ID: ALA3775484

Max Phase: Preclinical

Molecular Formula: C132H177N55O31

Molecular Weight: 3030.22

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(=O)Oc1c(C)c(C)c2c(c1Cn1cc(CCC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(N)=O)C(=O)Cn3cnc4c(=O)[nH]c(N)nc43)C(=O)Cn3ccc(N)nc3=O)C(=O)Cn3cnc4c(N)ncnc43)C(=O)Cn3ccc(N)nc3=O)C(=O)Cn3cnc4c(=O)[nH]c(N)nc43)C(=O)Cn3cnc4c(N)ncnc43)C(=O)Cn3ccc(N)nc3=O)C(=O)Cn3cc(C)c(=O)[nH]c3=O)C(=O)Cn3cc(C)c(=O)[nH]c3=O)nn1)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O2

Standard InChI:  InChI=1S/C132H177N55O31/c1-76(2)14-11-15-77(3)16-12-17-78(4)18-13-25-132(10)26-21-85-86(113(217-83(9)188)81(7)82(8)114(85)218-132)51-187-50-84(167-168-187)19-20-91(190)141-27-40-173(103(202)64-181-48-79(5)121(208)165-130(181)215)56-95(194)146-32-44-174(104(203)65-182-49-80(6)122(209)166-131(182)216)57-96(195)143-29-41-171(101(200)62-179-37-23-88(134)159-128(179)213)54-93(192)148-34-46-176(107(206)67-184-73-155-110-116(138)151-71-153-118(110)184)59-98(197)149-35-47-177(108(207)69-186-75-157-112-120(186)162-126(140)164-124(112)211)60-99(198)145-31-43-172(102(201)63-180-38-24-89(135)160-129(180)214)55-94(193)147-33-45-175(106(205)66-183-72-154-109-115(137)150-70-152-117(109)183)58-97(196)144-30-42-170(100(199)61-178-36-22-87(133)158-127(178)212)53-92(191)142-28-39-169(52-90(136)189)105(204)68-185-74-156-111-119(185)161-125(139)163-123(111)210/h22-24,36-38,48-50,70-78H,11-21,25-35,39-47,51-69H2,1-10H3,(H2,136,189)(H,141,190)(H,142,191)(H,143,195)(H,144,196)(H,145,198)(H,146,194)(H,147,193)(H,148,192)(H,149,197)(H2,133,158,212)(H2,134,159,213)(H2,135,160,214)(H2,137,150,152)(H2,138,151,153)(H,165,208,215)(H,166,209,216)(H3,139,161,163,210)(H3,140,162,164,211)

Standard InChI Key:  GCEUFDZCUXJLSB-UHFFFAOYSA-N

Associated Targets(Human)

Superoxide dismutase 173 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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

Properties

Molecular Weight: 3030.22Molecular Weight (Monoisotopic): 3028.3965AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Browne EC, Parakh S, Duncan LF, Langford SJ, Atkin JD, Abbott BM..  (2016)  Efficacy of peptide nucleic acid and selected conjugates against specific cellular pathologies of amyotrophic lateral sclerosis.,  24  (7): [PMID:26935939] [10.1016/j.bmc.2016.02.022]

Source