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(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:
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:
RDKit 2D
29 28 0 0 0 0 0 0 0 0999 V2000
19.6154 -11.2240 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
20.3231 -10.8154 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
21.0308 -12.0412 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
21.0308 -11.2240 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
20.3231 -9.9982 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
21.7344 -10.8154 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
22.4462 -11.2240 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
23.1539 -9.9982 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
23.1539 -10.8154 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
22.4462 -12.0412 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
23.1539 -12.4498 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
21.7344 -12.4498 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
23.8616 -11.2240 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
24.5693 -10.8154 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
25.2771 -12.0412 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
25.2771 -11.2240 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
24.5693 -9.9982 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
25.2771 -9.5896 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
23.8616 -9.5896 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
23.8616 -8.7724 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
25.9848 -10.8154 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
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
26.6925 -12.0412 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.4002 -10.8154 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.1079 -11.2240 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
21.0308 -9.5896 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
19.6154 -9.5896 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.4002 -12.4498 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4 6 1 0
9 13 1 0
16 21 1 0
25 26 1 0
1 2 1 0
2 4 1 0
4 3 2 0
2 5 1 1
6 7 1 0
7 9 1 0
9 8 2 0
7 10 1 6
10 11 1 0
10 12 1 0
13 14 1 0
14 16 1 1
16 15 2 0
14 17 1 0
17 18 1 6
17 19 1 0
19 20 1 0
21 22 1 0
22 25 1 0
25 23 2 0
22 24 1 6
5 27 1 0
5 28 1 0
24 29 1 0
M END Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 414.55Molecular Weight (Monoisotopic): 414.2842AlogP: 0.62#Rotatable Bonds: 12Polar Surface Area: 150.62Molecular Species: ACIDHBA: 5HBD: 5#RO5 Violations: ┄HBA (Lipinski): 9HBD (Lipinski): 6#RO5 Violations (Lipinski): 1CX Acidic pKa: 3.88CX Basic pKa: 8.21CX LogP: -0.82CX LogD: -0.88Aromatic 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 ]