NP-MRD: Showing NP-Card for Kanshone B (NP0061843)

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Record Information

Version

2.0

Created at

2022-04-28 06:33:01 UTC

Updated at

2022-04-28 06:33:01 UTC

NP-MRD ID

NP0061843

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Kanshone B

Description

Kanshone B belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Kanshone B is found in Nardostachys chinensis . Kanshone B was first documented in 2012 (PMID: 22079762). Based on a literature review a small amount of articles have been published on Kanshone B (PMID: 33220358) (PMID: 29616391).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 43  0  0  0  0  0  0  0  0999 V2000
    0.7937   -2.3727   -0.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0965   -0.8914   -0.6375 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6047   -0.6607   -0.4233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8529    0.7610   -0.9526 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6887    0.7635   -2.3191 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8843    1.6675   -0.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7989    1.2676    0.3430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1242    2.2150    1.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1563    3.3964    0.6219 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9456    1.6274    2.0897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6220    0.3697    1.7450 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9030    0.7147    1.2339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6084    1.2054    0.0233 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9754    0.0578   -0.5142 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5226    0.3736   -1.8771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1206   -0.9631   -0.6429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0740   -0.3556    0.5206 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3822   -0.1648    0.4451 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9586   -0.7309    1.7587 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7657   -2.9053   -0.7556 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1538   -2.6304   -1.5196 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2698   -2.7278    0.2435 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9324   -0.5245   -1.6571 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8701   -0.6424    0.6313 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1233   -1.4078   -1.0323 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8640    1.0906   -0.6243 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2050    1.5072   -2.7288 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0874    2.7467   -0.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6978    2.3976    2.3642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2756    1.5580    2.9969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7768   -0.2774    2.6056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7490    1.1444   -1.9746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4199    0.8127   -2.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3146   -0.5567   -2.4727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6778   -1.9622   -0.3667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4671   -1.0566   -1.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9216   -0.7705    0.0699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2331   -1.4517    0.7622 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6742   -0.0088    2.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1674   -0.8833    2.5213 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4119   -1.7319    1.6051 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
  4  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 14 17  1  0
 17 18  1  0
 18 19  1  1
 18  2  1  0
 18  7  1  0
 17 11  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  6
  3 24  1  0
  3 25  1  0
  4 26  1  6
  5 27  1  0
  6 28  1  0
 10 29  1  0
 10 30  1  0
 11 31  1  1
 15 32  1  0
 15 33  1  0
 15 34  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  1
 19 39  1  0
 19 40  1  0
 19 41  1  0
M  END


  Mrv1652304282208332D          

 19 21  0  0  1  0            999 V2000
    2.8571    0.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2470    1.5487    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8124    2.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9878    2.2242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5978    1.4972    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0325    0.7959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6425    0.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7732    1.4714    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3386    2.1727    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7286    2.8997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5532    2.9254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9432    3.6524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4626    1.9760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5232    1.1532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2406    0.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0186    0.0468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8053    0.2399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    0.7702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0716    1.5745    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  5  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  2  0  0  0  0
  9 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  5 18  1  1  0  0  0
  2 19  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0061843

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@H](O)C=C2C(=O)C[C@H]3OOC(C)(C)[C@H]3[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O4/c1-8-5-9(16)6-10-11(17)7-12-13(15(8,10)4)14(2,3)19-18-12/h6,8-9,12-13,16H,5,7H2,1-4H3/t8-,9-,12-,13+,15+/m1/s1

> <INCHI_KEY>
QLASPINFLLNESN-UVBAXCRRSA-N

> <FORMULA>
C15H22O4

> <MOLECULAR_WEIGHT>
266.337

> <EXACT_MASS>
266.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
28.421848298267918

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,7R,9R,9aR,9bS)-7-hydroxy-1,1,9,9a-tetramethyl-1H,3aH,4H,5H,7H,8H,9H,9aH,9bH-naphtho[2,1-c][1,2]dioxol-5-one

