NP-MRD: Showing NP-Card for (3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid (NP0213432)

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Record Information

Version

2.0

Created at

2022-09-05 12:25:09 UTC

Updated at

2022-09-05 12:25:09 UTC

NP-MRD ID

NP0213432

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid

Description

20-Hydroxy-3-oxolupan-28-oic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid was first documented in 2019 (PMID: 30678231). Based on a literature review very few articles have been published on 20-Hydroxy-3-oxolupan-28-oic acid (PMID: 34222220).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052214252D          

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M  END

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M  END


  Mrv1652309052214252D          

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    4.7647   -5.8267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9398   -5.8141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5382   -5.0935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6119   -5.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4868   -4.3477    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  2  5  1  0  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  6  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  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
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 19 18  1  1  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  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 19 32  1  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  6  0  0  0
 16 34  1  0  0  0  0
 34  5  1  1  0  0  0
  8 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0213432

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)C1CC[C@@]2(CC[C@]3(C)[C@H](CC[C@H]4[C@@]5(C)CCC(=O)C(C)(C)[C@H]5CC[C@@]34C)[C@H]12)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O4/c1-25(2)20-11-14-29(7)21(27(20,5)13-12-22(25)31)9-8-19-23-18(26(3,4)34)10-15-30(23,24(32)33)17-16-28(19,29)6/h18-21,23,34H,8-17H2,1-7H3,(H,32,33)/t18?,19-,20-,21+,23+,27+,28-,29-,30+/m1/s1

> <INCHI_KEY>
OWUOWYKFORUAIE-JCYQTYIMSA-N

> <FORMULA>
C30H48O4

> <MOLECULAR_WEIGHT>
472.71

> <EXACT_MASS>
472.355260026

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
55.31784374758079

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,5S,9R,10R,13S,14R,19S)-8-(2-hydroxypropan-2-yl)-1,2,14,18,18-pentamethyl-17-oxopentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5-carboxylic acid

> <JCHEM_LOGP>
6.1577516416666676

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
19.54364159948932

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.674285248745942

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8114125782247127

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
133.7848

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,9R,10R,13S,14R,19S)-8-(2-hydroxypropan-2-yl)-1,2,14,18,18-pentamethyl-17-oxopentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       2.449  -3.953   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.105  -5.454   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.604  -5.111   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.607  -5.797   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.762  -6.956   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.346  -7.561   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.484  -9.094   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.985  -9.438   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.061 -10.670   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.666 -12.086   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -0.468 -10.485   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.735 -10.783   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.275 -10.806   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.065  -9.484   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.814 -10.830   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.315  -8.139   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.105  -6.817   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.645  -6.841   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.395  -8.186   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.935  -8.209   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.185  -6.864   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.725  -6.888   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.265  -6.911   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.014  -8.256   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.554  -8.280   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      11.224  -9.578   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.663 -10.127   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.934 -11.090   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.684  -9.555   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.894 -10.876   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.354 -10.853   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.605  -9.508   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.742 -11.042   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.775  -8.116   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6   34                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   12   34                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   32                                             
CONECT   15   14                                                            
CONECT   16   14   17   34                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   32                                                  
CONECT   20   19   21   22   29                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   20   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   19   14   33                                             
CONECT   33   32                                                            
CONECT   34   16    5    8                                                  
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Value	Source
20-Hydroxy-3-oxolupan-28-Oate	Generator

Chemical Formula

C₃₀H₄₈O₄

Average Mass

472.7100 Da

Monoisotopic Mass

472.35526 Da

IUPAC Name

(1R,2R,5S,9R,10R,13S,14R,19S)-8-(2-hydroxypropan-2-yl)-1,2,14,18,18-pentamethyl-17-oxopentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5-carboxylic acid

Traditional Name

(1R,2R,5S,9R,10R,13S,14R,19S)-8-(2-hydroxypropan-2-yl)-1,2,14,18,18-pentamethyl-17-oxopentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(C)(O)C1CC[C@@]2(CC[C@]3(C)[C@H](CC[C@H]4[C@@]5(C)CCC(=O)C(C)(C)[C@H]5CC[C@@]34C)[C@H]12)C(O)=O

InChI Identifier

InChI=1S/C30H48O4/c1-25(2)20-11-14-29(7)21(27(20,5)13-12-22(25)31)9-8-19-23-18(26(3,4)34)10-15-30(23,24(32)33)17-16-28(19,29)6/h18-21,23,34H,8-17H2,1-7H3,(H,32,33)/t18?,19-,20-,21+,23+,27+,28-,29-,30+/m1/s1

InChI Key

OWUOWYKFORUAIE-JCYQTYIMSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
18-hydroxysteroid
18-oxosteroid
Oxosteroid
Hydroxysteroid
Steroid
Tertiary alcohol
Cyclic ketone
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	6.16	ChemAxon
pKa (Strongest Acidic)	4.67	ChemAxon
pKa (Strongest Basic)	-0.81	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	133.78 m³·mol⁻¹	ChemAxon
Polarizability	55.32 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

129317046

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yang X, Zhou J, He Y, Lv L, Cao Y, Hu W: 20-Hydroxy-3-Oxolupan-28-Oic Acid, a Minor Component From Mahonia bealei (Fort.) Carr. Leaves Alleviates Lipopolysaccharide-Induced Inflammatory in Murine Macrophages. Front Bioeng Biotechnol. 2021 Jun 17;9:701876. doi: 10.3389/fbioe.2021.701876. eCollection 2021. [PubMed:34222220 ]
Cao Y, Li F, Luo Y, Zhang L, Lu S, Xing R, Yan B, Zhang H, Hu W: 20-Hydroxy-3-Oxolupan-28-Oic Acid Attenuates Inflammatory Responses by Regulating PI3K(-)Akt and MAPKs Signaling Pathways in LPS-Stimulated RAW264.7 Macrophages. Molecules. 2019 Jan 22;24(3):386. doi: 10.3390/molecules24030386. [PubMed:30678231 ]
LOTUS database [Link]

Showing NP-Card for (3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid (NP0213432)

MOL for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)

3D MOL for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)

3D SDF for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)

3D-SDF for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)

PDB for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)

3D PDB for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)

SMILES for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)

INCHI for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)

Structure for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)

3D Structure for NP0213432 ((3as,5ar,5br,7as,11ar,11bs,13ar,13br)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid)