NP-MRD: Showing NP-Card for (1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one (NP0300221)

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Record Information

Version

2.0

Created at

2022-09-10 12:30:14 UTC

Updated at

2022-09-10 12:30:14 UTC

NP-MRD ID

NP0300221

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one

Description

Rivulalactone belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety. (1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one was first documented in 1997 (PMID: 9463110). Based on a literature review very few articles have been published on rivulalactone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
    2.4419   -1.1044   -0.3237 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3893   -0.2086    0.2844 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7326    1.2118   -0.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7442    2.2123    0.3891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6910    1.8572    0.1376 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1276    2.2021   -1.1256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9420    0.4605    0.4536 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2645   -0.1140    0.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0222   -1.6307    0.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5852   -1.7467    0.5449 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4838   -1.2241    1.9482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2681   -1.8810    2.9834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6862    0.1650    1.8280 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0143   -0.5343   -0.1844 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1015   -0.6260   -1.6510 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7118   -0.6714   -1.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0768   -2.1620   -0.4345 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3521   -1.0622    0.3225 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4248   -0.3520    1.3886 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8952    1.2686   -1.1681 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7110    1.4368    0.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9902    3.1924   -0.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8596    2.2963    1.5078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2944    2.4906    0.8541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9677    3.1240   -1.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6870    0.2010   -0.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9800    0.1151    0.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2904   -2.1154   -0.7888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6284   -2.1112    0.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0874   -2.6664    0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9277   -1.2488   -2.0341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8392   -1.1197   -2.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1480    0.3454   -2.1501 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 10 14  1  0
 14 15  1  6
 14  2  1  0
  7 13  1  1
 14  7  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  1
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  1
  6 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  1
 15 31  1  0
 15 32  1  0
 15 33  1  0
M  END


  Mrv1652309102214302D          

 15 17  0  0  1  0            999 V2000
    1.3202   -1.4408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8064   -0.5971    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6058   -0.3931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8288    0.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2525    0.9915    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4847    1.8406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4531    0.7875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6281    0.7835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2191    0.0671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6350   -0.6454    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4600   -0.6414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0605   -1.3987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8691    0.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2301   -0.0068    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5269    0.3622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  7 13  1  1  0  0  0
 10 14  1  0  0  0  0
  2 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0300221

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@@H](O)[C@]23CC[C@H](C(=O)O2)[C@]13C

> <INCHI_IDENTIFIER>
InChI=1S/C12H18O3/c1-7-3-4-9(13)12-6-5-8(10(14)15-12)11(7,12)2/h7-9,13H,3-6H2,1-2H3/t7-,8+,9+,11-,12-/m0/s1

> <INCHI_KEY>
INZNWRIFLOKNQB-MZQLCRGXSA-N

> <FORMULA>
C12H18O3

> <MOLECULAR_WEIGHT>
210.273

> <EXACT_MASS>
210.12559444

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
22.39911310531025

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,5S,6S,7S)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0^{1,6}]undecan-8-one

> <JCHEM_LOGP>
1.462371427333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.952306072956262

> <JCHEM_PKA_STRONGEST_BASIC>
-3.25706132368893

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
54.163000000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,6S,7S)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0^{1,6}]undecan-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       2.464  -2.690   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.372  -1.115   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.864  -0.734   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.281   0.749   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.205   1.851   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.638   3.436   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.713   1.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.173   1.463   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.409   0.125   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.185  -1.205   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.725  -1.197   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.846  -2.611   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       3.489   0.140   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.296  -0.013   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.984   0.676   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   13   14                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   14                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    7                                                       
CONECT   14   10    2    7   15                                             
CONECT   15   14                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₂H₁₈O₃

Average Mass

210.2730 Da

Monoisotopic Mass

210.12559 Da

IUPAC Name

(1R,2R,5S,6S,7S)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0^{1,6}]undecan-8-one

Traditional Name

(1R,2R,5S,6S,7S)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0^{1,6}]undecan-8-one

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@@H](O)[C@]23CC[C@H](C(=O)O2)[C@]13C

InChI Identifier

InChI=1S/C12H18O3/c1-7-3-4-9(13)12-6-5-8(10(14)15-12)11(7,12)2/h7-9,13H,3-6H2,1-2H3/t7-,8+,9+,11-,12-/m0/s1

InChI Key

INZNWRIFLOKNQB-MZQLCRGXSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Delta valerolactones

Direct Parent

Delta valerolactones

Alternative Parents

Substituents

Delta valerolactone
Delta_valerolactone
Gamma butyrolactone
Oxane
Cyclic alcohol
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
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	1.46	ChemAxon
pKa (Strongest Acidic)	13.95	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	54.16 m³·mol⁻¹	ChemAxon
Polarizability	22.4 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

Not Available

Chemspider ID

8831419

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10656064

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wu C, Gunatilaka AA, McCabe FL, Johnson RK, Spjut RW, Kingston DG: Bioactive and other sesquiterpenes from Chiloscyphus rivularis. J Nat Prod. 1997 Dec;60(12):1281-6. doi: 10.1021/np970251u. [PubMed:9463110 ]
LOTUS database [Link]

Showing NP-Card for (1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one (NP0300221)

MOL for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)

3D MOL for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)

3D SDF for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)

3D-SDF for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)

PDB for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)

3D PDB for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)

SMILES for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)

INCHI for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)

Structure for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)

3D Structure for NP0300221 ((1r,2r,5s,6s,7s)-2-hydroxy-5,6-dimethyl-9-oxatricyclo[5.2.2.0¹,⁶]undecan-8-one)