SCHEMBL500029

SCHEMBL500029

O=C(O)c1cc(F)c(F)cc1Br

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.50
LCK P06239 1/20 0.50
FYN P06241 1/20 0.50
CA12 O43570 1/20 0.48
CA1 P00915 1/20 0.48
CA2 P00918 1/20 0.48
CA3 P07451 1/20 0.48
CA4 P22748 1/20 0.48
CA6 P23280 1/20 0.48
CA5A P35218 1/20 0.48
CA7 P43166 1/20 0.48
CA9 Q16790 1/20 0.48
CA13 Q8N1Q1 1/20 0.48
CA14 Q9ULX7 1/20 0.48
CA5B Q9Y2D0 1/20 0.48
HSD17B10 Q99714 2/20 0.46
TSHR P16473 2/20 0.46
KEAP1 Q14145 2/20 0.45
NFE2L2 Q16236 1/20 0.45
AKR1C2 P52895 3/20 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
SCHEMBL6860298 0.88 SMN1; SMN2 (0.48) SMN1; SMN2LCKFYNCA12CA1
SCHEMBL31430795 0.88 SMN1; SMN2 (0.48) SMN1; SMN2LCKFYNCA12CA1
SCHEMBL27575950 0.88 CA12 (0.52) SMN1; SMN2LCKFYNCA12CA1
SCHEMBL2371182 0.88 LCK (0.48) SMN1; SMN2LCKFYNCA12CA1
SCHEMBL28799490 0.87 KEAP1 (0.46) SMN1; SMN2LCKFYNCA12CA1
SCHEMBL590353 0.84 AKR1C4 (0.47) SMN1; SMN2LCKFYNCA12CA1
SCHEMBL29851193 0.84 AKR1C4 (0.47) SMN1; SMN2LCKFYNCA12CA1
SCHEMBL1512601 0.83 CA12 (0.47) SMN1; SMN2LCKFYNCA12CA1
SCHEMBL15719837 0.83 LCK (0.48) SMN1; SMN2LCKFYNCA12CA1
SCHEMBL21050064 0.83 CA12 (0.47) SMN1; SMN2LCKFYNCA12CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240327419-A1 SYNTHESIS OF SUBSTITUTED TRICYCLIC AMIDES AND ANALOGUES THEREOF ARBUTUS BIOPHARMA CORP (CA) 2024-10-03 US claimed
EP-4373823-A1 SYNTHESIS OF SUBSTITUTED TRICYCLIC AMIDES AND ANALOGUES THEREOF Arbutus Biopharma Corporation (CA) 2024-05-29 EP claimed
CN-115181054-B Synthesis method of 3-benzyl indole compound 合肥工业大学 2024-04-05 CN claimed
CN-117730082-A Synthesis of substituted tricyclic amides and analogs thereof 爱彼特生物制药公司 2024-03-19 CN claimed
CN-116396159-A Synthesis method of 2,2' -biphenyl dicarboxylic acid compound 湖南大学 2023-07-07 CN claimed
WO-2023002323-A1 SYNTHESIS OF SUBSTITUTED TRICYCLIC AMIDES AND ANALOGUES THEREOF ARBUTUS BIOPHARMA CORPORATION (CA) 2023-01-26 WO claimed
CN-115181054-A Synthetic method of 3-benzyl indole compound 合肥工业大学 2022-10-14 CN claimed
WO-2021257669-A1 SYNTHESIS OF SUBSTITUTED ARYLMETHYLUREAS, ANALOGUES, AND CRYSTALLINE FORMS THEREOF AND METHODS OF USING SAME ARBUTUS BIOPHARMA CORPORATION (CA) 2021-12-23 WO claimed
US-20260132112-A1 COMPOUNDS CTXT PTY LTD (AU) 2026-05-14 US disclosed
EP-4734979-A2 TMEM175 AGONISTS, COMPOSITIONS, AND METHODS OF USE Caraway Therapeutics, Inc. (US) 2026-05-06 EP disclosed
US-12606522-B2 Sulfinylaminobenzamide and sulfonylaminobenzamide derivatives ORSOBIO, INC. (US) 2026-04-21 US disclosed
US-20250381179-A1 CHROMAN-BASED COMPOUNDS FOR TREATING CANCER ACCUTAR BIOTECHNOLOGY INC (US) 2025-12-18 US disclosed
EP-4077318-B1 BENZIMIDAZOLE DIMERS AS MODULATORS OF STING CTXT PTY LTD (AU) 2025-10-15 EP disclosed
US-12415785-B2 Compound modulators of sting CTXT PTY LTD (AU) 2025-09-16 US disclosed
EP-0342849-A2 Intermediates for preparing 1,4-dihydro-4-oxo-quinoline-3-carboxylic acid esters PFIZER INC. (US) 1989-11-23 EP disclosed
EP-0303291-A2 Fluorinated benzoyl compounds ASAHI GLASS COMPANY LTD. (JP) 1989-02-15 EP disclosed
US-4786649-A ANTISEPTICS OTSUKA PHARMACEUTICAL COMPANY LIMITED (JP) 1988-11-22 US disclosed
US-4684648-A Antimicrobial 1-substituted phenyl-4-oxoquinoline-3-carboxylic acid compounds and compositions thereof OTSUKA PHARMACEUTICAL COMPANY LIMITED (JP) 1987-08-04 US disclosed
EP-0228035-A2 Antimicrobial 1-thienyl-4-oxoquinoline-3-carboxylix acid compounds OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1987-07-08 EP disclosed
EP-0181521-A1 Antimicrobial 1-substituted Phenyl-4-oxoquinoline-3-carboxylic acid compounds OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1986-05-21 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 (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-20240327419-A1 SYNTHESIS OF SUBSTITUTED TRICYCLIC AMIDES AND ANALOGUES THEREOF HCCS, HDGF, GLS2 SMN1; SMN2 4698/4885LCK 2479/4885FYN 4422/4885
US-12415785-B2 Compound modulators of sting STING1, IRF3, MAVS SMN1; SMN2 3182/4885LCK 934/4885FYN 3193/4885
US-20250381179-A1 CHROMAN-BASED COMPOUNDS FOR TREATING CANCER BRCA1, CDYL, TP53 SMN1; SMN2 1797/4885LCK 434/4885FYN 868/4885
US-20260132112-A1 COMPOUNDS STING1, IRF3, CGAS SMN1; SMN2 521/4885LCK 872/4885FYN 1447/4885
US-12606522-B2 Sulfinylaminobenzamide and sulfonylaminobenzamide derivatives NR3C2, NR5A1, SRD5A2 SMN1; SMN2 286/4885LCK 3693/4885FYN 2490/4885

“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.