NP-MRD: Showing NP-Card for Dstramonin C (NP0331648)

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Record Information

Version

2.0

Created at

2023-05-26 16:00:41 UTC

Updated at

2024-09-03 04:16:22 UTC

NP-MRD ID

NP0331648

Natural Product DOI

https://doi.org/10.57994/0637

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Dstramonin C

Description

Dstramonin C belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. Dstramonin C was first documented in 2024 (PMID: 37198914). Based on a literature review very few articles have been published on Dstramonin C.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305262318002D          

 27 28  0  0  1  0            999 V2000
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303   -3.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303   -4.7570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2448   -5.1695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -5.1695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3461   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -3.9320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1808   -3.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9933   -3.0135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -2.2382    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7451   -1.6062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0273   -0.8310    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4970   -0.1990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7792    0.5762    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2489    1.2082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4364    1.0650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5916    0.7195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8738    1.4947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1219    0.0875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9344    0.2308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8398   -0.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3701   -1.3197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0879   -2.0950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111   -4.0752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -4.7570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6131   -5.1695    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  2  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 11 24  1  1  0  0  0
  8 25  1  6  0  0  0
  8 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END


  Mrv1652305262318002D          

 27 28  0  0  1  0            999 V2000
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303   -3.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303   -4.7570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2448   -5.1695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -5.1695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3461   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -3.9320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1808   -3.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9933   -3.0135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -2.2382    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7451   -1.6062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0273   -0.8310    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4970   -0.1990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7792    0.5762    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2489    1.2082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4364    1.0650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5916    0.7195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8738    1.4947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1219    0.0875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9344    0.2308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8398   -0.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3701   -1.3197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0879   -2.0950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111   -4.0752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -4.7570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6131   -5.1695    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  2  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 11 24  1  1  0  0  0
  8 25  1  6  0  0  0
  8 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0331648

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](O[C@H]1O[C@@H](CO)C(O)[C@@H](O)C1O)\C=C\[C@@]1(O)C(=C)CC(O)CC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C19H32O8/c1-10-7-12(21)8-18(3,4)19(10,25)6-5-11(2)26-17-16(24)15(23)14(22)13(9-20)27-17/h5-6,11-17,20-25H,1,7-9H2,2-4H3/b6-5+/t11-,12?,13-,14?,15+,16?,17-,19+/m0/s1

> <INCHI_KEY>
ODJOANBUUCOJRA-GHWZCYOWSA-N

> <FORMULA>
C19H32O8

> <MOLECULAR_WEIGHT>
388.457

> <EXACT_MASS>
388.20971799

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
40.84429125537546

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,4R,6S)-2-{[(2S,3E)-4-[(1S)-1,4-dihydroxy-2,2-dimethyl-6-methylidenecyclohexyl]but-3-en-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
-0.8611488883333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.034060675236542

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.186481875859126

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7248965496318203

> <JCHEM_POLAR_SURFACE_AREA>
139.84

> <JCHEM_REFRACTIVITY>
97.31940000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4R,6S)-2-{[(2S,3E)-4-[(1S)-1,4-dihydroxy-2,2-dimethyl-6-methylidenecyclohexyl]but-3-en-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.344  -6.570   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.990  -7.340   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.990  -8.880   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.324  -9.650   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.344  -9.650   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.646  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.677  -7.340   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.204  -5.893   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.721  -5.625   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.247  -4.178   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.258  -2.998   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.784  -1.551   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.794  -0.371   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.321   1.076   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.331   2.255   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.815   1.988   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.838   1.343   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.364   2.790   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.828   0.163   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.344   0.431   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.301  -1.284   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.291  -2.463   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.764  -3.911   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.194  -7.607   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.677  -8.880   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.011  -9.650   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7    8                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4   26                                                       
CONECT    7    2                                                            
CONECT    8    2    9   25   26                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   24                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   13   23                                                  
CONECT   23   22                                                            
CONECT   24   11                                                            
CONECT   25    8                                                            
CONECT   26    8    6   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₃₂O₈

Average Mass

388.4570 Da

Monoisotopic Mass

388.20972 Da

IUPAC Name

(2S,4R,6S)-2-{[(2S,3E)-4-[(1S)-1,4-dihydroxy-2,2-dimethyl-6-methylidenecyclohexyl]but-3-en-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2S,4R,6S)-2-{[(2S,3E)-4-[(1S)-1,4-dihydroxy-2,2-dimethyl-6-methylidenecyclohexyl]but-3-en-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

C[C@H](O[C@H]1O[C@@H](CO)C(O)[C@@H](O)C1O)\C=C\[C@@]1(O)C(=C)CC(O)CC1(C)C

InChI Identifier

InChI=1S/C19H32O8/c1-10-7-12(21)8-18(3,4)19(10,25)6-5-11(2)26-17-16(24)15(23)14(22)13(9-20)27-17/h5-6,11-17,20-25H,1,7-9H2,2-4H3/b6-5+/t11-,12?,13-,14?,15+,16?,17-,19+/m0/s1

InChI Key

ODJOANBUUCOJRA-GHWZCYOWSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View

Predicted Spectra

Not Available

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 600, CD₃OD, simulated)	570075670@qq.com	黑龙江中医药大学	Pan juan	2024-05-14	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
stramonium		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. These are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Cyclofarsesane sesquiterpenoid
Megastigmane sesquiterpenoid
Sesquiterpenoid
Fatty acyl glycoside of mono- or disaccharide
Ionone derivative
Alkyl glycoside
Fatty alcohol
Oxane
Monosaccharide
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	-0.86	ChemAxon
pKa (Strongest Acidic)	12.19	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	139.84 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	97.32 m³·mol⁻¹	ChemAxon
Polarizability	40.84 Å³	ChemAxon
Number of Rings	2	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pan J, Liu Y, Wang AF, Wu JT, Yang R, Guan W, Algradi AM, Kuang HX, Yang BY: Cytotoxicity sesquiterpenoids from the leaves of Datura stramonium L. Nat Prod Res. 2024 May;38(10):1639-1646. doi: 10.1080/14786419.2023.2214292. Epub 2023 May 17. [PubMed:37198914 ]

Showing NP-Card for Dstramonin C (NP0331648)

MOL for NP0331648 (Dstramonin C)

3D MOL for NP0331648 (Dstramonin C)

3D SDF for NP0331648 (Dstramonin C)

3D-SDF for NP0331648 (Dstramonin C)

PDB for NP0331648 (Dstramonin C)

3D PDB for NP0331648 (Dstramonin C)

SMILES for NP0331648 (Dstramonin C)

INCHI for NP0331648 (Dstramonin C)

Structure for NP0331648 (Dstramonin C)

3D Structure for NP0331648 (Dstramonin C)