NP-MRD: Showing NP-Card for pseuboyene B (NP0332947)

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Record Information

Version

2.0

Created at

2024-05-02 08:33:14 UTC

Updated at

2024-11-01 01:37:22 UTC

NP-MRD ID

NP0332947

Natural Product DOI

https://doi.org/10.57994/2229

Secondary Accession Numbers

None

Natural Product Identification

Common Name

pseuboyene B

Description

Pseuboyene B belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review very few articles have been published on pseuboyene B.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01142311102D          

 18 19  0  0  1  0            999 V2000
   -3.3410    1.0804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5367    1.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2935    2.0524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9755    0.6593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1712    0.8428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6101    0.2381    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8532   -0.5503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1942    0.4217    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1637    1.1650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1942   -0.4033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8393    0.9360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6436    0.7525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0015    0.0092    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8265    0.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6436   -0.7341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8393   -0.9177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6075    0.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1579    1.3975    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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
  8 11  1  6  0  0  0
 11 12  1  0  0  0  0
 13 12  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 12 18  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0332947

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC[C@@H](O)[C@@]1(C)OC2CC1C(=C)[C@H](O)C2

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O3/c1-9(2)5-6-14(17)15(4)12-7-11(18-15)8-13(16)10(12)3/h5,11-14,16-17H,3,6-8H2,1-2,4H3/t11?,12?,13-,14-,15+/m1/s1

> <INCHI_KEY>
RHJFPPCLZFUUQL-ODGNXRKOSA-N

> <FORMULA>
C15H24O3

> <MOLECULAR_WEIGHT>
252.354

> <EXACT_MASS>
252.172544633

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
28.98541234793303

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,7S)-7-[(1R)-1-hydroxy-4-methylpent-3-en-1-yl]-7-methyl-2-methylidene-6-oxabicyclo[3.2.1]octan-3-ol

> <JCHEM_LOGP>
1.3663755483333326

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.631174312851327

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.826511939524169

> <JCHEM_PKA_STRONGEST_BASIC>
-3.001345288336596

> <JCHEM_POLAR_SURFACE_AREA>
49.69

> <JCHEM_REFRACTIVITY>
72.1078

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3R,7S)-7-[(1R)-1-hydroxy-4-methylpent-3-en-1-yl]-7-methyl-2-methylidene-6-oxabicyclo[3.2.1]octan-3-ol

> <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      -6.237   2.017   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.735   2.360   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.281   3.831   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.688   1.231   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.186   1.573   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.139   0.444   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.593  -1.027   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.363   0.787   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.306   2.175   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.363  -0.753   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.567   1.747   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.068   1.405   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.736   0.017   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.276   0.017   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.068  -1.370   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.567  -1.713   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.134   0.017   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.028   2.609   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8   16                                                       
CONECT   11    8   12   17                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16   11                                                       
CONECT   18   12                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O₃

Average Mass

252.3540 Da

Monoisotopic Mass

252.17254 Da

IUPAC Name

(3R,7S)-7-[(1R)-1-hydroxy-4-methylpent-3-en-1-yl]-7-methyl-2-methylidene-6-oxabicyclo[3.2.1]octan-3-ol

Traditional Name

(3R,7S)-7-[(1R)-1-hydroxy-4-methylpent-3-en-1-yl]-7-methyl-2-methylidene-6-oxabicyclo[3.2.1]octan-3-ol

CAS Registry Number

Not Available

SMILES

CC(C)=CC[C@@H](O)[C@@]1(C)OC2CC1C(=C)[C@H](O)C2

InChI Identifier

InChI=1S/C15H24O3/c1-9(2)5-6-14(17)15(4)12-7-11(18-15)8-13(16)10(12)3/h5,11-14,16-17H,3,6-8H2,1-2,4H3/t11?,12?,13-,14-,15+/m1/s1

InChI Key

RHJFPPCLZFUUQL-ODGNXRKOSA-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)	m8545303@163.com	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C2D6OS, experimental)	m8545303@163.com	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C2D6OS, experimental)	m8545303@163.com	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C2D6OS, experimental)	m8545303@163.com	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	m8545303@163.com	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)	m8545303@163.com	Institute of Oceanology, Chinese Academy of Sciences	Linghong Meng	2024-05-02	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C2D6OS, experimental)	m8545303@163.com	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)	m8545303@163.com	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
boydii		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Oxepane
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	ChemAxon
pKa (Strongest Acidic)	13.83	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	49.69 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	72.11 m³·mol⁻¹	ChemAxon
Polarizability	28.99 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

Showing NP-Card for pseuboyene B (NP0332947)

MOL for NP0332947 (pseuboyene B)

3D MOL for NP0332947 (pseuboyene B)

3D SDF for NP0332947 (pseuboyene B)

3D-SDF for NP0332947 (pseuboyene B)

PDB for NP0332947 (pseuboyene B)

3D PDB for NP0332947 (pseuboyene B)

SMILES for NP0332947 (pseuboyene B)

INCHI for NP0332947 (pseuboyene B)

Structure for NP0332947 (pseuboyene B)

3D Structure for NP0332947 (pseuboyene B)