Drug

D0439 | Bafilomycin A1

Molecular Formula C35H58O9
Molecular Weight 622.8
Structure
State solid
Description macrolide antibiotics; ionophores (potassim); anti-tumor; anti-parasitic; immunosuppressant; anti-fungal; potent inhibitor of cellular autophagy; inhibitor of V-ATPases ;vacuolar ATPase inhibitor

Toxicity Dose Time Species Model Method Action Positive criterion Reference
TRANSPORT OF PROTONS BUT NOT CHARGE (K+) male Wistar rats liver mitochondria affect 199
MITOPHAGY 50 nM SH-SY5Y neuroblastoma cells Mitochondrial population levels were determined by flow cytometry using MitoTracker Deep Red (MTDR) dye. 252
APOPTOSIS pediatric B ALL cells induce 200
APOPTOSIS induce 200
AUTOPHAGY inhibit 200

Target Dose Time Species Model Method Action Positive criterion Reference
Apoptosis regulator Bcl-2 induce binding 200
Apoptosis-inducing factor 1, mitochondrial pediatric B ALL cells 200
Serine/threonine-protein kinase mTOR 200

Pictogram Signal Statements Precautionary Statement Codes
Warning

Aggregated GHS information provided by 40 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.


H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]


H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]


H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure


Respiratory tract irritation]


Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown.


P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501; (The corresponding statement to each P-code can be found at the GHS Classification page.)


  • (3Z,5E,7R,8S,9S,11E,13E,15S,16R)-16-[(1S,2R,3S)-3-[(2R,4R,5S,6R)-2,4-dihydroxy-6-isopropyl-5-methyl-tetrahydropyran-2-yl]-2-hydroxy-1-methyl-butyl]-8-hydroxy-3,15-dimethoxy-5,7,9,11-tetramethyl-1-oxacyclohexadeca-3,5,11,13-tetraen-2-one; (3Z,5E,7R,8S,9S,11E,13E,15S,16R)-16-{(2S,3R,4S)-4-[(2R,4R,5S,6R)-2,4-dihydroxy-6-isopropyl-5-methyltetrahydro-2H-pyran-2-yl]-3-hydroxypentan-2-yl}-8-hydroxy-3,15-dimethoxy-5,7,9,11-tetramethyloxacyclohexadeca-3,5,11,13-tetraen-2-one (3Z,5E,7R,8S,9S,11E,13E,15S,16R)-8-Hydroxy-16-[(1S,2R,3S)-2-hydroxy-1-methyl-3-[(2R,4R,5S,6R)-tetrahydro-2,4-dihydroxy-5-methyl-6-(1-methylethyl)-2H-pyran-2-yl]butyl]-3,15-dimethoxy-5,7,9,11-tetramethyloxacyclohexadeca-3,5,11,13-tetraen-2-one
    88899-55-2 ABP000610 ACon0_000813
    AKOS030213158 BDBM50064186 BSPBio_001470
    Bafilomycin A1(Baf-A1) Bafilomycin A1/ C35H58O9
    CHEBI:22689 CHEMBL290814 DB06733
    HMS3402J12 Hygrolidin, 21-O-de(3-carboxy-1-oxo-2-propenyl)-2-demethyl-2-methoxy-24-methyl- LS-178068
    MCULE-2359469972 MEGxm0_000385 MFCD06795130
    NCGC00163426-02 NSC 381866 NSC381866
    Q4841341 SCHEMBL13775181 ZINC169647947
    bafilomycin A1

    DrugBank Name Bafilomycin A1
    DrugBank DB06733
    CAS Number 88899-55-2
    PubChem Compound 6436223
    ChEBI 22689
    ChemSpider 10251049
    Wikipedia Bafilomycin