NP-MRD: Showing NP-Card for (3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol (NP0212536)

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Record Information

Version

2.0

Created at

2022-09-05 11:13:59 UTC

Updated at

2022-09-05 11:13:59 UTC

NP-MRD ID

NP0212536

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol

Description

Dihydroilludin M belongs to the class of organic compounds known as illudanes and illudins. These are sesquiterpenoids containing either the illudane moiety (based on a 3,6,6,7b-tetramethyl-decahydro-1H-cyclobuta[e]indene ring system), the illudin moiety (2',2',4',6'-tetramethyl-octahydrospiro[cyclopropane-1,5'-indene]), or a derivative thereof. (3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol is found in Granulobasidium vellereum and Omphalotus illudens. (3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol was first documented in 2015 (PMID: 26575435). Based on a literature review very few articles have been published on Dihydroilludin M.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -0.5023   -1.7746    2.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5995   -0.7899    0.8979 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4931   -0.1381    0.5275 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4604    0.8422   -0.5583 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6597    1.0584   -1.0199 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6432    0.2282   -0.2763 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8776    1.0639    0.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0524   -0.9857   -1.0654 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9120   -0.1540    0.9927 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2984   -1.4382    1.3505 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8445    1.4520   -0.9971 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1728    1.0974   -2.2855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9309    0.9838   -0.0487 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2552    1.4471   -0.5686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7072    1.6095    1.1791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8560   -0.4980    0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0609   -1.3184    0.3743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2213   -1.4628   -0.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4933   -1.9191    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0385   -2.6904    1.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1551   -1.2866    2.7872 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9471    1.7294   -1.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3932    1.2918   -0.8962 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5349    0.4631    0.6922 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5706    1.9962    0.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6193   -1.9085   -0.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1487   -1.1161   -1.0509 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7239   -0.9326   -2.1338 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0393    0.5861    1.7915 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4963   -1.5219    2.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7514    2.5583   -0.8929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1017    1.8960   -2.8914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2541    2.5708   -0.4968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3791    1.2094   -1.6501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1041    1.1135    0.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4258    1.2680    1.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0571   -0.9207    0.1888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0233   -2.1256    1.1265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6792   -2.4455   -0.9412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5670   -1.0383   -1.8281 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  9  1  0
  9 10  1  0
  9  6  1  0
  6  7  1  0
  6  8  1  0
  6  5  1  0
  5  4  2  0
  4 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  1
 13 16  1  0
 16 17  1  0
 17 18  1  0
 16  2  1  0
 18 16  1  0
  4  3  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  9 29  1  1
 10 30  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  8 28  1  0
  5 22  1  0
 11 31  1  6
 12 32  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  0
 17 37  1  0
 17 38  1  0
 18 39  1  0
 18 40  1  0
M  END


  Mrv1652309052213142D          

 18 20  0  0  1  0            999 V2000
    2.6689    1.0205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8840    0.2240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6813    0.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8964   -0.7844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7203   -0.8260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0145   -0.0552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7503   -0.4283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4624    0.6376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3723    0.4627    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4138    1.2867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3142   -1.3689    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5293   -2.1654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5169   -1.1570    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4466   -1.9790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6952   -1.2305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3018   -0.3605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5053   -0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7173    0.2217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  1  0  0  0
  4 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  6  0  0  0
 13 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0212536

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2[C@@H](O)C(C)(C)C=C2[C@@H](O)[C@](C)(O)C11CC1

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O3/c1-8-10-9(7-13(2,3)12(10)17)11(16)14(4,18)15(8)5-6-15/h7,11-12,16-18H,5-6H2,1-4H3/t11-,12-,14+/m1/s1

> <INCHI_KEY>
MBTBAQPUVNSQEB-BZPMIXESSA-N

> <FORMULA>
C15H22O3

> <MOLECULAR_WEIGHT>
250.338

> <EXACT_MASS>
250.156894568

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
28.081026444070975

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3'S,6'R,7'R)-2',2',4',6'-tetramethyl-2',3',6',7'-tetrahydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol

> <JCHEM_LOGP>
0.4207676313333327

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.961326991127553

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.071498692324436

> <JCHEM_PKA_STRONGEST_BASIC>
-3.226411518967974

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
70.4519

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3'S,6'R,7'R)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol

> <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       4.982   1.905   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.383   0.418   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.872   0.022   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.273  -1.464   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.811  -1.542   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.360  -0.103   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.734  -0.799   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.197   1.190   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.162   0.864   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.239   2.402   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.186  -2.555   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.588  -4.042   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.698  -2.160   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.567  -3.694   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.164  -2.297   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.297  -0.673   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.810  -1.075   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.206   0.414   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   16                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6    3   10                                                  
CONECT   10    9                                                            
CONECT   11    4   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13    2   17   18                                             
CONECT   17   16   18                                                       
CONECT   18   17   16                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₃

Average Mass

250.3380 Da

Monoisotopic Mass

250.15689 Da

IUPAC Name

(3'S,6'R,7'R)-2',2',4',6'-tetramethyl-2',3',6',7'-tetrahydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol

Traditional Name

(3'S,6'R,7'R)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol

CAS Registry Number

Not Available

SMILES

CC1=C2[C@@H](O)C(C)(C)C=C2[C@@H](O)[C@](C)(O)C11CC1

InChI Identifier

InChI=1S/C15H22O3/c1-8-10-9(7-13(2,3)12(10)17)11(16)14(4,18)15(8)5-6-15/h7,11-12,16-18H,5-6H2,1-4H3/t11-,12-,14+/m1/s1

InChI Key

MBTBAQPUVNSQEB-BZPMIXESSA-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
Granulobasidium vellereum	LOTUS Database	35616633
Omphalotus illudens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as illudanes and illudins. These are sesquiterpenoids containing either the illudane moiety (based on a 3,6,6,7b-tetramethyl-decahydro-1H-cyclobuta[e]indene ring system), the illudin moiety (2',2',4',6'-tetramethyl-octahydrospiro[cyclopropane-1,5'-indene]), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Illudanes and illudins

Alternative Parents

Substituents

Illudine sesquiterpenoid
Tertiary alcohol
Secondary alcohol
Polyol
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	0.42	ChemAxon
pKa (Strongest Acidic)	13.07	ChemAxon
pKa (Strongest Basic)	-3.2	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	0	ChemAxon
Refractivity	70.45 m³·mol⁻¹	ChemAxon
Polarizability	28.08 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

C00021442

Chemspider ID

142114

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

161813

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Nord C, Menkis A, Broberg A: Cytotoxic Illudane Sesquiterpenes from the Fungus Granulobasidium vellereum (Ellis and Cragin) Julich. J Nat Prod. 2015 Nov 25;78(11):2559-64. doi: 10.1021/acs.jnatprod.5b00500. Epub 2015 Nov 17. [PubMed:26575435 ]
LOTUS database [Link]

Showing NP-Card for (3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol (NP0212536)

MOL for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)

3D MOL for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)

3D SDF for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)

3D-SDF for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)

PDB for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)

3D PDB for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)

SMILES for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)

INCHI for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)

Structure for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)

3D Structure for NP0212536 ((3's,6'r,7'r)-2',2',4',6'-tetramethyl-3',7'-dihydrospiro[cyclopropane-1,5'-indene]-3',6',7'-triol)