NP-MRD: Showing NP-Card for Muzigadiolide (NP0063494)

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Record Information

Version

2.0

Created at

2022-04-28 07:53:52 UTC

Updated at

2022-04-28 07:53:52 UTC

NP-MRD ID

NP0063494

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Muzigadiolide

Description

Muzigadiolide belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. Muzigadiolide is found in Canella winterana , Warburgia salutaris, Warburgia stuhlmannii and Warburgia ugandensis. Muzigadiolide was first documented in 2005 (PMID: 16153670). Muzigadiolide is an extremely weak basic (essentially neutral) compound (based on its pKa) (PMID: 16920513).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
    2.2173    1.7390    0.7145 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6406    0.8623   -0.0676 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4468   -0.1262   -0.8042 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8700   -0.0456   -0.3600 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8393   -1.4895   -0.5542 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3844   -1.4540   -0.8903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4317   -0.5107   -0.0678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5932   -0.9552    1.3479 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1818    0.8675   -0.2058 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4947    1.8475    0.6915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9559    1.7401    0.4998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5494    0.7630   -0.1205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9176    0.4407   -0.4277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9077    1.2476   -0.3844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9978   -0.9222   -0.7887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7516   -1.4984   -0.3615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7891   -0.3949   -0.7219 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7135   -0.3131   -2.0922 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6402    2.4803    1.2721 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2800    1.7878    0.8573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3960    0.1218   -1.8894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9287   -0.1187    0.7432 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5081   -0.8111   -0.8600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3008    0.9267   -0.6545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0463   -1.7498    0.4981 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3123   -2.2684   -1.1784 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2960   -1.1847   -1.9672 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0010   -2.5109   -0.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4837   -0.4733    1.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7903   -2.0443    1.3443 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3226   -0.8041    1.9603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0552    1.1906   -1.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1972    1.7413    1.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1295    2.8698    0.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5646    2.5430    0.9126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8531   -1.6250    0.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5450   -2.4491   -0.8773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8917    0.5802   -2.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  6
 17  7  1  0
  7  8  1  1
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  2  3
  7  9  1  0
  2  9  1  0
 17 12  1  0
  9 32  1  6
 10 33  1  0
 10 34  1  0
 11 35  1  0
 16 36  1  0
 16 37  1  0
 18 38  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
  6 27  1  0
  6 28  1  0
  5 25  1  0
  5 26  1  0
  3 21  1  6
  4 22  1  0
  4 23  1  0
  4 24  1  0
  1 19  1  0
  1 20  1  0
M  END


  Mrv1652309272006292D          

 19 21  0  0  1  0            999 V2000
    1.6270   -0.0302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8522   -1.4785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3182    0.3818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6037    0.7944    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3182   -0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5905    1.6537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0756    1.6593    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3312    2.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6037   -0.8553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8892   -0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1086    0.6334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1086   -0.6944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3247    1.2070    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6036   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0690    0.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8892    0.3818    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8857    1.2068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7745    0.3818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7873    2.0667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 11  1  0  0  0  0
  1 12  1  0  0  0  0
  2 12  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  9  1  0  0  0  0
  6  8  1  0  0  0  0
  7  8  1  0  0  0  0
  9 10  2  0  0  0  0
 10 12  1  0  0  0  0
  3 13  1  1  0  0  0
  4 14  1  6  0  0  0
  3 15  1  0  0  0  0
 15  7  1  0  0  0  0
  4 16  1  0  0  0  0
 16 11  1  0  0  0  0
 16 10  1  0  0  0  0
 16 17  1  1  0  0  0
 15 18  2  0  0  0  0
  7 19  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0063494

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CC=C3C(=O)OC[C@]3(O)[C@@]1(C)CC[C@H](C)C2=C

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O3/c1-9-6-7-14(3)11(10(9)2)4-5-12-13(16)18-8-15(12,14)17/h5,9,11,17H,2,4,6-8H2,1,3H3/t9-,11-,14-,15+/m0/s1

> <INCHI_KEY>
OUBGLUCJLDERNN-LHAJWOIZSA-N

> <FORMULA>
C15H20O3

> <MOLECULAR_WEIGHT>
248.322

> <EXACT_MASS>
248.141244504

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
26.8357091593836

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5aS,7S,9aS,9bS)-9b-hydroxy-7,9a-dimethyl-6-methylidene-1H,3H,5H,5aH,6H,7H,8H,9H,9aH,9bH-naphtho[1,2-c]furan-3-one

> <ALOGPS_LOGP>
2.72

> <JCHEM_LOGP>
2.3230008783333336

> <ALOGPS_LOGS>
-2.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.757194419528965

