SCHEMBL7200660

SCHEMBL7200660

CC1(C)O[C@H]2[C@H]3C[C@@](O)(C[C@H]2O1)C(=O)O3

nearest known ligand 0.40

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ MGAM O43451 1/20 0.40
▸ CA1 P00915 1/20 0.40
▸ CA2 P00918 1/20 0.40
▸ GAA P10253 1/20 0.40
▸ SI P14410 1/20 0.40
▸ ACHE P22303 1/20 0.40
▸ MGAM2 Q2M2H8 1/20 0.40
▸ NPC1 O15118 1/20 0.30
▸ MITF O75030 1/20 0.30
▸ MAPT P10636 1/20 0.30
▸ HTT P42858 1/20 0.30
▸ RAB9A P51151 1/20 0.30
▸ KMT2A Q03164 1/20 0.30

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
SCHEMBL16602936 1.00 MGAM (0.40) MGAMCA1CA2GAASI
SCHEMBL10100000 1.00 MGAM (0.40) MGAMCA1CA2GAASI
SCHEMBL10063791 1.00 MGAM (0.40) MGAMCA1CA2GAASI
SCHEMBL13825709 1.00 MGAM (0.40) MGAMCA1CA2GAASI
SCHEMBL14403895 0.82 MGAM (0.39) MGAMCA1CA2GAASI
SCHEMBL14232901 0.82 MGAM (0.39) MGAMCA1CA2GAASI
SCHEMBL12510719 0.82 MGAM (0.39) MGAMCA1CA2GAASI
SCHEMBL13300885 0.80 — —
SCHEMBL13321423 0.80 — —
SCHEMBL14403629 0.79 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250313574-A1 SIALIC ACID DERIVATIVES AND METHODS OF USING SAME EISAI R&D MANAGEMENT CO., LTD. (JP) 2025-10-09 — — US disclosed
US-20200048183-A1 ANTIMICROBIAL AGENTS UNIV WARWICK (GB) 2020-02-13 — — US disclosed
EP-2949652-B1 Intermediates for the preparation of halichondrin B EISAI R&D MAN CO LTD (JP) 2019-08-07 — — EP disclosed
US-RE46965-E1 Intermediates for the preparation of analogs of Halichondrin B EISAI R&D MANAGEMENT CO., LTD. (JP) 2018-07-24 — — US disclosed
US-9475752-B2 Method for manufacturing 3,4,5-tricaffeoylquinic acid FUJIFILM CORPORATION (JP) 2016-10-25 — — US disclosed
US-9475752-B2 Method for manufacturing 3,4,5-tricaffeoylquinic acid FUJIFILM CORPORATION (JP) 2016-10-25 — — US disclosed
US-9303050-B2 Intermediates for the preparation of analogs of Halichondrin B EISAI R&D MANAGEMENT CO., LTD. (JP) 2016-04-05 — — US disclosed
US-20160023986-A1 METHOD FOR MANUFACTURING 3,4,5-TRICAFFEOYLQUINIC ACID FUJIFILM CORPORATION (JP) 2016-01-28 — — US disclosed
US-20160023986-A1 METHOD FOR MANUFACTURING 3,4,5-TRICAFFEOYLQUINIC ACID FUJIFILM CORPORATION (JP) 2016-01-28 — — US disclosed
EP-2949652-A1 Intermediates for the preparation of halichondrin B Eisai R&D Management Co., Ltd. (JP) 2015-12-02 — — EP disclosed
US-20120283331-A1 Anti-Inflammatory Quinic Acid Derivatives for Radioprotection/Radiomitigation UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2012-11-08 — — US disclosed
US-8115031-B2 Anti-inflammatory quinic acid derivatives for oral administration THE UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION 2012-02-14 — — US disclosed
US-8115031-B2 Anti-inflammatory quinic acid derivatives for oral administration THE UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION 2012-02-14 — — US disclosed
US-7982060-B2 Intermediates for the preparation of analogs of Halichondrin B EISAI R&D MANAGEMENT CO., LTD. (JP) 2011-07-19 — — US disclosed
WO-2010132504-A1 ANTI-INFLAMMATORY QUINIC ACID DERIVATIVES FOR RADIOPROTECTION/RADIOMITIGATION UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2010-11-18 — — WO disclosed
US-20090234015-A1 Anti-Inflammatory Quinic Acid Derivatives for Oral Administration THE UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION 2009-09-17 — — US disclosed
US-20090234015-A1 Anti-Inflammatory Quinic Acid Derivatives for Oral Administration THE UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION 2009-09-17 — — US disclosed
WO-2009062200-A1 ANTI-INFLAMMATORY QUINIC ACID DERIVATIVES FOR ORAL ADMINISTRATION UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2009-05-14 — — WO disclosed
US-20070244187-A1 Intermediates for the Preparation of Halichondrin B EISAI CO., LTD (JP) 2007-10-18 — — US disclosed
US-6593314-B1 Useful in the inhibition of neuraminidase enzymes from disease- causing microorganisms, especially influenza neuraminidase, pharmaceutical formulations containing same, processes and intermediates for preparing said compounds, ABBOTT LABORATORIES 2003-07-15 — — US 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 (6 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-20160023986-A1 METHOD FOR MANUFACTURING 3,4,5-TRICAFFEOYLQUINIC ACID HAAO, CUL5, ACMSD MGAM 1088/4885CA1 3855/4885CA2 3279/4885
US-20090234015-A1 Anti-Inflammatory Quinic Acid Derivatives for Oral Administration NFKBIA, NFRKB, IKBKB MGAM 1927/4885CA1 2232/4885CA2 2313/4885
US-20070244187-A1 Intermediates for the Preparation of Halichondrin B CDK4, CCNB1, CDK14 MGAM 4853/4885CA1 3967/4885CA2 3356/4885
US-20200048183-A1 ANTIMICROBIAL AGENTS C3AR1, HCAR3, C5AR1 MGAM 4097/4885CA1 1543/4885CA2 907/4885
US-20120283331-A1 Anti-Inflammatory Quinic Acid Derivatives for Radioprotection/Radiomitigation NQO2, SQSTM1, CTSA MGAM 1796/4885CA1 2228/4885CA2 3340/4885
US-20250313574-A1 SIALIC ACID DERIVATIVES AND METHODS OF USING SAME NEU1, NEU2, NEU4 MGAM 193/4885CA1 95/4885CA2 1654/4885

“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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