SCHEMBL6833949

SCHEMBL6833949

CC(=O)N[C@H]1[C@@H](OCc2ccccc2)O[C@@H]2COC(c3ccccc3)O[C@H]2[C@@H]1OC(C)C(=O)O

nearest known ligand 0.77

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 3/20 0.77
▸ KMT2A Q03164 3/20 0.42
▸ MEN1 O00255 1/20 0.42
▸ SELP P16109 1/20 0.41
▸ ALDH1A1 P00352 3/20 0.39
▸ PKM P14618 1/20 0.38
▸ POLB P06746 1/20 0.37
▸ MAPK1 P28482 1/20 0.37
▸ MAG P20916 1/20 0.36
▸ LMNA P02545 1/20 0.34
▸ KLK7 P49862 1/20 0.33
▸ KLK5 Q9Y337 1/20 0.33
▸ TACR1 P25103 1/20 0.33
▸ HRAS P01112 1/20 0.33
▸ BCHE P06276 1/20 0.32

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
SCHEMBL15513804 1.00 L3MBTL1 (0.77) L3MBTL1KMT2AMEN1SELPALDH1A1
SCHEMBL10545105 1.00 L3MBTL1 (0.77) L3MBTL1KMT2AMEN1SELPALDH1A1
SCHEMBL11565600 1.00 L3MBTL1 (0.77) L3MBTL1KMT2AMEN1SELPALDH1A1
SCHEMBL10543455 1.00 L3MBTL1 (0.77) L3MBTL1KMT2AMEN1SELPALDH1A1
SCHEMBL8571903 1.00 L3MBTL1 (0.77) L3MBTL1KMT2AMEN1SELPALDH1A1
SCHEMBL8332499 1.00 L3MBTL1 (0.77) L3MBTL1KMT2AMEN1SELPALDH1A1
SCHEMBL10542172 1.00 L3MBTL1 (0.77) L3MBTL1KMT2AMEN1SELPALDH1A1
SCHEMBL14612249 0.93 L3MBTL1 (0.74) L3MBTL1KMT2AMEN1SELPALDH1A1
SCHEMBL22607623 0.93 L3MBTL1 (0.74) L3MBTL1KMT2AMEN1SELPALDH1A1
SCHEMBL8334325 0.93 L3MBTL1 (0.74) L3MBTL1KMT2AMEN1SELPALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040028702-A1 Muramic acid derivative compounds MALETIC MILANA M (US) 2004-02-12 — — US disclosed
US-6562514-B1 Stabilized vanadium electrolyte solutions for all-vanadium redox cells and batteries PINNACLE VRB LIMITED (AU) 2003-05-13 — — US disclosed
US-6468688-B2 CHARGING, DISCHARGING EFFICIENCY; VANADIUM ELECTROLYTE PINNACLE VRB LIMITED (AU) 2002-10-22 — — US disclosed
US-20010028977-A1 Charging, discharging efficiency; vanadium electrolyte JD HOLDING INC. (KY) 2001-10-11 — — US disclosed
US-6143443-A ALL-VANADIUM REDOX BATTERY, COMPRISING THE STABILIZED ELECTROLYTE PINNACLE ARB LIMITED (AU) 2000-11-07 — — US disclosed
EP-0829104-A1 HIGH ENERGY DENSITY VANADIUM ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND ALL-VANADIUM REDOX CELLS AND BATTERIES CONTAINING HIGH ENERGY VANADIUM ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1998-03-18 — — EP disclosed
EP-0729648-A4 STABILISED ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND REDOX CELLS AND BATTERIES CONTAINING STABILISED ELECTROLYTE SOLUTIONS UNISEARCH LTD (AU) 1997-01-02 — — EP disclosed
WO-1996035239-A1 HIGH ENERGY DENSITY VANADIUM ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND ALL-VANADIUM REDOX CELLS AND BATTERIES CONTAINING HIGH ENERGY VANADIUM ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1996-11-07 — — WO disclosed
EP-0729648-A1 STABILISED ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND REDOX CELLS AND BATTERIES CONTAINING STABILISED ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1996-09-04 — — EP disclosed
WO-1995012219-A1 STABILISED ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND REDOX CELLS AND BATTERIES CONTAINING STABILISED ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1995-05-04 — — WO disclosed
US-4377570-A Immunologically active dipeptidyl saccharides and methods of preparation MERCK & CO., INC. (US) 1983-03-22 — — US disclosed
US-4369178-A Glucosamine peptide derivatives, their production and use TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1983-01-18 — — US disclosed
EP-0014984-B1 GLUCOSAMINE-PEPTIDE DERIVATIVES, THEIR PRODUCTION AND USE Takeda Chemical Industries, Ltd. (JP) 1982-12-01 — — EP disclosed
EP-0014159-B1 IMMUNOLOGICALLY ACTIVE DIPEPTIDYL SACCHARIDES AND METHODS OF PREPARATION MERCK & CO. INC. (US) 1982-07-14 — — EP disclosed
US-4256735-A BACTERICIDES MERCK & CO., INC. (US) 1981-03-17 — — US disclosed
EP-0014984-A1 Glucosamine-peptide derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1980-09-03 — — EP disclosed
EP-0014159-A1 Immunologically active dipeptidyl saccharides and methods of preparation MERCK & CO. INC. (US) 1980-08-06 — — EP disclosed
US-4172125-A Oil-free adjuvant compositions containing N-acetyl-muramyl-L-alanyl-D-glutamic acid and method of use AGENCE NATIONALE DE VALORISATION DE LA RECHERCHE (ANVAR) (FR) 1979-10-23 — — US disclosed
EP-0002677-A1 Glucosamine-peptide derivatives and their pharmaceutical compositions Takeda Chemical Industries, Ltd. (JP) 1979-07-11 — — EP disclosed
US-4082736-A NOVEL IMMUNOLOGICAL ADJUVANT COMPOUNDS AND METHODS OF PREPARATION THEREOF SYNTEX (U.S.A.) INC. (US) 1978-04-04 — — 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 (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-20040028702-A1 Muramic acid derivative compounds APEH, PEPD, OGT L3MBTL1 3336/4885KMT2A 1922/4885MEN1 3763/4885

“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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