NP-MRD: Showing NP-Card for 2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid (NP0252887)

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Record Information

Version

2.0

Created at

2022-09-07 16:34:11 UTC

Updated at

2022-09-07 16:34:11 UTC

NP-MRD ID

NP0252887

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid

Description

SCHEMBL3264337 belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid is found in Monascus pilosus. SCHEMBL3264337 is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
    3.5685    0.2063   -0.3781 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2233    0.0963    0.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0138   -1.4709    0.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1367    0.5896   -0.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2047    0.5916    0.0197 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1268    1.6532    1.1470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9471    1.6702    2.0899 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8954    2.5953    1.0811 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4030    0.9145   -0.8627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9875   -0.4037   -0.3292 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3507   -1.4207   -1.3377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1408   -0.0833    0.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5202    1.1139    0.8349 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7508   -1.2203    1.1631 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7685   -0.5636    0.3867 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9266    1.2336   -0.4348 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3342   -0.4154    0.1668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4283   -0.1523   -1.4454 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1575    0.5058    1.2617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7521   -1.7237   -0.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2560   -1.7600    1.0318 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9766   -1.8988    0.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3898    1.6295   -0.9333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1533   -0.0272   -1.5733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8930    3.4229    1.6912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2046    0.8742   -1.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9967    1.7589   -0.5115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8601   -1.3329   -2.3086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4610   -1.3423   -1.5456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2479   -2.4955   -0.9068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2020   -1.6420    1.9734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9329   -0.9034    1.3567 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  9  1  0
  9 10  1  0
 10 11  1  0
 10 15  1  0
 10 12  1  1
 12 14  1  0
 12 13  2  0
  5  6  1  1
  6  8  1  0
  6  7  2  0
 15  5  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  9 26  1  0
  9 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 15 32  1  0
 14 31  1  0
  8 25  1  0
M  END


  Mrv1533004171515362D          

 15 15  0  0  0  0            999 V2000
   -1.1813    0.5688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9678    1.3657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5511    1.9491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1709    1.5792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9959    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -0.1709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9959   -0.7542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1709    0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1709   -0.7542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0427   -1.5511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9678   -0.5407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9959    1.5792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7928    1.3657    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7823    2.3761    0.0000 O   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
  2  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
  7  9  1  0  0  0  0
  5  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
  5 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252887

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC1(CC(C)(N1)C(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C10H17NO4/c1-6(2)4-10(8(14)15)5-9(3,11-10)7(12)13/h6,11H,4-5H2,1-3H3,(H,12,13)(H,14,15)

> <INCHI_KEY>
DTLNBWQUOUXKIO-UHFFFAOYSA-N

> <FORMULA>
C10H17NO4

> <MOLECULAR_WEIGHT>
215.249

> <EXACT_MASS>
215.115758031

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
22.00712757598669

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid

> <ALOGPS_LOGP>
-0.60

> <JCHEM_LOGP>
-1.5084215754662533

> <ALOGPS_LOGS>
-1.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
3.469997739300722

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.7558364646935294

> <JCHEM_PKA_STRONGEST_BASIC>
9.052873679241657

> <JCHEM_POLAR_SURFACE_AREA>
86.63000000000001

> <JCHEM_REFRACTIVITY>
52.34980000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.69e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -2.205   1.062   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.806   2.549   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.895   3.638   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.319   2.948   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.770   1.859   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.859   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.770  -0.319   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.859  -1.408   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -0.319   0.770   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -0.319  -1.408   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.080  -2.895   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -1.806  -1.009   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.859   2.948   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.346   2.549   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       1.460   4.435   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    9   13                                             
CONECT    6    5    7                                                       
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7    5                                                       
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    5   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₀H₁₇NO₄

Average Mass

215.2490 Da

Monoisotopic Mass

215.11576 Da

IUPAC Name

2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid

Traditional Name

2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid

CAS Registry Number

Not Available

SMILES

CC(C)CC1(CC(C)(N1)C(O)=O)C(O)=O

InChI Identifier

InChI=1S/C10H17NO4/c1-6(2)4-10(8(14)15)5-9(3,11-10)7(12)13/h6,11H,4-5H2,1-3H3,(H,12,13)(H,14,15)

InChI Key

DTLNBWQUOUXKIO-UHFFFAOYSA-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
Monascus pilosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids

Alternative Parents

Substituents

Alpha-amino acid
Azetidinecarboxylic acid
Dicarboxylic acid or derivatives
Azetidine
Amino acid
Carboxylic acid
Secondary aliphatic amine
Secondary amine
Organoheterocyclic compound
Azacycle
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Amine
Organic oxygen compound
Organic oxide
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	-0.6	ALOGPS
logP	-1.5	ChemAxon
logS	-1.1	ALOGPS
pKa (Strongest Acidic)	2.76	ChemAxon
pKa (Strongest Basic)	9.05	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.63 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	52.35 m³·mol⁻¹	ChemAxon
Polarizability	22.01 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

44129378

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid (NP0252887)

MOL for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)

3D MOL for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)

3D SDF for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)

3D-SDF for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)

PDB for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)

3D PDB for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)

SMILES for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)

INCHI for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)

Structure for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)

3D Structure for NP0252887 (2-methyl-4-(2-methylpropyl)azetidine-2,4-dicarboxylic acid)