NP-MRD: Showing NP-Card for Gerbeloidanol M (NP0351026)

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Record Information

Version

2.0

Created at

2025-05-16 07:57:24 UTC

Updated at

2025-07-30 21:37:15 UTC

NP-MRD ID

NP0351026

Natural Product DOI

https://doi.org/10.57994/4013

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Gerbeloidanol M

Description

Not Available

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 02262310232D          

 25 28  0  0  1  0            999 V2000
    6.1064    1.5807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7946    0.8169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6483    0.0049    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8309   -0.1069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4720    0.6360    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6601    0.7822    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4944    1.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8429   -1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2295   -0.5732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8904    1.5744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0676    1.2069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2192   -0.5906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5868    0.5866    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  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
  8 18  1  0  0  0  0
 12 18  1  0  0  0  0
 10 19  2  0  0  0  0
 20  9  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  1  0  0  0
  6 22  1  1  0  0  0
  5 23  1  6  0  0  0
  2 23  1  0  0  0  0
  3 24  1  1  0  0  0
  2 25  1  0  0  0  0
M  END


  Mrv2104 02262310232D          

 25 28  0  0  1  0            999 V2000
    6.1064    1.5807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7946    0.8169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6483    0.0049    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8309   -0.1069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4720    0.6360    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6601    0.7822    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4944    1.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8429   -1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2295   -0.5732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8904    1.5744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0676    1.2069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2192   -0.5906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5868    0.5866    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  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
  8 18  1  0  0  0  0
 12 18  1  0  0  0  0
 10 19  2  0  0  0  0
 20  9  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  1  0  0  0
  6 22  1  1  0  0  0
  5 23  1  6  0  0  0
  2 23  1  0  0  0  0
  3 24  1  1  0  0  0
  2 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0351026

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2C3=C([C@H](O)[C@](C)(O3)[C@H]3C[C@H](O)C(C)(C)O3)C(=O)OC2=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H22O6/c1-9-6-5-7-10-13(9)15-14(17(22)23-10)16(21)19(4,25-15)12-8-11(20)18(2,3)24-12/h5-7,11-12,16,20-21H,8H2,1-4H3/t11-,12+,16-,19+/m0/s1

> <INCHI_KEY>
HUAJXXSNUYCQKI-YFZTVDGESA-N

> <FORMULA>
C19H22O6

> <MOLECULAR_WEIGHT>
346.379

> <EXACT_MASS>
346.141638428

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
35.54052618569163

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S)-3-hydroxy-2-[(2R,4S)-4-hydroxy-5,5-dimethyloxolan-2-yl]-2,9-dimethyl-2H,3H,4H-furo[3,2-c]chromen-4-one

> <JCHEM_LOGP>
0.9674698010000002

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.965004261051206

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.901069160388262

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2706591591516525

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
90.0043

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S)-3-hydroxy-2-[(2R,4S)-4-hydroxy-5,5-dimethyloxolan-2-yl]-2,9-dimethyl-3H-furo[3,2-c]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-FEB-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-FEB-23         0                                  
HETATM    1  C   UNK     0      11.399   2.951   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.817   1.525   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.544   0.009   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.018  -0.199   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.348   1.187   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.832   1.460   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.406   2.042   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.412   0.866   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.223  -0.443   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.495  -1.800   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.956  -1.848   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.145  -0.539   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.606  -0.587   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.206   0.722   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.522   2.079   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.062   2.127   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.790   3.484   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.873   0.818   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.307  -3.109   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.719  -0.076   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.895  -1.070   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.262   2.939   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.459   2.253   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      11.609  -1.102   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      12.295   1.095   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23   25                                             
CONECT    3    2    4   24                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7   20   22                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10   20                                                  
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    8   12                                                  
CONECT   19   10                                                            
CONECT   20    9    6   21                                                  
CONECT   21   20                                                            
CONECT   22    6                                                            
CONECT   23    5    2                                                       
CONECT   24    3                                                            
CONECT   25    2                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₂O₆

Average Mass

346.3790 Da

Monoisotopic Mass

346.14164 Da

IUPAC Name

(2S,3S)-3-hydroxy-2-[(2R,4S)-4-hydroxy-5,5-dimethyloxolan-2-yl]-2,9-dimethyl-2H,3H,4H-furo[3,2-c]chromen-4-one

Traditional Name

(2S,3S)-3-hydroxy-2-[(2R,4S)-4-hydroxy-5,5-dimethyloxolan-2-yl]-2,9-dimethyl-3H-furo[3,2-c]chromen-4-one

CAS Registry Number

Not Available

SMILES

CC1=C2C3=C([C@H](O)[C@](C)(O3)[C@H]3C[C@H](O)C(C)(C)O3)C(=O)OC2=CC=C1

InChI Identifier

InChI=1S/C19H22O6/c1-9-6-5-7-10-13(9)15-14(17(22)23-10)16(21)19(4,25-15)12-8-11(20)18(2,3)24-12/h5-7,11-12,16,20-21H,8H2,1-4H3/t11-,12+,16-,19+/m0/s1

InChI Key

HUAJXXSNUYCQKI-YFZTVDGESA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CD3OD, experimental)	cslhh0608@163.com	PUMC	shilin chen	2025-05-16	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CD3OD, experimental)	cslhh0608@163.com	PUMC	shilin chen	2025-05-16	View Spectrum
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CD3OD, experimental)	cslhh0608@163.com	PUMC	shilin chen	2025-05-16	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CD3OD, experimental)	cslhh0608@163.com	PUMC	shilin chen	2025-05-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD3OD, experimental)	cslhh0608@163.com	PUMC	shilin chen	2025-05-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD3OD, experimental)	cslhh0608@163.com	PUMC	shilin chen	2025-05-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, CD3OD, experimental)	cslhh0608@163.com	PUMC	shilin chen	2025-05-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD3OD, experimental)	cslhh0608@163.com	PUMC	shilin chen	2025-05-16	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Gerbera Gerbera piloselloides		Not Available

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	0.97	ChemAxon
pKa (Strongest Acidic)	12.9	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	90 m³·mol⁻¹	ChemAxon
Polarizability	35.54 Å³	ChemAxon
Number of Rings	4	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Gerbeloidanol M (NP0351026)

MOL for NP0351026 (Gerbeloidanol M)

3D MOL for NP0351026 (Gerbeloidanol M)

3D SDF for NP0351026 (Gerbeloidanol M)

3D-SDF for NP0351026 (Gerbeloidanol M)

PDB for NP0351026 (Gerbeloidanol M)

3D PDB for NP0351026 (Gerbeloidanol M)

SMILES for NP0351026 (Gerbeloidanol M)

INCHI for NP0351026 (Gerbeloidanol M)

Structure for NP0351026 (Gerbeloidanol M)

3D Structure for NP0351026 (Gerbeloidanol M)