SCHEMBL736623

SCHEMBL736623

CCCCCCCCCCCCO[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O

nearest known ligand 0.66

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ GBA1 P04062 5/20 0.59
▸ SLC2A1 P11166 1/20 0.54
▸ MAPK1 P28482 1/20 0.53
▸ LGALS8 O00214 1/20 0.46
▸ LGALS3 P17931 1/20 0.46
▸ LGALS4 P56470 1/20 0.46
▸ GJB2 P29033 1/20 0.46
▸ ADORA2A P29274 1/20 0.41
▸ ADORA2B P29275 1/20 0.41
▸ TNF P01375 1/20 0.40
▸ CETP P11597 1/20 0.39
▸ PTPN1 P18031 1/20 0.39

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
SCHEMBL4910764 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3
SCHEMBL8017553 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3
SCHEMBL6565021 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3
SCHEMBL1134697 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3
SCHEMBL4803964 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3
SCHEMBL4351721 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3
SCHEMBL23646744 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3
SCHEMBL4595842 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3
SCHEMBL10715427 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3
SCHEMBL3389904 1.00 GBA1 (0.59) GBA1SLC2A1MAPK1LGALS8LGALS3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119139931-B Preparation method of efficient boron-removing reverse osmosis membrane 山东纳飞博科技发展有限公司 2025-04-04 — — CN disclosed
CN-119139931-A Preparation method of efficient boron-removing reverse osmosis membrane 山东纳飞博科技发展有限公司 2024-12-17 — — CN disclosed
EP-4397374-A2 IMPROVED PEPTIDE PHARMACEUTICALS FOR INSULIN RESISTANCE Mederis Diabetes, LLC (US) 2024-07-10 — — EP disclosed
US-11911447-B2 Peptide pharmaceuticals for insulin resistance MEDERIS DIABETES LLC (US) 2024-02-27 — — US disclosed
EP-3155017-B1 IMPROVED PEPTIDE PHARMACEUTICALS FOR INSULIN RESISTANCE MEDERIS DIABETES LLC (US) 2024-01-10 — — EP disclosed
EP-4286400-A2 IMPROVED PEPTIDE PHARMACEUTICALS Eumederis Pharmaceuticals, Inc. (US) 2023-12-06 — — EP disclosed
EP-2709645-B1 IMPROVED PEPTIDE PHARMACEUTICALS EUMEDERIS PHARMACEUTICALS INC (US) 2023-08-09 — — EP disclosed
US-20230218564-A1 PEPTIDE PHARMACEUTICALS FOR TREATMENT OF NASH AND OTHER DISORDERS MEDERIS DIABETES LLC (US) 2023-07-13 — — US disclosed
US-11541028-B2 Peptide pharmaceuticals for treatment of NASH and other disorders ALTIMMUNE INC. (US) 2023-01-03 — — US disclosed
EP-3444281-B1 IMPROVED PEPTIDE PHARMACEUTICALS EUMEDERIS PHARMACEUTICALS INC (US) 2021-11-03 — — EP disclosed
WO-2012158965-A2 IMPROVED PEPTIDE PHARMACEUTICALS FOR INSULIN RESISTANCE MEDERIS DIABETES, LLC (US) 2012-11-22 — — WO disclosed
WO-2012158964-A2 IMPROVED PEPTIDE PHARMACEUTICALS FOR OSTEOPOROSIS EUMEDERIS PHARMACEUTICALS, INC. (US) 2012-11-22 — — WO disclosed
US-8137975-B2 Method for a rapid antibody-based analysis of platelet populations BECKMAN COULTER, INC. (US) 2012-03-20 — — US disclosed
US-7674598-B2 Method for a fully automated monoclonal antibody-based extended differential BECKMAN COULTER, INC. (US) 2010-03-09 — — US disclosed
US-20090111118-A1 METHOD FOR A RAPID ANTIBODY-BASED ANALYSIS OF PLATELET POPULATIONS BECKMAN COULTER, INC. (US) 2009-04-30 — — US disclosed
WO-2008002745-A2 METHOD FOR A FULLY AUTOMATED MONOCLONAL ANTIBODY-BASED EXTENDED DIFFERENTIAL BECKMAN COULTER, INC. (US) 2008-01-03 — — WO disclosed
US-20060269970-A1 Method for a fully automated monoclonal antibody-based extended differential BECKMAN COULTER, INC. (US) 2006-11-30 — — US disclosed
EP-0378710-A1 Process for the preparation of alkyl glycosides UNILEVER N.V. (NL) 1990-07-25 — — EP disclosed
EP-0187798-A1 PROCESS FOR THE SYNTHESIS OF ALDOSIDES OR OLIGOALDOSIDES OF ALKYL, CYCLOALKYL OR ALKENYL. BEGHIN SAY SA (FR) 1986-07-23 — — EP disclosed
WO-1986000906-A1 PROCESS FOR THE SYNTHESIS OF ALDOSIDES OR POLYALDOSIDES OF ALKYL, CYCLOALKYL OR ALKENYL BEGHIN-SAY SA (FR) 1986-02-13 — — 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 (3 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-11911447-B2 Peptide pharmaceuticals for insulin resistance IAPP, GLP1R, PTMS GBA1 2974/4885SLC2A1 125/4885MAPK1 2392/4885
US-20230218564-A1 PEPTIDE PHARMACEUTICALS FOR TREATMENT OF NASH AND OTHER DISORDERS GLP1R, IAPP, GPR119 GBA1 3581/4885SLC2A1 269/4885MAPK1 3386/4885
US-11541028-B2 Peptide pharmaceuticals for treatment of NASH and other disorders GLP1R, IAPP, GPR119 GBA1 3581/4885SLC2A1 269/4885MAPK1 3386/4885

“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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