NP-MRD: Showing NP-Card for Teucrolivin H (NP0072445)

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Record Information

Version

2.0

Created at

2022-04-28 17:47:29 UTC

Updated at

2022-04-28 17:47:29 UTC

NP-MRD ID

NP0072445

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Teucrolivin H

Description

[(1'R,2R,6'R,7'S,9'S,11'R,13'R)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]Tetradecane]-6'-yl]methyl acetate belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Teucrolivin H is found in Teucrium orientale. Based on a literature review very few articles have been published on [(1'R,2R,6'R,7'S,9'S,11'R,13'R)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]Tetradecane]-6'-yl]methyl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652304282219472D          

 30 35  0  0  1  0            999 V2000
   -0.2128    0.3960    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5657    0.0098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1454    0.6396    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4614    1.1271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2834    1.8694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0157    2.3526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7870    2.0119    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8598    1.1617    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6554    0.8534    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8002    0.0356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5770   -0.2423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1742   -0.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4058   -0.1940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9636    1.6187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4722    0.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1030    1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073    2.1336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1505    2.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9548    3.1056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5893    3.5268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4583    2.4913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1407    2.5771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4921    1.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5059    0.8934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1453    1.5885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8519   -0.1258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8053   -0.9495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5743   -1.2483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0961   -0.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6496    0.0845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  3 13  1  0  0  0  0
  9 14  1  6  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
  8 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  7 21  1  6  0  0  0
  5 22  1  6  0  0  0
  5 23  1  0  0  0  0
  1 23  1  0  0  0  0
  4 24  1  0  0  0  0
  1 24  1  0  0  0  0
  4 25  1  1  0  0  0
  1 26  1  6  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 26 30  1  0  0  0  0
M  END


  Mrv1652304282219472D          

 30 35  0  0  1  0            999 V2000
   -0.2128    0.3960    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5657    0.0098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1454    0.6396    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4614    1.1271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2834    1.8694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0157    2.3526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7870    2.0119    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8598    1.1617    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6554    0.8534    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8002    0.0356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5770   -0.2423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1742   -0.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4058   -0.1940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9636    1.6187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4722    0.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1030    1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073    2.1336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1505    2.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9548    3.1056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5893    3.5268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4583    2.4913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1407    2.5771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4921    1.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5059    0.8934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1453    1.5885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8519   -0.1258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8053   -0.9495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5743   -1.2483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0961   -0.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6496    0.0845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  3 13  1  0  0  0  0
  9 14  1  6  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
  8 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  7 21  1  6  0  0  0
  5 22  1  6  0  0  0
  5 23  1  0  0  0  0
  1 23  1  0  0  0  0
  4 24  1  0  0  0  0
  1 24  1  0  0  0  0
  4 25  1  1  0  0  0
  1 26  1  6  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 26 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0072445

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@@]12[C@@H](O)C[C@]3(C)O[C@@]4(C[C@@]3(C)[C@@]1(CCC(=O)[C@]21CO1)O4)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O8/c1-13(23)27-11-19-16(25)8-18(3)17(2)10-21(29-18,14-5-7-26-9-14)30-22(17,19)6-4-15(24)20(19)12-28-20/h5,7,9,16,25H,4,6,8,10-12H2,1-3H3/t16-,17+,18-,19-,20+,21+,22+/m0/s1

> <INCHI_KEY>
YJFASSMQGOHSIM-OVMODOJMSA-N

> <FORMULA>
C22H26O8

> <MOLECULAR_WEIGHT>
418.442

> <EXACT_MASS>
418.162767797

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
43.578403049052646

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1'R,2R,6'R,7'S,9'S,11'R,13'R)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0^{1,6}.0^{9,13}]tetradecane]-6'-yl]methyl acetate

> <ALOGPS_LOGP>
1.27

> <JCHEM_LOGP>
0.9476781219999992

> <ALOGPS_LOGS>
-3.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.129476457341895

