NP-MRD: Showing NP-Card for Repandiol (NP0004721)

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Record Information

Version

2.0

Created at

2020-12-09 02:08:45 UTC

Updated at

2021-07-15 16:49:58 UTC

NP-MRD ID

NP0004721

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Repandiol

Provided By

NPAtlas

Description

Repandiol is found in Russula subnigricans. Repandiol was first documented in 1992 (PMID: 1294319). Based on a literature review very few articles have been published on [(2R,3R)-3-{4-[(2R,3R)-3-(hydroxymethyl)oxiran-2-yl]buta-1,3-diyn-1-yl}oxiran-2-yl]methanol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118083D          

 24 25  0  0  0  0            999 V2000
    5.9180   -0.0862    1.2794 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6815    0.0867   -0.0835 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2417    0.3680   -0.3781 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9166    0.5525   -1.7010 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3765   -0.6195   -1.0478 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9287   -0.5689   -0.7748 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7446   -0.5256   -0.5324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472   -0.4786   -0.2238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8221   -0.4441    0.0569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2401   -0.3994    0.4198 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7466    0.8596    0.8425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1744    0.2948   -0.4191 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.6656   -0.0465   -0.3457 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4076    1.1049   -0.0841 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0655    0.1517    1.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0575   -0.8087   -0.6048 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2898    0.9636   -0.4412 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7403    1.0099    0.3889 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7513   -1.5368   -1.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5881   -1.2191    1.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8265    0.8827   -1.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7850   -0.7780    0.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9956   -0.5340   -1.2778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8133    1.7709    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  3  0  0  0  0
  7  8  1  0  0  0  0
  8  9  3  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5  3  1  0  0  0  0
 12 10  1  0  0  0  0
  1 15  1  0  0  0  0
  2 16  1  0  0  0  0
  2 17  1  0  0  0  0
  3 18  1  1  0  0  0
  5 19  1  6  0  0  0
 10 20  1  1  0  0  0
 12 21  1  6  0  0  0
 13 22  1  0  0  0  0
 13 23  1  0  0  0  0
 14 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0004721

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@@]1([H])O[C@]1([H])C#CC#C[C@@]1([H])O[C@]1([H])C([H])([H])O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C10H10O4/c11-5-9-7(13-9)3-1-2-4-8-10(6-12)14-8/h7-12H,5-6H2/t7-,8-,9-,10-/m1/s1

> <INCHI_KEY>
BQWDCZPSFPXRCB-ZYUZMQFOSA-N

> <FORMULA>
C10H10O4

> <MOLECULAR_WEIGHT>
194.186

> <EXACT_MASS>
194.057908802

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
24

> <JCHEM_AVERAGE_POLARIZABILITY>
19.826143567732913

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3R)-3-{4-[(2R,3R)-3-(hydroxymethyl)oxiran-2-yl]buta-1,3-diyn-1-yl}oxiran-2-yl]methanol

> <ALOGPS_LOGP>
-0.50

> <JCHEM_LOGP>
-0.45892371466666676

> <ALOGPS_LOGS>
-2.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.85751374528855

