NP-MRD: Showing NP-Card for (-)-Ovalicin (NP0051797)

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Record Information

Version

2.0

Created at

2022-04-27 23:01:38 UTC

Updated at

2022-04-27 23:01:38 UTC

NP-MRD ID

NP0051797

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Ovalicin

Description

Ovalicin 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 ). (-)-Ovalicin is found in Graphium, Pseudeurotium ovalis and Sporothrix sp. FO-4649. (-)-Ovalicin was first documented in 2019 (PMID: 30837307). Based on a literature review a small amount of articles have been published on Ovalicin (PMID: 35366116) (PMID: 35208983) (PMID: 34946641) (PMID: 34497158).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
   -2.4986   -3.0120   -0.5873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5940   -1.7542   -1.1078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3613   -0.7134   -0.2069 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6211    0.0612   -0.0653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5964   -0.2620   -0.6847 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6634    1.2192    0.8335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3091    1.8902    0.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7198    1.6487   -0.5731 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3486    2.3849   -1.6775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0646    2.6499   -1.2430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2863    0.2042   -0.7488 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2353   -0.0602   -2.1423 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0777   -0.0877   -0.2224 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2212    0.6377   -0.9460 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1455    0.1764    1.2266 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4364   -1.1374    0.6629 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8468   -1.5834    0.8704 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7664   -0.5584    1.3804 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9089   -0.1650    0.8684 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7152    0.9261    1.5626 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5237   -0.7122   -0.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2077   -3.2059    0.2566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8872   -3.7135   -1.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4651   -3.3448   -0.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1182   -1.1001    0.8189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4684    1.9561    0.5343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9513    0.9447    1.8788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7164    1.4717    1.6243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5069    2.9769    0.9402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5200    1.9566   -2.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0739    3.1934   -1.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1265   -0.0419   -2.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9099   -0.0815   -1.3799 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7425    1.2607   -1.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7586    1.3287   -0.3000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3019   -1.8922    1.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2767   -2.0616   -0.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9024   -2.4286    1.6359 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4418   -0.0627    2.3169 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0305    1.6476    0.7643 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1193    1.4431    2.3139 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6275    0.4894    1.9960 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8527    0.1200   -1.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8723   -1.3498   -0.9548 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4664   -1.2591   -0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  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
  8 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  3
 19 20  1  0
 19 21  1  0
 11  3  1  0
 16 13  1  0
  8 10  1  1
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  1
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  9 30  1  0
  9 31  1  0
 12 32  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 16 36  1  1
 17 37  1  0
 17 38  1  0
 18 39  1  0
 20 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  0
 21 44  1  0
 21 45  1  0
M  END


  Mrv1652304282201012D          

 21 23  0  0  1  0            999 V2000
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0982   -1.1265    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7891   -1.8914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9039   -2.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6689   -3.0174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7837   -3.8344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5486   -4.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1336   -4.3423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2812   -1.2413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9052   -1.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4273   -0.7392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  7  9  1  0  0  0  0
  6 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 11 17  1  0  0  0  0
 10 17  1  1  0  0  0
 10 18  1  1  0  0  0
  6 19  1  1  0  0  0
  5 20  1  1  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0051797

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1C(=O)CC[C@]2(CO2)[C@@]1(O)[C@@]1(C)O[C@@H]1CC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C16H24O5/c1-10(2)5-6-12-14(3,21-12)16(18)13(19-4)11(17)7-8-15(16)9-20-15/h5,12-13,18H,6-9H2,1-4H3/t12-,13-,14+,15+,16+/m1/s1

> <INCHI_KEY>
NESRXFGQJARQNM-OWYFMNJBSA-N

> <FORMULA>
C16H24O5

> <MOLECULAR_WEIGHT>
296.363

> <EXACT_MASS>
296.162373873

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
31.612829803367106

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4R,5S)-4-hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one

> <ALOGPS_LOGP>
1.37

> <JCHEM_LOGP>
1.2611042726666666

> <ALOGPS_LOGS>
-2.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.883374979118631

