NP-MRD: Showing NP-Card for 11-decyltetracosane (NP0171076)

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Record Information

Version

2.0

Created at

2022-09-03 07:26:09 UTC

Updated at

2022-09-03 07:26:09 UTC

NP-MRD ID

NP0171076

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-decyltetracosane

Description

11-Decyltetracosane belongs to the class of organic compounds known as branched alkanes. These are acyclic branched hydrocarbons having the general formula CnH2n+2. 11-decyltetracosane is found in Streptomyces sparsus. Based on a literature review very few articles have been published on 11-Decyltetracosane.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032209262D          

 34 33  0  0  0  0            999 V2000
    4.9500  -10.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0125  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 31 32  1  0  0  0  0
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 33 34  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309032209262D          

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   11.9625  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750  -14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2000  -14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6125  -15.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4375  -15.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8500  -15.7184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6750  -15.7184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0875  -16.4328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9125  -16.4328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3250  -17.1473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1500  -17.1473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5625  -17.8618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3875  -17.8618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6125  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4375  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8500  -12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6750  -12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0875  -12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9125  -12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3250  -11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1500  -11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5625  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3875  -10.7171    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  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
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171076

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCC(CCCCCCCCCC)CCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C34H70/c1-4-7-10-13-16-19-20-21-24-27-30-33-34(31-28-25-22-17-14-11-8-5-2)32-29-26-23-18-15-12-9-6-3/h34H,4-33H2,1-3H3

> <INCHI_KEY>
BVMGLUHWZZEDRX-UHFFFAOYSA-N

> <FORMULA>
C34H70

> <MOLECULAR_WEIGHT>
478.934

> <EXACT_MASS>
478.547752254

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
70.75801747416328

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
11-decyltetracosane

> <ALOGPS_LOGP>
11.29

> <JCHEM_LOGP>
15.421510943999998

> <ALOGPS_LOGS>
-8.03

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
158.1838

> <JCHEM_ROTATABLE_BOND_COUNT>
30

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.47e-06 g/l

> <JCHEM_TRADITIONAL_IUPAC>
tetracosane, 11-decyl-

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       9.240 -18.672   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.780 -18.672   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.550 -20.005   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.090 -20.005   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.860 -21.339   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.400 -21.339   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.170 -22.673   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.710 -22.673   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.480 -24.006   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.020 -24.006   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.790 -25.340   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      22.330 -25.340   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      23.100 -26.674   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      24.640 -26.674   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      25.410 -28.007   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      26.950 -28.007   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      27.720 -29.341   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      29.260 -29.341   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      30.030 -30.675   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      31.570 -30.675   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      32.340 -32.008   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      33.880 -32.008   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      34.650 -33.342   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      36.190 -33.342   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      25.410 -25.340   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      26.950 -25.340   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      27.720 -24.006   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      29.260 -24.006   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      30.030 -22.673   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      31.570 -22.673   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      32.340 -21.339   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      33.880 -21.339   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      34.650 -20.005   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      36.190 -20.005   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   25                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   14   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₇₀

Average Mass

478.9340 Da

Monoisotopic Mass

478.54775 Da

IUPAC Name

11-decyltetracosane

Traditional Name

tetracosane, 11-decyl-

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCC(CCCCCCCCCC)CCCCCCCCCC

InChI Identifier

InChI=1S/C34H70/c1-4-7-10-13-16-19-20-21-24-27-30-33-34(31-28-25-22-17-14-11-8-5-2)32-29-26-23-18-15-12-9-6-3/h34H,4-33H2,1-3H3

InChI Key

BVMGLUHWZZEDRX-UHFFFAOYSA-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
Streptomyces sparsus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as branched alkanes. These are acyclic branched hydrocarbons having the general formula CnH2n+2.

Kingdom

Organic compounds

Super Class

Hydrocarbons

Class

Saturated hydrocarbons

Sub Class

Alkanes

Direct Parent

Branched alkanes

Alternative Parents

Not Available

Substituents

Branched alkane
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	11.29	ALOGPS
logP	15.42	ChemAxon
logS	-8	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	30	ChemAxon
Refractivity	158.18 m³·mol⁻¹	ChemAxon
Polarizability	70.76 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

259995

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

294707

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11-decyltetracosane (NP0171076)

MOL for NP0171076 (11-decyltetracosane)

3D MOL for NP0171076 (11-decyltetracosane)

3D SDF for NP0171076 (11-decyltetracosane)

3D-SDF for NP0171076 (11-decyltetracosane)

PDB for NP0171076 (11-decyltetracosane)

3D PDB for NP0171076 (11-decyltetracosane)

SMILES for NP0171076 (11-decyltetracosane)

INCHI for NP0171076 (11-decyltetracosane)

Structure for NP0171076 (11-decyltetracosane)

3D Structure for NP0171076 (11-decyltetracosane)