fluopsin

CHEBI:231919 ·resolve ·ANTIBACTERIAL ·EXACT SEEDED

A thiocarbonyl compound that is ammonia in which the hydrogens are substituted by methyl, hydroxy, and carbonothioyl groups. — ChEBI

Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.

Classification

Strictly broader compounds or drug classes this molecule belongs to.

CHEBI:24709 CHEBI:24709
CHEBI:50492 CHEBI:50492

Chemical structure

Computed structure properties
Molecular formula	C2H5NOS
Charge	0
Average mass	91.135 Da
Monoisotopic mass	91.00918 Da
Source	ChEBI
InChIKey	LSLVHNSGLHQBDX-UHFFFAOYSA-N

SMILES

CN(O)C=S

InChI

InChI=1S/C2H5NOS/c1-3(4)2-5/h2,4H,1H3

Also called

N-hydroxy-N-methylthioformamide (EXACT_SYNONYM)— chebi
N-methyl-N-(thioformyl)hydroxylamine (EXACT_SYNONYM)— chebi
N-methyl-N-hydroxythioxomethylamine (EXACT_SYNONYM)— chebi
N-methyl-N-thioformylhydroxylamine (EXACT_SYNONYM)— chebi
thioformin (EXACT_SYNONYM)— chebi

Cross-references

Equivalent identifiers for this same structure in other resources.

cas:31335-60-1

Activity roles

Every antimicrobial role a source asserts for this compound — the unreduced evidence behind its antimicrobial_class.

CHEBI:33282 CHEBI:33282

Source concepts

Every upstream concept that resolved to this record. The merge is the product: this is what shows ChEBI and CARD are describing the same structure.

Upstream concepts merged into this record
Source	Native ID	Label	Minted CURIE	Version
CHEBI	`CHEBI:231919`	fluopsin	`antibioticmech:chebi-0e6afcd6c5`	2026-08-30

Curation history

SEEDED_FROM_SOURCES 2026-08-30 · seed_from_sources
Seeded from data/raw/ inventories (CHEBI)
RESEEDED_FROM_SOURCES 2026-08-30 · seed_from_sources
Re-seeded from updated data/raw/ inventories
RESEEDED_FROM_SOURCES 2026-08-30 · seed_from_sources
Re-seeded from updated data/raw/ inventories

Provenance

Seeded by scripts/seed_from_sources.py from the committed inventories in data/raw/. View the record.