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.255482903388081

> <JCHEM_PKA_STRONGEST_BASIC>
-2.992723048817595

> <JCHEM_POLAR_SURFACE_AREA>
65.52

> <JCHEM_REFRACTIVITY>
48.510200000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.35e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3R)-3-{4-[(2R,3R)-3-(hydroxymethyl)oxiran-2-yl]buta-1,3-diyn-1-yl}oxiran-2-yl]methanol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  O   UNK     0       5.918  -0.086   1.279  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.681   0.087  -0.084  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.242   0.368  -0.378  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.917   0.553  -1.701  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.377  -0.620  -1.048  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.929  -0.569  -0.775  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.745  -0.526  -0.532  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.647  -0.479  -0.224  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.822  -0.444   0.057  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.240  -0.399   0.420  0.00  0.00           C+0
HETATM   11  O   UNK     0      -3.747   0.860   0.843  0.00  0.00           O+0
HETATM   12  C   UNK     0      -4.174   0.295  -0.419  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.666  -0.047  -0.346  0.00  0.00           C+0
HETATM   14  O   UNK     0      -6.408   1.105  -0.084  0.00  0.00           O+0
HETATM   15  H   UNK     0       5.066   0.152   1.742  0.00  0.00           H+0
HETATM   16  H   UNK     0       6.058  -0.809  -0.605  0.00  0.00           H+0
HETATM   17  H   UNK     0       6.290   0.964  -0.441  0.00  0.00           H+0
HETATM   18  H   UNK     0       3.740   1.010   0.389  0.00  0.00           H+0
HETATM   19  H   UNK     0       3.751  -1.537  -1.510  0.00  0.00           H+0
HETATM   20  H   UNK     0      -3.588  -1.219   1.071  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.826   0.883  -1.293  0.00  0.00           H+0
HETATM   22  H   UNK     0      -5.785  -0.778   0.487  0.00  0.00           H+0
HETATM   23  H   UNK     0      -5.996  -0.534  -1.278  0.00  0.00           H+0
HETATM   24  H   UNK     0      -5.813   1.771   0.360  0.00  0.00           H+0
CONECT    1    2   15                                                       
CONECT    2    1    3   16   17                                             
CONECT    3    2    4    5   18                                             
CONECT    4    3    5                                                       
CONECT    5    4    6    3   19                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   20                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   10   21                                             
CONECT   13   12   14   22   23                                             
CONECT   14   13   24                                                       
CONECT   15    1                                                            
CONECT   16    2                                                            
CONECT   17    2                                                            
CONECT   18    3                                                            
CONECT   19    5                                                            
CONECT   20   10                                                            
CONECT   21   12                                                            
CONECT   22   13                                                            
CONECT   23   13                                                            
CONECT   24   14                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₀H₁₀O₄

Average Mass

194.1860 Da

Monoisotopic Mass

194.05791 Da

IUPAC Name

[(2R,3R)-3-{4-[(2R,3R)-3-(hydroxymethyl)oxiran-2-yl]buta-1,3-diyn-1-yl}oxiran-2-yl]methanol

Traditional Name

[(2R,3R)-3-{4-[(2R,3R)-3-(hydroxymethyl)oxiran-2-yl]buta-1,3-diyn-1-yl}oxiran-2-yl]methanol

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@H]1C#CC#C[C@H]1O[C@@H]1CO

InChI Identifier

InChI=1S/C10H10O4/c11-5-9-7(13-9)3-1-2-4-8-10(6-12)14-8/h7-12H,5-6H2/t7-,8-,9-,10-/m1/s1

InChI Key

BQWDCZPSFPXRCB-ZYUZMQFOSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Agaricus bisporus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...
Pleurotus ostreatus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...
Russula subnigricans	NPAtlas	1294319

Chemical Taxonomy

Classification

Not classified

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	-0.5	ALOGPS
logP	-0.46	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	14.26	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	65.52 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	48.51 m³·mol⁻¹	ChemAxon
Polarizability	19.83 Å³	ChemAxon
Number of Rings	2	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

NPAtlas ID

NPA017171

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9302253

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11127133

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Takahashi A, Endo T, Nozoe S: Repandiol, a new cytotoxic diepoxide from the mushrooms Hydnum repandum and H. repandum var. album. Chem Pharm Bull (Tokyo). 1992 Dec;40(12):3181-4. doi: 10.1248/cpb.40.3181. [PubMed:1294319 ]

Showing NP-Card for Repandiol (NP0004721)

MOL for NP0004721 (Repandiol)

3D MOL for NP0004721 (Repandiol)

3D SDF for NP0004721 (Repandiol)

3D-SDF for NP0004721 (Repandiol)

PDB for NP0004721 (Repandiol)

3D PDB for NP0004721 (Repandiol)

SMILES for NP0004721 (Repandiol)

INCHI for NP0004721 (Repandiol)

Structure for NP0004721 (Repandiol)

3D Structure for NP0004721 (Repandiol)