ARCHAZOLID F

ID: ALA1784269

Max Phase: Preclinical

Molecular Formula: C41H60N2O7S

Molecular Weight: 725.01

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): Archazolid F
Synonyms from Alternative Forms(1):

    Canonical SMILES:  CNC(=O)O[C@@H](CC(C)C)c1nc([C@H]2OC(=O)C/C=C/C(C)=C/[C@@H](O)[C@@H](C)/C=C(C)\C=C(C)/C=C/[C@@H](O)[C@H](C)[C@H](OC)/C(C)=C/C=C/[C@@H]2C)cs1

    Standard InChI:  InChI=1S/C41H60N2O7S/c1-25(2)20-36(49-41(47)42-10)40-43-33(24-51-40)39-30(7)16-13-15-29(6)38(48-11)32(9)34(44)19-18-27(4)21-28(5)22-31(8)35(45)23-26(3)14-12-17-37(46)50-39/h12-16,18-19,21-25,30-32,34-36,38-39,44-45H,17,20H2,1-11H3,(H,42,47)/b14-12+,16-13+,19-18+,26-23+,27-21-,28-22-,29-15+/t30-,31-,32-,34+,35+,36-,38+,39-/m0/s1

    Standard InChI Key:  WRJITTKUXGEQBF-KJKBHKFMSA-N

    Associated Targets(Human)

    U-937 (7138 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    SK-OV-3 (52876 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    A-431 (6446 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    PC-3 (62116 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    MCF7 (126967 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    ELANE Tclin Leukocyte elastase (8173 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    P2RX3 Tclin P2X purinoceptor 3 (1991 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    PRSS1 Tclin Trypsin (2137 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    CTSB Tchem Cathepsin B (3822 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    CTSL Tclin Cathepsin L (3852 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    CTRC Tchem Chymotrypsin (134 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Associated Targets(non-human)

    L929 (3802 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    VHA55 V-type proton ATPase subunit B (6 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: 725.01Molecular Weight (Monoisotopic): 724.4121AlogP: 8.67#Rotatable Bonds: 6
    Polar Surface Area: 127.21Molecular Species: NEUTRALHBA: 9HBD: 3
    #RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
    CX Acidic pKa: CX Basic pKa: 0.78CX LogP: 7.26CX LogD: 7.26
    Aromatic Rings: 1Heavy Atoms: 51QED Weighted: 0.25Np Likeness Score: 1.45

    References

    1. Horstmann N, Essig S, Bockelmann S, Wieczorek H, Huss M, Sasse F, Menche D..  (2011)  Archazolid A-15-O-β-D-glucopyranoside and iso-archazolid B: potent V-ATPase inhibitory polyketides from the myxobacteria Cystobacter violaceus and Archangium gephyra.,  74  (5): [PMID:21513292] [10.1021/np200036v]
    2. Scheeff S, Rivière S, Ruiz J, Abdelrahman A, Schulz-Fincke AC, Köse M, Tiburcy F, Wieczorek H, Gütschow M, Müller CE, Menche D..  (2020)  Synthesis of Novel Potent Archazolids: Pharmacology of an Emerging Class of Anticancer Drugs.,  63  (4): [PMID:31990540] [10.1021/acs.jmedchem.9b01887]

    Source