NP-MRD: Showing NP-Card for pseuboyene F (NP0332951)

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Record Information

Version

2.0

Created at

2024-05-02 09:08:27 UTC

Updated at

2026-02-06 11:08:04 UTC

NP-MRD ID

NP0332951

Natural Product DOI

https://doi.org/10.57994/2233

Secondary Accession Numbers

None

Natural Product Identification

Common Name

pseuboyene F

Description

pseuboyene F was first documented in 2024 (PMID: 38701173). Based on a literature review very few articles have been published on pseuboyene F.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01142311452D          

 21 22  0  0  0  0            999 V2000
   -2.2414   -2.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2414   -1.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9559   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269   -0.2692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -0.2692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165    0.9683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3309   -0.2692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.9683    0.0000 C   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
   -1.6249    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1552    1.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8731    2.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0606    2.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303    1.7435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2822    1.8868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1924    1.4211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9677    1.3137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2414    0.1433    0.0000 O   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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 17  1  0  0  0  0
 17 19  1  0  0  0  0
 13 19  1  0  0  0  0
 14 20  2  0  0  0  0
  5 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0332951

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC(=O)C(OC(C)=O)C1(C)C2CC1(O)CCC2=C

> <INCHI_IDENTIFIER>
InChI=1/C17H24O4/c1-10(2)8-14(19)15(21-12(4)18)16(5)13-9-17(16,20)7-6-11(13)3/h8,13,15,20H,3,6-7,9H2,1-2,4-5H3

> <INCHI_KEY>
PJGJOAWDIKTPHN-UHFFFAOYNA-N

> <FORMULA>
C17H24O4

> <MOLECULAR_WEIGHT>
292.375

> <EXACT_MASS>
292.167459253

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
31.487260255615624

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-{1-hydroxy-6-methyl-4-methylidenebicyclo[3.1.1]heptan-6-yl}-4-methyl-2-oxopent-3-en-1-yl acetate

> <JCHEM_LOGP>
2.2665039973333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.121583155925215

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.325629413671813

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0936876702761653

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
80.08829999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-{1-hydroxy-6-methyl-4-methylidenebicyclo[3.1.1]heptan-6-yl}-4-methyl-2-oxopent-3-en-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-JAN-23         0                                  
HETATM    1  C   UNK     0      -4.184  -4.353   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.184  -2.813   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.518  -2.043   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.850  -2.043   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.850  -0.503   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.517   0.267   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.183  -0.503   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.151   0.267   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.151   1.807   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.484  -0.503   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.517   1.807   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.033   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.023   2.720   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.496   4.167   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.980   4.434   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.990   3.255   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.527   3.522   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.226   2.653   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.540   2.452   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.184   0.267   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12   13   17                                             
CONECT   12   11                                                            
CONECT   13   11   14   19                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   11   19                                             
CONECT   18   17                                                            
CONECT   19   17   13                                                       
CONECT   20   14                                                            
CONECT   21    5                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₄O₄

Average Mass

292.3750 Da

Monoisotopic Mass

292.16746 Da

IUPAC Name

1-{1-hydroxy-6-methyl-4-methylidenebicyclo[3.1.1]heptan-6-yl}-4-methyl-2-oxopent-3-en-1-yl acetate

Traditional Name

1-{1-hydroxy-6-methyl-4-methylidenebicyclo[3.1.1]heptan-6-yl}-4-methyl-2-oxopent-3-en-1-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)=CC(=O)C(OC(C)=O)C1(C)C2CC1(O)CCC2=C

InChI Identifier

InChI=1/C17H24O4/c1-10(2)8-14(19)15(21-12(4)18)16(5)13-9-17(16,20)7-6-11(13)3/h8,13,15,20H,3,6-7,9H2,1-2,4-5H3

InChI Key

PJGJOAWDIKTPHN-UHFFFAOYNA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	[email protected]	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C2D6OS, experimental)	[email protected]	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C2D6OS, experimental)	[email protected]	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C2D6OS, experimental)	[email protected]	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	[email protected]	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	[email protected]	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C2D6OS, experimental)	[email protected]	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	[email protected]	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Pseudallescheria boydii		Not Available
Pseudallescheria boydii CS-793		Not Available

Chemical Taxonomy

Classification

Not classified

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	2.27	ChemAxon
pKa (Strongest Acidic)	14.33	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	80.09 m³·mol⁻¹	ChemAxon
Polarizability	31.49 Å³	ChemAxon
Number of Rings	2	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

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

Ying Z, Li XM, Yang SQ, Li HL, Li X, Wang BG, Meng LH: Antifungal Pseuboyenes A-J, Bergamotene-Derived Sesquiterpenoids from a Cold-Seep-Derived Pseudallescheria boydii. J Nat Prod. 2024 May 24;87(5):1347-1357. doi: 10.1021/acs.jnatprod.3c01175. Epub 2024 May 3. [PubMed:38701173 ]
DOI: 10.1021/acs.jnatprod.3c01175
PMID: 38701173

Showing NP-Card for pseuboyene F (NP0332951)

MOL for NP0332951 (pseuboyene F)

3D MOL for NP0332951 (pseuboyene F)

3D SDF for NP0332951 (pseuboyene F)

3D-SDF for NP0332951 (pseuboyene F)

PDB for NP0332951 (pseuboyene F)

3D PDB for NP0332951 (pseuboyene F)

SMILES for NP0332951 (pseuboyene F)

INCHI for NP0332951 (pseuboyene F)

Structure for NP0332951 (pseuboyene F)

3D Structure for NP0332951 (pseuboyene F)