NP-MRD: Showing NP-Card for Chlorohyssopifolin B (NP0063576)

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Record Information

Version

2.0

Created at

2022-04-28 07:57:32 UTC

Updated at

2022-04-28 07:57:32 UTC

NP-MRD ID

NP0063576

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Chlorohyssopifolin B

Description

(3AR,4S,6aR,8S,9S,9aS,9bR)-9-(chloromethyl)-4,8,9-trihydroxy-3,6-dimethylidene-dodecahydroazuleno[4,5-b]furan-2-one belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative. Chlorohyssopifolin B is found in Centaurea linifolia. Based on a literature review very few articles have been published on (3aR,4S,6aR,8S,9S,9aS,9bR)-9-(chloromethyl)-4,8,9-trihydroxy-3,6-dimethylidene-dodecahydroazuleno[4,5-b]furan-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
    0.0276   -2.9900   -0.3331 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3267   -1.9696    0.4517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7709   -1.7287    0.7221 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4131   -0.7118   -0.1252 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7543   -0.6069    0.2790 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8321    0.6716   -0.0419 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1890    1.2714   -1.3765 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1073    2.1522   -1.6417 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383    0.6032   -2.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3081    0.6017   -3.5391 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2595   -0.0195   -1.4647 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3339    0.7047   -0.2596 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4929    0.2903    0.8464 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7737   -1.1837    0.9846 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1151   -1.3894    0.3059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8927   -0.1401    0.7030 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8198    0.1960   -0.2819 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8327    0.9238    0.8785 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0846    1.5010    2.1588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1031    2.0107   -0.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0921    1.4965   -1.7958 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.8303   -3.5857   -0.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9999   -3.2045   -0.5458 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9287   -1.4560    1.8019 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3308   -2.6857    0.5947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4581   -1.1036   -1.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8355   -0.6262    1.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1879    1.2522    0.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7226    2.5398   -0.8489 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2736    2.5100   -2.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0964    1.7577   -0.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0311    0.5824    1.8017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9296   -1.4576    2.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0465   -1.5004   -0.7797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6767   -2.2555    0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3827   -0.3498    1.6715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7161    0.2277    0.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6592    2.3945    2.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1581    2.3600    0.1081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4802    2.9173    0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
  9  7  1  0
  7  8  2  3
  7  6  1  0
  6  4  1  0
  4  5  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
 13 18  1  0
 18 19  1  1
 18 20  1  0
 20 21  1  0
 18 16  1  0
  2 14  1  0
  6 12  1  0
 17 37  1  0
 16 36  1  1
 15 34  1  0
 15 35  1  0
 14 33  1  1
 13 32  1  1
 12 31  1  6
  8 29  1  0
  8 30  1  0
  6 28  1  1
  4 26  1  6
  5 27  1  0
  3 24  1  0
  3 25  1  0
  1 22  1  0
  1 23  1  0
 19 38  1  0
 20 39  1  0
 20 40  1  0
M  END


  Mrv1652304282209572D          

 21 23  0  0  1  0            999 V2000
    4.9157    0.2321    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1204    0.4515    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6659   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1803   -0.8820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9527   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9967   -1.6863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6417   -2.2007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2534   -2.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5101   -1.6863    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3265   -0.8820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8409   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3864    0.4515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9461    0.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5541   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8656   -1.0466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8651   -2.2007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2470    1.2668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6043    1.7840    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.4887    0.9822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5607    0.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  1  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  3 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 10 15  1  1  0  0  0
 15 16  2  0  0  0  0
  9 17  1  6  0  0  0
  2 18  1  1  0  0  0
 18 19  1  0  0  0  0
  2 20  1  6  0  0  0
  1 21  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0063576

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@H]1C[C@@H]2[C@@H]([C@@H]3OC(=O)C(=C)[C@@H]3[C@@H](O)CC2=C)[C@@]1(O)CCl

> <INCHI_IDENTIFIER>
InChI=1S/C15H19ClO5/c1-6-3-9(17)11-7(2)14(19)21-13(11)12-8(6)4-10(18)15(12,20)5-16/h8-13,17-18,20H,1-5H2/t8-,9-,10-,11+,12-,13+,15+/m0/s1

