SCHEMBL29407493

SCHEMBL29407493

CO[C@H]1O[C@H](COS(=O)(=O)O)[C@@H](O[C@@H]2O[C@@H](C(=O)O)[C@@H](O[C@H]3O[C@H](COS(=O)(=O)O)[C@@H](O[C@@H]4O[C@H](C(=O)O)[C@@H](O[C@H]5O[C@H](COS(=O)(=O)O)[C@@H](OC)[C@H](OC)[C@H]5OS(=O)(=O)O)[C@H](OC)[C@H]4OC)[C@H](OS(=O)(=O)O)[C@H]3OS(=O)(=O)O)[C@H](OC)[C@H]2OS(=O)(=O)O)[C@H](OS(=O)(=O)O)[C@H]1OS(=O)(=O)O

nearest known ligand 0.85

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ SERPINC1 P01008 3/20 0.85
▸ FGF1 P05230 4/20 0.57
▸ F10 P00742 6/20 0.56
▸ F2 P00734 1/20 0.53
▸ FGF2 P09038 1/20 0.52
▸ HPSE Q9Y251 5/20 0.48
▸ BDNF P23560 2/20 0.41
▸ PTN P21246 1/20 0.41
▸ MDK P21741 1/20 0.41

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Idraparinux SCHEMBL427808 1.00 SERPINC1 (0.85) SERPINC1FGF1F10F2FGF2
Idraparinux SCHEMBL29382311 1.00 SERPINC1 (0.85) SERPINC1FGF1F10F2FGF2
SCHEMBL12458587 0.93 SERPINC1 (0.75) SERPINC1FGF1F10F2FGF2
SCHEMBL12729453 0.92 SERPINC1 (0.74) SERPINC1FGF1F10F2FGF2
SCHEMBL15896273 0.88 SERPINC1 (0.69) SERPINC1FGF1F10F2FGF2
SCHEMBL12799309 0.87 SERPINC1 (0.68) SERPINC1FGF1F10F2FGF2
SCHEMBL17660081 0.86 SERPINC1 (0.66) SERPINC1FGF1F10F2FGF2
SCHEMBL13551204 0.86 SERPINC1 (0.66) SERPINC1FGF1F10F2FGF2
SCHEMBL4732494 0.86 SERPINC1 (0.66) SERPINC1FGF1F10F2FGF2
SCHEMBL29890443 0.85 SERPINC1 (0.65) SERPINC1FGF1F10F2FGF2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 114 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122080097-A Fucosylated heparin pentasaccharide and preparation method and application thereof — 2026-05-26 — — CN claimed
US-20250188506-A1 ANTICOAGULANT HEPARIN-CHONDROITIN CHIMERIC SACCHARIDE MOLECULE AS WELL AS PREPARATION METHOD AND APPLICATION THEREOF SHANDONG UNIVERSITY (CN) 2025-06-12 — — US claimed
CN-119823200-A Preparation method of fondaparinux sodium heparin pentasaccharide and method for synthesizing fondaparinux sodium heparin pentasaccharide by taking naphthylmethyl as temporary protecting group 海南大学 2025-04-15 — — CN claimed
WO-2025054300-A1 POLYMERIC VENOUS VALVE SYSTEMS AND METHODS OF MAKING AND USING THEREOF ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA (US) 2025-03-13 — — WO claimed
CN-117777320-A Low molecular weight heparin mimics based on heparin pentasaccharide and preparation method and application thereof 中国科学院上海药物研究所 2024-03-29 — — CN claimed
CN-117777216-A Preparation method and application of neutralizable biotinylation heparin pentasaccharide 中国科学院上海药物研究所 2024-03-29 — — CN claimed
WO-2024061270-A1 HEPARIN PENTASACCHARIDE-BASED LOW MOLECULAR WEIGHT HEPARIN MIMETIC, PREPARATION METHOD THEREFOR AND USE THEREOF 中国科学院上海药物研究所 2024-03-28 — — WO claimed
WO-2024061271-A1 PREPARATION METHOD FOR BIOTINYLATED HEPARIN PENTASACCHARIDE CAPABLE OF BEING NEUTRALIZED AND USE 中国科学院上海药物研究所 2024-03-28 — — WO claimed
CN-117683830-A Anticoagulant heparin-chondroitin chimeric sugar molecule and preparation method and application thereof 山东大学 2024-03-12 — — CN claimed
WO-2024032575-A1 HEPARIN DODECASACCHARIDE CONTAINING DOUBLE ANTITHROMBIN BINDING SEQUENCE, PREPARATION METHOD THEREFOR, AND USE THEREOF 山东大学 2024-02-15 — — WO claimed
CN-114957354-B Heparin pentasaccharide structure compound 南开大学 2023-11-24 — — CN claimed
CN-113583151-B Heparin molecules containing AT binding sequences and continuous 2-O-glucuronic acid residues, and preparation method and application thereof 山东大学 2023-06-20 — — CN claimed
CN-115417937-B Heparin dodecasaccharide containing double antithrombin binding sequence and preparation method and application thereof 山东大学 2023-06-06 — — CN claimed
WO-2023280235-A1 HEPARIN MOLECULE CONTAINING AT BINDING SEQUENCE AND CONTINUOUS 2-O-GLUCURONIC ACID RESIDUE, AND PREPARATION METHOD THEREFOR AND USE THEREOF 山东大学 2023-01-12 — — WO claimed
CN-115417937-A Heparin decabiose containing double-antithrombin binding sequence and preparation method and application thereof 山东大学 2022-12-02 — — CN claimed
CN-114957354-A Heparin pentasaccharide structural compound 南开大学 2022-08-30 — — CN claimed
CN-122080097-A Fucosylated heparin pentasaccharide and preparation method and application thereof — 2026-05-26 — — CN disclosed
CN-122080097-A Fucosylated heparin pentasaccharide and preparation method and application thereof — 2026-05-26 — — CN disclosed
US-20220072032-A1 INHIBITORS OF PCSK9 FOR TREATMENT OF LIPOPROTEIN METABOLISM DISORDERS AARHUS UNIVERSITET (DK) 2022-03-10 — — US disclosed
CN-114053251-A Sulfated polysaccharide inhalation preparation and application thereof in preventing and treating new coronavirus related diseases 苏州融析生物科技有限公司 2022-02-18 — — CN disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20220072032-A1 INHIBITORS OF PCSK9 FOR TREATMENT OF LIPOPROTEIN METABOLISM DISORDERS PCSK9, PCSK6, PCSK7 SERPINC1 262/4885FGF1 3794/4885F10 3605/4885
US-20250188506-A1 ANTICOAGULANT HEPARIN-CHONDROITIN CHIMERIC SACCHARIDE MOLECULE AS WELL AS PREPARATION METHOD AND APPLICATION THEREOF HPSE, CD44, CSGALNACT1 SERPINC1 18/4885FGF1 1060/4885F10 46/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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