NP-MRD: Showing NP-Card for (7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione (NP0146071)

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Record Information

Version

2.0

Created at

2022-09-02 01:23:51 UTC

Updated at

2022-09-02 01:23:51 UTC

NP-MRD ID

NP0146071

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022203232D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309022203232D          

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 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  2  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  9 30  1  0  0  0  0
 30 31  2  0  0  0  0
 13 31  1  0  0  0  0
 18 31  1  0  0  0  0
 29 32  2  0  0  0  0
 24 32  1  0  0  0  0
 19 32  1  0  0  0  0
 20 33  1  0  0  0  0
 33 34  1  0  0  0  0
 17 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 16 39  1  0  0  0  0
 39 40  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0146071

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1O[C@H](C)[C@]2(O)OC3=CC(O)=C4C(=O)C5=C6C7=C8C(O[C@@]6(O)[C@@H](C)O[C@@H]5C)=CC(=O)C5=C(O)C1=C2C(C3=C47)=C85

> <INCHI_IDENTIFIER>
InChI=1S/C30H22O10/c1-7-15-25-23-19-13(39-29(25,35)9(3)37-7)6-12(32)18-22(19)24-20-14(5-11(31)17(21(20)23)27(15)33)40-30(36)10(4)38-8(2)16(26(24)30)28(18)34/h5-10,31,34-36H,1-4H3/t7-,8-,9-,10-,29+,30+/m1/s1

> <INCHI_KEY>
XFQZLNMJXFZDBL-NQLPKGGMSA-N

> <FORMULA>
C30H22O10

> <MOLECULAR_WEIGHT>
542.496

> <EXACT_MASS>
542.121296908

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
54.16199244903473

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(7R,9R,10R,18R,20R,21R)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1^{6,26}.0^{2,15}.0^{3,12}.0^{4,27}.0^{5,10}.0^{21,29}.0^{23,28}]triaconta-1,3,5,12,15,17(29),23,25,27-nonaene-14,30-dione

> <ALOGPS_LOGP>
3.04

> <JCHEM_LOGP>
3.719871924333332

> <ALOGPS_LOGS>
-3.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.006503169495444

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.609798582982293

> <JCHEM_PKA_STRONGEST_BASIC>
2.6184137279820177

> <JCHEM_POLAR_SURFACE_AREA>
151.98

> <JCHEM_REFRACTIVITY>
140.36119999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.07e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(7R,9R,10R,18R,20R,21R)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1^{6,26}.0^{2,15}.0^{3,12}.0^{4,27}.0^{5,10}.0^{21,29}.0^{23,28}]triaconta-1,3,5,12,15,17(29),23,25,27-nonaene-14,30-dione

> <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      -0.206   2.723   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.564   4.056   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.206   5.390   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.564   6.724   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.206   8.057   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.104   6.724   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.334   8.057   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       2.874   8.057   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.414   8.057   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.184   9.391   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.724   9.391   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.494  10.725   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.494   8.057   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.034   8.057   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.804   9.391   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.804   6.724   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.034   5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.494   5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.724   4.056   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.494   2.723   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.724   1.389   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.184   1.389   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.414   0.055   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.414   2.723   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.874   2.723   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.104   1.389   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.104   4.056   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.874   5.390   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.414   5.390   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.184   6.724   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.724   6.724   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.184   4.056   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       9.034   2.723   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       9.804   4.056   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      10.574   2.723   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      11.344   4.056   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.114   2.723   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      12.114   5.390   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      11.344   6.724   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      12.114   8.057   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8   28                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   30                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   31                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   39                                                  
CONECT   17   16   18   34                                                  
CONECT   18   17   19   31                                                  
CONECT   19   18   20   32                                                  
CONECT   20   19   21   33                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   32                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    2   28                                                  
CONECT   28   27    6   29                                                  
CONECT   29   28   30   32                                                  
CONECT   30   29    9   31                                                  
CONECT   31   30   13   18                                                  
CONECT   32   29   24   19                                                  
CONECT   33   20   34                                                       
CONECT   34   33   17   35   36                                             
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   16   40                                                  
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₂₂O₁₀

Average Mass

542.4960 Da

Monoisotopic Mass

542.12130 Da

IUPAC Name

(7R,9R,10R,18R,20R,21R)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1^{6,26}.0^{2,15}.0^{3,12}.0^{4,27}.0^{5,10}.0^{21,29}.0^{23,28}]triaconta-1,3,5,12,15,17(29),23,25,27-nonaene-14,30-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1O[C@H](C)[C@]2(O)OC3=CC(O)=C4C(=O)C5=C6C7=C8C(O[C@@]6(O)[C@@H](C)O[C@@H]5C)=CC(=O)C5=C(O)C1=C2C(C3=C47)=C85

InChI Identifier

InChI=1S/C30H22O10/c1-7-15-25-23-19-13(39-29(25,35)9(3)37-7)6-12(32)18-22(19)24-20-14(5-11(31)17(21(20)23)27(15)33)40-30(36)10(4)38-8(2)16(26(24)30)28(18)34/h5-10,31,34-36H,1-4H3/t7-,8-,9-,10-,29+,30+/m1/s1

InChI Key

XFQZLNMJXFZDBL-NQLPKGGMSA-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
Hamamelistes betulinus	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	3.04	ALOGPS
logP	3.72	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	6.61	ChemAxon
pKa (Strongest Basic)	2.62	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	151.98 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	140.36 m³·mol⁻¹	ChemAxon
Polarizability	54.16 Å³	ChemAxon
Number of Rings	9	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione (NP0146071)

MOL for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)

3D MOL for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)

3D SDF for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)

3D-SDF for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)

PDB for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)

3D PDB for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)

SMILES for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)

INCHI for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)

Structure for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)

3D Structure for NP0146071 ((7r,9r,10r,18r,20r,21r)-10,16,21,25-tetrahydroxy-7,9,18,20-tetramethyl-8,11,19,22-tetraoxanonacyclo[15.11.1.1⁶,²⁶.0²,¹⁵.0³,¹².0⁴,²⁷.0⁵,¹⁰.0²¹,²⁹.0²³,²⁸]triaconta-1(29),2(15),3,5,12,16,23,25,27-nonaene-14,30-dione)