SCHEMBL1140728

SCHEMBL1140728

CC(=O)OC[C@H]1O[C@H](O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP2D6 P10635 1/20 0.60
▸ THRB P10828 1/20 0.60
▸ HSD17B10 Q99714 1/20 0.60
▸ TSHR P16473 1/20 0.58
▸ NR3C1 P04150 1/20 0.58
▸ FYN P06241 1/20 0.58
▸ ADRA2A P08913 1/20 0.58
▸ ADORA3 P0DMS8 1/20 0.58
▸ ADRA2B P18089 1/20 0.58
▸ DRD4 P21917 1/20 0.58
▸ DRD3 P35462 1/20 0.58
▸ CA2 P00918 12/20 0.57
▸ CA12 O43570 11/20 0.57
▸ CA1 P00915 11/20 0.57
▸ CA9 Q16790 6/20 0.57
▸ PKM P14618 1/20 0.52
▸ PTPN1 P18031 1/20 0.52
▸ CA4 P22748 7/20 0.50
▸ CA5A P35218 7/20 0.50
▸ CA7 P43166 7/20 0.50

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
SCHEMBL1582590 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1
SCHEMBL133580 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1
SCHEMBL18652541 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1
SCHEMBL13465295 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1
SCHEMBL3188307 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1
SCHEMBL18880355 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1
SCHEMBL12569416 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1
SCHEMBL133581 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1
SCHEMBL22766232 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1
SCHEMBL17119468 1.00 CYP2D6 (0.60) CYP2D6THRBHSD17B10TSHRNR3C1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114773409-B Preparation method of 2,3,4, 6-tetra-O-acetyl-glucopyranose 江西艾立斯特生物科技有限公司 2023-12-15 — — CN claimed
CN-114773409-A Preparation method of 2,3,4, 6-tetra-O-acetyl-glucopyranose 江西艾立斯特生物科技有限公司 2022-07-22 — — CN claimed
US-20190048202-A1 METHOD FOR THE PREPARATION OF A COATING COMPRISING OLIGOMERIC ALKYNES ÉCOLE POLYTECHNIQUE FÉDÉRALE DE LAUSANNE (EPFL) EPFL-TTO (CH) 2019-02-14 — — US claimed
WO-2016174266-A2 METHOD FOR THE PREPARATION OF A COATING ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL) EPFL-TTO (CH) 2016-11-03 — — WO claimed
EP-0867431-B1 Process for the preparation of azide derivatives EISAI CO LTD (JP) 2002-06-05 — — EP claimed
US-5986088-A Process for the preparation of azide derivatives EISAI CO., LTD. (JP) 1999-11-16 — — US claimed
EP-0867431-A1 Process for the preparation of azide derivatives Eisai Chemical Co., Ltd. (JP) 1998-09-30 — — EP claimed
EP-0511917-B1 Glycosylated prodrugs, process for their preparation and uses thereof HOECHST SA LAB (FR) 1996-10-23 — — EP claimed
WO-1992019639-A1 GLYCOSYLATED PRODRUGS, METHOD OF PREPARATION AND USE LABORATOIRES HOECHST (FR) 1992-11-12 — — WO claimed
EP-0511917-A1 Glycosylated prodrugs, process for their preparation and uses thereof LABORATOIRES HOECHST S.A. (FR) 1992-11-04 — — EP claimed
US-20260109721-A1 IONIZABLE CATIONIC LIPIDS INCORPORATING SILICON: SYNTHESIS AND LNP FORMULATION ALDEXCHEM KFT (HU) 2026-04-23 — — US disclosed
US-12552823-B2 Glucosamine derivatives and pharmaceutical uses thereof Risen (Suzhou) Pharma Tech Co., Ltd. (CN) 2026-02-17 — — US disclosed
US-20260022140-A1 3'-KETOGLYCOSIDE COMPOUND FOR THE SLOW RELEASE OF A VOLATILE ALCOHOL GLYCOSCIENCE, S.L. (ES) 2026-01-22 — — US disclosed
US-20260008793-A1 IONIZABLE CATIONIC LIPIDS INCORPORATING SILICON ALDEXCHEM KFT (HU) 2026-01-08 — — US disclosed
US-12509482-B2 3′-ketoglycoside compound for the slow release of a volatile alcohol GLYCOSCIENCE, S.L. (ES) 2025-12-30 — — US disclosed
US-4868289-A INTERFERE WITH BINDING OF VIRUSES AND BACTERIA, USEFUL AGAINST INFECTION AND FOR DIAGNOSIS SYMBICOM AKTIEBOLAG (SE) 1989-09-19 — — US disclosed
US-4855417-A Anomeric deacetylation YEDA RESEARCH AND DEVELOPMENT COMPANY LTD (IL) 1989-08-08 — — US disclosed
US-4792615-A HYDROLYSIS OF A-DIHYDROPOLYPRENYL DICHLOROPHOSPHATE WITH ALKALI OR ALKALINE EARTH METAL HYDROXIDE; POLYISOPRENE NAKAGAWA NAOSHI (JP) 1988-12-20 — — US disclosed
EP-0208749-A1 GLYCOSIDIC DERIVATIVES. SYNTEK AB (SE) 1987-01-21 — — EP disclosed
WO-1986004065-A1 GLYCOSIDIC DERIVATIVES SYN-TEK AB (SE) 1986-07-17 — — 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 (5 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-20260022140-A1 3'-KETOGLYCOSIDE COMPOUND FOR THE SLOW RELEASE OF A VOLATILE ALCOHOL GPR35, DPY30, ERG28 CYP2D6 3066/4885THRB 3043/4885HSD17B10 1795/4885
US-12552823-B2 Glucosamine derivatives and pharmaceutical uses thereof SOST, FUT6, SLC5A1 CYP2D6 1419/4885THRB 819/4885HSD17B10 4261/4885
US-20260008793-A1 IONIZABLE CATIONIC LIPIDS INCORPORATING SILICON SGMS1, SGMS2, AGO2 CYP2D6 4447/4885THRB 3687/4885HSD17B10 2337/4885
US-12509482-B2 3′-ketoglycoside compound for the slow release of a volatile alcohol EBP, MGAT1, MGAT3 CYP2D6 2139/4885THRB 437/4885HSD17B10 700/4885
US-20260109721-A1 IONIZABLE CATIONIC LIPIDS INCORPORATING SILICON: SYNTHESIS AND LNP FORMULATION SGMS1, SGMS2, AGO2 CYP2D6 4702/4885THRB 2565/4885HSD17B10 3336/4885

“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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