NP-MRD: Showing NP-Card for (2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal (NP0142017)

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Record Information

Version

2.0

Created at

2022-09-01 20:27:55 UTC

Updated at

2022-09-01 20:27:55 UTC

NP-MRD ID

NP0142017

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal

Description

6,7-Dihydroxy-7-[3-(hydroxymethyl)oxiranyl]-2-(1-propenyl)-2,4-heptadienal belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. (2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal is found in Menisporopsis theobromae. Based on a literature review very few articles have been published on 6,7-Dihydroxy-7-[3-(hydroxymethyl)oxiranyl]-2-(1-propenyl)-2,4-heptadienal.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 36  0  0  0  0  0  0  0  0999 V2000
    6.5146    1.2469    0.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4702    0.1604    0.3946 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2081    0.4600    0.3471 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1705   -0.5541    0.2470 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5441   -1.9443    0.1978 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7802   -2.9284    0.1126 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8890   -0.1931    0.2015 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7830   -1.0993    0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4363   -0.5154    0.0717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6373   -1.3588   -0.0283 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8798   -1.6153   -1.3588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8308   -0.7752    0.6866 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5668   -0.5233    2.0258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3638    0.4516   -0.0216 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6778    0.3646   -1.3649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7569    0.4425   -0.4259 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5473    1.7260   -0.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6709    2.7930   -0.4384 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0296    2.1972    0.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3352    0.9887   -0.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9110    1.3197    1.5097 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8688   -0.8262    0.3663 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9237    1.4945    0.3833 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5966   -2.2050    0.2369 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7257    0.9008    0.2466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8229   -2.1719    0.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5611    0.5507    0.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3842   -2.3385    0.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308   -1.5746   -1.8645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6394   -1.5334    0.6681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8138   -1.0442    2.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9782    1.4406    0.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3797   -0.4543   -0.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3939    1.7350    0.0548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8555    1.7275   -1.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1691    3.6555   -0.5590 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  4  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 14  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  3 23  1  0
  5 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  1
 11 29  1  0
 12 30  1  1
 13 31  1  0
 14 32  1  6
 16 33  1  1
 17 34  1  0
 17 35  1  0
 18 36  1  0
M  END


  Mrv1652309012222272D          

 18 18  0  0  0  0            999 V2000
    3.0960    6.6638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0960    5.8388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3816    5.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3816    4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0960    4.1888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0960    3.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6671    4.1888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6671    3.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9526    2.9513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9526    2.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6671    1.7138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2382    1.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4763    2.1263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2382    0.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6507    0.1743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1743    0.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8888   -0.2382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8888   -1.0632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  4  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0142017

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C\C(\C=O)=C\C=C\C(O)C(O)C1OC1CO

> <INCHI_IDENTIFIER>
InChI=1S/C13H18O5/c1-2-4-9(7-14)5-3-6-10(16)12(17)13-11(8-15)18-13/h2-7,10-13,15-17H,8H2,1H3/b4-2+,6-3+,9-5-

> <INCHI_KEY>
VAEGPTFYQCVMTP-HUJNKONTSA-N

> <FORMULA>
C13H18O5

> <MOLECULAR_WEIGHT>
254.282

> <EXACT_MASS>
254.11542368

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
26.638972613584883

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z,4E)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1E)-prop-1-en-1-yl]hepta-2,4-dienal

> <ALOGPS_LOGP>
0.29

> <JCHEM_LOGP>
-0.4294594813333335

> <ALOGPS_LOGS>
-1.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.33526856925575

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.981509502385855

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9791427790931504

> <JCHEM_POLAR_SURFACE_AREA>
90.29

> <JCHEM_REFRACTIVITY>
69.14840000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.98e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z,4E)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1E)-prop-1-en-1-yl]hepta-2,4-dienal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-SEP-22         0                                  
HETATM    1  C   UNK     0       5.779  12.439   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.779  10.899   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.446  10.129   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.446   8.589   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.779   7.819   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.779   6.279   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.112   7.819   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.112   6.279   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.778   5.509   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.778   3.969   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.112   3.199   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.445   3.199   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.889   3.969   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.445   1.659   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.215   0.325   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.325   0.325   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.659  -0.445   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.659  -1.985   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14   16                                                       
CONECT   16   15   14   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₁₈O₅

Average Mass

254.2820 Da

Monoisotopic Mass

254.11542 Da

IUPAC Name

(2Z,4E)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1E)-prop-1-en-1-yl]hepta-2,4-dienal

Traditional Name

(2Z,4E)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1E)-prop-1-en-1-yl]hepta-2,4-dienal

CAS Registry Number

Not Available

SMILES

C\C=C\C(\C=O)=C\C=C\C(O)C(O)C1OC1CO

InChI Identifier

InChI=1S/C13H18O5/c1-2-4-9(7-14)5-3-6-10(16)12(17)13-11(8-15)18-13/h2-7,10-13,15-17H,8H2,1H3/b4-2+,6-3+,9-5-

InChI Key

VAEGPTFYQCVMTP-HUJNKONTSA-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
Menisporopsis theobromae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Alpha,beta-unsaturated aldehyde
Enal
1,2-diol
Secondary alcohol
Ether
Oxirane
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Alcohol
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Aldehyde
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	0.29	ALOGPS
logP	-0.43	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	12.98	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.29 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	69.15 m³·mol⁻¹	ChemAxon
Polarizability	26.64 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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78444426

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101426747

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal (NP0142017)

MOL for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)

3D MOL for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)

3D SDF for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)

3D-SDF for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)

PDB for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)

3D PDB for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)

SMILES for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)

INCHI for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)

Structure for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)

3D Structure for NP0142017 ((2z,4e)-6,7-dihydroxy-7-[3-(hydroxymethyl)oxiran-2-yl]-2-[(1e)-prop-1-en-1-yl]hepta-2,4-dienal)