NP-MRD: Showing NP-Card for (1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate (NP0284637)

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Record Information

Version

2.0

Created at

2022-09-09 12:26:34 UTC

Updated at

2022-09-09 12:26:34 UTC

NP-MRD ID

NP0284637

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate

Description

Turraparvin D belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group. (1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate is found in Turnera odorata. (1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate was first documented in 2003 (PMID: 12648531). Based on a literature review very few articles have been published on Turraparvin D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092214262D          

 34 38  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309092214262D          

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 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 27 31  1  0  0  0  0
 31 32  1  0  0  0  0
 26 33  1  0  0  0  0
 23 33  1  0  0  0  0
  5 33  1  0  0  0  0
 33 34  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0284637

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@@H]2[C@@]3(C)C=CC(=O)C(C)(C)[C@@H]3C[C@@H](O)[C@@]2(C)C2=CC[C@@H](C3=CCN=C3O)[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C28H37NO5/c1-15(30)34-23-14-20-26(4)11-9-21(31)25(2,3)19(26)13-22(32)28(20,6)18-8-7-17(27(18,23)5)16-10-12-29-24(16)33/h8-11,17,19-20,22-23,32H,7,12-14H2,1-6H3,(H,29,33)/t17-,19-,20+,22+,23-,26-,27-,28-/m0/s1

> <INCHI_KEY>
QJFDATLJUPEHJF-LXEMIKRWSA-N

> <FORMULA>
C28H37NO5

> <MOLECULAR_WEIGHT>
467.606

> <EXACT_MASS>
467.267173295

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
51.447030627785104

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,7R,9R,10R,14R,15S,16S)-9-hydroxy-14-(5-hydroxy-2H-pyrrol-4-yl)-2,6,6,10,15-pentamethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,11-dien-16-yl acetate

> <JCHEM_LOGP>
3.3362958160000007

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
16.4087405788317

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.107332276202514

> <JCHEM_PKA_STRONGEST_BASIC>
2.286618871828419

> <JCHEM_POLAR_SURFACE_AREA>
96.19000000000001

> <JCHEM_REFRACTIVITY>
131.3844

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,7R,9R,10R,14R,15S,16S)-9-hydroxy-14-(2-hydroxy-5H-pyrrol-3-yl)-2,6,6,10,15-pentamethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,11-dien-16-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       6.244  -1.307   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.728  -1.036   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.205   0.413   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.735  -2.213   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.184  -8.144   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.322  -8.817   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.835  -9.184   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.312  -7.735   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.758  -3.723   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.281  -2.274   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0      -0.065  -1.329   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       1.209  -2.193   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.658  -1.670   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.594  -3.453   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   33                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   21                                                  
CONECT    8    7    9   10   17                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14    8   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    7   22   23                                             
CONECT   22   21                                                            
CONECT   23   21   24   33                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   33                                                  
CONECT   27   26   28   31                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   27   32                                                  
CONECT   32   31                                                            
CONECT   33   26   23    5   34                                             
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₇NO₅

Average Mass

467.6060 Da

Monoisotopic Mass

467.26717 Da

IUPAC Name

(1R,2R,7R,9R,10R,14R,15S,16S)-9-hydroxy-14-(5-hydroxy-2H-pyrrol-4-yl)-2,6,6,10,15-pentamethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,11-dien-16-yl acetate

Traditional Name

(1R,2R,7R,9R,10R,14R,15S,16S)-9-hydroxy-14-(2-hydroxy-5H-pyrrol-3-yl)-2,6,6,10,15-pentamethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,11-dien-16-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@@H]2[C@@]3(C)C=CC(=O)C(C)(C)[C@@H]3C[C@@H](O)[C@@]2(C)C2=CC[C@@H](C3=CCN=C3O)[C@]12C

InChI Identifier

InChI=1S/C28H37NO5/c1-15(30)34-23-14-20-26(4)11-9-21(31)25(2,3)19(26)13-22(32)28(20,6)18-8-7-17(27(18,23)5)16-10-12-29-24(16)33/h8-11,17,19-20,22-23,32H,7,12-14H2,1-6H3,(H,29,33)/t17-,19-,20+,22+,23-,26-,27-,28-/m0/s1

InChI Key

QJFDATLJUPEHJF-LXEMIKRWSA-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
Turnera odorata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid esters

Direct Parent

Steroid esters

Alternative Parents

Substituents

Steroid ester
3-oxo-delta-1-steroid
3-oxosteroid
Hydroxysteroid
Oxosteroid
7-hydroxysteroid
3-oxo-5-alpha-steroid
Delta-1-steroid
Cyclohexenone
Cyclic alcohol
Pyrroline
Secondary carboxylic acid amide
Secondary alcohol
Cyclic ketone
Carboxamide group
Lactam
Ketone
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organic oxygen compound
Organopnictogen compound
Organic nitrogen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	3.34	ChemAxon
pKa (Strongest Acidic)	6.11	ChemAxon
pKa (Strongest Basic)	2.29	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	96.19 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	131.38 m³·mol⁻¹	ChemAxon
Polarizability	51.45 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

4479742

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5322179

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Cheplogoi PK, Mulholland DA: Tetranortriterpenoid derivatives from Turraea parvifolia (Meliaceae). Phytochemistry. 2003 Apr;62(8):1173-8. doi: 10.1016/s0031-9422(03)00028-1. [PubMed:12648531 ]
LOTUS database [Link]

Showing NP-Card for (1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate (NP0284637)

MOL for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D MOL for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D SDF for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D-SDF for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

PDB for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D PDB for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

SMILES for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

INCHI for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

Structure for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D Structure for NP0284637 ((1r,3br,4r,5ar,9ar,9br,11s,11as)-4-hydroxy-1-(2-hydroxy-5h-pyrrol-3-yl)-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)