> <JCHEM_PKA_STRONGEST_BASIC>
-3.779803160898031

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
68.6198

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.46e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5aS,7S,9aS,9bS)-9b-hydroxy-7,9a-dimethyl-6-methylidene-1H,5H,5aH,7H,8H,9H-naphtho[1,2-c]furan-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-20         0                                  
HETATM    1  O   UNK     0       3.037  -0.056   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0       3.457  -2.760   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.061   0.713   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.727   1.483   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.061  -0.827   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.702   3.087   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.474   3.097   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.085   3.900   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.727  -1.597   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.393  -0.827   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.936   1.182   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.936  -1.296   0.000  0.00  0.00           C+0
HETATM   13  H   UNK     0       8.073   2.253   0.000  0.00  0.00           H+0
HETATM   14  C   UNK     0       6.727  -0.057   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.462   1.493   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.393   0.713   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.387   2.253   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.779   0.713   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.803   3.858   0.000  0.00  0.00           C+0
CONECT    1   11   12                                                       
CONECT    2   12                                                            
CONECT    3    4    5   13   15                                             
CONECT    4    3    6   14   16                                             
CONECT    5    3    9                                                       
CONECT    6    4    8                                                       
CONECT    7    8   15   19                                                  
CONECT    8    6    7                                                       
CONECT    9    5   10                                                       
CONECT   10    9   12   16                                                  
CONECT   11    1   16                                                       
CONECT   12    1    2   10                                                  
CONECT   13    3                                                            
CONECT   14    4                                                            
CONECT   15    3    7   18                                                  
CONECT   16    4   11   10   17                                             
CONECT   17   16                                                            
CONECT   18   15                                                            
CONECT   19    7                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₃

Average Mass

248.3220 Da

Monoisotopic Mass

248.14124 Da

IUPAC Name

(5aS,7S,9aS,9bS)-9b-hydroxy-7,9a-dimethyl-6-methylidene-1H,3H,5H,5aH,6H,7H,8H,9H,9aH,9bH-naphtho[1,2-c]furan-3-one

Traditional Name

(5aS,7S,9aS,9bS)-9b-hydroxy-7,9a-dimethyl-6-methylidene-1H,5H,5aH,7H,8H,9H-naphtho[1,2-c]furan-3-one

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC=C3C(=O)OC[C@]3(O)[C@@]1(C)CC[C@H](C)C2=C

InChI Identifier

InChI=1S/C15H20O3/c1-9-6-7-14(3)11(10(9)2)4-5-12-13(16)18-8-15(12,14)17/h5,9,11,17H,2,4,6-8H2,1,3H3/t9-,11-,14-,15+/m0/s1

InChI Key

OUBGLUCJLDERNN-LHAJWOIZSA-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
Canella winterana	Plant	KNApSAcK
Warburgia salutaris	LOTUS Database	35616633
Warburgia stuhlmannii	Plant	KNApSAcK
Warburgia ugandensis	LOTUS Database	35616633

Chemical Taxonomy

Description

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
Sesquiterpenoid
Naphthofuran
Gamma butyrolactone
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Lactone
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Organic oxide
Organooxygen compound
Organic oxygen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
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	2.72	ALOGPS
logP	2.32	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	12.76	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	68.62 m³·mol⁻¹	ChemAxon
Polarizability	26.84 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

Not Available

Chemspider ID

552320

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

636559

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Rugutt JK, Ngigi AN, Rugutt KJ, Ndalut PK: Native Kenyan plants as possible alternatives to methyl bromide in soil fumigation. Phytomedicine. 2006 Sep;13(8):576-83. doi: 10.1016/j.phymed.2003.08.005. Epub 2005 Jun 24. [PubMed:16920513 ]
Wube AA, Bucar F, Gibbons S, Asres K: Sesquiterpenes from Warburgia ugandensis and their antimycobacterial activity. Phytochemistry. 2005 Oct;66(19):2309-15. doi: 10.1016/j.phytochem.2005.07.018. [PubMed:16153670 ]

Showing NP-Card for Muzigadiolide (NP0063494)

MOL for NP0063494 (Muzigadiolide)

3D MOL for NP0063494 (Muzigadiolide)

3D SDF for NP0063494 (Muzigadiolide)

3D-SDF for NP0063494 (Muzigadiolide)

PDB for NP0063494 (Muzigadiolide)

3D PDB for NP0063494 (Muzigadiolide)

SMILES for NP0063494 (Muzigadiolide)

INCHI for NP0063494 (Muzigadiolide)

Structure for NP0063494 (Muzigadiolide)

3D Structure for NP0063494 (Muzigadiolide)