NP-MRD: Showing NP-Card for (2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol (NP0161246)

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Record Information

Version

2.0

Created at

2022-09-02 19:22:30 UTC

Updated at

2022-09-02 19:22:30 UTC

NP-MRD ID

NP0161246

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol

Description

(2R)-2-[(1R,2R,5S,6S,9R,10S,13R,14S,19S)-9-(hydroxymethyl)-1,2,14,18,18-pentamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-6-yl]propan-1-ol belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30). (2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol is found in Lophosoria quadripinnata. Based on a literature review very few articles have been published on (2R)-2-[(1R,2R,5S,6S,9R,10S,13R,14S,19S)-9-(hydroxymethyl)-1,2,14,18,18-pentamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-6-yl]propan-1-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022221222D          

 32 36  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309022221222D          

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    0.4685    1.9434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1378    1.1206    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5611    1.8287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3860    1.8162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7876    1.0955    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7139    1.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  2  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 20 28  1  0  0  0  0
 28 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 19 31  1  0  0  0  0
 14 31  1  0  0  0  0
 31 32  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0161246

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](CO)[C@H]1CC[C@@]2(CO)[C@H]1CC[C@]1(C)[C@@H]2CC[C@@H]2[C@@]3(C)CCCC(C)(C)[C@@H]3CC[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H52O2/c1-20(18-31)21-10-17-30(19-32)22(21)11-15-29(6)25(30)9-8-24-27(4)14-7-13-26(2,3)23(27)12-16-28(24,29)5/h20-25,31-32H,7-19H2,1-6H3/t20-,21+,22-,23-,24+,25-,27-,28+,29+,30+/m0/s1

> <INCHI_KEY>
IIGGBARDSBQECF-MKDCHBEHSA-N

> <FORMULA>
C30H52O2

> <MOLECULAR_WEIGHT>
444.744

> <EXACT_MASS>
444.396730914

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
55.81444884149395

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-2-[(1R,2R,5S,6S,9R,10S,13R,14S,19S)-9-(hydroxymethyl)-1,2,14,18,18-pentamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-6-yl]propan-1-ol

> <ALOGPS_LOGP>
5.84

> <JCHEM_LOGP>
6.387007315666667

> <ALOGPS_LOGS>
-6.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.233616595515162

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.685661618596644

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8641082588563512

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
133.2417

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.50e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-[(1R,2R,5S,6S,9R,10S,13R,14S,19S)-9-(hydroxymethyl)-1,2,14,18,18-pentamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-6-yl]propan-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      12.187   4.156   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.484   2.645   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.941   2.146   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      15.101   3.159   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.324   1.632   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.462   0.098   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.046  -0.507   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.033   0.653   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.385  -0.744   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.271  -2.004   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.823   1.975   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.073   3.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.534   3.343   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.743   2.022   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.994   3.367   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.493   0.676   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.703  -0.645   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.163  -0.622   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.413   0.723   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.874   0.747   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.623  -0.599   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.083  -0.575   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.543  -0.552   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.206   0.793   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.584   2.115   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.855   2.664   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.875   3.628   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.124   2.092   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.914   3.414   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.454   3.390   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.204   2.045   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.066   3.579   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    5                                                  
CONECT    3    2    4                                                       
CONECT    4    3                                                            
CONECT    5    2    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   11   16                                             
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8    5   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   31                                             
CONECT   15   14                                                            
CONECT   16   14    8   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   31                                                  
CONECT   20   19   21   22   28                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   20   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   19   14   32                                             
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₅₂O₂

Average Mass

444.7440 Da

Monoisotopic Mass

444.39673 Da

IUPAC Name

(2R)-2-[(1R,2R,5S,6S,9R,10S,13R,14S,19S)-9-(hydroxymethyl)-1,2,14,18,18-pentamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-6-yl]propan-1-ol

Traditional Name

(2R)-2-[(1R,2R,5S,6S,9R,10S,13R,14S,19S)-9-(hydroxymethyl)-1,2,14,18,18-pentamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-6-yl]propan-1-ol

CAS Registry Number

Not Available

SMILES

C[C@@H](CO)[C@H]1CC[C@@]2(CO)[C@H]1CC[C@]1(C)[C@@H]2CC[C@@H]2[C@@]3(C)CCCC(C)(C)[C@@H]3CC[C@@]12C

InChI Identifier

InChI=1S/C30H52O2/c1-20(18-31)21-10-17-30(19-32)22(21)11-15-29(6)25(30)9-8-24-27(4)14-7-13-26(2,3)23(27)12-16-28(24,29)5/h20-25,31-32H,7-19H2,1-6H3/t20-,21+,22-,23-,24+,25-,27-,28+,29+,30+/m0/s1

InChI Key

IIGGBARDSBQECF-MKDCHBEHSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Lophosoria quadripinnata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Hopanoids

Direct Parent

Hopanoids

Alternative Parents

Substituents

Triterpenoid
Hopane-skeleton
21-hydroxysteroid
Hydroxysteroid
Steroid
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
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	5.84	ALOGPS
logP	6.39	ChemAxon
logS	-6.9	ALOGPS
pKa (Strongest Acidic)	17.69	ChemAxon
pKa (Strongest Basic)	-0.86	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	133.24 m³·mol⁻¹	ChemAxon
Polarizability	55.81 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

162878448

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol (NP0161246)

MOL for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)

3D MOL for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)

3D SDF for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)

3D-SDF for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)

PDB for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)

3D PDB for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)

SMILES for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)

INCHI for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)

Structure for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)

3D Structure for NP0161246 ((2r)-2-[(3s,3as,5ar,5br,7as,11as,11br,13as,13br)-13b-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol)