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Chemical substance record

Natamycin

7681-93-8C33H47NO13665.733 g/mol

A macrolide antibiotic that has formula C33H47NO13, produced by several Streptomyces species including Streptomyces natalensis. It exhibits broad spectrum antifungal activity and used in eye drops, and as a food preservative, and also as a postharvest biofungicide for citrus and other fruit crops. — ChEBI

Safety references

Safety documents & references

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Identity & molecular properties

Source-linked values
CAS number7681-93-8ChEBI ↗
Molecular formulaC33H47NO13ChEBI ↗
Molar mass665.733 g/molChEBI ↗
Monoisotopic mass665.30474 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:7488ChEBI ↗

Cross-source molecular data

PubChem
Molar mass665.7 g/molPubChem ↗
Exact mass665.30474055 DaPubChem ↗
Computed XLogP-1.3PubChem ↗
Topological polar surface area (Ų)231PubChem ↗
H-bond donors7PubChem ↗
H-bond acceptors14PubChem ↗
Rotatable bonds3PubChem ↗

PubChem computed values are shown separately from the ChEBI record. An exact InChIKey match was used to connect the records. Molecular descriptors do not describe a supplied product’s purity, particle size or performance.

Names & structural identifiers

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natamycin
(1R,3S,5R,7R,8E,12R,14E,16E,18E,20E,22R,24S,25R,26S)-22-[(3-amino-3,6-dideoxy-beta-D-mannopyranosyl)oxy]-1,3,26-trihydroxy-12-methyl-10-oxo-6,11,28-trioxatricyclo[22.3.1.0(5,7)]octacosa-8,14,16,18,20-pentaene-25-carboxylic acid
NCXMLFZGDNKEPB-FFPOYIOWSA-N
[H][C@@]12C[C@H](O)C[C@]3(O)C[C@H](O)[C@@H](C(=O)O)[C@]([H])(C[C@@H](O[C@@H]4O[C@H](C)[C@@H](O)[C@H](N)[C@@H]4O)/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]1O2)O3
InChI=1S/C33H47NO13/c1-18-10-8-6-4-3-5-7-9-11-21(45-32-30(39)28(34)29(38)19(2)44-32)15-25-27(31(40)41)22(36)17-33(42,47-25)16-20(35)14-24-23(46-24)12-13-26(37)43-18/h3-9,11-13,18-25,27-30,32,35-36,38-39,42H,10,14-17,34H2,1-2H3,(H,40,41)/b4-3+,7-5+,8-6+,11-9+,13-12+/t18-,19-,20+,21+,22+,23-,24-,25+,27-,28+,29-,30+,32+,33-/m1/s1

Names & synonyms

DelvocidDelvolanDelvoposMycophytMyprozineMyuprozineNatacynNatajenNatamatrixNatamaxnatamicinanatamycine

Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

antimicrobial food preservativeophthalmology drugapoptosis inducerbacterial metaboliteantifungal agrochemical

Database role annotations describe reported biological or chemical roles; they are not product approvals or recommendations for use.

Mass ↔ amount of substance

Calculated from sourced mass
Equivalent amount
0.0015021 mol

Uses 665.733 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.

Elemental composition

Theoretical mass fractions
C
Carbon · 33 atoms
59.54%
O
Oxygen · 13 atoms
31.24%
H
Hydrogen · 47 atoms
7.12%
N
Nitrogen · 1 atom
2.10%

Calculated theoretical mass fractions from the reported formula and PubChem periodic-table atomic masses. These are not assay or purity results.

Research & patent references

Selected source associations

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:7488

Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0

NCBI PubChem · CID 5284447 · retrieved 2026-09-27

PubCAS formats source data, connects references and computes explicitly labelled conversions. CAS cross-references are supplied by ChEBI; they do not constitute CAS verification or endorsement.