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.50277529161838

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7462992967283735

> <JCHEM_POLAR_SURFACE_AREA>
71.59

> <JCHEM_REFRACTIVITY>
76.70150000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.66e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4R,5S)-4-hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.954   0.770   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.050  -2.103   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.473  -3.531   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.687  -5.056   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.115  -5.633   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.330  -7.158   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.757  -7.734   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.116  -8.106   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.525  -2.317   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.556  -2.423   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.798  -1.380   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       4.414  -1.897   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.954  -1.897   0.000  0.00  0.00           C+0
CONECT    1    2    7                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   20                                                  
CONECT    6    5    7   10   19                                             
CONECT    7    6    1    8    9                                             
CONECT    8    7    9                                                       
CONECT    9    8    7                                                       
CONECT   10    6   11   17   18                                             
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   11   10                                                       
CONECT   18   10                                                            
CONECT   19    6                                                            
CONECT   20    5   21                                                       
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₄O₅

Average Mass

296.3630 Da

Monoisotopic Mass

296.16237 Da

IUPAC Name

(3S,4R,5S)-4-hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one

Traditional Name

(3S,4R,5S)-4-hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one

CAS Registry Number

Not Available

SMILES

CO[C@@H]1C(=O)CC[C@]2(CO2)[C@@]1(O)[C@@]1(C)O[C@@H]1CC=C(C)C

InChI Identifier

InChI=1S/C16H24O5/c1-10(2)5-6-12-14(3,21-12)16(18)13(19-4)11(17)7-8-15(16)9-20-15/h5,12-13,18H,6-9H2,1-4H3/t12-,13-,14+,15+,16+/m1/s1

InChI Key

NESRXFGQJARQNM-OWYFMNJBSA-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
Graphium	-	KNApSAcK
Pseudeurotium ovalis	Fungi	KNApSAcK
Sporothrix sp. FO-4649	Fungi	KNApSAcK

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
Cyclic ketone
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxide
Hydrocarbon derivative
Carbonyl group
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	1.37	ALOGPS
logP	1.26	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	11.5	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	71.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	76.7 m³·mol⁻¹	ChemAxon
Polarizability	31.61 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

C00003137

Chemspider ID

9132647

KEGG Compound ID

C09674

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10957430

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

rw1491431

References

General References

Wei J, Zhou X, Dong M, Yang L, Zhao C, Lu R, Bao G, Hu F: Metabolites and novel compounds with anti-microbial or antiaging activities from Cordyceps fumosorosea. AMB Express. 2022 Apr 2;12(1):40. doi: 10.1186/s13568-022-01379-w. [PubMed:35366116 ]
Sorres J, Hebra T, Elie N, Leman-Loubiere C, Grayfer T, Grellier P, Touboul D, Stien D, Eparvier V: Antiparasitic Ovalicin Derivatives from Pseudallescheria boydii, a Mutualistic Fungus of French Guiana Termites. Molecules. 2022 Feb 10;27(4). pii: molecules27041182. doi: 10.3390/molecules27041182. [PubMed:35208983 ]
Jenssen M, Kristoffersen V, Motiram-Corral K, Isaksson J, Rama T, Andersen JH, Hansen EH, Hansen KO: Chlovalicin B, a Chlorinated Sesquiterpene Isolated from the Marine Mushroom Digitatispora marina. Molecules. 2021 Dec 13;26(24). pii: molecules26247560. doi: 10.3390/molecules26247560. [PubMed:34946641 ]
Hwang SH, Yang Y, Jeong Y, Kim Y: Ovalicin attenuates atopic dermatitis symptoms by inhibiting IL-31 signaling and intracellular calcium influx. J Biomed Res. 2021 Jun 16;35(6):448-458. doi: 10.7555/JBR.35.20210012. [PubMed:34497158 ]
Pillalamarri V, Arya T, Haque N, Bala SC, Marapaka AK, Addlagatta A: Discovery of natural product ovalicin sensitive type 1 methionine aminopeptidases: molecular and structural basis. Biochem J. 2019 Mar 22;476(6):991-1003. doi: 10.1042/BCJ20180874. [PubMed:30837307 ]

Showing NP-Card for (-)-Ovalicin (NP0051797)

MOL for NP0051797 ((-)-Ovalicin)

3D MOL for NP0051797 ((-)-Ovalicin)

3D SDF for NP0051797 ((-)-Ovalicin)

3D-SDF for NP0051797 ((-)-Ovalicin)

PDB for NP0051797 ((-)-Ovalicin)

3D PDB for NP0051797 ((-)-Ovalicin)

SMILES for NP0051797 ((-)-Ovalicin)

INCHI for NP0051797 ((-)-Ovalicin)

Structure for NP0051797 ((-)-Ovalicin)

3D Structure for NP0051797 ((-)-Ovalicin)