SCHEMBL6883728

SCHEMBL6883728

Cc1ccc(OCCCC(=O)O)cc1

nearest known ligand 0.82

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 2/20 0.82
▸ FFAR4 Q5NUL3 1/20 0.65
▸ TSHR P16473 1/20 0.62
▸ MEN1 O00255 2/20 0.57
▸ KMT2A Q03164 2/20 0.57
▸ HPGD P15428 2/20 0.56
▸ HTT P42858 1/20 0.56
▸ ALDH1A1 P00352 1/20 0.56
▸ PPARG P37231 1/20 0.56
▸ PPARA Q07869 2/20 0.56
▸ CYP1A2 P05177 1/20 0.55
▸ CYP3A4 P08684 1/20 0.55
▸ CYP2C9 P11712 1/20 0.55
▸ CYP2C19 P33261 1/20 0.55
▸ PLA2G4B P0C869 1/20 0.54
▸ LMNA P02545 1/20 0.53
▸ DRD2 P14416 1/20 0.52
▸ DRD4 P21917 1/20 0.52
▸ DRD3 P35462 1/20 0.52
▸ NPC1 O15118 1/20 0.51

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
SCHEMBL4257143 0.94 L3MBTL1 (0.79) L3MBTL1FFAR4TSHRMEN1KMT2A
SCHEMBL14570555 0.93 L3MBTL1 (0.77) L3MBTL1FFAR4TSHRPPARGPPARA
SCHEMBL29335714 0.93 L3MBTL1 (0.77) L3MBTL1FFAR4TSHRPPARGPPARA
SCHEMBL13450803 0.93 L3MBTL1 (0.77) L3MBTL1FFAR4TSHRPPARGPPARA
SCHEMBL7691552 0.93 L3MBTL1 (0.77) L3MBTL1FFAR4TSHRPPARGPPARA
SCHEMBL8357754 0.93 L3MBTL1 (0.77) L3MBTL1FFAR4TSHRPPARGPPARA
SCHEMBL1806524 0.90 L3MBTL1 (1.00) L3MBTL1FFAR4TSHRMEN1KMT2A
SCHEMBL31448501 0.90 PPARA (0.65) L3MBTL1FFAR4PPARAPLA2G4BLMNA
SCHEMBL13940016 0.89 L3MBTL1 (0.66) L3MBTL1FFAR4TSHRMEN1KMT2A
SCHEMBL29089242 0.86 PLA2G4B (0.68) L3MBTL1TSHRPPARAPLA2G4BLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4327886-A2 PYRIMIDO- PYRIDAZINONE COMPOUNDS AND USE THEREOF Libertas Bio, Inc. (US) 2024-02-28 — — EP disclosed
EP-3392252-B1 PYRIMIDO- PYRIDAZINONE COMPOUNDS AND USE THEREOF LIBERTAS BIO INC (US) 2023-10-04 — — EP disclosed
EP-4216946-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS Achillion Pharmaceuticals, Inc. (US) 2023-08-02 — — EP disclosed
CN-116437913-A Pharmaceutical compounds for treating complement-mediated disorders 艾其林医药公司 2023-07-14 — — CN disclosed
WO-2022066774-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS ACHILLION PHARMACEUTICALS, INC. (US) 2022-03-31 — — WO disclosed
EP-2748166-B1 PYRIMIDO-PYRIDAZINONE COMPOUNDS AND USE THEREOF ASANA BIOSCIENCES LLC (US) 2018-07-11 — — EP disclosed
WO-2017095898-A1 USES OF PYRIMIDO-PYRIMIDAZINONES TO TREAT CANCER ASANA BIOSCIENCES, LLC (US) 2017-06-08 — — WO disclosed
US-20170157126-A1 USES OF PYRIMIDO-PYRIDAZINONES TO TREAT CANCER ASANA BIOSCIENCES, LLC (US) 2017-06-08 — — US disclosed
US-20160348107-A1 Compositions and Methods for Inhibiting Gene Expression of Hif2alpha SIXTH STREETLENDING PARTNERS, AS THE ADMINISTRATIVE AGENT 2016-12-01 — — US disclosed
US-20160347793-A1 Biologically Cleavable Tetrapeptide Linking Agents SIXTH STREETLENDING PARTNERS, AS THE ADMINISTRATIVE AGENT 2016-12-01 — — US disclosed
US-20080119465-A1 Novel Indoline Compounds LABORATORIES FOURNIER S.A. (FR) 2008-05-22 — — US disclosed
US-20080119465-A1 Novel Indoline Compounds LABORATORIES FOURNIER S.A. (FR) 2008-05-22 — — US disclosed
WO-2007000550-A2 NOVEL INDOLINE COMPOUNDS LABORATOIRES FOURNIER S.A. (FR) 2007-01-04 — — WO disclosed
CN-1200915-C Process for preparing organic compound MITSUI CHEMICALS INC (JP) 2005-05-11 — — CN disclosed
US-20040260039-A1 Process for producing organic compound epoxy resin composition, cured article obtained from the epoxy resin, and semiconductor device obtained with epoxy resin MITSUI CHEMICALS, INC. (JP) 2004-12-23 — — US disclosed
EP-0950649-B1 A process for preparing oxyalkylene derivatives in the presence of phosphine oxides MITSUI CHEMICALS INC (JP) 2003-03-26 — — EP disclosed
US-6130346-A ESTERIFICATION, CARBONATION, SULFONATION, ETHERIFICATION MITSUI CHEMICALS, INC. (JP) 2000-10-10 — — US disclosed
CN-1235141-A Process for preparing organic compound MITSUI CHEMICALS INC (JP) 1999-11-17 — — CN disclosed
EP-0950649-A1 A process for preparing oxyalkylene derivatives in the presence of phosphine oxides Mitsui Chemicals, Inc. (JP) 1999-10-20 — — EP disclosed
US-4563436-A Catalyst component for α-olefin polymerization and method of producing the same MITSUBISHI PETROCHEMICAL CO., LTD. (JP) 1986-01-07 — — 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 (4 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-20080119465-A1 Novel Indoline Compounds GPR119, INSR, IRS1 L3MBTL1 1493/4885FFAR4 125/4885TSHR 681/4885
US-20170157126-A1 USES OF PYRIMIDO-PYRIDAZINONES TO TREAT CANCER MKI67, DPYD, TYMP L3MBTL1 4282/4885FFAR4 3714/4885TSHR 2720/4885
US-20160348107-A1 Compositions and Methods for Inhibiting Gene Expression of Hif2alpha EPAS1, HIF1AN, EGLN2 L3MBTL1 1063/4885FFAR4 3499/4885TSHR 3954/4885
US-20160347793-A1 Biologically Cleavable Tetrapeptide Linking Agents DNPEP, VIP, ANPEP L3MBTL1 99/4885FFAR4 4513/4885TSHR 2805/4885

“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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