NP-MRD: Showing NP-Card for (1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid (NP0305682)

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Record Information

Version

2.0

Created at

2022-09-10 21:42:37 UTC

Updated at

2022-09-10 21:42:37 UTC

NP-MRD ID

NP0305682

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid

Description

(1S,4S,5S,8R,9S,10R,11S,13S,14R,17R,18S,22R)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]Tetracosane-9-carboxylic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid is found in Atroxima afzeliana. Based on a literature review very few articles have been published on (1S,4S,5S,8R,9S,10R,11S,13S,14R,17R,18S,22R)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]Tetracosane-9-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102223422D          

 36 41  0  0  1  0            999 V2000
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  2 36  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309102223422D          

 36 41  0  0  1  0            999 V2000
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    5.5338   -0.1875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5557    0.6372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2297    0.2555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9614   -0.1257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1941    1.0797    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4773   -0.9191    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0774   -1.6475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2434   -1.6591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7527   -0.9614    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0043   -1.4598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2909   -0.9548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1549   -1.6490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2481   -0.4766    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9505   -0.0438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2718   -1.3013    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
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  6  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 15 27  1  0  0  0  0
 10 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  9 30  1  0  0  0  0
  5 30  1  0  0  0  0
 30 31  1  1  0  0  0
 31 32  1  0  0  0  0
  6 32  1  1  0  0  0
 32 33  2  0  0  0  0
  6 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
  2 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0305682

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C[C@@H]2[C@@]34CC[C@H]5[C@](C)(CC[C@@H]6[C@@]5(C)C[C@H](O)[C@H](O)[C@@]6(C)C(O)=O)[C@@H]3CC[C@]2([C@H](O)C1)C(=O)O4

> <INCHI_IDENTIFIER>
InChI=1S/C29H44O7/c1-24(2)13-19-28(20(31)14-24)10-7-18-25(3)9-6-17-26(4,12-15(30)21(32)27(17,5)22(33)34)16(25)8-11-29(18,19)36-23(28)35/h15-21,30-32H,6-14H2,1-5H3,(H,33,34)/t15-,16-,17+,18-,19-,20+,21-,25-,26-,27-,28-,29+/m0/s1

> <INCHI_KEY>
VDUTWZBXKDNVIK-XXFQTEAJSA-N

> <FORMULA>
C29H44O7

> <MOLECULAR_WEIGHT>
504.664

> <EXACT_MASS>
504.308703757

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
55.30660243861202

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4S,5S,8R,9S,10R,11S,13S,14R,17R,18S,22R)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosane-9-carboxylic acid

> <JCHEM_LOGP>
3.091515079333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.567150673764438

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.3097482553142745

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0503381446548676

> <JCHEM_POLAR_SURFACE_AREA>
124.29

> <JCHEM_REFRACTIVITY>
130.9295

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,5S,8R,9S,10R,11S,13S,14R,17R,18S,22R)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosane-9-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.219  -4.388   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.804  -3.237   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.759  -4.444   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.372  -2.460   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.203  -0.966   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.892  -0.158   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.893   1.127   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.489   1.076   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.153  -0.404   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.710  -0.389   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.928   0.938   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.469   0.952   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.009   0.964   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.790  -0.363   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.031  -1.703   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.272  -3.043   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.812  -3.030   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.352  -3.017   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.133  -4.344   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      11.111  -1.677   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.651  -1.664   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.330  -0.350   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.371   1.189   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.629   0.477   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      12.995  -0.235   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      11.562   2.016   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.491  -1.716   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.745  -3.075   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.188  -3.097   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.272  -1.795   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.875  -2.725   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       0.543  -1.782   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.289  -3.078   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -0.463  -0.890   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -1.774  -0.082   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -0.507  -2.429   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   36                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   30                                                  
CONECT    6    5    7   32   34                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   30                                                  
CONECT   10    9   11   12   27                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14   16   17   27                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   14   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   15   10   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    9    5   31                                             
CONECT   31   30   32                                                       
CONECT   32   31    6   33                                                  
CONECT   33   32                                                            
CONECT   34    6   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34    2                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

View in JSmol

Synonyms

Value	Source
(1S,4S,5S,8R,9S,10R,11S,13S,14R,17R,18S,22R)-10,11,22-Trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0,.0,.0,.0,]tetracosane-9-carboxylate	Generator

Chemical Formula

C₂₉H₄₄O₇

Average Mass

504.6640 Da

Monoisotopic Mass

504.30870 Da

IUPAC Name

(1S,4S,5S,8R,9S,10R,11S,13S,14R,17R,18S,22R)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosane-9-carboxylic acid

Traditional Name

(1S,4S,5S,8R,9S,10R,11S,13S,14R,17R,18S,22R)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosane-9-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1(C)C[C@@H]2[C@@]34CC[C@H]5[C@](C)(CC[C@@H]6[C@@]5(C)C[C@H](O)[C@H](O)[C@@]6(C)C(O)=O)[C@@H]3CC[C@]2([C@H](O)C1)C(=O)O4

InChI Identifier

InChI=1S/C29H44O7/c1-24(2)13-19-28(20(31)14-24)10-7-18-25(3)9-6-17-26(4,12-15(30)21(32)27(17,5)22(33)34)16(25)8-11-29(18,19)36-23(28)35/h15-21,30-32H,6-14H2,1-5H3,(H,33,34)/t15-,16-,17+,18-,19-,20+,21-,25-,26-,27-,28-,29+/m0/s1

InChI Key

VDUTWZBXKDNVIK-XXFQTEAJSA-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
Atroxima afzeliana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Steroid lactone
12-alpha-hydroxysteroid
12-hydroxysteroid
15-hydroxysteroid
Hydroxysteroid
Steroid
Caprolactone
Beta-hydroxy acid
Oxepane
Dicarboxylic acid or derivatives
Gamma butyrolactone
Hydroxy acid
Cyclic alcohol
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid
Carboxylic acid derivative
Polyol
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
Organooxygen compound
Organic oxygen 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	3.09	ChemAxon
pKa (Strongest Acidic)	4.31	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	124.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	130.93 m³·mol⁻¹	ChemAxon
Polarizability	55.31 Å³	ChemAxon
Number of Rings	6	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

162915684

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid (NP0305682)

MOL for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D MOL for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D SDF for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D-SDF for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

PDB for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D PDB for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

SMILES for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

INCHI for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

Structure for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D Structure for NP0305682 ((1s,4s,5s,8r,9s,10r,11s,13s,14r,17r,18s,22r)-10,11,22-trihydroxy-5,9,13,20,20-pentamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)