General
Preferred name
GRISEOFULVIN
Synonyms
Amudane ()
Fulvicin ()
Grisactin ()
Griseofulvin126-07-8 ()
Griseofulvin-d3 ()
NSC-755822 ()
Ultragris-330 ()
Fulvicin P/G ()
Grifulvin ()
Grivate ()
Grisol AF ()
Fulcin 125 ()
Griseofulvin, Ultramicrosize ()
Fulcin 500 ()
Griseofulvin permeability diameter ()
Fulvicin P/G 165 ()
NSC-34533 ()
Fulvicin-U/F ()
Fulvicin P/G 330 ()
Griseofulvinum ()
Griseofulvin,Ultramicrosize ()
Griseofulvin microsize ()
Grisactin v ()
Grifulvin V ()
Ultragris-165 ()
Grisactin Ultra ()
Fulsovin ()
Gris-Peg ()
Griseofulvin,microsize ()
Fulcin ()
P&D ID
PD002235
CAS
126-07-8
107912-37-8
1279033-22-5
Tags
natural product
drug
available
Approved by
FDA
First approval
1962
Drug indication
Ringworm infection
Antifungal
Drug Status
investigational
vet_approved
approved
Max Phase
4.0
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Cell lines
10
Organisms
7
Compound Sets
23
AdooQ Bioactive Compound Library
Cayman Chemical Bioactives
ChEMBL Approved Drugs
ChEMBL Drugs
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine BioReference Compounds
Mcule NIBR MoA Box Subset
MedChem Express Bioactive Compound Library
NCATS Inxight Approved Drugs
NIH Clinical Collections (NCC)
Novartis Chemogenetic Library (NIBR MoA Box)
NPC Screening Collection
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
The Spectrum Collection
External IDs
52
Properties
(calculated by RDKit )
Molecular Weight
352.07
Hydrogen Bond Acceptors
6
Hydrogen Bond Donors
0
Rotatable Bonds
3
Ring Count
3
Aromatic Ring Count
1
cLogP
2.81
TPSA
71.06
Fraction CSP3
0.41
Chiral centers
2.0
Largest ring
6.0
QED
0.83
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Pathway
Cytoskeletal Signaling
Anti-infection
Apoptosis
Metabolic Enzyme/Protease
Target
Tubulin chain
KRT12
antibiotic
Endogenous Metabolite
Fungal
Microtubule Associated
Member status
member
MOA
Keratin 12 modulator
tubulin polymerization inhibitor
Indication
ringworm, tinea pedis
Therapeutic Class
Antifungal Agents
Source data