NP-MRD: Showing NP-Card for Enanderinanin H (NP0075322)

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Record Information

Version

2.0

Created at

2022-04-28 20:36:53 UTC

Updated at

2022-04-28 20:36:53 UTC

NP-MRD ID

NP0075322

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Enanderinanin H

Description

(1R,2S,3S,6S,7S,8R,12S,16S,18S,21R)-6,7,21-trihydroxy-9,9,14,14-tetramethyl-19-methylidene-5,13,15-trioxahexacyclo[16.2.1.0¹,⁶.0²,¹⁶.0³,⁸.0³,¹²]Henicosan-20-one belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Enanderinanin H is found in Isodon enanderianus. Based on a literature review very few articles have been published on (1R,2S,3S,6S,7S,8R,12S,16S,18S,21R)-6,7,21-trihydroxy-9,9,14,14-tetramethyl-19-methylidene-5,13,15-trioxahexacyclo[16.2.1.0¹,⁶.0²,¹⁶.0³,⁸.0³,¹²]Henicosan-20-one.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652304282222362D          

 30 35  0  0  1  0            999 V2000
    0.9471    0.9337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2768    0.4329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7667   -0.2443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6255   -0.2378    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3968    0.1900    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8004    0.8652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7622    1.7213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1113    2.4845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9476    2.3897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3413    1.6269    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0206    0.7989    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3741    0.0034    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6242   -0.6795    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8639   -1.0385    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5274   -1.7917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1653    0.0061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1569   -1.3199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0754   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2268   -0.2617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3542   -1.0768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9266    0.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7027   -0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7020    1.0494    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1907    1.7353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9941    0.5964    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4842    1.2449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052    2.9111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1100    3.3095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0976   -0.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7743   -1.0693    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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  1  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  1  0  0  0
 13 16  1  1  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  1  0  0  0
 12 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 23 21  1  1  0  0  0
 23 24  1  0  0  0  0
 10 24  1  1  0  0  0
 23 25  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  6  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
M  END


  Mrv1652304282222362D          

 30 35  0  0  1  0            999 V2000
    0.9471    0.9337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2768    0.4329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7667   -0.2443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6255   -0.2378    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3968    0.1900    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8004    0.8652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7622    1.7213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1113    2.4845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9476    2.3897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3413    1.6269    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0206    0.7989    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3741    0.0034    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6242   -0.6795    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8639   -1.0385    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5274   -1.7917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1653    0.0061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1569   -1.3199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0754   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2268   -0.2617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3542   -1.0768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9266    0.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7027   -0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7020    1.0494    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1907    1.7353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9941    0.5964    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4842    1.2449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052    2.9111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1100    3.3095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0976   -0.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7743   -1.0693    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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  1  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  1  0  0  0
 13 16  1  1  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  1  0  0  0
 12 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 23 21  1  1  0  0  0
 23 24  1  0  0  0  0
 10 24  1  1  0  0  0
 23 25  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  6  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0075322

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CC[C@@H]2OC(C)(C)O[C@H]3C[C@@H]4[C@@H](O)[C@]5([C@@H]3[C@@]22CO[C@]5(O)[C@@H](O)[C@H]12)C(=O)C4=C

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O7/c1-10-11-8-12-14-21-9-28-23(27,22(14,16(10)24)17(11)25)18(26)15(21)19(2,3)7-6-13(21)30-20(4,5)29-12/h11-15,17-18,25-27H,1,6-9H2,2-5H3/t11-,12-,13-,14-,15+,17+,18-,21+,22-,23+/m0/s1

> <INCHI_KEY>
ZMQMQOGLLZCWSG-BMAXGERGSA-N

> <FORMULA>
C23H32O7

> <MOLECULAR_WEIGHT>
420.502

> <EXACT_MASS>
420.21480337

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
46.132124784678496

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,3S,6S,7S,8R,12S,16S,18S,21R)-6,7,21-trihydroxy-9,9,14,14-tetramethyl-19-methylidene-5,13,15-trioxahexacyclo[16.2.1.0^{1,6}.0^{2,16}.0^{3,8}.0^{3,12}]henicosan-20-one

> <ALOGPS_LOGP>
0.91

> <JCHEM_LOGP>
0.9342680126666658

> <ALOGPS_LOGS>
-2.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.627408801874367

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.508780609176045

> <JCHEM_PKA_STRONGEST_BASIC>
-3.223621747064257

> <JCHEM_POLAR_SURFACE_AREA>
105.45

> <JCHEM_REFRACTIVITY>
105.67680000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.28e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,6S,7S,8R,12S,16S,18S,21R)-6,7,21-trihydroxy-9,9,14,14-tetramethyl-19-methylidene-5,13,15-trioxahexacyclo[16.2.1.0^{1,6}.0^{2,16}.0^{3,8}.0^{3,12}]henicosan-20-one

> <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       1.768   1.743   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.517   0.808   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.431  -0.456   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.034  -0.444   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.474   0.355   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.361   1.615   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.289   3.213   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.941   4.638   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.502   4.461   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.237   3.037   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.638   1.491   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.298   0.006   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.899  -1.268   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.479  -1.939   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.851  -3.345   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       4.042   0.011   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       5.893  -2.464   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.741  -0.885   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.890  -0.488   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.128  -2.010   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.196   0.427   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.645  -0.095   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.777   1.959   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.823   3.239   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.456   1.113   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.504   2.324   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.623   5.434   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.939   6.178   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.182  -1.357   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.445  -1.996   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   29   30                                             
CONECT    4    3    5   14                                                  
CONECT    5    4    6   11   18                                             
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   27   28                                             
CONECT    9    8   10                                                       
CONECT   10    9   11   24                                                  
CONECT   11   10    5   12                                                  
CONECT   12   11   13   19   25                                             
CONECT   13   12   14   16   17                                             
CONECT   14   13    4   15                                                  
CONECT   15   14                                                            
CONECT   16   13                                                            
CONECT   17   13   18                                                       
CONECT   18   17    5                                                       
CONECT   19   12   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23   10                                                       
CONECT   25   23   12   26                                                  
CONECT   26   25                                                            
CONECT   27    8                                                            
CONECT   28    8                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₇

Average Mass

420.5020 Da

Monoisotopic Mass

420.21480 Da

IUPAC Name

(1R,2S,3S,6S,7S,8R,12S,16S,18S,21R)-6,7,21-trihydroxy-9,9,14,14-tetramethyl-19-methylidene-5,13,15-trioxahexacyclo[16.2.1.0^{1,6}.0^{2,16}.0^{3,8}.0^{3,12}]henicosan-20-one

Traditional Name

(1R,2S,3S,6S,7S,8R,12S,16S,18S,21R)-6,7,21-trihydroxy-9,9,14,14-tetramethyl-19-methylidene-5,13,15-trioxahexacyclo[16.2.1.0^{1,6}.0^{2,16}.0^{3,8}.0^{3,12}]henicosan-20-one

CAS Registry Number

Not Available

SMILES

CC1(C)CC[C@@H]2OC(C)(C)O[C@H]3C[C@@H]4[C@@H](O)[C@]5([C@@H]3[C@@]22CO[C@]5(O)[C@@H](O)[C@H]12)C(=O)C4=C

InChI Identifier

InChI=1S/C23H32O7/c1-10-11-8-12-14-21-9-28-23(27,22(14,16(10)24)17(11)25)18(26)15(21)19(2,3)7-6-13(21)30-20(4,5)29-12/h11-15,17-18,25-27H,1,6-9H2,2-5H3/t11-,12-,13-,14-,15+,17+,18-,21+,22-,23+/m0/s1

InChI Key

ZMQMQOGLLZCWSG-BMAXGERGSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Isodon enanderianus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Ketal
Dioxepane
1,3-dioxepane
Oxane
Cyclic alcohol
Secondary alcohol
Ketone
Hemiacetal
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	0.91	ALOGPS
logP	0.93	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	10.51	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.45 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	105.68 m³·mol⁻¹	ChemAxon
Polarizability	46.13 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

162940617

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Enanderinanin H (NP0075322)

MOL for NP0075322 (Enanderinanin H)

3D MOL for NP0075322 (Enanderinanin H)

3D SDF for NP0075322 (Enanderinanin H)

3D-SDF for NP0075322 (Enanderinanin H)

PDB for NP0075322 (Enanderinanin H)

3D PDB for NP0075322 (Enanderinanin H)

SMILES for NP0075322 (Enanderinanin H)

INCHI for NP0075322 (Enanderinanin H)

Structure for NP0075322 (Enanderinanin H)

3D Structure for NP0075322 (Enanderinanin H)