> <ALOGPS_LOGP>
2.17

> <JCHEM_LOGP>
1.7323186479999992

> <ALOGPS_LOGS>
-2.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.32007090917661

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.826374186922557

> <JCHEM_PKA_STRONGEST_BASIC>
-2.873870990143728

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
70.6306

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.37e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,7R,9R,9aR,9bS)-7-hydroxy-1,1,9,9a-tetramethyl-3aH,4H,7H,8H,9H,9bH-naphtho[2,1-c][1,2]dioxol-5-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       5.333   1.534   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.061   2.891   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.250   4.200   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.711   4.152   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.983   2.795   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.794   1.486   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.066   0.129   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.443   2.747   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.632   4.056   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.360   5.413   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.899   5.461   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.627   6.818   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -0.863   3.689   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -0.977   2.153   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.449   1.571   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.035   0.087   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.503   0.448   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.255   1.438   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.600   2.939   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6    8   18                                             
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   15                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10    4   12                                                  
CONECT   12   11                                                            
CONECT   13    9   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    8   16   17                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18    5                                                            
CONECT   19    2                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₄

Average Mass

266.3370 Da

Monoisotopic Mass

266.15181 Da

IUPAC Name

(3aR,7R,9R,9aR,9bS)-7-hydroxy-1,1,9,9a-tetramethyl-1H,3aH,4H,5H,7H,8H,9H,9aH,9bH-naphtho[2,1-c][1,2]dioxol-5-one

Traditional Name

(3aR,7R,9R,9aR,9bS)-7-hydroxy-1,1,9,9a-tetramethyl-3aH,4H,7H,8H,9H,9bH-naphtho[2,1-c][1,2]dioxol-5-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@H](O)C=C2C(=O)C[C@H]3OOC(C)(C)[C@H]3[C@@]12C

InChI Identifier

InChI=1S/C15H22O4/c1-8-5-9(16)6-10-11(17)7-12-13(15(8,10)4)14(2,3)19-18-12/h6,8-9,12-13,16H,5,7H2,1-4H3/t8-,9-,12-,13+,15+/m1/s1

InChI Key

QLASPINFLLNESN-UVBAXCRRSA-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
Nardostachys jatamansi	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Nardosinane sesquiterpenoid
Sesquiterpenoid
Ortho-dioxolane
Dialkyl peroxide
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	2.17	ALOGPS
logP	1.73	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	14.83	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	70.63 m³·mol⁻¹	ChemAxon
Polarizability	28.42 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

C00017479

Chemspider ID

28487931

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14021478

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li R, Wang ZM, Wang Y, Dong X, Zhang LH, Wang T, Zhu Y, Gao XM, Wu HH, Xu YT: Antidepressant activities and regulative effects on serotonin transporter of Nardostachys jatamansi DC. J Ethnopharmacol. 2021 Mar 25;268:113601. doi: 10.1016/j.jep.2020.113601. Epub 2020 Nov 18. [PubMed:33220358 ]
Hwang JS, Lee SA, Hong SS, Han XH, Lee C, Lee D, Lee CK, Hong JT, Kim Y, Lee MK, Hwang BY: Inhibitory constituents of Nardostachys chinensis on nitric oxide production in RAW 264.7 macrophages. Bioorg Med Chem Lett. 2012 Jan 1;22(1):706-8. doi: 10.1016/j.bmcl.2011.10.043. Epub 2011 Oct 18. [PubMed:22079762 ]
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Showing NP-Card for Kanshone B (NP0061843)

MOL for NP0061843 (Kanshone B)

3D MOL for NP0061843 (Kanshone B)

3D SDF for NP0061843 (Kanshone B)

3D-SDF for NP0061843 (Kanshone B)

PDB for NP0061843 (Kanshone B)

3D PDB for NP0061843 (Kanshone B)

SMILES for NP0061843 (Kanshone B)

INCHI for NP0061843 (Kanshone B)

Structure for NP0061843 (Kanshone B)

3D Structure for NP0061843 (Kanshone B)