NP-MRD: Showing NP-Card for 10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one (NP0237928)

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Record Information

Version

2.0

Created at

2022-09-06 21:12:35 UTC

Updated at

2022-09-06 21:12:35 UTC

NP-MRD ID

NP0237928

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one

Description

10-Hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]Nonacosan-12-one 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. 10-Hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]Nonacosan-12-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261512372D          

 39 46  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004261512372D          

 39 46  0  0  0  0            999 V2000
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    6.4638   -1.0738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9268    0.2521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3238    1.2080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8233    0.9545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2996    1.6281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2677    0.2265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6076   -0.2591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8587   -1.0450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7626    1.1785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1650    0.7513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2653    0.5537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960    0.8536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2296    1.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8708    1.8906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4480    1.5735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9031    0.9143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2075    1.2663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7345    1.7219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9508    1.9797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3496    2.2717    0.0000 C   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
  8  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  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
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  2  0  0  0  0
 23 28  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  1  0  0  0  0
 21 29  1  0  0  0  0
 29 30  1  0  0  0  0
 13 30  1  0  0  0  0
 30 31  1  0  0  0  0
 10 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 12 35  1  0  0  0  0
 35 36  1  0  0  0  0
 10 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237928

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2(OC34CCCCCCCC(C)C5C6C7(OC5(C)OC7=O)C(O)C5(CO)OC5C(C2O3)C16O4)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O9/c1-15(2)26-13-17(4)29-19-21(26)35-28(38-26,39-29)12-10-8-6-7-9-11-16(3)18-20(29)30(24(33)36-25(18,5)37-30)23(32)27(14-31)22(19)34-27/h16-23,31-32H,1,6-14H2,2-5H3

> <INCHI_KEY>
XRYQMTUHMOLDGS-UHFFFAOYSA-N

> <FORMULA>
C30H42O9

> <MOLECULAR_WEIGHT>
546.657

> <EXACT_MASS>
546.282882932

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
57.776548979847945

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one

> <ALOGPS_LOGP>
3.20

> <JCHEM_LOGP>
3.9713317449999987

> <ALOGPS_LOGS>
-3.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.302536747364393

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.481256280121649

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1497666333959096

> <JCHEM_POLAR_SURFACE_AREA>
116.21000000000001

> <JCHEM_REFRACTIVITY>
135.54680000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.74e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      11.322  -0.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.960   0.408   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.047  -1.071   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.320  -2.546   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.744  -3.508   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.265  -4.124   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.944  -3.229   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.172  -1.814   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.069  -0.171   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.278   1.004   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.502  -0.446   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.753  -0.183   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.310  -0.261   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.954  -1.612   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.241  -3.126   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.408  -2.120   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.352  -3.338   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.769  -4.763   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.769  -1.173   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.066  -2.004   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      11.063   0.471   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      11.804   2.255   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.737   1.782   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.626   3.039   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.566   0.423   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      12.334  -0.484   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.803  -1.951   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      10.757   2.200   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.641   1.402   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.962   1.034   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.339   1.593   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.895   2.560   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.092   3.529   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.436   2.937   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.419   1.707   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       4.121   2.364   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       5.104   3.214   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.642   3.696   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.253   4.241   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   31   36                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   35                                                  
CONECT   13   12   14   30                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14   16                                                       
CONECT   16   15   14   17   19                                             
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   26   29                                             
CONECT   22   21   23                                                       
CONECT   23   22   24   25   28                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   21   27                                                  
CONECT   27   26                                                            
CONECT   28   23    2   29                                                  
CONECT   29   28   21   30                                                  
CONECT   30   29   13   31   32                                             
CONECT   31   30   10                                                       
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   12   36   37                                             
CONECT   36   35   10                                                       
CONECT   37   35   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₂O₉

Average Mass

546.6570 Da

Monoisotopic Mass

546.28288 Da

IUPAC Name

10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one

Traditional Name

10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one

CAS Registry Number

Not Available

SMILES

CC1CC2(OC34CCCCCCCC(C)C5C6C7(OC5(C)OC7=O)C(O)C5(CO)OC5C(C2O3)C16O4)C(C)=C

InChI Identifier

InChI=1S/C30H42O9/c1-15(2)26-13-17(4)29-19-21(26)35-28(38-26,39-29)12-10-8-6-7-9-11-16(3)18-20(29)30(24(33)36-25(18,5)37-30)23(32)27(14-31)22(19)34-27/h16-23,31-32H,1,6-14H2,2-5H3

InChI Key

XRYQMTUHMOLDGS-UHFFFAOYSA-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 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
Ketal
1,3-dioxepane
Carboxylic acid orthoester
Delta valerolactone
Dioxepane
Delta_valerolactone
Ortho ester
Meta-dioxane
Oxane
Meta-dioxolane
Cyclic alcohol
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Orthocarboxylic acid derivative
Lactone
Ether
Oxirane
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Acetal
Monocarboxylic acid or derivatives
Primary alcohol
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Organooxygen compound
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
logP	3.2	ALOGPS
logP	3.97	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	12.48	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	116.21 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	135.55 m³·mol⁻¹	ChemAxon
Polarizability	57.78 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

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

75082455

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one (NP0237928)

MOL for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)

3D MOL for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)

3D SDF for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)

3D-SDF for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)

PDB for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)

3D PDB for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)

SMILES for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)

INCHI for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)

Structure for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)

3D Structure for NP0237928 (10-hydroxy-9-(hydroxymethyl)-2,14,16-trimethyl-4-(prop-1-en-2-yl)-8,13,25,27,28,29-hexaoxaoctacyclo[13.10.1.1⁴,²⁴.1⁵,²⁴.1¹¹,¹⁴.0¹,⁶.0⁷,⁹.0¹¹,²⁶]nonacosan-12-one)