EcoDrugPlus


Trade Names	MYCIFRADIN NEO-FRADIN NEO-RX NEOBIOTIC NEOMYCIN SULFATE
Synonyms	Biomydrin Biosol Bykomycin Cicatrene Cicatrin Endomixin Fradiomycin Sulfate Fradiomycin sulfate Framycetin sulfate Framycetin sulphate Fraquinol Gppe nsl gel Graneodin Myacine Mycifradin Myciguent NSC-757240 Naseptin Neo-fradin Neo-rx Neobacrin Neobiotic Neobrettin Neomix Neomycin b sulfate Neomycin b sulphate Neomycin b, sulfate (salt) Neomycin b, sulphate (salt) Neomycin sulfate Neosporin Neosulf Nivemycin Soframycin Tribiotic Tuttomycin Vibrocil
Status
Molecule Category	UNKNOWN
UNII	057Y626693
Parent Compound:	NEOMYCIN

Trade Names

MYCIFRADIN

NEO-FRADIN

NEO-RX

NEOBIOTIC

NEOMYCIN SULFATE

Synonyms

Biomydrin

Biosol

Bykomycin

Cicatrene

Cicatrin

Endomixin

Fradiomycin Sulfate

Fradiomycin sulfate

Framycetin sulfate

Framycetin sulphate

Fraquinol

Gppe nsl gel

Graneodin

Myacine

Mycifradin

Myciguent

NSC-757240

Naseptin

Neo-fradin

Neo-rx

Neobacrin

Neobiotic

Neobrettin

Neomix

Neomycin b sulfate

Neomycin b sulphate

Neomycin b, sulfate (salt)

Neomycin b, sulphate (salt)

Neomycin sulfate

Neosporin

Neosulf

Nivemycin

Soframycin

Tribiotic

Tuttomycin

Vibrocil

Status

Molecule Category

UNKNOWN

UNII

057Y626693

Parent Compound:

NEOMYCIN


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70

Mechanism of Action	Action	Reference
Bacterial 70S ribosome inhibitor	INHIBITOR	PubMed PubMed PubMed PubMed Wikipedia

Mechanism of Action

Action

Reference

Bacterial 70S ribosome inhibitor

INHIBITOR

PubMed PubMed PubMed PubMed Wikipedia

Targets	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Enzyme Hydrolase	-	-	-	-
Transporter Electrochemical transporter SLC superfamily of solute carriers SLC21/SLCO family of organic anion transporting polypeptides	-	-	-	-	80

Targets

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Enzyme Hydrolase

Transporter Electrochemical transporter SLC superfamily of solute carriers SLC21/SLCO family of organic anion transporting polypeptides

Resources	Reference
ChEMBL	CHEMBL3989769
FDA SRS	057Y626693

Resources

Reference

ChEMBL

CHEMBL3989769

FDA SRS

057Y626693


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

NEOMYCIN SULFATE

Bioactivity

Cross References