SCHEMBL641903

SCHEMBL641903

CCOC(=O)c1cccc(F)c1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.62
SMN1; SMN2 Q16637 1/20 0.62
TDP1 Q9NUW8 1/20 0.62
LMNA P02545 1/20 0.60
NPC1 O15118 1/20 0.60
ELANE P08246 1/20 0.56
CYP4F2 P78329 1/20 0.56
CYP4A11 Q02928 1/20 0.56
THRB P10828 1/20 0.56
ADRB2 P07550 1/20 0.56
ADRB1 P08588 1/20 0.56
ADRB3 P13945 1/20 0.56
CES2 O00748 1/20 0.55
CES1 P23141 1/20 0.55
CA12 O43570 1/20 0.54
CA1 P00915 1/20 0.54
CA2 P00918 1/20 0.54
CA7 P43166 1/20 0.54
CA9 Q16790 1/20 0.54
CA14 Q9ULX7 1/20 0.54

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
SCHEMBL31237097 1.00 POLB (0.62) POLBSMN1; SMN2TDP1LMNANPC1
SCHEMBL7471102 0.91 POLB (0.54) POLBSMN1; SMN2TDP1LMNANPC1
SCHEMBL23817385 0.87 NPC1 (0.52) POLBSMN1; SMN2TDP1LMNANPC1
SCHEMBL110276 0.87 CYP4F2 (0.65) SMN1; SMN2LMNANPC1CYP4F2CYP4A11
SCHEMBL522694 0.86 LMNA (0.64) POLBSMN1; SMN2TDP1LMNANPC1
SCHEMBL6028173 0.86 RAB9A (0.66) POLBSMN1; SMN2TDP1LMNANPC1
SCHEMBL29427226 0.85 CYP4F2 (0.63) POLBSMN1; SMN2NPC1CYP4F2CYP4A11
SCHEMBL28376879 0.85 CYP4F2 (0.63) POLBSMN1; SMN2NPC1CYP4F2CYP4A11
SCHEMBL17479491 0.84 LMNA (0.52) POLBSMN1; SMN2TDP1LMNANPC1
SCHEMBL17459869 0.84 CES2 (0.57) POLBSMN1; SMN2TDP1LMNANPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117946303-A Catalyst, preparation method thereof, method for regulating and controlling ethylene polymerization kinetics behavior and application 中国石油化工股份有限公司 2024-04-30 CN claimed
WO-2023212597-A1 CARBON DIOXIDE CAPTURE AND UTILIZATION AS A CLEAN FEEDSTOCK MICHIGAN TECHNOLOGICAL UNIVERSITY (US) 2023-11-02 WO claimed
US-10224485-B2 Process for preparing a crystalline organic semiconductor material BASF SE (DE) 2019-03-05 US claimed
US-20170012208-A1 ORGANIC SEMICONDUCTOR FORMULATIONS USINVEST LLC 2017-01-12 US claimed
EP-0647615-B1 Process for the preparation of 5-fluoroanthranilic acid alkyl esters and or 5-fluoroanthranilic acid HOECHST AG (DE) 1997-05-28 EP claimed
US-5543550-A NITRATING ALKYL ESTER OF 3-FLUOROBENZOIC ACID DISSOLVED IN SOLVENT-FREE SULFURIC ACID, THEN ADDING WATER, SEPARATION, HYDROLYSIS, PRESSURIZED CATALYTIC HYDROGENATION OF THE NITRATED ACID HOECHST AKTIENGESELLSCHAFT (DE) 1996-08-06 US claimed
US-20250188626-A1 CARBON DIOXIDE CAPTURE AND UTILIZATION AS A CLEAN FEEDSTOCK UNIV MICHIGAN TECH (US) 2025-06-12 US disclosed
CN-120058445-A Method for generating aryl phenol compound by hydroxylation of uranium photocatalytic aryl fluorine compound and application of method 华东师范大学 2025-05-30 CN disclosed
CN-117946303-A Catalyst, preparation method thereof, method for regulating and controlling ethylene polymerization kinetics behavior and application 中国石油化工股份有限公司 2024-04-30 CN disclosed
CN-117946304-A Spherical catalyst component containing fluoroester electron donor, preparation method, catalyst and application thereof in ethylene polymerization 中国石油化工股份有限公司 2024-04-30 CN disclosed
WO-2023212597-A1 CARBON DIOXIDE CAPTURE AND UTILIZATION AS A CLEAN FEEDSTOCK MICHIGAN TECHNOLOGICAL UNIVERSITY (US) 2023-11-02 WO disclosed
EP-3183250-B1 PROCESS FOR PREPARING CRYSTALLINE ORGANIC SEMICONDUCTOR MATERIAL CLAP CO LTD (KR) 2023-10-04 EP disclosed
CN-113912597-B ROR gamma inhibitor, preparation method and medical application thereof 赛诺哈勃药业(成都)有限公司 2023-06-13 CN disclosed
US-20020161227-A1 PROCESS FOR PREPARATION OF SUBSTITUTED AROMATIC COMPOUND MITSUI CHEMICALS, INC. (JP) 2002-10-31 US disclosed
US-6469224-B1 REACTING A PHOSPHAZENIUM COMPOUND WITH A HALOGENATED AROMATIC COMPOUNDS, ESPECIALLY CHLORINATED AROMATIC COMPOUNDS MITSUI CHEMICALS, INC. (JP) 2002-10-22 US disclosed
US-5543550-A NITRATING ALKYL ESTER OF 3-FLUOROBENZOIC ACID DISSOLVED IN SOLVENT-FREE SULFURIC ACID, THEN ADDING WATER, SEPARATION, HYDROLYSIS, PRESSURIZED CATALYTIC HYDROGENATION OF THE NITRATED ACID HOECHST AKTIENGESELLSCHAFT (DE) 1996-08-06 US disclosed
US-5446190-A Process for the preparation of alkyl fluorobenzoates in high purity and high yield HOECHST AKTIENGESELLSCHAFT (DE) 1995-08-29 US disclosed
US-4333940-A Ring-fluorinated 4-(monosubstituted-amino) phenyl compounds in inhibiting atherosclerotic lesion development AMERICAN CYANAMID COMPANY (US) 1982-06-08 US disclosed
US-4243609-A ANTILIPEMIC AGENTS, ANTIATHEROSCLEROTIC AGENTS AMERICAN CYANAMID COMPANY (US) 1981-01-06 US disclosed
EP-0003663-A2 Amino-substituted phenyl and heteroaryl compounds, process for their preparation and pharmaceutical compositions containing them AMERICAN CYANAMID COMPANY (US) 1979-08-22 EP 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 (2 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-10224485-B2 Process for preparing a crystalline organic semiconductor material STOM, SPOP, TTR POLB 1829/4885SMN1; SMN2 4265/4885TDP1 3713/4885
US-20020161227-A1 PROCESS FOR PREPARATION OF SUBSTITUTED AROMATIC COMPOUND H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, AFF1, PAH POLB 460/4885SMN1; SMN2 3858/4885TDP1 2061/4885

“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.