(S)-2-((2S,3S)-2-((S)-2-((S)-2-amino-3-methylbutanamido)-3-methylbutanamido)-3-methylpentanamido)butanoic acid

ID: ALA4743678

PubChem CID: 162646178

Max Phase: Preclinical

Molecular Formula: C20H38N4O5

Molecular Weight: 414.55

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  CC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](N)C(C)C)C(C)C)[C@@H](C)CC)C(=O)O

Standard InChI:  InChI=1S/C20H38N4O5/c1-8-12(7)16(19(27)22-13(9-2)20(28)29)24-18(26)15(11(5)6)23-17(25)14(21)10(3)4/h10-16H,8-9,21H2,1-7H3,(H,22,27)(H,23,25)(H,24,26)(H,28,29)/t12-,13-,14-,15-,16-/m0/s1

Standard InChI Key:  RVXICZAVXBJLNH-QXKUPLGCSA-N

Molfile:  

 
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   21.0308  -12.0412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   25.2771  -12.0412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   26.6925  -11.2240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.4002   -9.9982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

Alternative Forms

  1. Parent:

    ALA4743678

    ---

Associated Targets(Human)

APP Tclin Amyloid-beta A4 protein (8510 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

PC-12 (7051 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 414.55Molecular Weight (Monoisotopic): 414.2842AlogP: 0.62#Rotatable Bonds: 12
Polar Surface Area: 150.62Molecular Species: ACIDHBA: 5HBD: 5
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: 3.88CX Basic pKa: 8.21CX LogP: -0.82CX LogD: -0.88
Aromatic Rings: Heavy Atoms: 29QED Weighted: 0.32Np Likeness Score: 0.14

References

1. Kapadia A,Sharma KK,Maurya IK,Singh V,Khullar M,Jain R.  (2021)  Structural and mechanistic insights into the inhibition of amyloid-β aggregation by Aβ fragment derived synthetic peptides.,  212  [PMID:33395622] [10.1016/j.ejmech.2020.113126]

Source