N-(indole-3-acetyl)-L-aspartic acid

Identification

Generic Name
N-(indole-3-acetyl)-L-aspartic acid
DrugBank Accession Number
DB07951
Background

Not Available

Type
Small Molecule
Groups
Experimental
Structure
Weight
Average: 290.2714
Monoisotopic: 290.090271568
Chemical Formula
C14H14N2O5
Synonyms
  • IAASP
  • N-(indol-3-ylacetyl)-L-aspartic acid
  • N-(indol-3-ylacetyl)aspartic acid
  • N-(indole-3-acetyl)aspartic acid

Pharmacology

Indication

Not Available

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Pharmacodynamics

Not Available

Mechanism of action
TargetActionsOrganism
UTryptophan synthase alpha chainNot AvailableSalmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720)
UTryptophan synthase beta chainNot AvailableSalmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720)
Absorption

Not Available

Volume of distribution

Not Available

Protein binding

Not Available

Metabolism
Not Available
Route of elimination

Not Available

Half-life

Not Available

Clearance

Not Available

Adverse Effects
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Toxicity

Not Available

Pathways
Not Available
Pharmacogenomic Effects/ADRs
Not Available

Interactions

Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Not Available
Food Interactions
Not Available

Categories

Drug Categories
Chemical TaxonomyProvided by Classyfire
Description
This compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
Kingdom
Organic compounds
Super Class
Organic acids and derivatives
Class
Carboxylic acids and derivatives
Sub Class
Amino acids, peptides, and analogues
Direct Parent
Aspartic acid and derivatives
Alternative Parents
N-acyl-L-alpha-amino acids / 3-alkylindoles / Substituted pyrroles / Dicarboxylic acids and derivatives / Benzenoids / Heteroaromatic compounds / Secondary carboxylic acid amides / Carboxylic acids / Azacyclic compounds / Organopnictogen compounds
show 4 more
Substituents
3-alkylindole / Aromatic heteropolycyclic compound / Aspartic acid or derivatives / Azacycle / Benzenoid / Carbonyl group / Carboxamide group / Carboxylic acid / Dicarboxylic acid or derivatives / Heteroaromatic compound
show 16 more
Molecular Framework
Aromatic heteropolycyclic compounds
External Descriptors
Not Available
Affected organisms
Not Available

Chemical Identifiers

UNII
5V1L30W0M7
CAS number
2456-73-7
InChI Key
VAFNMNRKDDAKRM-NSHDSACASA-N
InChI
InChI=1S/C14H14N2O5/c17-12(16-11(14(20)21)6-13(18)19)5-8-7-15-10-4-2-1-3-9(8)10/h1-4,7,11,15H,5-6H2,(H,16,17)(H,18,19)(H,20,21)/t11-/m0/s1
IUPAC Name
(2S)-2-[2-(1H-indol-3-yl)acetamido]butanedioic acid
SMILES
OC(=O)C[C@H](NC(=O)CC1=CNC2=CC=CC=C12)C(O)=O

References

General References
Not Available
PubChem Compound
446620
PubChem Substance
99444422
ChemSpider
393931
ChEBI
21484
ZINC
ZINC000000056756
PDBe Ligand
IAD
PDB Entries
1k3u

Clinical Trials

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PhaseStatusPurposeConditionsCountStart DateWhy Stopped100+ additional columns

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
Not Available
Prices
Not Available
Patents
Not Available

