NP-MRD: Showing NP-Card for (1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol (NP0324998)

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Record Information

Version

2.0

Created at

2022-09-12 05:25:19 UTC

Updated at

2022-09-12 05:25:19 UTC

NP-MRD ID

NP0324998

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol

Description

(23R,24S)-16beta,23:16Alpha,24-Diepoxycycloartane-3beta,6alpha,7beta,25-tetrol, also known as (23R,24S)-16β,23:16α,24-Diepoxycycloartane-3β,6α,7β,25-tetrol, belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. Based on a literature review very few articles have been published on (23R,24S)-16beta,23:16Alpha,24-Diepoxycycloartane-3beta,6alpha,7beta,25-tetrol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122207252D          

 36 42  0  0  1  0            999 V2000
    5.6501    3.9405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0887    1.1694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4035    1.6422    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.6021    1.4462    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309122207252D          

 36 42  0  0  1  0            999 V2000
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    2.2303    1.8461    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4612    2.6381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0317    2.0421    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2626    2.8342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0639    3.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6355    2.4379    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9430    3.2035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4679    2.4707    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4339    1.0136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2266    1.3828    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9490    0.9844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6715    0.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5507    0.2619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3474    1.7068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 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
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 15 23  1  1  0  0  0
 23 24  1  1  0  0  0
 25 24  1  1  0  0  0
 10 25  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  8 28  1  0  0  0  0
 28 29  1  1  0  0  0
 30 28  1  1  0  0  0
  2 30  1  0  0  0  0
  6 30  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  1  0  0  0  0
  4 32  1  0  0  0  0
 32 33  1  1  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0324998

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H]2O[C@]3(C[C@@]4(C)[C@@H]5[C@@H](O)[C@H](O)[C@@H]6[C@]7(C[C@@]57CC[C@]4(C)[C@@H]13)CC[C@H](O)C6(C)C)O[C@@H]2C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O6/c1-15-12-16-23(25(4,5)34)36-30(35-16)13-27(7)22-19(33)18(32)21-24(2,3)17(31)8-9-28(21)14-29(22,28)11-10-26(27,6)20(15)30/h15-23,31-34H,8-14H2,1-7H3/t15-,16-,17+,18+,19+,20-,21+,22+,23+,26-,27+,28-,29+,30-/m1/s1

> <INCHI_KEY>
IZLOVIRIHSPYRC-SRSYERAPSA-N

> <FORMULA>
C30H48O6

> <MOLECULAR_WEIGHT>
504.708

> <EXACT_MASS>
504.345089266

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
57.924663724174344

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3S,4S,5R,6R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0^{1,18}.0^{3,17}.0^{4,14}.0^{7,12}.0^{12,14}]tetracosane-5,6,9-triol

> <JCHEM_LOGP>
2.508511394666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.159926133933865

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.494630375211322

> <JCHEM_PKA_STRONGEST_BASIC>
-2.92760392577122

> <JCHEM_POLAR_SURFACE_AREA>
99.38000000000001

> <JCHEM_REFRACTIVITY>
134.8245

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,4S,5R,6R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0^{1,18}.0^{3,17}.0^{4,14}.0^{7,12}.0^{12,14}]tetracosane-5,6,9-triol

> <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      10.547   7.356   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.144   5.936   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.720   5.685   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.285   4.179   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      11.987   3.679   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.812   3.069   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.499   2.183   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.220   3.065   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.941   1.551   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.724   2.699   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.293   1.221   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.358   0.109   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.797   0.855   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.366  -0.623   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.732   1.968   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.236   1.602   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.857   0.192   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.956   0.746   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.171   2.714   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.324   2.348   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.602   4.192   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.098   4.558   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.163   3.446   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.594   4.924   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.659   3.812   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.090   5.290   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.586   5.656   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.653   4.551   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.227   5.980   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.207   4.612   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.010   1.892   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      13.490   2.581   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.838   1.838   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      16.187   1.094   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.095   0.489   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      15.582   3.186   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   32                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   30   31                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   10   28                                             
CONECT    9    8                                                            
CONECT   10    8   11   25                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   23                                                  
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   15   24   25                                             
CONECT   24   23   25                                                       
CONECT   25   24   10   23   26                                             
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27    8   29   30                                             
CONECT   29   28                                                            
CONECT   30   28    2    6                                                  
CONECT   31    6   32                                                       
CONECT   32   31    4   33                                                  
CONECT   33   32   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   84    0
END

View in JSmol

Synonyms

Value	Source
(23R,24S)-16b,23:16a,24-Diepoxycycloartane-3b,6a,7b,25-tetrol	Generator
(23R,24S)-16Β,23:16α,24-diepoxycycloartane-3β,6α,7β,25-tetrol	Generator

Chemical Formula

C₃₀H₄₈O₆

Average Mass

504.7080 Da

Monoisotopic Mass

504.34509 Da

IUPAC Name

(1R,3S,4S,5R,6R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0^{1,18}.0^{3,17}.0^{4,14}.0^{7,12}.0^{12,14}]tetracosane-5,6,9-triol

Traditional Name

(1R,3S,4S,5R,6R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0^{1,18}.0^{3,17}.0^{4,14}.0^{7,12}.0^{12,14}]tetracosane-5,6,9-triol

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H]2O[C@]3(C[C@@]4(C)[C@@H]5[C@@H](O)[C@H](O)[C@@H]6[C@]7(C[C@@]57CC[C@]4(C)[C@@H]13)CC[C@H](O)C6(C)C)O[C@@H]2C(C)(C)O

InChI Identifier

InChI=1S/C30H48O6/c1-15-12-16-23(25(4,5)34)36-30(35-16)13-27(7)22-19(33)18(32)21-24(2,3)17(31)8-9-28(21)14-29(22,28)11-10-26(27,6)20(15)30/h15-23,31-34H,8-14H2,1-7H3/t15-,16-,17+,18+,19+,20-,21+,22+,23+,26-,27+,28-,29+,30-/m1/s1

InChI Key

IZLOVIRIHSPYRC-SRSYERAPSA-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 cycloartanols and derivatives. These are steroids containing a cycloartanol moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cycloartanols and derivatives

Direct Parent

Cycloartanols and derivatives

Alternative Parents

Substituents

Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Cycloartane-skeleton
Triterpenoid
3-hydroxysteroid
6-hydroxysteroid
Hydroxysteroid
3-beta-hydroxysteroid
7-hydroxysteroid
Oxepane
Ketal
Oxane
Meta-dioxolane
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Polyol
Acetal
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Alcohol
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	2.51	ChemAxon
pKa (Strongest Acidic)	13.49	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	99.38 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	134.82 m³·mol⁻¹	ChemAxon
Polarizability	57.92 Å³	ChemAxon
Number of Rings	7	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

14376709

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol (NP0324998)

MOL for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)

3D MOL for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)

3D SDF for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)

3D-SDF for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)

PDB for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)

3D PDB for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)

SMILES for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)

INCHI for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)

Structure for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)

3D Structure for NP0324998 ((1r,3s,4s,5r,6r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosane-5,6,9-triol)