L-β-ethynylserine zwitterion
CHEBI:144729
·resolve ·ANTIBACTERIAL
·EXACT
SEEDED
An L-α-amino acid zwitterion obtained by transfer of a proton from the carboxy group to the amino group of L-β-ethynylserine. The major species at pH 7.3. — 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.
Chemical structure
Computed structure properties
| Molecular formula | C5H7NO3 |
|---|
| Charge | 0 |
|---|
| Average mass | 129.115 Da |
|---|
| Monoisotopic mass | 129.04259 Da |
|---|
| Source | ChEBI |
|---|
| InChIKey | RBWXRFBKVDBXEG-DMTCNVIQSA-N |
SMILES
C#C[C@@H](O)[C@H]([NH3+])C(=O)[O-]
InChI
InChI=1S/C5H7NO3/c1-2-3(7)4(6)5(8)9/h1,3-4,7H,6H2,(H,8,9)/t3-,4+/m1/s1
Also called
- 2-azaniumyl-2,4,5-trideoxy-D-threo-pent-4-ynonate (EXACT_SYNONYM)— chebi
- (2S,3R)-2-azaniumyl-3-hydroxypent-4-ynoate (EXACT_SYNONYM)— chebi
Activity roles
Every antimicrobial role a source asserts for this compound — the
unreduced evidence behind its antimicrobial_class.
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:144729 |
L-β-ethynylserine zwitterion |
antibioticmech:chebi-e8012d1da1 |
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.