NP-MRD: Showing NP-Card for Trichosorbicillin H (NP0019450)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-01-06 04:57:40 UTC

Updated at

2021-07-15 17:31:00 UTC

NP-MRD ID

NP0019450

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Trichosorbicillin H

Provided By

NPAtlas

Description

4-(2,4-Dihydroxy-5-methylphenyl)-4-oxobutanoic acid belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Trichosorbicillin H is found in Trichoderma and Trichoderma reesei. Based on a literature review very few articles have been published on 4-(2,4-dihydroxy-5-methylphenyl)-4-oxobutanoic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242120163D          

 28 28  0  0  0  0            999 V2000
   -4.0014    0.6583   -1.0761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7658    0.3814   -0.2895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5654    0.4915   -0.9215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4012    0.2398   -0.2141 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8570    0.3621   -0.9118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8894    0.6936   -2.1310 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1319    0.1013   -0.2116 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2761    0.3335   -1.2003 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5796    0.0856   -0.5506 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6112    0.2417   -1.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6768   -0.3024    0.7767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4509   -0.1155    1.1042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6937   -0.3686    1.8214 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6929   -0.2186    1.7177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8596    0.0278    1.0304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0990   -0.0710    1.6276 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1902   -0.2137   -1.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8667    1.5433   -1.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8344    0.8392   -0.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4670    0.7711   -1.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2448    0.8278    0.6176 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1754   -0.9398    0.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0784   -0.3623   -2.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2774    1.3867   -1.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9837   -0.9514    1.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6151   -0.6281    2.7920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7249   -0.4988    2.7557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1709   -0.3369    2.6207 H   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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  4 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15  2  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  3 20  1  0  0  0  0
  7 21  1  0  0  0  0
  7 22  1  0  0  0  0
  8 23  1  0  0  0  0
  8 24  1  0  0  0  0
 11 25  1  0  0  0  0
 13 26  1  0  0  0  0
 14 27  1  0  0  0  0
 16 28  1  0  0  0  0
M  END


  Mrv1652306242120163D          

 28 28  0  0  0  0            999 V2000
   -4.0014    0.6583   -1.0761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7658    0.3814   -0.2895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5654    0.4915   -0.9215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4012    0.2398   -0.2141 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8570    0.3621   -0.9118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8894    0.6936   -2.1310 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1319    0.1013   -0.2116 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2761    0.3335   -1.2003 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5796    0.0856   -0.5506 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6112    0.2417   -1.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6768   -0.3024    0.7767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4509   -0.1155    1.1042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6937   -0.3686    1.8214 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6929   -0.2186    1.7177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8596    0.0278    1.0304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0990   -0.0710    1.6276 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1902   -0.2137   -1.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8667    1.5433   -1.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8344    0.8392   -0.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4670    0.7711   -1.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2448    0.8278    0.6176 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1754   -0.9398    0.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0784   -0.3623   -2.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2774    1.3867   -1.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9837   -0.9514    1.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6151   -0.6281    2.7920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7249   -0.4988    2.7557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1709   -0.3369    2.6207 H   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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  4 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15  2  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  3 20  1  0  0  0  0
  7 21  1  0  0  0  0
  7 22  1  0  0  0  0
  8 23  1  0  0  0  0
  8 24  1  0  0  0  0
 11 25  1  0  0  0  0
 13 26  1  0  0  0  0
 14 27  1  0  0  0  0
 16 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0019450

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C([H])([H])C([H])([H])C(=O)C1=C(O[H])C([H])=C(O[H])C(=C1[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C11H12O5/c1-6-4-7(10(14)5-9(6)13)8(12)2-3-11(15)16/h4-5,13-14H,2-3H2,1H3,(H,15,16)

> <INCHI_KEY>
NWXNGGQNAGTBJM-UHFFFAOYSA-N

> <FORMULA>
C11H12O5

> <MOLECULAR_WEIGHT>
224.212

> <EXACT_MASS>
224.068473486

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
22.305568806064016

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(2,4-dihydroxy-5-methylphenyl)-4-oxobutanoic acid

