SCHEMBL5120243

SCHEMBL5120243

COC(=O)COc1ccc(Cl)cc1

nearest known ligand 0.81

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ PTGS2 P35354 1/20 0.81
▸ L3MBTL1 Q9Y468 3/20 0.59
▸ ALDH1A1 P00352 2/20 0.59
▸ CYP2C19 P33261 2/20 0.59
▸ MEN1 O00255 1/20 0.59
▸ KMT2A Q03164 1/20 0.59
▸ CYP1A2 P05177 1/20 0.59
▸ CYP3A4 P08684 1/20 0.59
▸ BLM P54132 1/20 0.58
▸ PMP22 Q01453 1/20 0.58
▸ SMN1; SMN2 Q16637 1/20 0.55
▸ ATF4 P18848 4/20 0.54
▸ MAPT P10636 2/20 0.54
▸ LMNA P02545 2/20 0.54
▸ KDM4E B2RXH2 1/20 0.54
▸ TDP1 Q9NUW8 1/20 0.54
▸ NPSR1 Q6W5P4 1/20 0.53
▸ CYP2C9 P11712 1/20 0.53

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
SCHEMBL11872199 0.95 PTGS2 (0.74) PTGS2L3MBTL1ALDH1A1CYP2C19MEN1
SCHEMBL23605967 0.90 PTGS2 (0.68) PTGS2L3MBTL1ALDH1A1MAPTTDP1
SCHEMBL2116437 0.90 PTGS2 (0.66) PTGS2L3MBTL1ALDH1A1CYP2C19MEN1
SCHEMBL24805907 0.85 PTGS2 (0.62) PTGS2L3MBTL1ALDH1A1MEN1KMT2A
SCHEMBL17365269 0.84 PTGS2 (0.60) PTGS2L3MBTL1ALDH1A1CYP2C19MEN1
SCHEMBL12061812 0.84 GAA (0.66) PTGS2L3MBTL1ALDH1A1CYP2C19MEN1
SCHEMBL3913180 0.84 PTGS2 (0.60) PTGS2L3MBTL1ALDH1A1CYP2C19MEN1
SCHEMBL11151346 0.83 PTGS2 (0.59) PTGS2L3MBTL1ALDH1A1CYP2C19MEN1
SCHEMBL13935133 0.82 PTGS2 (0.58) PTGS2L3MBTL1ALDH1A1CYP2C19MEN1
SCHEMBL7068289 0.82 LMNA (0.59) PTGS2L3MBTL1CYP2C19CYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101391969-B Method for preparing N-methyl-2-(2,4-dichlorophenoxy) acetamide SHANGHAI INST TECHNOLOGY 2012-05-09 — — CN claimed
CN-101391968-A N-ethyl-2-(4-chlorophenoxy) acetamide and preparation method thereof SHANGHAI INST TECHNOLOGY (CN) 2009-03-25 — — CN claimed
CN-101391969-A Method for preparing N-methyl-2-(2,4-dichlorophenoxy) acetamide SHANGHAI INST TECHNOLOGY (CN) 2009-03-25 — — CN claimed
US-4145432-A 6-ACYLORYALKYL-1,4-DIHYDROPYRIDINE DERIVATIVES AND A METHOD OF EFFECTING VASODILATION THEREWITH FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1979-03-20 — — US claimed
US-20240327323-A1 Methods of Treating of Halogen- Containing Waste Plastic to Produce Halogenated Products U. S. DEPARTMENT OF ENERGY 2024-10-03 — — US disclosed
CN-111201245-B Compounds, compositions, and methods 戴纳立制药公司 2024-04-05 — — CN disclosed
CN-117736082-A Preparation method of phenoxy carboxylic acid herbicide 山东润博生物科技有限公司 2024-03-22 — — CN disclosed
CN-117645540-A Preparation method of chlorophenoxycarboxylate 山东润博生物科技有限公司 2024-03-05 — — CN disclosed
CN-117466730-A Preparation method of phenoxy carboxylate herbicide 山东润博生物科技有限公司 2024-01-30 — — CN disclosed
CN-115260049-B Method for preparing 2-chloro-N-methylacetanilide by taking wheat straw lignin as raw material 宿州学院 2023-11-07 — — CN disclosed
US-20230165848-A1 CHEMICAL COMPOUNDS GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED (GB) 2023-06-01 — — US disclosed
US-20230165848-A1 CHEMICAL COMPOUNDS GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED (GB) 2023-06-01 — — US disclosed
US-7169794-B2 6-substituted pyrido-pyrimidines ROCHE PALO ALTO LLC (US) 2007-01-30 — — US disclosed
EP-1361880-B1 6-SUBSTITUTED PYRIDO-PYRIMIDINES HOFFMANN LA ROCHE (CH) 2005-09-28 — — EP disclosed
US-20040116698-A1 6-Substituted pyrido-pyrimidines CHEN JIAN JEFFREY (US) 2004-06-17 — — US disclosed
US-6696566-B2 SELECTIVE P38 KINASE INHIBITORS RELATIVE TO CYCLIN-DEPENDENT KINASES AND TYROSINE KINASES SYNTEX (U.S.A.) LLC 2004-02-24 — — US disclosed
EP-1361880-A2 6-SUBSTITUTED PYRIDO-PYRIMIDINES F. HOFFMANN-LA ROCHE AG (CH) 2003-11-19 — — EP disclosed
US-20030171584-A1 Treating p38 mediated disorders such as arthritis, Crohns disease, irritable bowel syndrome adult respiratory distress syndrome or chronic obstructive pulmonary disease. SYNTEX (U.S.A.) LLC 2003-09-11 — — US disclosed
WO-2002064594-A2 6-SUBSTITUTED PYRIDO-PYRIMIDINES F. HOFFMANN-LA ROCHE AG (CH) 2002-08-22 — — WO disclosed
US-5185341-A Antiamnestic, antihypoxic compounds ARZNEIMITTELWERK DRESDEN GMBH (DE) 1993-02-09 — — 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 (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-20240327323-A1 Methods of Treating of Halogen- Containing Waste Plastic to Produce Halogenated Products VCL, SLC6A12, TPO PTGS2 4104/4885L3MBTL1 1845/4885ALDH1A1 1975/4885
US-20230165848-A1 CHEMICAL COMPOUNDS ATF4, XBP1, EIF2B5 PTGS2 1508/4885L3MBTL1 260/4885ALDH1A1 3046/4885
US-20030171584-A1 Treating p38 mediated disorders such as arthritis, Crohns disease, irritable bowel syndrome adult respiratory distress syndrome or chronic obstructive pulmonary disease. ARRB1, MAPK1, MAPK8 PTGS2 391/4885L3MBTL1 3254/4885ALDH1A1 1614/4885

“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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