SCHEMBL255259

SCHEMBL255259

CC(C)c1ccccc1Br

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GABRA1 P14867 4/20 0.50
GABRB2 P47870 2/20 0.50
GABRG2 P18507 2/20 0.46
GABRB3 P28472 2/20 0.46
CYP3A4 P08684 2/20 0.46
FAAH O00519 2/20 0.46
CA1 P00915 2/20 0.46
CA2 P00918 2/20 0.46
GABRB1 P18505 2/20 0.46
LMNA P02545 1/20 0.46
CYP1A2 P05177 1/20 0.46
HPGD P15428 1/20 0.46
TSHR P16473 1/20 0.46
PTGS1 P23219 1/20 0.46
SLC6A2 P23975 1/20 0.46
HTR2C P28335 1/20 0.46
GABRA5 P31644 1/20 0.46
GABRA3 P34903 1/20 0.46
HTR2B P41595 1/20 0.46
GABRA2 P47869 1/20 0.46

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
SCHEMBL29428538 1.00 GABRA1 (0.50) GABRA1GABRB2GABRG2GABRB3CYP3A4
SCHEMBL4659907 0.97 GABRA1 (0.48) GABRA1GABRB2GABRG2GABRB3CYP3A4
SCHEMBL5713283 0.83 HTT (0.44) GABRA1GABRB2GABRG2GABRB3CYP3A4
SCHEMBL1044900 0.81 HTT (0.47) GABRA1GABRB2GABRG2GABRB3CYP3A4
SCHEMBL1368986 0.81 HTT (0.43) GABRA1GABRB2GABRG2GABRB3CYP3A4
SCHEMBL3293339 0.81 HTT (0.43) GABRA1GABRB2GABRG2GABRB3CYP3A4
SCHEMBL3296582 0.81 HTT (0.43) GABRA1GABRB2GABRG2GABRB3CYP3A4
SCHEMBL4427313 0.80 CA1 (0.46) GABRA1GABRB2GABRG2GABRB3CYP3A4
SCHEMBL1454663 0.79 CYP3A4 (0.45) CYP3A4LMNACYP1A2HIF1AHTT
SCHEMBL22416798 0.79 HTT (0.42) GABRA1GABRB2GABRG2GABRB3CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260028482-A1 Substitution at the Central Position of Heptamethine Dyes By Aryllithium Addition for Improved Fluorophores UNIV ARKANSAS (US) 2026-01-29 US claimed
CN-111205317-A Novel [ ONN ] tridentate fourth subgroup metal complex and preparation method and application thereof 山东京博中聚新材料有限公司 2020-05-29 CN claimed
CN-106146710-B Cationic polymerization method 中国石油化工股份有限公司 2018-12-28 CN claimed
CN-106146710-A Cationic polymerization method 中国石油化工股份有限公司 2016-11-23 CN claimed
CN-102304056-B 3-methyl-4-aryl-3-alkenyl-butyryl-pentafluoroaniline derivatives and preparation method thereof UNIV ZHEJIANG 2013-12-11 CN claimed
CN-102304056-A 3-methyl-4-aryl-3-alkenyl-butyryl-pentafluoroaniline derivatives and preparation method thereof UNIV ZHEJIANG 2012-01-04 CN claimed
JP-7278031-A None JP disclosed
EP-4216951-B1 KRAS G12D INHIBITORS MIRATI THERAPEUTICS INC (US) 2026-04-01 EP disclosed
US-12577251-B2 Modulators of the sigma-2 receptor and their method of use Temple University—Of the Commonwealth System of Higher Education (US) 2026-03-17 US disclosed
US-20260028482-A1 Substitution at the Central Position of Heptamethine Dyes By Aryllithium Addition for Improved Fluorophores UNIV ARKANSAS (US) 2026-01-29 US disclosed
US-20250270210-A1 BCL-2 Inhibitor BEIGENE, LTD. (KY) 2025-08-28 US disclosed
US-12338245-B2 5-hydroxytryptamine receptor 7 modulators and their use as therapeutic agents Temple University—Of the Commonwealth System of Higher Education (US) 2025-06-24 US disclosed
US-20250179045-A1 LPAR1 ANTAGONISTS AND USES THEREOF CONTINEUM THERAPEUTICS, INC. 2025-06-05 US disclosed
US-4996372-A In a basic aqueous solution, then acid cleaving in the presence of hydrogen peroxide MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1991-02-26 US disclosed
EP-0144729-B1 11-Substituted 5H,11H-pyrrolo[2,1-c][1,4]benzoxazepines, a process for their preparation and their use in medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1989-11-08 EP disclosed
US-4681879-A 11-substituted 5H,11H-pyrrolo[2,1-c][1,4]benzoxazepines as antipsychotic and analgesic agents HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1987-07-21 US disclosed
US-4608374-A 11-substituted 5H,11H-pyrrolo[2,1-c][1,4]benzoxazepines as antipsychotic and analgesic agents HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1986-08-26 US disclosed
EP-0144729-A1 11-Substituted 5H,11H-pyrrolo[2,1-c][1,4]benzoxazepines, a process for their preparation and their use in medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1985-06-19 EP disclosed
EP-0005385-B1 PIPERAZINE METHANE IMINE DERIVATIVES, METHODS FOR THEIR PREPARATION AND THEIR THERAPEUTICAL USE LAROCHE NAVARRON S.A. Société dite: (FR) 1982-09-01 EP disclosed
US-3962307-A HERBICIDES E. I. DU PONT DE NEMOURS AND COMPANY (US) 1976-06-08 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 (5 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-20250179045-A1 LPAR1 ANTAGONISTS AND USES THEREOF LPAR1, LPAR2, LPAR3 GABRA1 474/4885GABRB2 697/4885GABRG2 745/4885
US-20250270210-A1 BCL-2 Inhibitor BCL2, BCL2A1, BCL2L1 GABRA1 2982/4885GABRB2 923/4885GABRG2 1221/4885
US-12338245-B2 5-hydroxytryptamine receptor 7 modulators and their use as therapeutic agents HTR7, HTR6, HTR5A GABRA1 484/4885GABRB2 417/4885GABRG2 695/4885
US-12577251-B2 Modulators of the sigma-2 receptor and their method of use SIGMAR1, CHRNA6, NR3C2 GABRA1 103/4885GABRB2 59/4885GABRG2 181/4885
US-20260028482-A1 Substitution at the Central Position of Heptamethine Dyes By Aryllithium Addition for Improved Fluorophores KCNK5, KCNA7, KCNA4 GABRA1 1607/4885GABRB2 1007/4885GABRG2 2750/4885

“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.