NP-MRD: Showing NP-Card for Floricaline (NP0140926)

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Record Information

Version

2.0

Created at

2022-06-29 21:58:51 UTC

Updated at

2022-06-29 21:58:51 UTC

NP-MRD ID

NP0140926

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Floricaline

Description

Floricaline belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. Based on a literature review very few articles have been published on Floricaline.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292223582D          

 34 35  0  0  1  0            999 V2000
    5.9213    2.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0964    2.0124    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6947    1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8698    1.2794    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4680    0.5588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8912   -0.1494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6431    0.5464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2200    1.2546    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4626    0.9275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6957    1.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3686    1.9891    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6729    2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4302    3.0831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1985    2.6834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6217    1.9752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4466    1.9876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6002    3.4040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4252    3.4164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8483    2.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9469    1.8891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6732    2.7206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3662    3.1682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6897    3.5454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4122    3.9436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4286    4.7684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1183    3.5170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4563    1.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4517    0.6946    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2362   -0.1018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2491    0.9062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8311    0.3214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6285    0.5330    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6156   -0.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1091    0.4899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  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
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  2  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 11 27  1  0  0  0  0
  4 28  1  6  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
  4 34  1  1  0  0  0
M  END

     RDKit          3D

 67 68  0  0  0  0  0  0  0  0999 V2000
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   -2.7049    4.4102   -0.0977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5644    5.8620    0.3008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8575    3.9132   -0.0727 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3848    1.8988   -1.5009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4896    1.2437   -2.5737 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8171    2.2178   -1.0088 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8023    1.7806   -0.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5411    0.5298   -0.4536 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7612    0.8296    0.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9537    0.1931    0.6688 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8582   -1.2398    0.7445 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2019   -1.7585    0.9072 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2431   -1.8904   -0.3604 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0252   -2.6620    0.0235 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0428   -1.7237    0.8525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0095   -0.8913    1.1557 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6121   -1.4453   -1.4833 H   0  0  0  0  0  0  0  0  0  0  0  0
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 33 34  2  0
 31  7  1  0
 33 22  1  0
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  5 38  1  1
  1 35  1  0
  1 36  1  0
  1 37  1  0
  8 42  1  0
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 29 67  1  6
M  END


  Mrv1652306292223582D          

 34 35  0  0  1  0            999 V2000
    5.9213    2.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0964    2.0124    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6947    1.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8698    1.2794    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4680    0.5588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8912   -0.1494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2200    1.2546    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.6217    1.9752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4563    1.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
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  8  9  1  6  0  0  0
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 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 11 27  1  0  0  0  0
  4 28  1  6  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
  4 34  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0140926

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](OC(C)=O)[C@@]1(O)C[C@@H](C)[C@@](C)(OC(C)=O)C(=O)OC\C2=C\CN(C)CC[C@@H](OC1=O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H33NO10/c1-13-11-23(30,14(2)32-15(3)25)21(29)33-18-8-10-24(6)9-7-17(19(18)27)12-31-20(28)22(13,5)34-16(4)26/h7,13-14,18,30H,8-12H2,1-6H3/b17-7-/t13-,14-,18-,22-,23+/m1/s1

> <INCHI_KEY>
IVVHMCWHYZBIAK-CARZHQTMSA-N

> <FORMULA>
C23H33NO10

> <MOLECULAR_WEIGHT>
483.514

> <EXACT_MASS>
483.210446267

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0      11.053   3.780   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.513   3.756   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.763   2.411   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.224   2.388   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.474   1.043   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.264  -0.279   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       4.934   1.020   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.144   2.342   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.730   1.731   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.299   2.299   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       0.688   3.713   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       1.256   5.145   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.670   5.755   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.104   5.009   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.894   3.687   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.434   3.710   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.854   6.354   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.394   6.377   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.184   5.055   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.367   3.526   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.723   5.078   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.017   5.914   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.754   6.618   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.103   7.361   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.133   8.901   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      11.421   6.565   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.852   3.690   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.310   1.297   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.908  -0.190   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.798   1.692   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      10.885   0.600   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      12.373   0.995   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      10.482  -0.887   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       7.670   0.914   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   28   34                                             
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   27                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14    8   16                                                  
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    2   22   23                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   11                                                            
CONECT   28    4   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34    4                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₃NO₁₀

Average Mass

483.5140 Da

Monoisotopic Mass

483.21045 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H](OC(C)=O)[C@@]1(O)C[C@@H](C)[C@@](C)(OC(C)=O)C(=O)OC\C2=C\CN(C)CC[C@@H](OC1=O)C2=O

InChI Identifier

InChI=1S/C23H33NO10/c1-13-11-23(30,14(2)32-15(3)25)21(29)33-18-8-10-24(6)9-7-17(19(18)27)12-31-20(28)22(13,5)34-16(4)26/h7,13-14,18,30H,8-12H2,1-6H3/b17-7-/t13-,14-,18-,22-,23+/m1/s1

InChI Key

IVVHMCWHYZBIAK-CARZHQTMSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tetracarboxylic acids and derivatives

Direct Parent

Tetracarboxylic acids and derivatives

Alternative Parents

Substituents

Tetracarboxylic acid or derivatives
Alpha-acyloxy ketone
Tertiary alcohol
Tertiary aliphatic amine
Tertiary amine
Lactone
Ketone
Carboxylic acid ester
Amino acid or derivatives
Oxacycle
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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

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

111307106

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

134714991

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Floricaline (NP0140926)

MOL for NP0140926 (Floricaline)

3D MOL for NP0140926 (Floricaline)

3D SDF for NP0140926 (Floricaline)

3D-SDF for NP0140926 (Floricaline)

PDB for NP0140926 (Floricaline)

3D PDB for NP0140926 (Floricaline)

SMILES for NP0140926 (Floricaline)

INCHI for NP0140926 (Floricaline)

Structure for NP0140926 (Floricaline)

3D Structure for NP0140926 (Floricaline)