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.32980035163865

> <JCHEM_PKA_STRONGEST_BASIC>
-2.858578060909478

> <JCHEM_POLAR_SURFACE_AREA>
107.73

> <JCHEM_REFRACTIVITY>
100.1376

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.51e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,2R,6'R,7'S,9'S,11'R,13'R)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0^{1,6}.0^{9,13}]tetradecane]-6'-ylmethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -0.397   0.739   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.056   0.018   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.138   1.194   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.861   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.529   3.490   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.896   4.392   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.336   3.756   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.472   2.168   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.957   1.593   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.227   0.067   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.677  -0.452   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.059  -0.934   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.624  -0.362   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.532   3.022   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.481   1.809   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.926   3.640   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.427   3.983   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.881   5.454   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.382   5.797   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.833   6.583   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.589   4.650   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.263   4.811   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.919   2.706   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.944   1.668   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.138   2.965   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.590  -0.235   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.503  -1.772   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -2.939  -2.330   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -3.913  -1.137   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.079   0.158   0.000  0.00  0.00           C+0
CONECT    1    2   23   24   26                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    8   13                                             
CONECT    4    3    5   24   25                                             
CONECT    5    4    6   22   23                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   21                                                  
CONECT    8    7    3    9   16                                             
CONECT    9    8   10   14   15                                             
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12    3                                                       
CONECT   14    9   15                                                       
CONECT   15   14    9                                                       
CONECT   16    8   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21    7                                                            
CONECT   22    5                                                            
CONECT   23    5    1                                                       
CONECT   24    4    1                                                       
CONECT   25    4                                                            
CONECT   26    1   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   26                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   70    0
END

View in JSmol

Synonyms

Value	Source
[(1'r,2R,6'r,7's,9's,11'r,13'r)-11'-(Furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0,.0,]tetradecane]-6'-yl]methyl acetic acid	Generator

Chemical Formula

C₂₂H₂₆O₈

Average Mass

418.4420 Da

Monoisotopic Mass

418.16277 Da

IUPAC Name

[(1'R,2R,6'R,7'S,9'S,11'R,13'R)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0^{1,6}.0^{9,13}]tetradecane]-6'-yl]methyl acetate

Traditional Name

(1'R,2R,6'R,7'S,9'S,11'R,13'R)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0^{1,6}.0^{9,13}]tetradecane]-6'-ylmethyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@@]12[C@@H](O)C[C@]3(C)O[C@@]4(C[C@@]3(C)[C@@]1(CCC(=O)[C@]21CO1)O4)C1=COC=C1

InChI Identifier

InChI=1S/C22H26O8/c1-13(23)27-11-19-16(25)8-18(3)17(2)10-21(29-18,14-5-7-26-9-14)30-22(17,19)6-4-15(24)20(19)12-28-20/h5,7,9,16,25H,4,6,8,10-12H2,1-3H3/t16-,17+,18-,19-,20+,21+,22+/m0/s1

InChI Key

YJFASSMQGOHSIM-OVMODOJMSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Teucrium orientale	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Ketal
Meta-dioxane
Heteroaromatic compound
Tetrahydrofuran
Furan
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	1.27	ALOGPS
logP	0.95	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	14.33	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	107.73 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	100.14 m³·mol⁻¹	ChemAxon
Polarizability	43.58 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

162890338

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Teucrolivin H (NP0072445)

MOL for NP0072445 (Teucrolivin H)

3D MOL for NP0072445 (Teucrolivin H)

3D SDF for NP0072445 (Teucrolivin H)

3D-SDF for NP0072445 (Teucrolivin H)

PDB for NP0072445 (Teucrolivin H)

3D PDB for NP0072445 (Teucrolivin H)

SMILES for NP0072445 (Teucrolivin H)

INCHI for NP0072445 (Teucrolivin H)

Structure for NP0072445 (Teucrolivin H)

3D Structure for NP0072445 (Teucrolivin H)