NP-MRD: Showing NP-Card for methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate (NP0326193)

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Record Information

Version

2.0

Created at

2022-09-12 07:32:30 UTC

Updated at

2022-09-12 07:32:30 UTC

NP-MRD ID

NP0326193

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate

Description

methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate is found in Ligularia sibirica.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 32  0  0  0  0  0  0  0  0999 V2000
    3.7760    0.5735    1.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7867    0.0679    0.3160 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5486    0.6777    0.1539 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3900    1.7104    0.8535 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5719    0.1096   -0.7657 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7164    0.8057   -0.8874 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1137    1.6854    0.2506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6466    1.5910    0.1544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7876    0.1005   -0.0847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7620   -0.1587   -1.0468 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1874   -1.4722   -0.9377 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2188   -1.3362   -0.4611 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3991   -1.6678    0.9903 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0379   -2.2070   -1.1943 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2994    1.1240    2.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3864    1.2914    0.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4648   -0.2085    1.5374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0513    0.0815   -1.7894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7365    1.4552   -1.8131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8473    2.7389    0.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8729    1.2822    1.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0047    2.1521   -0.7344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1292    1.8817    1.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6172   -0.4267    0.8889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8116   -0.0696   -0.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7977   -2.1416   -0.2685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2211   -1.9401   -1.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0568   -2.7042    1.1435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1321   -0.9633    1.6608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5002   -1.6779    1.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8962   -2.3548   -0.7078 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  6
 12  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  1  0
 10  6  1  0
  5  6  1  0
  6 19  1  6
  7 20  1  0
  7 21  1  0
  8 22  1  0
  8 23  1  0
  9 24  1  0
  9 25  1  0
 11 26  1  0
 11 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
 14 31  1  0
  5 18  1  6
  1 15  1  0
  1 16  1  0
  1 17  1  0
M  END


  Mrv1652307301919582D          

 15 16  0  0  0  0            999 V2000
    2.6673    2.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4849    1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    1.9049    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5692    2.1599    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8242    2.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    1.4924    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7846    1.0799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2721    3.5576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6673    0.9404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6312    3.1160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0437    3.8305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    2.7299    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0  0  0  0
  4  2  1  0  0  0  0
  6  3  1  0  0  0  0
  7  6  1  0  0  0  0
  7  8  1  1  0  0  0
  9  1  1  1  0  0  0
  9  5  1  0  0  0  0
  9  7  1  0  0  0  0
 10  4  1  0  0  0  0
 10  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  8  2  0  0  0  0
 12  9  1  0  0  0  0
 13  8  1  0  0  0  0
 13 14  1  0  0  0  0
  6 15  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0326193

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CCCN1C[C@@](C)(O)[C@@H]2C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C10H17NO3/c1-10(13)6-11-5-3-4-7(11)8(10)9(12)14-2/h7-8,13H,3-6H2,1-2H3/t7-,8-,10+/m0/s1

> <INCHI_KEY>
LADVYSUMGRTFSZ-OYNCUSHFSA-N

> <FORMULA>
C10H17NO3

> <MOLECULAR_WEIGHT>
199.25

> <EXACT_MASS>
199.120843411

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
20.941262278716028

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,2S,7aS)-2-hydroxy-2-methyl-hexahydro-1H-pyrrolizine-1-carboxylate

> <JCHEM_LOGP>
-0.05234198033333363

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.108130537212993

> <JCHEM_PKA_STRONGEST_BASIC>
9.586492143448568

> <JCHEM_POLAR_SURFACE_AREA>
49.77000000000001

> <JCHEM_REFRACTIVITY>
51.441

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,2S,7aS)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 30-JUL-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   30-JUL-19         0                                  
HETATM    1  C   UNK     0       4.979   3.816   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.905   2.786   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   4.032   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.929   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.465   3.556   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.929   4.032   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.405   5.496   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.835   2.786   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       1.465   2.016   0.000  0.00  0.00           N+0
HETATM   11  O   UNK     0       2.375   6.641   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       4.979   1.755   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       4.912   5.817   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.682   7.150   0.000  0.00  0.00           C+0
HETATM   15  H   UNK     0       1.465   5.096   0.000  0.00  0.00           H+0
CONECT    1    9                                                            
CONECT    2    3    4                                                       
CONECT    3    2    6                                                       
CONECT    4    2   10                                                       
CONECT    5    9   10                                                       
CONECT    6    3    7   10   15                                             
CONECT    7    6    8    9                                                  
CONECT    8    7   11   13                                                  
CONECT    9    1    5    7   12                                             
CONECT   10    4    5    6                                                  
CONECT   11    8                                                            
CONECT   12    9                                                            
CONECT   13    8   14                                                       
CONECT   14   13                                                            
CONECT   15    6                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   32    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₀H₁₇NO₃

Average Mass

199.2500 Da

Monoisotopic Mass

199.12084 Da

IUPAC Name

methyl (1R,2S,7aS)-2-hydroxy-2-methyl-hexahydro-1H-pyrrolizine-1-carboxylate

Traditional Name

methyl (1R,2S,7aS)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate

CAS Registry Number

Not Available

SMILES

[H][C@@]12CCCN1C[C@@](C)(O)[C@@H]2C(=O)OC

InChI Identifier

InChI=1S/C10H17NO3/c1-10(13)6-11-5-3-4-7(11)8(10)9(12)14-2/h7-8,13H,3-6H2,1-2H3/t7-,8-,10+/m0/s1

InChI Key

LADVYSUMGRTFSZ-OYNCUSHFSA-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
Ligularia sibirica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolizidines. Pyrrolizidines are compounds containing a pyrrolizidine, which is a bicyclic ring system made up of two fused pyrrolidine ring sharing a nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolizidines

Sub Class

Not Available

Direct Parent

Pyrrolizidines

Alternative Parents

Substituents

Pyrrolidine carboxylic acid
Pyrrolidine carboxylic acid or derivatives
Pyrrolizidine
N-alkylpyrrolidine
Pyrrolidine
Tertiary alcohol
Methyl ester
Amino acid or derivatives
Carboxylic acid ester
1,2-aminoalcohol
Tertiary amine
Tertiary aliphatic amine
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Azacycle
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Alcohol
Amine
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	-0.052	ChemAxon
pKa (Strongest Acidic)	14.11	ChemAxon
pKa (Strongest Basic)	9.59	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.77 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	51.44 m³·mol⁻¹	ChemAxon
Polarizability	20.94 Å³	ChemAxon
Number of Rings	2	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

FDB008495

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

10899620

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate (NP0326193)

MOL for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)

3D MOL for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)

3D SDF for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)

3D-SDF for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)

PDB for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)

3D PDB for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)

SMILES for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)

INCHI for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)

Structure for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)

3D Structure for NP0326193 (methyl (1r,2s,7as)-2-hydroxy-2-methyl-hexahydropyrrolizine-1-carboxylate)