NH2-CGTGCTGAA-H

ID: ALA3775382

PubChem CID: 127032320

Max Phase: Preclinical

Molecular Formula: C97H122N54O27

Molecular Weight: 2476.39

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1cn(CC(=O)N(CCNC(=O)CN(CCNC(=O)CN(CCN)C(=O)Cn2ccc(N)nc2=O)C(=O)Cn2cnc3c(=O)[nH]c(N)nc32)CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(=O)NCCN(CC(N)=O)C(=O)Cn2cnc3c(N)ncnc32)C(=O)Cn2cnc3c(N)ncnc32)C(=O)Cn2cnc3c(=O)[nH]c(N)nc32)C(=O)Cn2cc(C)c(=O)[nH]c2=O)C(=O)Cn2ccc(N)nc2=O)C(=O)Cn2cnc3c(=O)[nH]c(N)nc32)c(=O)[nH]c1=O

Standard InChI:  InChI=1S/C97H122N54O27/c1-52-25-145(96(177)132-86(52)170)38-67(163)137(30-59(155)113-13-24-142(73(169)44-151-51-123-78-85(151)128-93(106)131-90(78)174)35-64(160)114-11-21-139(70(166)41-148-48-120-75-80(103)116-46-118-82(75)148)32-61(157)107-6-17-135(27-56(101)152)69(165)40-147-47-119-74-79(102)115-45-117-81(74)147)19-8-110-58(154)29-136(66(162)37-144-15-4-55(100)125-95(144)176)18-7-109-62(158)33-141(72(168)43-150-50-122-77-84(150)127-92(105)130-89(77)173)23-12-112-60(156)31-138(68(164)39-146-26-53(2)87(171)133-97(146)178)20-9-111-63(159)34-140(71(167)42-149-49-121-76-83(149)126-91(104)129-88(76)172)22-10-108-57(153)28-134(16-5-98)65(161)36-143-14-3-54(99)124-94(143)175/h3-4,14-15,25-26,45-51H,5-13,16-24,27-44,98H2,1-2H3,(H2,101,152)(H,107,157)(H,108,153)(H,109,158)(H,110,154)(H,111,159)(H,112,156)(H,113,155)(H,114,160)(H2,99,124,175)(H2,100,125,176)(H2,102,115,117)(H2,103,116,118)(H,132,170,177)(H,133,171,178)(H3,104,126,129,172)(H3,105,127,130,173)(H3,106,128,131,174)

Standard InChI Key:  BHLCVRZRBUNWQH-UHFFFAOYSA-N

Molfile:  

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M  END

Alternative Forms

  1. Parent:

    ALA3775382

    ---

Associated Targets(Human)

SOD1 Tchem 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

Calculated Properties

Molecular Weight: 2476.39Molecular Weight (Monoisotopic): 2474.9833AlogP: #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