SCHEMBL659294

SCHEMBL659294

N#Cc1nn(C2CCCCO2)c2ccc(Br)cc12

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ATR Q13535 2/20 0.38
RET P07949 1/20 0.35
SMN1; SMN2 Q16637 2/20 0.35
RXRA P19793 1/20 0.35
RXRB P28702 1/20 0.35
RXRG P48443 1/20 0.35
MAPT P10636 3/20 0.35
TP53 P04637 2/20 0.34
ALDH1A1 P00352 1/20 0.34
LMNA P02545 1/20 0.34
MAPK1 P28482 1/20 0.34
HTT P42858 1/20 0.34
NPSR1 Q6W5P4 1/20 0.34
CYP3A4 P08684 1/20 0.33
DPP4 P27487 1/20 0.33
CYP4F2 P78329 2/20 0.33
CYP4A11 Q02928 2/20 0.33
GAA P10253 1/20 0.33
XDH P47989 1/20 0.32
ELANE P08246 2/20 0.32

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
SCHEMBL14658464 0.91 ATR (0.36) ATRRETRXRARXRBRXRG
SCHEMBL29502036 0.91 ATR (0.36) ATRRETRXRARXRBRXRG
SCHEMBL30182911 0.84 MAPT (0.38) ATRRETSMN1; SMN2RXRARXRB
SCHEMBL25473050 0.83 ATR (0.36) ATRRETRXRARXRBRXRG
SCHEMBL19204829 0.83 ELANE (0.43) ATRRETMAPTALDH1A1MAPK1
SCHEMBL29167963 0.83 ELANE (0.34) MAPTELANECTSK
SCHEMBL29959666 0.83 ELANE (0.43) ATRRETMAPTALDH1A1MAPK1
SCHEMBL30673140 0.82 RET (0.34) RETSMN1; SMN2RXRARXRBRXRG
SCHEMBL26924343 0.82 RET (0.34) RETSMN1; SMN2RXRARXRBRXRG
SCHEMBL767404 0.81 CYP4F2 (0.39) ATRRETSMN1; SMN2RXRARXRB

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260069571-A1 DDR1 AND DDR2 INHIBITORS FOR THE TREATEMENT OF CANCER AND FIBROTIC DISEASES REDX PHARMA PLC (GB) 2026-03-12 US disclosed
EP-4426688-B1 DDR1 AND DDR2 INHIBITORS FOR THE TREATEMENT OF CANCER AND FIBROTIC DISEASES REDX PHARMA LTD (GB) 2025-12-03 EP disclosed
EP-4426688-A1 DDR1 AND DDR2 INHIBITORS FOR THE TREATEMENT OF CANCER AND FIBROTIC DISEASES Redx Pharma Plc (GB) 2024-09-11 EP disclosed
CN-118201918-A DDR1 and DDR2 inhibitors for the treatment of cancer and fibrotic diseases 莱德克斯制药公共有限公司 2024-06-14 CN disclosed
WO-2023079291-A1 DDR1 AND DDR2 INHIBITORS FOR THE TREATEMENT OF CANCER AND FIBROTIC DISEASES REDX PHARMA PLC (GB) 2023-05-11 WO disclosed
US-8378104-B2 7-aminofuropyridine derivatives OSI Pharmaceuticals, LLC (US) 2013-02-19 US disclosed
US-20120046267-A1 7-AMINOFUROPYRIDINE DERIVATIVES OSI PHARMACEUTICALS, INC. 2012-02-23 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 (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-20120046267-A1 7-AMINOFUROPYRIDINE DERIVATIVES MAP3K5, STK17A, MAPKAPK5 ATR 1630/4885RET 588/4885SMN1; SMN2 1807/4885
US-20260069571-A1 DDR1 AND DDR2 INHIBITORS FOR THE TREATEMENT OF CANCER AND FIBROTIC DISEASES DDR1, DDR2, TGFBR2 ATR 457/4885RET 300/4885SMN1; SMN2 1766/4885

“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.