> <ALOGPS_LOGP>
1.33

> <JCHEM_LOGP>
1.9120468276666664

> <ALOGPS_LOGS>
-2.24

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.182736028669307

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.645158065406847

> <JCHEM_PKA_STRONGEST_BASIC>
-4.859387645917779

> <JCHEM_POLAR_SURFACE_AREA>
94.83000000000001

> <JCHEM_REFRACTIVITY>
56.35710000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.29e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-(2,4-dihydroxy-5-methylphenyl)-4-oxobutanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.001   0.658  -1.076  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.766   0.381  -0.290  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.565   0.492  -0.922  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.401   0.240  -0.214  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.857   0.362  -0.912  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.889   0.694  -2.131  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.132   0.101  -0.212  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.276   0.334  -1.200  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.580   0.086  -0.551  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.611   0.242  -1.256  0.00  0.00           O+0
HETATM   11  O   UNK     0       4.677  -0.302   0.777  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.451  -0.116   1.104  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.694  -0.369   1.821  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.693  -0.219   1.718  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.860   0.028   1.030  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.099  -0.071   1.628  0.00  0.00           O+0
HETATM   17  H   UNK     0      -4.190  -0.214  -1.739  0.00  0.00           H+0
HETATM   18  H   UNK     0      -3.867   1.543  -1.745  0.00  0.00           H+0
HETATM   19  H   UNK     0      -4.834   0.839  -0.369  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.467   0.771  -1.969  0.00  0.00           H+0
HETATM   21  H   UNK     0       2.245   0.828   0.618  0.00  0.00           H+0
HETATM   22  H   UNK     0       2.175  -0.940   0.182  0.00  0.00           H+0
HETATM   23  H   UNK     0       3.078  -0.362  -2.050  0.00  0.00           H+0
HETATM   24  H   UNK     0       3.277   1.387  -1.540  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.984  -0.951   1.127  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.615  -0.628   2.792  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.725  -0.499   2.756  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.171  -0.337   2.621  0.00  0.00           H+0
CONECT    1    2   17   18   19                                             
CONECT    2    1    3   15                                                  
CONECT    3    2    4   20                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   21   22                                             
CONECT    8    7    9   23   24                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   25                                                       
CONECT   12    4   13   14                                                  
CONECT   13   12   26                                                       
CONECT   14   12   15   27                                                  
CONECT   15   14   16    2                                                  
CONECT   16   15   28                                                       
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    3                                                            
CONECT   21    7                                                            
CONECT   22    7                                                            
CONECT   23    8                                                            
CONECT   24    8                                                            
CONECT   25   11                                                            
CONECT   26   13                                                            
CONECT   27   14                                                            
CONECT   28   16                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol View NMR Assignments

Synonyms

Value	Source
4-(2,4-Dihydroxy-5-methylphenyl)-4-oxobutanoate	Generator

Chemical Formula

C₁₁H₁₂O₅

Average Mass

224.2120 Da

Monoisotopic Mass

224.06847 Da

IUPAC Name

4-(2,4-dihydroxy-5-methylphenyl)-4-oxobutanoic acid

Traditional Name

4-(2,4-dihydroxy-5-methylphenyl)-4-oxobutanoic acid

CAS Registry Number

Not Available

SMILES

CC1=C(O)C=C(O)C(=C1)C(=O)CCC(O)=O

InChI Identifier

InChI=1S/C11H12O5/c1-6-4-7(10(14)5-9(6)13)8(12)2-3-11(15)16/h4-5,13-14H,2-3H2,1H3,(H,15,16)

InChI Key

NWXNGGQNAGTBJM-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Trichoderma	NPAtlas	30920218
Trichoderma reesei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Butyrophenone
Aryl alkyl ketone
Resorcinol
P-cresol
O-cresol
Gamma-keto acid
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Toluene
Phenol
Benzenoid
Keto acid
Monocyclic benzene moiety
Vinylogous acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	1.33	ALOGPS
logP	1.91	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	3.65	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	56.36 m³·mol⁻¹	ChemAxon
Polarizability	22.31 Å³	ChemAxon
Number of Rings	1	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

NPAtlas ID

NPA025064

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

73930417

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

145720836

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Trichosorbicillin H (NP0019450)

MOL for NP0019450 (Trichosorbicillin H)

3D MOL for NP0019450 (Trichosorbicillin H)

3D SDF for NP0019450 (Trichosorbicillin H)

3D-SDF for NP0019450 (Trichosorbicillin H)

PDB for NP0019450 (Trichosorbicillin H)

3D PDB for NP0019450 (Trichosorbicillin H)

SMILES for NP0019450 (Trichosorbicillin H)

INCHI for NP0019450 (Trichosorbicillin H)

Structure for NP0019450 (Trichosorbicillin H)

3D Structure for NP0019450 (Trichosorbicillin H)