    0.1093   -2.0475 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9750    1.6734   -1.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9410    0.4454   -1.9697 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  9  1  6
  8 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
  8  6  1  0
  6  7  1  1
  6 18  1  0
 18 19  1  0
 19  2  1  0
  2  1  1  0
  2  3  1  6
  2  4  1  0
  4  5  2  0
 15  8  1  0
 15 17  1  6
  5  6  1  0
  9 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  1
 12 35  1  0
 13 36  1  6
 14 37  1  0
 16 38  1  0
 16 39  1  0
  7 26  1  0
  7 27  1  0
  7 28  1  0
 18 40  1  0
 18 41  1  0
 19 42  1  0
 19 43  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  4 24  1  0
  5 25  1  0
M  END


  Mrv1652309122209452D          

 19 21  0  0  1  0            999 V2000
    1.4157    4.1734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0801    3.4197    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3962    3.8810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8806    3.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1080    2.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5350    1.8336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2189    1.3723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1994    1.0799    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4849    1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9840    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9840    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6515   -0.4849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1994   -0.2549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9445   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7345    2.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5071    2.8262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  6  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  1  0  0  0
  8  9  1  6  0  0  0
  8 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 17  1  6  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0326314

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]1(C[C@@H](O)[C@@H](O)[C@@]11CO1)[C@@]1(C)CC[C@](C)(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O4/c1-12(4-6-13(2,18)7-5-12)14(3)8-10(16)11(17)15(14)9-19-15/h4,6,10-11,16-18H,5,7-9H2,1-3H3/t10-,11-,12-,13-,14-,15+/m1/s1

> <INCHI_KEY>
FPANWDWGPATUTH-OJVARPOJSA-N

> <FORMULA>
C15H24O4

> <MOLECULAR_WEIGHT>
268.353

> <EXACT_MASS>
268.167459253

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
28.413424809226008

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4R,5R,7R)-7-[(1S,4S)-4-hydroxy-1,4-dimethylcyclohex-2-en-1-yl]-7-methyl-1-oxaspiro[2.4]heptane-4,5-diol

> <JCHEM_LOGP>
0.414120452666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.95791064479413

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.94472693373702

> <JCHEM_PKA_STRONGEST_BASIC>
-1.449088415223788

> <JCHEM_POLAR_SURFACE_AREA>
73.22

> <JCHEM_REFRACTIVITY>
71.8348

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4R,5R,7R)-7-[(1S,4S)-4-hydroxy-1,4-dimethylcyclohex-2-en-1-yl]-7-methyl-1-oxaspiro[2.4]heptane-4,5-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       2.643   7.790   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.016   6.383   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.740   7.245   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.511   6.011   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.935   4.531   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.865   3.423   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.142   2.562   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.239   2.016   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.905   2.786   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.703   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.703   0.000   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.949  -0.905   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.239  -0.476   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.763  -1.941   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.371   3.795   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.947   5.276   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   19                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   18                                             
CONECT    7    6                                                            
CONECT    8    6    9   10   15                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    8   16   17                                             
CONECT   16   15   17                                                       
CONECT   17   16   15                                                       
CONECT   18    6   19                                                       
CONECT   19   18    2                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O₄

Average Mass

268.3530 Da

Monoisotopic Mass

268.16746 Da

IUPAC Name

(3S,4R,5R,7R)-7-[(1S,4S)-4-hydroxy-1,4-dimethylcyclohex-2-en-1-yl]-7-methyl-1-oxaspiro[2.4]heptane-4,5-diol

Traditional Name

(3S,4R,5R,7R)-7-[(1S,4S)-4-hydroxy-1,4-dimethylcyclohex-2-en-1-yl]-7-methyl-1-oxaspiro[2.4]heptane-4,5-diol

CAS Registry Number

Not Available

SMILES

C[C@@]1(C[C@@H](O)[C@@H](O)[C@@]11CO1)[C@@]1(C)CC[C@](C)(O)C=C1

InChI Identifier

InChI=1S/C15H24O4/c1-12(4-6-13(2,18)7-5-12)14(3)8-10(16)11(17)15(14)9-19-15/h4,6,10-11,16-18H,5,7-9H2,1-3H3/t10-,11-,12-,13-,14-,15+/m1/s1

InChI Key

FPANWDWGPATUTH-OJVARPOJSA-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
Fusarium sporotrichioides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Tertiary alcohols

Alternative Parents

Substituents

Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Hydrocarbon derivative
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	0.41	ChemAxon
pKa (Strongest Acidic)	12.94	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	73.22 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	71.83 m³·mol⁻¹	ChemAxon
Polarizability	28.41 Å³	ChemAxon
Number of Rings	3	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

C00012655

Chemspider ID

10204911

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21587788

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kimura M, Kaneko I, Komiyama M, Takatsuki A, Koshino H, Yoneyama K, Yamaguchi I: Trichothecene 3-O-acetyltransferase protects both the producing organism and transformed yeast from related mycotoxins. Cloning and characterization of Tri101. J Biol Chem. 1998 Jan 16;273(3):1654-61. doi: 10.1074/jbc.273.3.1654. [PubMed:9430709 ]
Senter LH, Sanson DR, Corley DG, Tempesta MS, Rottinghaus AA, Rottinghaus GE: Cytotoxicity of trichothecene mycotoxins isolated from Fusarium sporotrichioides (MC-72083) and Fusarium sambucinum in baby hamster kidney (BHK-21) cells. Mycopathologia. 1991 Feb;113(2):127-31. doi: 10.1007/BF00442425. [PubMed:2034260 ]
McCormick SP, Taylor SL, Plattner RD, Beremand MN: Bioconversion of possible T-2 toxin precursors by a mutant strain of Fusarium sporotrichioides NRRL 3299. Appl Environ Microbiol. 1990 Mar;56(3):702-6. doi: 10.1128/aem.56.3.702-706.1990. [PubMed:2317042 ]
LOTUS database [Link]

Showing NP-Card for trichotriol (NP0326314)

MOL for NP0326314 (trichotriol)

3D MOL for NP0326314 (trichotriol)

3D SDF for NP0326314 (trichotriol)

3D-SDF for NP0326314 (trichotriol)

PDB for NP0326314 (trichotriol)

3D PDB for NP0326314 (trichotriol)

SMILES for NP0326314 (trichotriol)

INCHI for NP0326314 (trichotriol)

Structure for NP0326314 (trichotriol)

3D Structure for NP0326314 (trichotriol)