5,11,17,23-Tetra-tert-butyl-25,26,27,28-tetrakis(4-guanidiniumbutoxy)calix[4]arene

ID: ALA4072822

Chembl Id: CHEMBL4072822

PubChem CID: 137640204

Max Phase: Preclinical

Molecular Formula: C64H104Cl4N12O4

Molecular Weight: 1101.58

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)(C)c1cc2c(OCCCCNC(=N)N)c(c1)Cc1cc(C(C)(C)C)cc(c1OCCCCNC(=N)N)Cc1cc(C(C)(C)C)cc(c1OCCCCNC(=N)N)Cc1cc(C(C)(C)C)cc(c1OCCCCNC(=N)N)C2.Cl.Cl.Cl.Cl

Standard InChI:  InChI=1S/C64H100N12O4.4ClH/c1-61(2,3)49-33-41-29-43-35-50(62(4,5)6)37-45(54(43)78-26-18-14-22-74-58(67)68)31-47-39-52(64(10,11)12)40-48(56(47)80-28-20-16-24-76-60(71)72)32-46-38-51(63(7,8)9)36-44(55(46)79-27-19-15-23-75-59(69)70)30-42(34-49)53(41)77-25-17-13-21-73-57(65)66;;;;/h33-40H,13-32H2,1-12H3,(H4,65,66,73)(H4,67,68,74)(H4,69,70,75)(H4,71,72,76);4*1H

Standard InChI Key:  FWPHQNSLJDXGMD-UHFFFAOYSA-N

Associated Targets(Human)

TLR4 Tchem Toll-like receptor 4/MD-2/CD14 (27 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TLR4 Tchem Toll-like receptor 4 (970 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: 1101.58Molecular Weight (Monoisotopic): 1100.7990AlogP: #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. Sestito SE, Facchini FA, Morbioli I, Billod JM, Martin-Santamaria S, Casnati A, Sansone F, Peri F..  (2017)  Amphiphilic Guanidinocalixarenes Inhibit Lipopolysaccharide (LPS)- and Lectin-Stimulated Toll-like Receptor 4 (TLR4) Signaling.,  60  (12): [PMID:28471658] [10.1021/acs.jmedchem.7b00095]

Source