NP-MRD: Showing NP-Card for (1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate (NP0146230)

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Record Information

Version

2.0

Created at

2022-09-02 01:35:14 UTC

Updated at

2022-09-02 01:35:14 UTC

NP-MRD ID

NP0146230

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate

Description

CHEMBL502799 belongs to the class of organic compounds known as phorbol esters. These are tigliane diterpenoids which are esters of phorbol. (1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate is found in Croton ciliatoglandulifer. Based on a literature review very few articles have been published on CHEMBL502799.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022203352D          

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M  END

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M  END


  Mrv1652309022203352D          

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    1.5323    2.3612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6875    0.7730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9342   -0.0142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5105    0.5761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7271   -0.2420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3775    0.2656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7555   -1.0665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4392   -1.5282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9801   -1.3483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4725   -0.6980    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7172   -0.3483    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5207   -0.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0299    0.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3059   -0.2821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  6  5  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 10 14  1  6  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 17  6  1  0  0  0  0
 17 18  1  6  0  0  0
 19 17  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 27 26  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 34 33  1  1  0  0  0
 34 27  1  0  0  0  0
 19 34  1  0  0  0  0
 21 35  1  0  0  0  0
 35  5  1  0  0  0  0
 35 36  1  1  0  0  0
  5 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146230

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H](N(C)C)C(=O)O[C@@H]1[C@@H](C)[C@]2(O)[C@@H]3C=C(C)C(=O)[C@]3(O)CC(CO)=C[C@H]2[C@@H]2C(C)(C)[C@]12OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C29H43NO8/c1-14(2)21(30(8)9)25(34)37-24-16(4)28(36)19(22-26(6,7)29(22,24)38-17(5)32)11-18(13-31)12-27(35)20(28)10-15(3)23(27)33/h10-11,14,16,19-22,24,31,35-36H,12-13H2,1-9H3/t16-,19+,20-,21-,22-,24-,27+,28-,29-/m1/s1

> <INCHI_KEY>
NNQZZZKSYAIGAN-XUSXYMRCSA-N

> <FORMULA>
C29H43NO8

> <MOLECULAR_WEIGHT>
533.662

> <EXACT_MASS>
533.298867349

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
57.62452876107588

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,6S,10S,11R,13S,14R,15R)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0^{2,6}.0^{11,13}]pentadeca-3,8-dien-14-yl (2R)-2-(dimethylamino)-3-methylbutanoate

> <ALOGPS_LOGP>
2.31

> <JCHEM_LOGP>
1.4491260283333327

> <ALOGPS_LOGS>
-3.31

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.933224684425827

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.570370773829492

> <JCHEM_PKA_STRONGEST_BASIC>
6.725862734159687

> <JCHEM_POLAR_SURFACE_AREA>
133.60000000000002

> <JCHEM_REFRACTIVITY>
140.99890000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.64e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,6S,10S,11R,13S,14R,15R)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0^{2,6}.0^{11,13}]pentadeca-3,8-dien-14-yl (2R)-2-(dimethylamino)-3-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.733  -1.229   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.384  -2.729   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -5.508  -3.781   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -2.910  -3.176   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.786  -2.124   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.734  -3.248   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.181  -4.721   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.681  -5.071   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.733  -3.947   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -3.128  -6.545   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.628  -6.894   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.075  -8.368   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.680  -5.770   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      -2.076  -7.669   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -0.576  -7.319   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.523  -9.142   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.766  -2.898   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.819  -4.023   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.214  -1.425   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.179  -2.625   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.161  -0.301   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.384   1.223   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.714   1.999   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.592   3.534   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.860   4.408   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.150   1.443   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.610  -0.027   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.686   1.075   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.091  -0.452   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.305   0.496   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.144  -1.991   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.420  -2.853   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.696  -2.517   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.749  -1.303   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.339  -0.650   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.839  -1.000   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -3.789   0.212   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -4.304  -0.527   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   35   36                                             
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   14                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   10   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    6   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21   34                                             
CONECT   20   19                                                            
CONECT   21   19   22   35                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28   29   34                                             
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   27   19                                                  
CONECT   35   21    5   36                                                  
CONECT   36   35    5   37   38                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₃NO₈

Average Mass

533.6620 Da

Monoisotopic Mass

533.29887 Da

IUPAC Name

(1S,2S,6S,10S,11R,13S,14R,15R)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0^{2,6}.0^{11,13}]pentadeca-3,8-dien-14-yl (2R)-2-(dimethylamino)-3-methylbutanoate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H](N(C)C)C(=O)O[C@@H]1[C@@H](C)[C@]2(O)[C@@H]3C=C(C)C(=O)[C@]3(O)CC(CO)=C[C@H]2[C@@H]2C(C)(C)[C@]12OC(C)=O

InChI Identifier

InChI=1S/C29H43NO8/c1-14(2)21(30(8)9)25(34)37-24-16(4)28(36)19(22-26(6,7)29(22,24)38-17(5)32)11-18(13-31)12-27(35)20(28)10-15(3)23(27)33/h10-11,14,16,19-22,24,31,35-36H,12-13H2,1-9H3/t16-,19+,20-,21-,22-,24-,27+,28-,29-/m1/s1

InChI Key

NNQZZZKSYAIGAN-XUSXYMRCSA-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
Croton ciliatoglandulifer	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phorbol esters. These are tigliane diterpenoids which are esters of phorbol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Phorbol esters

Alternative Parents

Substituents

Phorbol ester
Alpha-amino acid ester
Valine or derivatives
Alpha-amino acid or derivatives
Fatty acid ester
Fatty acyl
Dicarboxylic acid or derivatives
Tertiary alcohol
Cyclic alcohol
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Ketone
Carboxylic acid derivative
Alcohol
Organonitrogen compound
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organopnictogen compound
Amine
Organic oxygen compound
Organic nitrogen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	2.31	ALOGPS
logP	1.45	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	12.57	ChemAxon
pKa (Strongest Basic)	6.73	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	133.6 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	141 m³·mol⁻¹	ChemAxon
Polarizability	57.62 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

9694209

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11519421

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate (NP0146230)

MOL for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)

3D MOL for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)

3D SDF for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)

3D-SDF for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)

PDB for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)

3D PDB for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)

SMILES for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)

INCHI for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)

Structure for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)

3D Structure for NP0146230 ((1s,2s,6s,10s,11r,13s,14r,15r)-13-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-14-yl (2r)-2-(dimethylamino)-3-methylbutanoate)