NP-MRD: Showing NP-Card for heterodendrin (NP0294840)

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Record Information

Version

2.0

Created at

2022-09-10 03:33:35 UTC

Updated at

2022-09-10 03:33:35 UTC

NP-MRD ID

NP0294840

Secondary Accession Numbers

None

Natural Product Identification

Common Name

heterodendrin

Description

heterodendrin is found in Vachellia hebeclada, Acacia pulchella, Rhodiola sachalinensis, Rhodiola sacra and Vachellia sieberiana.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 37  0  0  0  0  0  0  0  0999 V2000
    4.3892    0.1856   -0.0972 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0729   -0.1271    0.6057 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4966    1.1314    1.1869 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1261   -0.7155   -0.4245 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6680   -1.8915   -1.0616 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1027   -2.8192   -1.5842 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9283   -1.0067    0.1868 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1401   -0.2703   -0.3308 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6730    0.4486    0.7033 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9492    0.8673    0.5879 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4233    1.3377    1.9592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6035    2.3834    2.3800 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9267   -0.1945    0.1349 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2003    0.3133    0.0865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4335   -0.6235   -1.2539 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2746   -1.5406   -1.8300 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0697   -1.2249   -0.9953 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4871   -1.7099   -2.1590 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6635   -0.6630   -0.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1671    0.4465    0.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1826    1.0527   -0.7722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2227   -0.8564    1.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9180    0.9507    2.1203 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8108    1.6113    0.4562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3083    1.8481    1.4750 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9510    0.0571   -1.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3003    0.3808   -1.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0950    1.7458   -0.0902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3224    0.5314    2.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4747    1.6470    1.9514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6554    3.1043    1.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8385   -1.1120    0.7651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8362   -0.4592    0.2073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2935    0.2905   -1.8748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7804   -1.9983   -2.5571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2310   -2.0905   -0.3140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5996   -1.0305   -2.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  4  5  1  0
  5  6  3  0
 17  8  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  6
  8 27  1  6
 10 28  1  6
 11 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  1
 14 33  1  0
 15 34  1  6
 16 35  1  0
 17 36  1  1
 18 37  1  0
M  END

 
  Mrv1652307301920052D          
 
 18 18  0  0  1  0            999 V2000
   16.8831   -9.5291    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.1677   -9.1389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8933  -10.3473    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.5986   -9.1116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4624   -9.5532    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.1984  -10.7615    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.5951  -10.7444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3174   -9.5224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4488  -10.3679    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.7470   -9.1594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1984  -11.5762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.0363   -9.1116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3140  -10.3542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7778  -10.7820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0520   -9.5737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.7517   -9.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0329   -8.2797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3482  -11.1860    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  0  0  0  0
  1  4  1  1  0  0  0
  2  5  1  0  0  0  0
  3  6  1  0  0  0  0
  3  7  1  6  0  0  0
  4  8  1  0  0  0  0
  5  9  1  0  0  0  0
  5 10  1  1  0  0  0
  6 11  1  1  0  0  0
  8 12  1  0  0  0  0
  8 13  1  1  0  0  0
  9 14  1  6  0  0  0
 10 15  1  0  0  0  0
 12 16  1  0  0  0  0
 12 17  1  0  0  0  0
 13 18  3  0  0  0  0
  6  9  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0294840

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C11H19NO6/c1-5(2)6(3-12)17-11-10(16)9(15)8(14)7(4-13)18-11/h5-11,13-16H,4H2,1-2H3/t6-,7-,8-,9+,10-,11-/m1/s1

> <INCHI_KEY>
CQWWASNOGSDPRL-MPVQUNCYSA-N

> <FORMULA>
C11H19NO6

> <MOLECULAR_WEIGHT>
261.274

> <EXACT_MASS>
261.121237336

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
25.507492335364617

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-3-methyl-2-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanenitrile

> <JCHEM_LOGP>
-1.2972210756666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.199438603722836

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.20888349244165

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981084073599132

> <JCHEM_POLAR_SURFACE_AREA>
123.17000000000002

> <JCHEM_REFRACTIVITY>
59.228

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
heterodendrin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 30-JUL-19   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   30-JUL-19         0                                  
HETATM    1  C   UNK     0      31.515 -17.788   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      30.180 -17.059   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      31.534 -19.315   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      32.851 -17.008   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      28.863 -17.833   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      30.237 -20.088   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      32.844 -20.056   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      34.193 -17.775   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      28.838 -19.353   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      27.528 -17.098   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      30.237 -21.609   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      35.534 -17.008   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      34.186 -19.328   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      27.585 -20.126   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      26.230 -17.871   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      36.870 -17.775   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      35.528 -15.455   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      34.250 -20.880   0.000  0.00  0.00           N+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5                                                       
CONECT    3    1    6    7                                                  
CONECT    4    1    8                                                       
CONECT    5    2    9   10                                                  
CONECT    6    3   11    9                                                  
CONECT    7    3                                                            
CONECT    8    4   12   13                                                  
CONECT    9    5   14    6                                                  
CONECT   10    5   15                                                       
CONECT   11    6                                                            
CONECT   12    8   16   17                                                  
CONECT   13    8   18                                                       
CONECT   14    9                                                            
CONECT   15   10                                                            
CONECT   16   12                                                            
CONECT   17   12                                                            
CONECT   18   13                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₉NO₆

Average Mass

261.2740 Da

Monoisotopic Mass

261.12124 Da

IUPAC Name

(2S)-3-methyl-2-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanenitrile

Traditional Name

heterodendrin

CAS Registry Number

Not Available

SMILES

CC(C)[C@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C#N

InChI Identifier

InChI=1S/C11H19NO6/c1-5(2)6(3-12)17-11-10(16)9(15)8(14)7(4-13)18-11/h5-11,13-16H,4H2,1-2H3/t6-,7-,8-,9+,10-,11-/m1/s1

InChI Key

CQWWASNOGSDPRL-MPVQUNCYSA-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
Acacia hebeclada	LOTUS Database	35616633
Acacia pulchella	LOTUS Database	35616633
Rhodiola sachalinensis	LOTUS Database	35616633
Rhodiola sacra	LOTUS Database	35616633
Vachellia sieberiana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyanogenic glycosides. These are glycosides in which the aglycone moiety contains a cyanide group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Cyanogenic glycosides

Alternative Parents

Substituents

Cyanogenic glycoside
Hexose monosaccharide
O-glycosyl compound
Monosaccharide
Oxane
Secondary alcohol
Polyol
Organoheterocyclic compound
Oxacycle
Nitrile
Carbonitrile
Acetal
Primary alcohol
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic nitrogen compound
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

cyanogenic glycoside (CHEBI:5687 )
Cyanogenic glucosides derived from leucine (C08332 )

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	-1.3	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	123.17 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	59.23 m³·mol⁻¹	ChemAxon
Polarizability	25.51 Å³	ChemAxon
Number of Rings	1	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

FDB017849

KNApSAcK ID

C00001445

Chemspider ID

Not Available

KEGG Compound ID

C08332

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

181804

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for heterodendrin (NP0294840)

MOL for NP0294840 (heterodendrin)

3D MOL for NP0294840 (heterodendrin)

3D SDF for NP0294840 (heterodendrin)

3D-SDF for NP0294840 (heterodendrin)

PDB for NP0294840 (heterodendrin)

3D PDB for NP0294840 (heterodendrin)

SMILES for NP0294840 (heterodendrin)

INCHI for NP0294840 (heterodendrin)

Structure for NP0294840 (heterodendrin)

3D Structure for NP0294840 (heterodendrin)