NP-MRD: Showing NP-Card for Jungianol (NP0063442)

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Record Information

Version

2.0

Created at

2022-04-28 07:51:29 UTC

Updated at

2022-04-28 07:51:29 UTC

NP-MRD ID

NP0063442

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Jungianol

Description

Epi-Jungianol, also known as jungianol, belongs to the class of organic compounds known as indanes. Indanes are compounds containing an indane moiety, which consists of a cyclopentane fused to a benzene ring. Jungianol is found in Jungia malvaefolia. Jungianol was first documented in 2003 (PMID: 14502619). Based on a literature review a small amount of articles have been published on epi-Jungianol (PMID: 26182950) (PMID: 23317410).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 37  0  0  0  0  0  0  0  0999 V2000
    2.6554    0.5876    1.9284 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8322    0.3829    0.4554 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0271    0.9377   -0.1962 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8889   -0.2960   -0.1871 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6992   -0.8460    0.4737 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3635   -2.2478   -0.0252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0956   -2.3463    0.2669 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8265   -3.2995   -0.6445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5834   -0.9524    0.1299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8634   -0.4517   -0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1130    0.9037   -0.1862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0525    1.7754   -0.0624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3215    3.2326   -0.1681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7812    1.2790    0.1540 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2491    2.2228    0.2700 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5292   -0.0717    0.2523 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0684   -0.2926    2.4766 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2872    1.4522    2.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6263    0.8374    2.2055 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8275    0.1477   -0.1892 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4415    1.7949    0.3670 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8262    1.2603   -1.2233 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0196   -0.4425   -1.2530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8868   -0.9513    1.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6093   -2.3420   -1.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9045   -3.0123    0.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2403   -2.6915    1.3123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8777   -2.9532   -0.7512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7994   -4.3035   -0.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3482   -3.3437   -1.6561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6832   -1.1658   -0.1819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1306    1.2683   -0.3580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5658    3.6304   -0.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1555    3.6711    0.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3373    3.4184   -0.5126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0914    3.2073    0.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
  5 16  1  0
 16 14  2  0
 14 15  1  0
 14 12  1  0
 12 13  1  0
 12 11  2  0
 11 10  1  0
 10  9  2  0
  9  7  1  0
  9 16  1  0
  8 28  1  0
  8 29  1  0
  8 30  1  0
  7 27  1  1
  6 25  1  0
  6 26  1  0
  5 24  1  1
  4 23  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
 15 36  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 11 32  1  0
 10 31  1  0
M  END


  Mrv1652304282209512D          

 16 17  0  0  1  0            999 V2000
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8838    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -0.1006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -0.8853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752    0.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  7 14  1  6  0  0  0
  3 15  1  0  0  0  0
  2 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0063442

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C[C@@H](C=C(C)C)C2=C(O)C(C)=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O/c1-9(2)7-12-8-11(4)13-6-5-10(3)15(16)14(12)13/h5-7,11-12,16H,8H2,1-4H3/t11-,12+/m0/s1

> <INCHI_KEY>
RDMPWGDHXGLLAE-NWDGAFQWSA-N

> <FORMULA>
C15H20O

> <MOLECULAR_WEIGHT>
216.324

> <EXACT_MASS>
216.151415264

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
26.26748623636681

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3S)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-2,3-dihydro-1H-inden-4-ol

> <ALOGPS_LOGP>
4.96

> <JCHEM_LOGP>
4.535402562333333

> <ALOGPS_LOGS>
-4.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.71355638004473

> <JCHEM_PKA_STRONGEST_BASIC>
-6.00357639061922

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
69.6591

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.69e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-2,3-dihydro-1H-inden-4-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.126   1.597   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.650   0.132   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.143  -0.188   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.333  -1.652   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.887   0.957   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.650   5.553   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.924  -0.237   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.591   1.303   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   16                                                  
CONECT    3    2    4   15                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   14                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    7                                                            
CONECT   15    3                                                            
CONECT   16    2                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

View in JSmol

Synonyms

Value	Source
Jungianol	MeSH

Chemical Formula

C₁₅H₂₀O

Average Mass

216.3240 Da

Monoisotopic Mass

216.15142 Da

IUPAC Name

(1S,3S)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-2,3-dihydro-1H-inden-4-ol

Traditional Name

(1S,3S)-1,5-dimethyl-3-(2-methylprop-1-en-1-yl)-2,3-dihydro-1H-inden-4-ol

CAS Registry Number

Not Available

SMILES

C[C@H]1C[C@@H](C=C(C)C)C2=C(O)C(C)=CC=C12

InChI Identifier

InChI=1S/C15H20O/c1-9(2)7-12-8-11(4)13-6-5-10(3)15(16)14(12)13/h5-7,11-12,16H,8H2,1-4H3/t11-,12+/m0/s1

InChI Key

RDMPWGDHXGLLAE-NWDGAFQWSA-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
Jungia malvaefolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indanes. Indanes are compounds containing an indane moiety, which consists of a cyclopentane fused to a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Indanes

Sub Class

Not Available

Direct Parent

Indanes

Alternative Parents

Substituents

Indane
1-hydroxy-4-unsubstituted benzenoid
Phenol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	4.96	ALOGPS
logP	4.54	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	9.71	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	69.66 m³·mol⁻¹	ChemAxon
Polarizability	26.27 Å³	ChemAxon
Number of Rings	2	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

Not Available

Chemspider ID

9508352

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11333406

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Dethe DH, Murhade GM, Ghosh S: FeCl3-Catalyzed Intramolecular Michael Reaction of Styrenes for the Synthesis of Highly Substituted Indenes. J Org Chem. 2015 Aug 21;80(16):8367-76. doi: 10.1021/acs.joc.5b01071. Epub 2015 Jul 31. [PubMed:26182950 ]
Dethe DH, Murhade G: FeCl3 catalyzed Prins-type cyclization for the synthesis of highly substituted indenes: application to the total synthesis of (+/-)-jungianol and epi-jungianol. Org Lett. 2013 Feb 1;15(3):429-31. doi: 10.1021/ol3032347. Epub 2013 Jan 14. [PubMed:23317410 ]
Hashmi AS, Ding L, Bats JW, Fischer P, Frey W: Gold catalysis: efficient synthesis and structural assignment of jungianol and epi-jungianol. Chemistry. 2003 Sep 22;9(18):4339-45. doi: 10.1002/chem.200305092. [PubMed:14502619 ]

Showing NP-Card for Jungianol (NP0063442)

MOL for NP0063442 (Jungianol)

3D MOL for NP0063442 (Jungianol)

3D SDF for NP0063442 (Jungianol)

3D-SDF for NP0063442 (Jungianol)

PDB for NP0063442 (Jungianol)

3D PDB for NP0063442 (Jungianol)

SMILES for NP0063442 (Jungianol)

INCHI for NP0063442 (Jungianol)

Structure for NP0063442 (Jungianol)

3D Structure for NP0063442 (Jungianol)