Properties

State
Solid
Experimental Properties
Not Available
Predicted Properties
PropertyValueSource
Water Solubility0.228 mg/mLALOGPS
logP1.04ALOGPS
logP0.53Chemaxon
logS-3.1ALOGPS
pKa (Strongest Acidic)3.74Chemaxon
pKa (Strongest Basic)-2.8Chemaxon
Physiological Charge-2Chemaxon
Hydrogen Acceptor Count5Chemaxon
Hydrogen Donor Count4Chemaxon
Polar Surface Area119.49 Å2Chemaxon
Rotatable Bond Count6Chemaxon
Refractivity71.78 m3·mol-1Chemaxon
Polarizability27.68 Å3Chemaxon
Number of Rings2Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon
Predicted ADMET Features
PropertyValueProbability
Human Intestinal Absorption+0.7083
Blood Brain Barrier+0.7842
Caco-2 permeable-0.8312
P-glycoprotein substrateNon-substrate0.6458
P-glycoprotein inhibitor INon-inhibitor0.9791
P-glycoprotein inhibitor IINon-inhibitor0.9701
Renal organic cation transporterNon-inhibitor0.9376
CYP450 2C9 substrateNon-substrate0.7988
CYP450 2D6 substrateNon-substrate0.8157
CYP450 3A4 substrateNon-substrate0.6506
CYP450 1A2 substrateNon-inhibitor0.9639
CYP450 2C9 inhibitorNon-inhibitor0.9322
CYP450 2D6 inhibitorNon-inhibitor0.9461
CYP450 2C19 inhibitorNon-inhibitor0.9575
CYP450 3A4 inhibitorNon-inhibitor0.9575
CYP450 inhibitory promiscuityLow CYP Inhibitory Promiscuity0.9494
Ames testNon AMES toxic0.9123
CarcinogenicityNon-carcinogens0.9519
BiodegradationNot ready biodegradable0.6864
Rat acute toxicity1.7237 LD50, mol/kg Not applicable
hERG inhibition (predictor I)Weak inhibitor0.9896
hERG inhibition (predictor II)Non-inhibitor0.9376
ADMET data is predicted using admetSAR, a free tool for evaluating chemical ADMET properties. (23092397)

Spectra

Mass Spec (NIST)
Not Available
Spectra
SpectrumSpectrum TypeSplash Key
GC-MS Spectrum - GC-MS (4 TMS)GC-MSsplash10-0ufr-1691010000-3ce91028a03b237b4357
GC-MS Spectrum - GC-MS (3 TMS)GC-MSsplash10-0udi-0290000000-5f6d2dce4b9b88102702
Predicted GC-MS Spectrum - GC-MSPredicted GC-MSsplash10-052g-4970000000-a08e5dbc762684766fa8
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSsplash10-0a4j-0690000000-e4f3bdfe3d24c8472833
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSsplash10-03ki-5910000000-1849f791763422090e9e
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSsplash10-0a4i-1900000000-6715e25fa4b6d70df8b1
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSsplash10-01pa-6920000000-bbffd13483f05f56f352
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSsplash10-001i-0900000000-78794d870323a7e214f7
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSsplash10-0006-9820000000-bab6a445ee2eda93151f
Predicted 1H NMR Spectrum1D NMRNot Applicable
Predicted 13C NMR Spectrum1D NMRNot Applicable
Chromatographic Properties
Collision Cross Sections (CCS)
AdductCCS Value (Å2)Source typeSource
[M-H]-172.7944689
predicted
DarkChem Lite v0.1.0
[M-H]-172.5236689
predicted
DarkChem Lite v0.1.0
[M-H]-156.41672
predicted
DeepCCS 1.0 (2019)
[M+H]+173.4724689
predicted
DarkChem Lite v0.1.0
[M+H]+172.6848689
predicted
DarkChem Lite v0.1.0
[M+H]+158.77502
predicted
DeepCCS 1.0 (2019)
[M+Na]+172.7274689
predicted
DarkChem Lite v0.1.0
[M+Na]+172.7675689
predicted
DarkChem Lite v0.1.0
[M+Na]+164.86816
predicted
DeepCCS 1.0 (2019)

Targets

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Kind
Protein
Organism
Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720)
Pharmacological action
Unknown
General Function
Tryptophan synthase activity
Specific Function
The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3-phosphate.
Gene Name
trpA
Uniprot ID
P00929
Uniprot Name
Tryptophan synthase alpha chain
Molecular Weight
28670.485 Da
References
  1. Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. [Article]
Kind
Protein
Organism
Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720)
Pharmacological action
Unknown
General Function
Tryptophan synthase activity
Specific Function
The beta subunit is responsible for the synthesis of L-tryptophan from indole and L-serine.
Gene Name
trpB
Uniprot ID
P0A2K1
Uniprot Name
Tryptophan synthase beta chain
Molecular Weight
42867.63 Da
References
  1. Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. [Article]

Drug created at September 15, 2010 21:27 / Updated at June 12, 2020 16:52