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Compounds
ALA2262900

(S)-3-(4-acetylphenyl)-6-((3aR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)dihydropyrimidine-2,4(1H,3H)-dione

ID: ALA2262900

Chembl Id: CHEMBL2262900

PubChem CID: 76319480

Max Phase: Preclinical

Molecular Formula: C26H28N2O7

Molecular Weight: 480.52

Molecule Type: Small molecule

Associated Items:

Bioactivity Summary Target Summary Assay Summary

Names and Identifiers

Canonical SMILES: CC(=O)c1ccc(N2C(=O)C[C@@H]([C@H]3O[C@@H]4OC(C)(C)O[C@@H]4[C@H]3OCc3ccccc3)NC2=O)cc1

Standard InChI: InChI=1S/C26H28N2O7/c1-15(29)17-9-11-18(12-10-17)28-20(30)13-19(27-25(28)31)21-22(32-14-16-7-5-4-6-8-16)23-24(33-21)35-26(2,3)34-23/h4-12,19,21-24H,13-14H2,1-3H3,(H,27,31)/t19-,21+,22-,23+,24+/m0/s1

Standard InChI Key: WBNSLOIHIDYPMS-LKAHAZCJSA-N

Alternative Forms

Parent:

ALA2262900
(6S)-6-[(3aR,5R,6S,6aR)-2,2-dimethyl-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-3-(4-acetylphenyl)-1,3-diazinane-2,4-dione

Associated Targets(non-human)

Gsr Glutathione reductase, mitochondrial (107 Activities)

Discover Target: Gsr

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

trxr-2 Probable glutathione reductase 2 (91 Activities)

Discover Target: trxr-2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Gclc Glutamate--cysteine ligase catalytic subunit (107 Activities)

Discover Target: Gclc

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

gcs-1 Glutamate--cysteine ligase (130 Activities)

Discover Target: gcs-1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Molecule Features

Natural Product: No	Oral: No	Chemical Probe: No	Parenteral: No
Molecule Type: Small molecule	Topical: No	First In Class: No	Black Box: No
Chirality: No	Availability: No	Prodrug: 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: 480.52	Molecular Weight (Monoisotopic): 480.1897	AlogP: 3.17	#Rotatable Bonds: 6
Polar Surface Area: 103.40	Molecular Species: NEUTRAL	HBA: 7	HBD: 1
#RO5 Violations: ┄	HBA (Lipinski): 9	HBD (Lipinski): 1	#RO5 Violations (Lipinski): ┄
CX Acidic pKa: ┄	CX Basic pKa: ┄	CX LogP: 2.57	CX LogD: 2.57
Aromatic Rings: 2	Heavy Atoms: 35	QED Weighted: 0.63	Np Likeness Score: 0.06

References

1. Arora K, Mishra R, Tripathi R, Srivastava AK, Walter RD. (2004) GLUTATHIONE SYNTHESIS IN FILARIAL WORMS: AN ATTRACTIVE TARGET FOR THE DESIGN AND SYNTHESIS OF NEW ANTIFILARIALS, 13 (8): [10.1007/s00044-004-0111-x]

Source

Source(1):

Scientific Literature