[1-Hydroxy-2-(4'-methoxy-biphenyl-4-yl)-1-phosphono-ethyl]-phosphonic acid

ID: ALA198066

PubChem CID: 5277499

Max Phase: Preclinical

Molecular Formula: C15H18O8P2

Molecular Weight: 388.25

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccc(-c2ccc(CC(O)(P(=O)(O)O)P(=O)(O)O)cc2)cc1

Standard InChI:  InChI=1S/C15H18O8P2/c1-23-14-8-6-13(7-9-14)12-4-2-11(3-5-12)10-15(16,24(17,18)19)25(20,21)22/h2-9,16H,10H2,1H3,(H2,17,18,19)(H2,20,21,22)

Standard InChI Key:  JLDCYROWPBFECT-UHFFFAOYSA-N

Molfile:  

     RDKit          2D

 25 26  0  0  0  0  0  0  0  0999 V2000
   -2.1712   -5.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1723   -6.2324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4578   -6.6450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7418   -6.2319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7446   -5.4019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4596   -4.9929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0322   -4.9829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0267   -4.1583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0199   -3.3376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8513   -4.1521    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.7979   -4.1605    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    1.6234   -4.1755    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6746   -4.1507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8475   -3.3275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8563   -4.9767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065   -3.3360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7881   -4.9851    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8869   -6.6480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6009   -6.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3148   -6.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3159   -7.4699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5972   -7.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8862   -7.4692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0298   -7.8825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7442   -7.4707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0
 10 13  2  0
  1  2  2  0
 10 14  1  0
  5  7  1  0
 10 15  1  0
  3  4  2  0
 11 16  1  0
  7  8  1  0
 11 17  1  0
  8  9  1  0
 18 19  2  0
  4  5  1  0
 19 20  1  0
  8 10  1  0
 20 21  2  0
  2  3  1  0
 21 22  1  0
  8 11  1  0
 22 23  2  0
 23 18  1  0
  2 18  1  0
  5  6  2  0
 21 24  1  0
 11 12  2  0
 24 25  1  0
M  END

Associated Targets(Human)

MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-268 (49410 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

PPase1 Vacuolar-type proton translocating pyrophosphatase 1 (115 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: 388.25Molecular Weight (Monoisotopic): 388.0477AlogP: 1.91#Rotatable Bonds: 6
Polar Surface Area: 144.52Molecular Species: ACIDHBA: 4HBD: 5
#RO5 Violations: HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski):
CX Acidic pKa: 0.69CX Basic pKa: CX LogP: 0.90CX LogD: -4.03
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.47Np Likeness Score: 0.06

References

1. Kotsikorou E, Song Y, Chan JM, Faelens S, Tovian Z, Broderick E, Bakalara N, Docampo R, Oldfield E..  (2005)  Bisphosphonate inhibition of the exopolyphosphatase activity of the Trypanosoma brucei soluble vacuolar pyrophosphatase.,  48  (19): [PMID:16162013] [10.1021/jm058220g]
2. Song Y, Chan JM, Tovian Z, Secrest A, Nagy E, Krysiak K, Bergan K, Parniak MA, Oldfield E..  (2008)  Bisphosphonate inhibitors of ATP-mediated HIV-1 reverse transcriptase catalyzed excision of chain-terminating 3'-azido, 3'-deoxythymidine: a QSAR investigation.,  16  (19): [PMID:18789701] [10.1016/j.bmc.2008.08.047]

Source