NP-MRD: Showing NP-Card for (+)-Angustanal (NP0082989)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-29 04:03:03 UTC

Updated at

2022-04-29 04:03:03 UTC

NP-MRD ID

NP0082989

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Angustanal

Description

Angustanal belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (+)-Angustanal is found in Illicium angustisepalum . Based on a literature review very few articles have been published on Angustanal.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
    5.5655   -0.8887    0.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7372    0.1203    0.2172 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2759    1.4838    0.4532 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2887   -0.1073    0.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4643    0.9046    0.2602 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0040    0.7899    0.1904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5099   -0.4154   -0.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3247   -1.6153    0.2374 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7669   -1.4664   -0.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9094   -0.4736   -0.5151 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9103    0.0597   -1.9015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3828   -1.8874   -0.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8544   -1.9521   -0.8478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7148   -1.1120    0.0270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1902    0.2848    0.2511 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8221    0.7423    1.5794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6706    1.2437   -0.7725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6502    1.9822   -0.5850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7107    0.3255    0.4713 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2694    1.7430    0.6151 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1727    2.0029    0.3500 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2278   -1.9031   -0.0867 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6417   -0.7219    0.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7763    2.1881   -0.2723 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1364    1.8222    1.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3528    1.5337    0.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8845    1.9048    0.4326 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1775   -1.9154    1.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9432   -2.5014   -0.3504 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9562   -1.7750   -1.1454 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3344   -2.1550    0.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8296    1.1637   -1.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7367   -0.3484   -2.5449 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0276   -0.3247   -2.4035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8682   -2.5183   -1.2826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2518   -2.3291    0.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0628   -1.7622   -1.9104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1557   -3.0272   -0.6737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7257   -1.0898   -0.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7495   -1.6142    1.0377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2436    0.2770    2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7305    1.8462    1.6624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9063    0.4990    1.6016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2083    1.3717   -1.7519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5331   -0.1706    1.4733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5215    2.0709    1.6671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9035    2.4339   -0.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6214    2.5860    1.2081 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3221    2.6945   -0.5309 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  2  0
 15 19  1  0
 19 20  1  0
 20 21  1  0
  9  4  1  0
 19 10  1  0
 21  6  1  0
  3 24  1  0
  3 25  1  0
  3 26  1  0
  1 22  1  0
  1 23  1  0
  5 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 11 32  1  0
 11 33  1  0
 11 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 19 45  1  1
 20 46  1  0
 20 47  1  0
 21 48  1  0
 21 49  1  0
M  END


  Mrv1652304292206032D          

 21 23  0  0  1  0            999 V2000
    2.7770   -0.3020    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
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3977    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1261    1.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
  2 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
 12 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 17 20  1  1  0  0  0
 13 21  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0082989

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C1=CC2=C(CC1)[C@@]1(C)CCC[C@](C)(C=O)[C@@H]1CC2

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O/c1-14(2)15-6-8-17-16(12-15)7-9-18-19(3,13-21)10-5-11-20(17,18)4/h12-13,18H,1,5-11H2,2-4H3/t18-,19+,20+/m0/s1

> <INCHI_KEY>
NIEZTTVUVNKESL-XUVXKRRUSA-N

> <FORMULA>
C20H28O

> <MOLECULAR_WEIGHT>
284.443

> <EXACT_MASS>
284.214015522

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
34.76647314206316

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4aS,10aR)-1,4a-dimethyl-7-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,9,10,10a-decahydrophenanthrene-1-carbaldehyde

> <ALOGPS_LOGP>
4.78

> <JCHEM_LOGP>
4.402645172333335

> <ALOGPS_LOGS>
-4.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.0973878924104845

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
89.79969999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.02e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4aS,10aR)-1,4a-dimethyl-7-(prop-1-en-2-yl)-2,3,4,5,6,9,10,10a-octahydrophenanthrene-1-carbaldehyde

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.742   2.920   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.102   2.197   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.510   3.643   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   13                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    3   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12    2   14   21                                             
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12   18   20                                             
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17                                                            
CONECT   21   13                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O

Average Mass

284.4430 Da

Monoisotopic Mass

284.21402 Da

IUPAC Name

(1S,4aS,10aR)-1,4a-dimethyl-7-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,9,10,10a-decahydrophenanthrene-1-carbaldehyde

Traditional Name

(1S,4aS,10aR)-1,4a-dimethyl-7-(prop-1-en-2-yl)-2,3,4,5,6,9,10,10a-octahydrophenanthrene-1-carbaldehyde

CAS Registry Number

Not Available

SMILES

CC(=C)C1=CC2=C(CC1)[C@@]1(C)CCC[C@](C)(C=O)[C@@H]1CC2

InChI Identifier

InChI=1S/C20H28O/c1-14(2)15-6-8-17-16(12-15)7-9-18-19(3,13-21)10-5-11-20(17,18)4/h12-13,18H,1,5-11H2,2-4H3/t18-,19+,20+/m0/s1

InChI Key

NIEZTTVUVNKESL-XUVXKRRUSA-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
Illicium angustisepalum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Abietane diterpenoid
Phenanthrene
Hydrophenanthrene
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	4.78	ALOGPS
logP	4.4	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	89.8 m³·mol⁻¹	ChemAxon
Polarizability	34.77 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00049983

Chemspider ID

9025939

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10850645

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Angustanal (NP0082989)

MOL for NP0082989 ((+)-Angustanal)

3D MOL for NP0082989 ((+)-Angustanal)

3D SDF for NP0082989 ((+)-Angustanal)

3D-SDF for NP0082989 ((+)-Angustanal)

PDB for NP0082989 ((+)-Angustanal)

3D PDB for NP0082989 ((+)-Angustanal)

SMILES for NP0082989 ((+)-Angustanal)

INCHI for NP0082989 ((+)-Angustanal)

Structure for NP0082989 ((+)-Angustanal)

3D Structure for NP0082989 ((+)-Angustanal)