AntibioticMech

halistanol sulfonic acid G

CHEBI:72479 ·resolve ·ANTIVIRAL ·EXACT SEEDED

A steroid sulfate that is 5α-ergostane substituted by sulfate groups at positions 2, 3 and 6 (the (2β,3α,6α stereoisomer). — ChEBI

Classification

Strictly broader compounds or drug classes this molecule belongs to.

• CHEBI:16158 CHEBI:16158

Chemical structure

Computed structure properties

Molecular formula	C28H50O12S3
Charge	0
Average mass	674.897 Da
Monoisotopic mass	674.24644 Da
Source	ChEBI
InChIKey	WBHAMVHLRVKJRH-VZAWWNCJSA-N

SMILES

[H][C@@]12C[C@H](OS(=O)(=O)O)[C@@]3([H])C[C@H](OS(=O)(=O)O)[C@@H](OS(=O)(=O)O)C[C@]3(C)[C@@]1([H])CC[C@@]1(C)[C@@]2([H])CC[C@]1([H])[C@H](C)CC[C@H](C)C(C)C

InChI

InChI=1S/C28H50O12S3/c1-16(2)17(3)7-8-18(4)20-9-10-21-19-13-24(38-41(29,30)31)23-14-25(39-42(32,33)34)26(40-43(35,36)37)15-28(23,6)22(19)11-12-27(20,21)5/h16-26H,7-15H2,1-6H3,(H,29,30,31)(H,32,33,34)(H,35,36,37)/t17-,18+,19-,20+,21-,22-,23+,24-,25-,26-,27+,28+/m0/s1

Also called

• (2β,3α,5α,6α)-ergostane-2,3,6-triyl tris(hydrogen sulfate) (EXACT_SYNONYM)— chebi

Activity roles

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

• CHEBI:64947 CHEBI:64947
• CHEBI:64949 CHEBI:64949

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:72479	halistanol sulfonic acid G	antibioticmech:chebi-59b7bde878	2026-08-30

Curation history

1. SEEDED_FROM_SOURCES 2026-08-30 · seed_from_sources

   Seeded from data/raw/ inventories (CHEBI)

2. RESEEDED_FROM_SOURCES 2026-08-30 · seed_from_sources

   Re-seeded from updated data/raw/ inventories

3. 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.