SCHEMBL3675243

SCHEMBL3675243

CCOC(=O)C1=CC(O)C(O)C(O)C1

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.38
FUCA1 P04066 2/20 0.37
GLB1 P16278 1/20 0.37
MEN1 O00255 2/20 0.36
LMNA P02545 2/20 0.36
KMT2A Q03164 2/20 0.36
CYP3A4 P08684 1/20 0.36
CA12 O43570 3/20 0.36
CA1 P00915 3/20 0.36
CA2 P00918 3/20 0.36
CA7 P43166 3/20 0.36
CA9 Q16790 3/20 0.36
CA14 Q9ULX7 3/20 0.36
ESR1 P03372 1/20 0.36
ESR2 Q92731 1/20 0.36
KDM4E B2RXH2 2/20 0.35
MAPT P10636 1/20 0.35
ALOX15 P16050 1/20 0.35
NR1H2 P55055 1/20 0.35
NR1H3 Q13133 1/20 0.35

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
SCHEMBL30468187 1.00 TSHR (0.38) TSHRFUCA1GLB1MEN1LMNA
SCHEMBL3650538 1.00 TSHR (0.38) TSHRFUCA1GLB1MEN1LMNA
SCHEMBL15144345 1.00 TSHR (0.38) TSHRFUCA1GLB1MEN1LMNA
SCHEMBL13984986 1.00 TSHR (0.38) TSHRFUCA1GLB1MEN1LMNA
SCHEMBL2829330 0.85 LMNA (0.43) TSHRMEN1LMNAKMT2ACYP3A4
SCHEMBL24418103 0.84 MEN1 (0.40) TSHRFUCA1GLB1MEN1LMNA
Hydrochloric Acid SCHEMBL2829328 0.84 LMNA (0.42) TSHRMEN1LMNAKMT2ACYP3A4
SCHEMBL23084653 0.83 MIF (0.32)
SCHEMBL3277593 0.82 SLC7A5 (0.31)
SCHEMBL14905976 0.81 CHRM3 (0.36) TSHRFUCA1LMNAKMT2AMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122079832-A Selective reduction method of ketal (acetal) for preparing darifene epoxy intermediate 2026-05-26 CN claimed
CN-113677658-B Flow synthesis method for producing oseltamivir 纳尔逊·曼德拉大学 2024-12-10 CN claimed
EP-3938343-B1 FLOW SYNTHESIS PROCESS FOR THE PRODUCTION OF OSELTAMIVIR NELSON MANDELA UNIV (ZA) 2024-10-09 EP claimed
CN-118580147-A Synthesis process of ethyl shikimate catalyzed by cation exchange resin 浙江得乐康食品股份有限公司 2024-09-03 CN claimed
CN-118084963-A Preparation method of prostaglandin intermediate protected by silicon reagent 华东理工大学 2024-05-28 CN claimed
CN-116836075-A Preparation method of oseltamivir phosphate catalyzed by azide-free palladium-free catalyst 华东理工大学 2023-10-03 CN claimed
CN-113677658-A Flow synthesis method for producing oseltamivir 纳尔逊·曼德拉大学 2021-11-19 CN claimed
CN-102816078-A Preparation method of N-(5-methoxycarbonyl-2-hydroxyphenyl) amino acid ester compounds CAS GUANGZHOU CHEMISTRY CO LTD 2012-12-12 CN claimed
CN-101538221-A Preparation method of Oseltamivir phosphate UNIV EAST CHINA SCIENCE & TECH 2009-09-23 CN claimed
CN-122079832-A Selective reduction method of ketal (acetal) for preparing darifene epoxy intermediate 2026-05-26 CN disclosed
CN-122079832-A Selective reduction method of ketal (acetal) for preparing darifene epoxy intermediate 2026-05-26 CN disclosed
CN-113677658-B Flow synthesis method for producing oseltamivir 纳尔逊·曼德拉大学 2024-12-10 CN disclosed
CN-118580147-A Synthesis process of ethyl shikimate catalyzed by cation exchange resin 浙江得乐康食品股份有限公司 2024-09-03 CN disclosed
CN-118580147-A Synthesis process of ethyl shikimate catalyzed by cation exchange resin 浙江得乐康食品股份有限公司 2024-09-03 CN disclosed
WO-2009079876-A1 3-ACYLATED SHIKIMIC ACID OR METHYL (ETHYL) SHIKIMATE JIANGNAN UNIVERSITY (CN) 2009-07-02 WO disclosed
WO-2009079876-A1 3-ACYLATED SHIKIMIC ACID OR METHYL (ETHYL) SHIKIMATE JIANGNAN UNIVERSITY (CN) 2009-07-02 WO disclosed
CN-101351438-A Epoxide intermediate in the tamiflu synthesis ROCHE PALO ALTO LLC (CH) 2009-01-21 CN disclosed
US-7473798-B2 Derivatives of unsaturated, cyclic organic acids ROCHE PALO ALTO LLC (US) 2009-01-06 US disclosed
US-20070197807-A1 Derivatives of unsaturated, cyclic organic acids GABEL RICHARD A 2007-08-23 US disclosed
WO-2007074091-A2 EPOXIDE INTERMEDIATE IN THE TAMIFLU SYNTHESIS F. HOFFMANN-LA ROCHE AG (CH) 2007-07-05 WO 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 (1 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-20070197807-A1 Derivatives of unsaturated, cyclic organic acids ALOX5, VKORC1, ELOVL5 TSHR 4005/4885FUCA1 3922/4885GLB1 1945/4885

“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.