SCHEMBL799467

SCHEMBL799467

O=C(O)[C@H]1C[C@@H]1c1ccc(Br)cc1

nearest known ligand 0.59

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
FFAR1 O14842 7/20 0.59
KDM1A O60341 5/20 0.50
HRH3 Q9Y5N1 2/20 0.50
KCNH2 Q12809 2/20 0.50
MAOB P27338 2/20 0.50
RCOR1 Q9UKL0 2/20 0.50
HDAC4 P56524 1/20 0.50
KDM1B Q8NB78 1/20 0.50
ALDH1A1 P00352 1/20 0.44
HTR2C P28335 2/20 0.44
HTR2B P41595 2/20 0.44
AGTR2 P50052 1/20 0.43

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
SCHEMBL4719284 1.00 FFAR1 (0.59) FFAR1KDM1AHRH3KCNH2MAOB
SCHEMBL455245 1.00 FFAR1 (0.59) FFAR1KDM1AHRH3KCNH2MAOB
SCHEMBL806142 1.00 FFAR1 (0.59) FFAR1KDM1AHRH3KCNH2MAOB
SCHEMBL455246 1.00 FFAR1 (0.59) FFAR1KDM1AHRH3KCNH2MAOB
SCHEMBL437376 1.00 FFAR1 (0.59) FFAR1KDM1AHRH3KCNH2MAOB
SCHEMBL21501045 1.00 FFAR1 (0.59) FFAR1KDM1AHRH3KCNH2MAOB
SCHEMBL24890441 0.84 KDM1A (0.50) FFAR1KDM1AHRH3KCNH2MAOB
SCHEMBL799464 0.82 HRH3 (0.49) FFAR1KDM1AHRH3KCNH2MAOB
SCHEMBL4133964 0.82 KDM1A (0.53) FFAR1KDM1AHRH3KCNH2MAOB
SCHEMBL4133967 0.82 KDM1A (0.53) FFAR1KDM1AHRH3KCNH2MAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260108546-A1 GIP RECEPTOR AGONIST COMPOUNDS LILLY CO ELI (US) 2026-04-23 US disclosed
EP-4709708-A1 NOVEL CARBOXAMIDE DERIVATIVES ANGELINI PHARMA S.P.A. (IT) 2026-03-18 EP disclosed
WO-2025264700-A1 GIP RECEPTOR AGONIST COMPOUNDS ELI LILLY AND COMPANY (US) 2025-12-26 WO disclosed
WO-2025106910-A1 DEGRADER MOLECULES TARGETING ANDROGEN RECEPTOR FLARE THERAPEUTICS INC. (US) 2025-05-22 WO disclosed
WO-2024233603-A1 NOVEL CARBOXAMIDE DERIVATIVES ICAGEN, LLC (US) 2024-11-14 WO disclosed
WO-2023284651-A1 N-(2-AMINOPHENYL)BENZAMIDE COMPOUND AND APPLICATION THEREOF 南京明德新药研发有限公司 2023-01-19 WO disclosed
US-11021427-B2 Pd(II)-catalyzed enantioselective C—H arylation of free carboxylic acids THE SCRIPPS RESEARCH INSTITUTE (US) 2021-06-01 US disclosed
US-10329256-B2 (Hetero)aryl cyclopropylamine compounds as LSD1 inhibitors ORYZON GENOMICS, S.A. (ES) 2019-06-25 US disclosed
US-10233178-B2 Arylcyclopropylamine based demethylase inhibitors of LSD1 and their medical use ORYZON GENOMICS, S.A. (ES) 2019-03-19 US disclosed
US-20180127406-A1 ARYLCYCLOPROPYLAMINE BASED DEMETHYLASE INHIBITORS OF LSD1 AND THEIR MEDICAL USE ORYZON GENOMICS SA (ES) 2018-05-10 US disclosed
US-20120071651-A1 Processes for Preparing 1,2-Substituted Cyclopropyl Derivatives ABBOTT LABORATORIES (US) 2012-03-22 US disclosed
US-20120071651-A1 Processes for Preparing 1,2-Substituted Cyclopropyl Derivatives ABBOTT LABORATORIES (US) 2012-03-22 US disclosed
US-20110201622-A1 Solid Forms Comprising A Cyclopropyl Amide Derivative ASTRAZENECA PHARMACEUTICALS LP 2011-08-18 US disclosed
US-20110201622-A1 Solid Forms Comprising A Cyclopropyl Amide Derivative ASTRAZENECA PHARMACEUTICALS LP 2011-08-18 US disclosed
US-20110201623-A1 Crystalline Form Of A Cyclopropyl Benzamide Derivative ASTRAZENECA PHARMACEUTICALS LP 2011-08-18 US disclosed
US-20110201623-A1 Crystalline Form Of A Cyclopropyl Benzamide Derivative ASTRAZENECA PHARMACEUTICALS LP 2011-08-18 US disclosed
US-20110201623-A1 Crystalline Form Of A Cyclopropyl Benzamide Derivative ASTRAZENECA PHARMACEUTICALS LP 2011-08-18 US disclosed
US-20100216812-A1 Cyclopropyl Amide Derivatives ASTRAZENECA AB (SE) 2010-08-26 US disclosed
US-20100216812-A1 Cyclopropyl Amide Derivatives ASTRAZENECA AB (SE) 2010-08-26 US disclosed
US-20100216812-A1 Cyclopropyl Amide Derivatives ASTRAZENECA AB (SE) 2010-08-26 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 (9 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-20110201622-A1 Solid Forms Comprising A Cyclopropyl Amide Derivative SFPQ, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, SBDS FFAR1 2695/4885KDM1A 878/4885HRH3 1977/4885
US-10233178-B2 Arylcyclopropylamine based demethylase inhibitors of LSD1 and their medical use KDM6A, KDM1B, KDM1A FFAR1 2820/4885KDM1A 3/4885HRH3 730/4885
US-20180127406-A1 ARYLCYCLOPROPYLAMINE BASED DEMETHYLASE INHIBITORS OF LSD1 AND THEIR MEDICAL USE KDM6A, KDM1B, KDM1A FFAR1 2820/4885KDM1A 3/4885HRH3 730/4885
US-20100216812-A1 Cyclopropyl Amide Derivatives HRH4, HRH2, HRH3 FFAR1 48/4885KDM1A 760/4885HRH3 3/4885
US-20260108546-A1 GIP RECEPTOR AGONIST COMPOUNDS GIPR, GLP1R, GCGR FFAR1 65/4885KDM1A 4614/4885HRH3 600/4885
US-11021427-B2 Pd(II)-catalyzed enantioselective C—H arylation of free carboxylic acids PDCD1, PDK3, PDCD1LG2 FFAR1 119/4885KDM1A 1577/4885HRH3 49/4885
US-20120071651-A1 Processes for Preparing 1,2-Substituted Cyclopropyl Derivatives HRH3, HRH4, HRH1 FFAR1 211/4885KDM1A 1116/4885HRH3 1/4885
US-10329256-B2 (Hetero)aryl cyclopropylamine compounds as LSD1 inhibitors KDM1B, KDM1A, KDM2A FFAR1 3080/4885KDM1A 2/4885HRH3 435/4885
US-20110201623-A1 Crystalline Form Of A Cyclopropyl Benzamide Derivative GBA1, BAK1, BBC3 FFAR1 854/4885KDM1A 2260/4885HRH3 653/4885

“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.