NP-MRD: Showing NP-Card for Dolichocarpol Q (NP0333634)

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Record Information

Version

2.0

Created at

2024-07-31 18:58:46 UTC

Updated at

2026-02-04 16:59:11 UTC

NP-MRD ID

NP0333634

Natural Product DOI

https://doi.org/10.57994/3113

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Dolichocarpol Q

Description

Dolichocarpol Q belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. Dolichocarpol Q was first documented in 2025 (PMID: 39826808). Based on a literature review very few articles have been published on Dolichocarpol Q.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 04142321322D          

 20 21  0  0  1  0            999 V2000
    0.2603   -1.3072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0762   -1.1844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0143   -2.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7749   -0.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1875    0.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0034    0.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8278    0.9215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5911    0.6085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0247   -0.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -0.9161    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7644   -0.7207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3964   -1.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4293   -1.5453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6278   -1.7408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8645   -1.4277    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5860   -2.2043    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5462   -0.9631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6080   -0.1405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3760    0.1608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8262    0.1020    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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
 10  9  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  1  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  0  0  0  0
 15  2  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  2  0  0  0  0
  9 20  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0333634

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CC[C@@](C)(O)C(=O)CCC(=CCC1(C)C)C(=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O4/c1-14(2)8-6-10-4-5-11(16)15(3,18)9-7-12(14)19-13(10)17/h6,12,18H,4-5,7-9H2,1-3H3/t12-,15-/m1/s1

> <INCHI_KEY>
ATBNINQLVCIJDY-IUODEOHRSA-N

> <FORMULA>
C15H22O4

> <MOLECULAR_WEIGHT>
266.337

> <EXACT_MASS>
266.151809188

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
28.370718187362616

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4R)-4-hydroxy-4,11,11-trimethyl-12-oxabicyclo[6.3.2]tridec-8-ene-5,13-dione

> <JCHEM_LOGP>
2.599929376333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.67185068143293

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.270419316931159

> <JCHEM_PKA_STRONGEST_BASIC>
-3.555318431872809

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
71.62069999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R)-4-hydroxy-4,11,11-trimethyl-12-oxabicyclo[6.3.2]tridec-8-ene-5,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-APR-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-APR-23         0                                  
HETATM    1  C   UNK     0       0.486  -2.440   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.009  -2.211   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.893  -3.747   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.446  -0.777   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.217   0.556   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.740   0.785   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.279   1.720   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.703   1.136   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.513  -0.174   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.397  -1.710   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.894  -1.345   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.207  -3.020   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.401  -2.885   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.905  -3.249   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.480  -2.665   0.000  0.00  0.00           C+0
HETATM   16  H   UNK     0       2.961  -4.115   0.000  0.00  0.00           H+0
HETATM   17  O   UNK     0       4.753  -1.798   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.868  -0.262   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.302   0.300   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       9.009   0.190   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   15                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   20                                                  
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    2   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    6   19                                                  
CONECT   19   18                                                            
CONECT   20    9                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₄

Average Mass

266.3370 Da

Monoisotopic Mass

266.15181 Da

IUPAC Name

(1R,4R)-4-hydroxy-4,11,11-trimethyl-12-oxabicyclo[6.3.2]tridec-8-ene-5,13-dione

Traditional Name

(1R,4R)-4-hydroxy-4,11,11-trimethyl-12-oxabicyclo[6.3.2]tridec-8-ene-5,13-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC[C@@](C)(O)C(=O)CCC(=CCC1(C)C)C(=O)O2

InChI Identifier

InChI=1S/C15H22O4/c1-14(2)8-6-10-4-5-11(16)15(3,18)9-7-12(14)19-13(10)17/h6,12,18H,4-5,7-9H2,1-3H3/t12-,15-/m1/s1

InChI Key

ATBNINQLVCIJDY-IUODEOHRSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View

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, 500.0, Chloroform-d, simulated)	epoynton@sfu.ca	Not Available	Not Available	2026-02-04	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125.0, Chloroform-d, simulated)	epoynton@sfu.ca	Not Available	Not Available	2026-02-04	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Anaxagorea Anaxagorea dolichocarpa		Not Available
Anaxagorea dolichocarpa		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Farsesane sesquiterpenoid
Sesquiterpenoid
Fatty acid ester
Fatty acyl
Acyloin
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Alpha-hydroxy ketone
Cyclic ketone
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
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	2.6	ChemAxon
pKa (Strongest Acidic)	13.27	ChemAxon
pKa (Strongest Basic)	-3.6	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	0	ChemAxon
Refractivity	71.62 m³·mol⁻¹	ChemAxon
Polarizability	28.37 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

DOI: 10.1016/j.phytochem.2025.114406

Showing NP-Card for Dolichocarpol Q (NP0333634)

MOL for NP0333634 (Dolichocarpol Q)

3D MOL for NP0333634 (Dolichocarpol Q)

3D SDF for NP0333634 (Dolichocarpol Q)

3D-SDF for NP0333634 (Dolichocarpol Q)

PDB for NP0333634 (Dolichocarpol Q)

3D PDB for NP0333634 (Dolichocarpol Q)

SMILES for NP0333634 (Dolichocarpol Q)

INCHI for NP0333634 (Dolichocarpol Q)

Structure for NP0333634 (Dolichocarpol Q)

3D Structure for NP0333634 (Dolichocarpol Q)