NP-MRD: Showing NP-Card for (1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol (NP0150316)

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Record Information

Version

2.0

Created at

2022-09-02 06:22:29 UTC

Updated at

2022-09-02 06:22:29 UTC

NP-MRD ID

NP0150316

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol

Description

28-Noroleana-16,21-diene-3alpha,19alpha,23,29-tetrol belongs to the class of organic compounds known as steroids and steroid derivatives. Steroids and steroid derivatives are compounds based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred. (1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol is found in Phlomoides spectabilis. Based on a literature review very few articles have been published on 28-Noroleana-16,21-diene-3alpha,19alpha,23,29-tetrol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022208222D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309022208222D          

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    1.1270   -3.8230    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395   -3.1086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  1  0  0  0
  3  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 22 26  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 15 29  1  0  0  0  0
 10 29  1  0  0  0  0
 29 30  1  6  0  0  0
 12 31  1  0  0  0  0
 31  7  1  1  0  0  0
 31 32  1  0  0  0  0
  2 32  1  0  0  0  0
 32 33  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0150316

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]1(CO)C=CC2=CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@@H](O)[C@@](C)(CO)[C@@H]5CC[C@@]34C)[C@@H]2[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C29H46O4/c1-25(16-30)12-8-18-9-14-28(4)19(23(18)24(25)33)6-7-21-26(2)13-11-22(32)27(3,17-31)20(26)10-15-29(21,28)5/h8-9,12,19-24,30-33H,6-7,10-11,13-17H2,1-5H3/t19-,20-,21-,22-,23-,24+,25+,26+,27+,28-,29-/m1/s1

> <INCHI_KEY>
MDSHPYCQLTVNFB-IOKRWCHISA-N

> <FORMULA>
C29H46O4

> <MOLECULAR_WEIGHT>
458.683

> <EXACT_MASS>
458.339609961

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
54.13437184303177

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,6aR,6bR,8aR,9R,10R,12aR,12bR,14aR,14bS)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,2,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-octadecahydropicene-1,10-diol

> <ALOGPS_LOGP>
4.00

> <JCHEM_LOGP>
3.0267724073333335

> <ALOGPS_LOGS>
-4.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.55619448125286

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.020293770042358

> <JCHEM_PKA_STRONGEST_BASIC>
-2.785442497988596

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
133.53670000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.49e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,6aR,6bR,8aR,9R,10R,12aR,12bR,14aR,14bS)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1H-picene-1,10-diol

> <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       0.831  -5.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.564  -7.136   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.883  -6.610   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.151  -5.093   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.206  -8.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.564  -9.804   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.104  -9.804   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.874 -11.137   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.414 -11.137   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.184  -9.804   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.954 -11.137   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.414  -8.470   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.184  -7.136   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.724  -7.136   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.494  -8.470   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.034  -8.470   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.264  -7.136   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.804  -7.136   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.344  -7.136   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.114  -8.470   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      13.654  -8.470   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.344  -9.804   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.076 -11.320   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.791 -10.330   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.058 -11.847   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.804  -9.804   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.034 -11.137   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.494 -11.137   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.724  -9.804   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.885 -11.335   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.874  -8.470   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.104  -7.136   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.874  -5.803   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    5   32                                             
CONECT    3    2    4                                                       
CONECT    4    3                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   31                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   29                                             
CONECT   11   10                                                            
CONECT   12   10   13   31                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   29                                                  
CONECT   16   15   17   18   26                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24   26                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   22   16   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   15   10   30                                             
CONECT   30   29                                                            
CONECT   31   12    7   32                                                  
CONECT   32   31    2   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Value	Source
28-Noroleana-16,21-diene-3a,19a,23,29-tetrol	Generator
28-Noroleana-16,21-diene-3α,19α,23,29-tetrol	Generator

Chemical Formula

C₂₉H₄₆O₄

Average Mass

458.6830 Da

Monoisotopic Mass

458.33961 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@]1(CO)C=CC2=CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@@H](O)[C@@](C)(CO)[C@@H]5CC[C@@]34C)[C@@H]2[C@@H]1O

InChI Identifier

InChI=1S/C29H46O4/c1-25(16-30)12-8-18-9-14-28(4)19(23(18)24(25)33)6-7-21-26(2)13-11-22(32)27(3,17-31)20(26)10-15-29(21,28)5/h8-9,12,19-24,30-33H,6-7,10-11,13-17H2,1-5H3/t19-,20-,21-,22-,23-,24+,25+,26+,27+,28-,29-/m1/s1

InChI Key

MDSHPYCQLTVNFB-IOKRWCHISA-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
Phlomoides spectabilis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroids and steroid derivatives. Steroids and steroid derivatives are compounds based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Not Available

Direct Parent

Steroids and steroid derivatives

Alternative Parents

Substituents

Steroid
Cyclic alcohol
Secondary alcohol
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

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

101630392

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol (NP0150316)

MOL for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)

3D MOL for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)

3D SDF for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)

3D-SDF for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)

PDB for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)

3D PDB for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)

SMILES for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)

INCHI for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)

Structure for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)

3D Structure for NP0150316 ((1s,2s,6ar,6br,8ar,9r,10r,12ar,12br,14ar,14bs)-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-6,7,8,8a,10,11,12,12b,13,14,14a,14b-dodecahydro-1h-picene-1,10-diol)