NP-MRD: Showing NP-Card for Grisechelin F (NP0332998)

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Record Information

Version

2.0

Created at

2024-05-03 06:27:44 UTC

Updated at

2025-02-11 15:43:58 UTC

NP-MRD ID

NP0332998

Natural Product DOI

https://doi.org/10.57994/2287

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Grisechelin F

Description

Grisechelin F belongs to the class of organic compounds known as o-hydroxybenzoic acid esters. These are benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group. Grisechelin F was first documented in 2024 (PMID: 38301035). Based on a literature review very few articles have been published on Grisechelin F.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01152309042D          

 29 32  0  0  0  0            999 V2000
    0.0000   -1.6500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3731    0.8205    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1800    0.9920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5156    1.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3361    1.8319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6716    2.5856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4921    2.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8277    3.4255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3427    4.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6481    3.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1331    2.8443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7975    2.0906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9770    2.0044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1867    3.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5925    0.2775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0405   -0.3356    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 14 20  1  0  0  0  0
 13 21  2  0  0  0  0
 10 22  2  0  0  0  0
 22 23  1  0  0  0  0
  8 23  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
  5 28  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
  2 29  1  0  0  0  0
M  END


  Mrv2104 01152309042D          

 29 32  0  0  0  0            999 V2000
    0.0000   -1.6500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3731    0.8205    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1800    0.9920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5156    1.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3361    1.8319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6716    2.5856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4921    2.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8277    3.4255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3427    4.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6481    3.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1331    2.8443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7975    2.0906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9770    2.0044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1867    3.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5925    0.2775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0405   -0.3356    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 14 20  1  0  0  0  0
 13 21  2  0  0  0  0
 10 22  2  0  0  0  0
 22 23  1  0  0  0  0
  8 23  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
  5 28  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
  2 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0332998

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=C(C=CC=C1)C(=O)OCC1=CSC(=N1)C1=NC2=CC=C(Cl)C=C2C(Cl)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H12Cl2N2O4S/c21-10-5-6-14-13(7-10)16(22)18(26)17(24-14)19-23-11(9-29-19)8-28-20(27)12-3-1-2-4-15(12)25/h1-7,9,25-26H,8H2

> <INCHI_KEY>
JTPYETSFGNADBE-UHFFFAOYSA-N

> <FORMULA>
C20H12Cl2N2O4S

> <MOLECULAR_WEIGHT>
447.29

> <EXACT_MASS>
445.9894834

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
43.526774006318334

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[2-(4,6-dichloro-3-hydroxyquinolin-2-yl)-1,3-thiazol-4-yl]methyl 2-hydroxybenzoate

> <JCHEM_LOGP>
6.260694507666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.714814193124043

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.866948760388176

> <JCHEM_PKA_STRONGEST_BASIC>
-1.217946187339032

> <JCHEM_POLAR_SURFACE_AREA>
92.54

> <JCHEM_REFRACTIVITY>
119.60439999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[2-(4,6-dichloro-3-hydroxyquinolin-2-yl)-1,3-thiazol-4-yl]methyl 2-hydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-JAN-23         0                                  
HETATM    1 Cl   UNK     0       0.000  -3.080   0.000  0.00  0.00          Cl+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       5.335   0.000   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       8.163   1.532   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       9.669   1.852   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.296   3.259   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.827   3.420   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      12.454   4.826   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.985   4.987   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.612   6.394   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.706   7.640   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      16.143   6.555   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      17.048   5.309   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.422   3.903   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.890   3.742   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.549   6.072   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.439   0.518   0.000  0.00  0.00           C+0
HETATM   23  S   UNK     0       9.409  -0.626   0.000  0.00  0.00           S+0
HETATM   24  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   27 Cl   UNK     0       5.335  -4.620   0.000  0.00  0.00          Cl+0
HETATM   28  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   24                                                  
CONECT    8    7    9   23                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   22                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   14                                                       
CONECT   21   13                                                            
CONECT   22   10   23                                                       
CONECT   23   22    8                                                       
CONECT   24    7   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28    5   26   29                                                  
CONECT   29   28    2                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₂Cl₂N₂O₄S