> <INCHI_KEY>
YIFQICREHIVCKL-UXJUNDEPSA-N

> <FORMULA>
C15H19ClO5

> <MOLECULAR_WEIGHT>
314.76

> <EXACT_MASS>
314.0921014

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
30.317129480855492

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,4S,6aR,8S,9S,9aS,9bR)-9-(chloromethyl)-4,8,9-trihydroxy-3,6-dimethylidene-dodecahydroazuleno[4,5-b]furan-2-one

> <ALOGPS_LOGP>
0.23

> <JCHEM_LOGP>
-0.0410867173333343

> <ALOGPS_LOGS>
-1.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.43567639463518

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.792700916621307

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9241395004084065

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
75.38109999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.15e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,4S,6aR,8S,9S,9aS,9bR)-9-(chloromethyl)-4,8,9-trihydroxy-3,6-dimethylidene-octahydroazuleno[4,5-b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       9.176   0.433   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.691   0.843   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.843  -0.442   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.803  -1.646   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.245  -1.105   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.461  -3.148   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.665  -4.108   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.073  -3.816   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.686  -3.148   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.343  -1.646   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.303  -0.442   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.455   0.843   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.970   0.433   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.766   1.393   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.901  -1.105   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.616  -1.954   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.482  -4.108   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.928   2.365   0.000  0.00  0.00           C+0
HETATM   19 Cl   UNK     0       6.728   3.330   0.000  0.00  0.00          Cl+0
HETATM   20  O   UNK     0       6.512   1.833   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      10.380   1.393   0.000  0.00  0.00           O+0
CONECT    1    2    5   21                                                  
CONECT    2    1    3   18   20                                             
CONECT    3    2    4   11                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   17                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10    3   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   10   16                                                  
CONECT   16   15                                                            
CONECT   17    9                                                            
CONECT   18    2   19                                                       
CONECT   19   18                                                            
CONECT   20    2                                                            
CONECT   21    1                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₉ClO₅

Average Mass

314.7600 Da

Monoisotopic Mass

314.09210 Da

IUPAC Name

(3aR,4S,6aR,8S,9S,9aS,9bR)-9-(chloromethyl)-4,8,9-trihydroxy-3,6-dimethylidene-dodecahydroazuleno[4,5-b]furan-2-one

Traditional Name

(3aR,4S,6aR,8S,9S,9aS,9bR)-9-(chloromethyl)-4,8,9-trihydroxy-3,6-dimethylidene-octahydroazuleno[4,5-b]furan-2-one

CAS Registry Number

Not Available

SMILES

O[C@H]1C[C@@H]2[C@@H]([C@@H]3OC(=O)C(=C)[C@@H]3[C@@H](O)CC2=C)[C@@]1(O)CCl

InChI Identifier

InChI=1S/C15H19ClO5/c1-6-3-9(17)11-7(2)14(19)21-13(11)12-8(6)4-10(18)15(12,20)5-16/h8-13,17-18,20H,1-5H2/t8-,9-,10-,11+,12-,13+,15+/m0/s1

InChI Key

YIFQICREHIVCKL-UXJUNDEPSA-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
Centaurea linifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Guaianolides and derivatives

Alternative Parents

Substituents

Guaianolide-skeleton
Sesquiterpenoid
Guaiane sesquiterpenoid
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Lactone
Halohydrin
Chlorohydrin
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organohalogen compound
Carbonyl group
Alkyl halide
Alkyl chloride
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	0.23	ALOGPS
logP	-0.041	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	12.79	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	75.38 m³·mol⁻¹	ChemAxon
Polarizability	30.32 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

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

162899721

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Chlorohyssopifolin B (NP0063576)

MOL for NP0063576 (Chlorohyssopifolin B)

3D MOL for NP0063576 (Chlorohyssopifolin B)

3D SDF for NP0063576 (Chlorohyssopifolin B)

3D-SDF for NP0063576 (Chlorohyssopifolin B)

PDB for NP0063576 (Chlorohyssopifolin B)

3D PDB for NP0063576 (Chlorohyssopifolin B)

SMILES for NP0063576 (Chlorohyssopifolin B)

INCHI for NP0063576 (Chlorohyssopifolin B)

Structure for NP0063576 (Chlorohyssopifolin B)

3D Structure for NP0063576 (Chlorohyssopifolin B)