NP-MRD: Showing NP-Card for methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate (NP0237994)

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Record Information

Version

2.0

Created at

2022-09-06 21:18:09 UTC

Updated at

2022-09-06 21:18:09 UTC

NP-MRD ID

NP0237994

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate

Description

94992-54-8 Belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open. methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate is found in Tocoyena formosa. Based on a literature review very few articles have been published on 94992-54-8.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 32  0  0  0  0  0  0  0  0999 V2000
    4.9288    1.0698    0.6833 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6305    0.7458    1.0790 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6045    0.3845    0.2139 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8916    0.3544   -1.0110 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2635    0.0552    0.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9656    0.0877    1.9681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3289   -0.2361    2.3500 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3880    0.3037    1.5782 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6468    1.6077    2.0531 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0702    0.3798    0.1061 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2143   -0.3226   -0.2632 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1971   -1.7543   -0.1328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5094   -1.8592   -0.3230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0765   -0.5114   -0.5944 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3386   -0.3499   -0.0272 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1084   -0.2311   -2.0876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0109   -1.1341   -2.6793 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6205    0.6540    1.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2084    0.6576   -0.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0745    2.1752    0.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7584    0.3677    2.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2948   -0.2797    1.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8549    1.6136    3.0043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1059    1.4172   -0.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4545   -0.0642   -1.3132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4330   -2.6204    0.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1246   -2.7615   -0.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6604    0.5426   -0.3126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1148   -0.4070   -2.5407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3961    0.8053   -2.2761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8219   -0.6900   -2.9991 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 11  5  1  0
 14 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  6 21  1  0
  8 22  1  6
  9 23  1  0
 10 24  1  6
 11 25  1  6
 12 26  1  0
 13 27  1  0
 15 28  1  0
 16 29  1  0
 16 30  1  0
 17 31  1  0
M  END


  Mrv1652309062223182D          

 17 18  0  0  1  0            999 V2000
    3.9934    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1726   -0.8134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9429   -1.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7248   -1.3268    0.0000 O   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
  5 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  1  0  0  0
 16 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237994

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CO[C@@H](O)[C@H]2[C@@H]1C=C[C@]2(O)CO

> <INCHI_IDENTIFIER>
InChI=1S/C11H14O6/c1-16-9(13)7-4-17-10(14)8-6(7)2-3-11(8,15)5-12/h2-4,6,8,10,12,14-15H,5H2,1H3/t6-,8-,10-,11+/m1/s1

> <INCHI_KEY>
CYFGAUDUKUUIEV-IALJFVCMSA-N

> <FORMULA>
C11H14O6

> <MOLECULAR_WEIGHT>
242.227

> <EXACT_MASS>
242.079038171

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
23.16489036209802

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1R,4aS,7R,7aS)-1,7-dihydroxy-7-(hydroxymethyl)-1H,4aH,7H,7aH-cyclopenta[c]pyran-4-carboxylate

> <JCHEM_LOGP>
-1.1425509889999994

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.323248498053069

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.961435341134498

> <JCHEM_PKA_STRONGEST_BASIC>
-3.099126499006994

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
57.3732

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,4aS,7R,7aS)-1,7-dihydroxy-7-(hydroxymethyl)-1H,4aH,7aH-cyclopenta[c]pyran-4-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       7.454   6.160   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.454   4.620   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.787   4.620   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.454   0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.121  -2.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.189  -1.518   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.627  -1.986   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.086  -2.477   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   14                                                  
CONECT   11   10    5   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   10   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₄O₆

Average Mass

242.2270 Da

Monoisotopic Mass

242.07904 Da

IUPAC Name

methyl (1R,4aS,7R,7aS)-1,7-dihydroxy-7-(hydroxymethyl)-1H,4aH,7H,7aH-cyclopenta[c]pyran-4-carboxylate

Traditional Name

methyl (1R,4aS,7R,7aS)-1,7-dihydroxy-7-(hydroxymethyl)-1H,4aH,7aH-cyclopenta[c]pyran-4-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CO[C@@H](O)[C@H]2[C@@H]1C=C[C@]2(O)CO

InChI Identifier

InChI=1S/C11H14O6/c1-16-9(13)7-4-17-10(14)8-6(7)2-3-11(8,15)5-12/h2-4,6,8,10,12,14-15H,5H2,1H3/t6-,8-,10-,11+/m1/s1

InChI Key

CYFGAUDUKUUIEV-IALJFVCMSA-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
Tocoyena formosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Iridoids and derivatives

Alternative Parents

Substituents

Iridoid-skeleton
Bicyclic monoterpenoid
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tertiary alcohol
1,2-diol
Carboxylic acid ester
Hemiacetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Organooxygen compound
Primary alcohol
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	-1.1	ChemAxon
pKa (Strongest Acidic)	11.96	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	57.37 m³·mol⁻¹	ChemAxon
Polarizability	23.16 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

161160

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

185378

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate (NP0237994)

MOL for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)

3D MOL for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)

3D SDF for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)

3D-SDF for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)

PDB for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)

3D PDB for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)

SMILES for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)

INCHI for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)

Structure for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)

3D Structure for NP0237994 (methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate)