NP-MRD: Showing NP-Card for Roscoeanane C (NP0341861)

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Record Information

Version

2.0

Created at

2024-09-30 14:51:56 UTC

Updated at

2025-06-11 06:35:32 UTC

NP-MRD ID

NP0341861

Natural Product DOI

https://doi.org/10.57994/3349

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Roscoeanane C

Description

Roscoeanane C belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Based on a literature review very few articles have been published on Roscoeanane C.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 06142317232D          

 24 26  0  0  1  0            999 V2000
    0.6257   -1.0731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4009   -1.3553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5442   -2.1678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4009   -0.2947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3329   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6021    0.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5206    0.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5966   -1.6455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    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
  4  2  1  6  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  8  7  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 11 10  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  0  0  0  0
 19 11  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21  7  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
  4 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0341861

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12C[C@@H](O)C3=C[C@](O)(CC[C@]3(O)[C@@]1(C)CCCC2(C)C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H34O3/c1-13(2)19(22)9-10-20(23)14(12-19)15(21)11-16-17(3,4)7-6-8-18(16,20)5/h12-13,15-16,21-23H,6-11H2,1-5H3/t15-,16+,18+,19-,20-/m1/s1

> <INCHI_KEY>
CTNOCMRDHMLGSQ-MEBIHWHUSA-N

> <FORMULA>
C20H34O3

> <MOLECULAR_WEIGHT>
322.489

> <EXACT_MASS>
322.250794955

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
37.8713773110792

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,4aS,4bS,8aS,10R)-4b,8,8-trimethyl-2-(propan-2-yl)-2,3,4,4a,4b,5,6,7,8,8a,9,10-dodecahydrophenanthrene-2,4a,10-triol

> <JCHEM_LOGP>
2.850902535666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.177692369449828

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.552056850271697

> <JCHEM_PKA_STRONGEST_BASIC>
-3.011402934634969

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
92.98769999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4aS,4bS,8aS,10R)-2-isopropyl-4b,8,8-trimethyl-3,4,5,6,7,8a,9,10-octahydrophenanthrene-2,4a,10-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-JUN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-JUN-23         0                                  
HETATM    1  C   UNK     0       1.168  -2.003   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.615  -2.530   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.882  -4.046   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.615  -0.550   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.105   2.461   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   12  H   UNK     0       9.955  -1.540   0.000  0.00  0.00           H+0
HETATM   13  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.457   1.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.172   0.320   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.645  -2.874   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.714  -3.072   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6   24                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   21                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13   19                                             
CONECT   12   11                                                            
CONECT   13   11   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   11   20   21                                             
CONECT   20   19                                                            
CONECT   21   19    7   22   23                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23    4                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₄O₃

Average Mass

322.4890 Da

Monoisotopic Mass

322.25079 Da

IUPAC Name

(2S,4aS,4bS,8aS,10R)-4b,8,8-trimethyl-2-(propan-2-yl)-2,3,4,4a,4b,5,6,7,8,8a,9,10-dodecahydrophenanthrene-2,4a,10-triol

Traditional Name

(2S,4aS,4bS,8aS,10R)-2-isopropyl-4b,8,8-trimethyl-3,4,5,6,7,8a,9,10-octahydrophenanthrene-2,4a,10-triol

CAS Registry Number

Not Available

SMILES

[H][C@@]12C[C@@H](O)C3=C[C@](O)(CC[C@]3(O)[C@@]1(C)CCCC2(C)C)C(C)C

InChI Identifier

InChI=1S/C20H34O3/c1-13(2)19(22)9-10-20(23)14(12-19)15(21)11-16-17(3,4)7-6-8-18(16,20)5/h12-13,15-16,21-23H,6-11H2,1-5H3/t15-,16+,18+,19-,20-/m1/s1

InChI Key

CTNOCMRDHMLGSQ-MEBIHWHUSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	ratchanaporn.ch@up.ac.th	University of Phayao	Ratchanaporn Chokchaisiri	2024-09-30	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	ratchanaporn.ch@up.ac.th	University of Phayao	Ratchanaporn Chokchaisiri	2024-09-30	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl3, experimental)	ratchanaporn.ch@up.ac.th	University of Phayao	Ratchanaporn Chokchaisiri	2024-09-30	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	ratchanaporn.ch@up.ac.th	University of Phayao	Ratchanaporn Chokchaisiri	2024-09-30	View Spectrum
HMQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	ratchanaporn.ch@up.ac.th	University of Phayao	Ratchanaporn Chokchaisiri	2024-09-30	View Spectrum
1D_DEPT NMR	¹³C NMR Spectrum (1D, 101 MHz, CDCl3, experimental)	ratchanaporn.ch@up.ac.th	University of Phayao	Ratchanaporn Chokchaisiri	2024-09-30	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, CDCl3, experimental)	ratchanaporn.ch@up.ac.th	University of Phayao	Ratchanaporn Chokchaisiri	2024-09-30	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl3, experimental)	ratchanaporn.ch@up.ac.th	University of Phayao	Ratchanaporn Chokchaisiri	2024-09-30	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
Kaempferia roscoeana		Not Available

Chemical Taxonomy

Description

This compound 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
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	2.85	ChemAxon
pKa (Strongest Acidic)	13.55	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	92.99 m³·mol⁻¹	ChemAxon
Polarizability	37.87 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

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 Roscoeanane C (NP0341861)

MOL for NP0341861 (Roscoeanane C)

3D MOL for NP0341861 (Roscoeanane C)

3D SDF for NP0341861 (Roscoeanane C)

3D-SDF for NP0341861 (Roscoeanane C)

PDB for NP0341861 (Roscoeanane C)

3D PDB for NP0341861 (Roscoeanane C)

SMILES for NP0341861 (Roscoeanane C)

INCHI for NP0341861 (Roscoeanane C)

Structure for NP0341861 (Roscoeanane C)

3D Structure for NP0341861 (Roscoeanane C)