Average Mass

447.2900 Da

Monoisotopic Mass

445.98948 Da

IUPAC Name

[2-(4,6-dichloro-3-hydroxyquinolin-2-yl)-1,3-thiazol-4-yl]methyl 2-hydroxybenzoate

Traditional Name

[2-(4,6-dichloro-3-hydroxyquinolin-2-yl)-1,3-thiazol-4-yl]methyl 2-hydroxybenzoate

CAS Registry Number

Not Available

SMILES

OC1=C(C=CC=C1)C(=O)OCC1=CSC(=N1)C1=NC2=CC=C(Cl)C=C2C(Cl)=C1O

InChI Identifier

InChI=1S/C20H12Cl2N2O4S/c21-10-5-6-14-13(7-10)16(22)18(26)17(24-14)19-23-11(9-29-19)8-28-20(27)12-3-1-2-4-15(12)25/h1-7,9,25-26H,8H2

InChI Key

JTPYETSFGNADBE-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 700 MHz, CDCl3, experimental)	[email protected]	Not Available	Not Available	2024-05-03	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 700 MHz, CDCl3, experimental)	[email protected]	Not Available	Not Available	2024-05-03	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 700 MHz, CDCl3, experimental)	[email protected]	Not Available	Not Available	2024-05-03	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl3, experimental)	[email protected]	Not Available	Not Available	2024-05-03	View Spectrum
1D_DEPT NMR	¹³C NMR Spectrum (1D, 176 MHz, CDCl3, experimental)	[email protected]	Not Available	Not Available	2024-05-03	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, CDCl3, experimental)	[email protected]	Not Available	Not Available	2024-05-03	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 700.184323611, CDCl₃, simulated)	[email protected]	South China Sea Institute of Oceanology, CAS	Wenjun Zhang	2024-05-03	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Streptomyces sp. SCSIO 40022		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as o-hydroxybenzoic acid esters. These are benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

o-Hydroxybenzoic acid esters

Alternative Parents

Substituents

O-hydroxybenzoic acid ester
Haloquinoline
Chloroquinoline
Salicylic acid or derivatives
Quinoline
Polyhalopyridine
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Hydroxypyridine
Phenol
Fatty acid ester
Fatty acyl
Pyridine
Heteroaromatic compound
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Thiazole
Secondary ketimine
Azole
Ketimine
Imidothioester
Carboxylic acid ester
Azacycle
Chloroalkene
Haloalkene
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Sulfenyl compound
Vinyl halide
Vinyl chloride
Monocarboxylic acid or derivatives
Imidothioic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Imine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	6.26	ChemAxon
pKa (Strongest Acidic)	6.87	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	92.54 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	119.6 m³·mol⁻¹	ChemAxon
Polarizability	43.53 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Liu W, Zhai S, Zhang L, Chen Y, Liu Z, Ma W, Zhang T, Zhang W, Ma L, Zhang C, Zhang W: Expanding the Chemical Diversity of Grisechelins via Heterologous Expression. J Nat Prod. 2024 Feb 23;87(2):371-380. doi: 10.1021/acs.jnatprod.3c01132. Epub 2024 Feb 1. [PubMed:38301035 ]
DOI: 10.1021/acs.jnatprod.3c01132

Showing NP-Card for Grisechelin F (NP0332998)

MOL for NP0332998 (Grisechelin F)

3D MOL for NP0332998 (Grisechelin F)

3D SDF for NP0332998 (Grisechelin F)

3D-SDF for NP0332998 (Grisechelin F)

PDB for NP0332998 (Grisechelin F)

3D PDB for NP0332998 (Grisechelin F)

SMILES for NP0332998 (Grisechelin F)

INCHI for NP0332998 (Grisechelin F)

Structure for NP0332998 (Grisechelin F)

3D Structure for NP0332998 (Grisechelin F)