NP-MRD: Showing NP-Card for (1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol (NP0242422)

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Record Information

Version

2.0

Created at

2022-09-07 02:44:13 UTC

Updated at

2022-09-07 02:44:14 UTC

NP-MRD ID

NP0242422

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol

Description

CHEMBL3586081 belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring. Based on a literature review very few articles have been published on CHEMBL3586081.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072204442D          

 32 37  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309072204442D          

 32 37  0  0  1  0            999 V2000
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M  END
> <DATABASE_ID>
NP0242422

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCO[C@H]1OC[C@]23CCC[C@@]1(C)C2CC[C@]1(C)C3CC[C@]2(C)OC3=CC=C(O)C=C3CC12

> <INCHI_IDENTIFIER>
InChI=1S/C28H40O4/c1-5-30-24-26(3)11-6-12-28(17-31-24)21-10-14-27(4)23(25(21,2)13-9-22(26)28)16-18-15-19(29)7-8-20(18)32-27/h7-8,15,21-24,29H,5-6,9-14,16-17H2,1-4H3/t21?,22?,23?,24-,25+,26-,27-,28-/m0/s1

> <INCHI_KEY>
ASXZDCUZAROTNW-HQTIXOHMSA-N

> <FORMULA>
C28H40O4

> <MOLECULAR_WEIGHT>
440.624

> <EXACT_MASS>
440.292659768

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
51.28142641931639

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,5S,15R,19S,20S)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0^{1,18}.0^{2,15}.0^{5,14}.0^{7,12}]pentacosa-7,9,11-trien-10-ol

> <JCHEM_LOGP>
5.983887548666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.003930619866058

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9618419712561397

> <JCHEM_POLAR_SURFACE_AREA>
47.92

> <JCHEM_REFRACTIVITY>
124.80099999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,5S,15R,19S,20S)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0^{1,18}.0^{2,15}.0^{5,14}.0^{7,12}]pentacosa-7,9,11-trien-10-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       5.289  -4.529   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.978  -3.021   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.517  -2.535   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.207  -1.027   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.726  -0.523   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.772   1.350   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.908   2.624   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.396   2.915   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.121   2.051   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.830   0.539   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.694  -0.736   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.847  -2.022   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.398   1.171   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.402   0.003   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.915   0.288   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.425   1.741   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.429   0.573   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.939   2.026   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.942   0.858   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.455   1.143   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.459  -0.026   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.972   0.259   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      13.976  -0.909   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      13.482   1.712   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.479   2.881   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.965   2.596   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.962   3.764   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.449   3.479   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.959   4.932   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.445   4.647   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.932   4.362   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.422   2.909   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   13   32                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    4   12   13                                             
CONECT   12   11                                                            
CONECT   13   11    7   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   32                                             
CONECT   17   16                                                            
CONECT   18   16   19   28                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   20   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   18   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    7   16                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₄₀O₄

Average Mass

440.6240 Da

Monoisotopic Mass

440.29266 Da

IUPAC Name

(1S,5S,15R,19S,20S)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0^{1,18}.0^{2,15}.0^{5,14}.0^{7,12}]pentacosa-7,9,11-trien-10-ol

Traditional Name

(1S,5S,15R,19S,20S)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0^{1,18}.0^{2,15}.0^{5,14}.0^{7,12}]pentacosa-7,9,11-trien-10-ol

CAS Registry Number

Not Available

SMILES

CCO[C@H]1OC[C@]23CCC[C@@]1(C)C2CC[C@]1(C)C3CC[C@]2(C)OC3=CC=C(O)C=C3CC12

InChI Identifier

InChI=1S/C28H40O4/c1-5-30-24-26(3)11-6-12-28(17-31-24)21-10-14-27(4)23(25(21,2)13-9-22(26)28)16-18-15-19(29)7-8-20(18)32-27/h7-8,15,21-24,29H,5-6,9-14,16-17H2,1-4H3/t21?,22?,23?,24-,25+,26-,27-,28-/m0/s1

InChI Key

ASXZDCUZAROTNW-HQTIXOHMSA-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 xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthenes

Alternative Parents

Substituents

Xanthene
Naphthopyran
Naphthalene
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Pyran
Oxane
Oxacycle
Ether
Acetal
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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
logP	5.98	ChemAxon
pKa (Strongest Acidic)	10	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	47.92 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	124.8 m³·mol⁻¹	ChemAxon
Polarizability	51.28 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's 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

122180074

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol (NP0242422)

MOL for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)

3D MOL for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)

3D SDF for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)

3D-SDF for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)

PDB for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)

3D PDB for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)

SMILES for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)

INCHI for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)

Structure for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)

3D Structure for NP0242422 ((1s,5s,15r,19s,20s)-20-ethoxy-5,15,19-trimethyl-6,21-dioxahexacyclo[17.3.3.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁷,¹²]pentacosa-7,9,11-trien-10-ol)