NP-MRD: Showing NP-Card for (4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione (NP0326437)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 07:59:12 UTC

Updated at

2022-09-12 07:59:12 UTC

NP-MRD ID

NP0326437

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione

Description

(4S,8R,13R,16R)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. (4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione is found in Pestalotiopsis fici. Based on a literature review very few articles have been published on (4S,8R,13R,16R)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309122209592D          

 23 23  0  0  1  0            999 V2000
    1.9184    2.2160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.4223    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7183    2.0140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5182    1.8119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7432    1.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5430    0.8161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1683    0.4265    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3684    0.6285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3932   -0.3673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8183   -0.9589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0184   -0.7569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0433   -1.7527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4684   -2.3444    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6933   -3.1381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6685   -2.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4435   -1.3486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6436   -1.1466    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0687   -1.7382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4187   -0.3528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9936    0.2389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7686    1.0326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0313    1.2346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3435    1.6243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  4  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  2 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0326437

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@@H](O)C=CC(=O)O[C@H](C)CCC(=O)[C@@H](O)CC(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C16H24O7/c1-10-3-5-12(17)6-8-15(20)22-11(2)4-7-13(18)14(19)9-16(21)23-10/h6,8,10-12,14,17,19H,3-5,7,9H2,1-2H3/t10-,11-,12-,14+/m1/s1

> <INCHI_KEY>
QERMLGGCVHACEI-BYNQJWBRSA-N

> <FORMULA>
C16H24O7

> <MOLECULAR_WEIGHT>
328.361

> <EXACT_MASS>
328.152203113

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
33.11888572791374

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S,8R,13R,16R)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione

> <JCHEM_LOGP>
0.9056342206666677

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.836083964480945

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.132452567605942

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8735890051723993

> <JCHEM_POLAR_SURFACE_AREA>
110.13

> <JCHEM_REFRACTIVITY>
81.64819999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4S,8R,13R,16R)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       3.581   4.137   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001   2.655   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.074   3.759   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.567   3.382   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.987   1.901   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.480   1.523   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.914   0.796   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.421   1.173   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.334  -0.686   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.261  -1.790   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.768  -1.413   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       5.681  -3.272   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.608  -4.376   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.028  -5.858   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.115  -3.999   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.695  -2.517   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.201  -2.140   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.128  -3.245   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.782  -0.659   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.855   0.446   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.435   1.928   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.058   2.305   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.508   3.032   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    2                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₄O₇

Average Mass

328.3610 Da

Monoisotopic Mass

328.15220 Da

IUPAC Name

(4S,8R,13R,16R)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione

Traditional Name

(4S,8R,13R,16R)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@@H](O)C=CC(=O)O[C@H](C)CCC(=O)[C@@H](O)CC(=O)O1

InChI Identifier

InChI=1S/C16H24O7/c1-10-3-5-12(17)6-8-15(20)22-11(2)4-7-13(18)14(19)9-16(21)23-10/h6,8,10-12,14,17,19H,3-5,7,9H2,1-2H3/t10-,11-,12-,14+/m1/s1

InChI Key

QERMLGGCVHACEI-BYNQJWBRSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Pestalotiopsis fici	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic ketone
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	0.91	ChemAxon
pKa (Strongest Acidic)	13.13	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	110.13 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	81.65 m³·mol⁻¹	ChemAxon
Polarizability	33.12 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584211

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione (NP0326437)

MOL for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)

3D MOL for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)

3D SDF for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)

3D-SDF for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)

PDB for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)

3D PDB for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)

SMILES for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)

INCHI for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)

Structure for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)

3D Structure for NP0326437 ((4s,8r,13r,16r)-4,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadec-11-ene-2,5,10-trione)