NP-MRD: Showing NP-Card for (6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid (NP0227468)

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Record Information

Version

2.0

Created at

2022-09-06 06:48:04 UTC

Updated at

2022-09-06 06:48:04 UTC

NP-MRD ID

NP0227468

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid

Description

Fumifungin belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. (6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid is found in Aspergillus fumigatus. (6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid was first documented in 2015 (PMID: 25737146). Based on a literature review very few articles have been published on Fumifungin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062208482D          

 30 29  0  0  0  0            999 V2000
    4.7586    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4730    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6164    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3309    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4743    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0467    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7612    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4756    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4756    4.8099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1901    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1901    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9046    2.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6190    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9046    1.5099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9046    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6190    3.5724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9046    4.8099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1901    5.2224    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.6190    5.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6190    6.0474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3335    4.8099    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  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
  7  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  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 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
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END

     RDKit          3D

 71 70  0  0  0  0  0  0  0  0999 V2000
    7.9859   -0.3070    3.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3361   -0.4764    2.1743 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6025   -1.7808    2.1590 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6038    0.8098    0.8286 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3428    0.0108   -0.0543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7019   -0.2148   -0.0049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3798   -1.1060   -1.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3649    0.3414    0.9049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5250    0.0202    1.4734 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7016    0.7061    2.3431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0240   -1.2633    2.0823 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9133   -2.1737    2.3624 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7396   -0.9581    3.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2806   -1.5451    4.4086 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8199   -0.1094    3.4726 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9282   -1.2010   -2.3119 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2418   -0.3653   -3.2067 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8296    0.7833   -1.6970 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622    1.8175   -2.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2906   -0.1629   -3.8364 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5169    0.8272   -4.6921 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4527    2.9372   -3.8710 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7643    2.9267   -2.9954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6318    2.1860   -1.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6194    0.8265   -3.7445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4503   -0.1293   -2.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
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 26 68  1  6
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 27 70  1  0
 30 71  1  0
M  END


  Mrv1652309062208482D          

 30 29  0  0  0  0            999 V2000
    4.7586    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4730    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6164    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3309    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4743    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0467    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7612    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4756    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4756    4.8099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1901    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1901    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9046    2.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6190    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9046    1.5099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9046    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6190    3.5724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9046    4.8099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1901    5.2224    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.6190    5.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6190    6.0474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3335    4.8099    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
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 28 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0227468

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCC(O)CCCCCC\C=C\C(O)C(OC(C)=O)C(O)C(N)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H41NO7/c1-3-4-5-10-13-17(25)14-11-8-6-7-9-12-15-18(26)21(30-16(2)24)20(27)19(23)22(28)29/h12,15,17-21,25-27H,3-11,13-14,23H2,1-2H3,(H,28,29)/b15-12+

> <INCHI_KEY>
OOEOVXMORBPOKC-NTCAYCPXSA-N

> <FORMULA>
C22H41NO7

> <MOLECULAR_WEIGHT>
431.57

> <EXACT_MASS>
431.288302664

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
49.512081993044205

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6E)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid

> <JCHEM_LOGP>
0.41915068662458294

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.309436426717355

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.9575539226623029

> <JCHEM_PKA_STRONGEST_BASIC>
8.610328428155448

> <JCHEM_POLAR_SURFACE_AREA>
150.30999999999997

> <JCHEM_REFRACTIVITY>
114.5054

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(6E)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       8.883   6.668   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.216   7.438   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.884   7.438   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.217   6.668   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.551   7.438   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.885   6.668   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      16.885   5.128   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      18.218   7.438   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.552   6.668   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.886   7.438   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      22.219   6.668   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      23.553   7.438   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      24.887   6.668   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      26.220   7.438   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      27.554   6.668   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      28.888   7.438   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      28.888   8.978   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      30.222   6.668   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      30.222   5.128   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      31.555   4.358   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      32.889   5.128   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      31.555   2.818   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      31.555   7.438   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      32.889   6.668   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      31.555   8.978   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0      30.222   9.748   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      32.889   9.748   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      32.889  11.288   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      34.223   8.978   0.000  0.00  0.00           O+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    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   58    0
END

View in JSmol

Synonyms

Value	Source
2-Amino-4-acetoxy-3,5,14-trihydroxyeicosenoic acid	MeSH

Chemical Formula

C₂₂H₄₁NO₇

Average Mass

431.5700 Da

Monoisotopic Mass

431.28830 Da

IUPAC Name

(6E)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid

Traditional Name

(6E)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid

CAS Registry Number

Not Available

SMILES

CCCCCCC(O)CCCCCC\C=C\C(O)C(OC(C)=O)C(O)C(N)C(O)=O

InChI Identifier

InChI=1S/C22H41NO7/c1-3-4-5-10-13-17(25)14-11-8-6-7-9-12-15-18(26)21(30-16(2)24)20(27)19(23)22(28)29/h12,15,17-21,25-27H,3-11,13-14,23H2,1-2H3,(H,28,29)/b15-12+

InChI Key

OOEOVXMORBPOKC-NTCAYCPXSA-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
Aspergillus fumigatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

Long-chain fatty acid
Alpha-amino acid
Alpha-amino acid or derivatives
Amino fatty acid
Beta-hydroxy acid
Hydroxy fatty acid
Unsaturated fatty acid
Dicarboxylic acid or derivatives
Hydroxy acid
Secondary alcohol
Amino acid
Amino acid or derivatives
Carboxylic acid ester
Polyol
Carboxylic acid derivative
Carboxylic acid
Organonitrogen compound
Hydrocarbon derivative
Organooxygen compound
Primary amine
Carbonyl group
Alcohol
Organic oxide
Amine
Organic oxygen compound
Primary aliphatic amine
Organic nitrogen compound
Organopnictogen compound
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	0.42	ChemAxon
pKa (Strongest Acidic)	1.96	ChemAxon
pKa (Strongest Basic)	8.61	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	150.31 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	114.51 m³·mol⁻¹	ChemAxon
Polarizability	49.51 Å³	ChemAxon
Number of Rings	0	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

Not Available

KNApSAcK ID

C00017875

Chemspider ID

4948070

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6444133

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Tamiya H, Ochiai E, Kikuchi K, Yahiro M, Toyotome T, Watanabe A, Yaguchi T, Kamei K: Secondary metabolite profiles and antifungal drug susceptibility of Aspergillus fumigatus and closely related species, Aspergillus lentulus, Aspergillus udagawae, and Aspergillus viridinutans. J Infect Chemother. 2015 May;21(5):385-91. doi: 10.1016/j.jiac.2015.01.005. Epub 2015 Jan 23. [PubMed:25737146 ]
LOTUS database [Link]

Showing NP-Card for (6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid (NP0227468)

MOL for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)

3D MOL for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)

3D SDF for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)

3D-SDF for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)

PDB for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)

3D PDB for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)

SMILES for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)

INCHI for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)

Structure for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)

3D Structure for NP0227468 ((6e)-4-(acetyloxy)-2-amino-3,5,14-trihydroxyicos-6-enoic acid)