SCHEMBL661822

SCHEMBL661822

Brc1cccn2cncc12

nearest known ligand 0.47

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
IDO1 P14902 3/20 0.47
QPCT Q16769 1/20 0.46
QPCTL Q9NXS2 1/20 0.46
TDO2 P48775 2/20 0.44
TBXAS1 P24557 1/20 0.43
SRC P12931 1/20 0.37
LCK P06239 6/20 0.36
CYP17A1 P05093 2/20 0.33
CYP1A2 P05177 1/20 0.33
AHR P35869 1/20 0.33
PRMT5 O14744 1/20 0.32
WDR77 Q9BQA1 1/20 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
SCHEMBL4550275 0.75 SRC (0.51) IDO1QPCTQPCTLTDO2TBXAS1
SCHEMBL18569895 0.75 IDO1 (0.47) IDO1QPCTQPCTLTDO2TBXAS1
SCHEMBL4219167 0.75 IDO1 (0.47) IDO1QPCTQPCTLTDO2TBXAS1
Hydrochloric Acid SCHEMBL23458904 0.73 IDO1 (0.46) IDO1QPCTQPCTLTDO2TBXAS1
SCHEMBL21355011 0.72 IDO1 (0.44) IDO1QPCTQPCTLTDO2TBXAS1
SCHEMBL10272961 0.71 QPCT (0.46) IDO1QPCTQPCTLTDO2TBXAS1
SCHEMBL11173928 0.71 IDO1 (0.44) IDO1QPCTQPCTLTDO2TBXAS1
SCHEMBL23065942 0.71 TBXAS1 (0.57) IDO1QPCTQPCTLTDO2TBXAS1
SCHEMBL20689814 0.71 QPCT (0.46) IDO1QPCTQPCTLTDO2TBXAS1
SCHEMBL24843280 0.71 IDO1 (0.43) IDO1QPCTQPCTLTDO2TBXAS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4688149-A1 IRAK4 PROTACS Astrazeneca AB (SE) 2026-02-11 EP disclosed
EP-4665729-A1 DDR1 AND DDR2 INHIBITORS HAVING A DIHYDROBENZIMIDAZOLONE CORE Redx Pharma Limited (GB) 2025-12-24 EP disclosed
US-20250333399-A1 INHIBITORS OF FIBROBLAST GROWTH FACTOR RECEPTOR KINASES KHORA SPV 1 LLC (US) 2025-10-30 US disclosed
US-12331039-B2 Inhibitors of fibroblast growth factor receptor kinases KHORA SPV 1, LLC (US) 2025-06-17 US disclosed
US-20250122195-A1 POLYHETEROCYCLIC COMPOUNDS AS METTL3 INHIBITORS STORM THERAPEUTICS LIMITED (GB) 2025-04-17 US disclosed
US-12195458-B2 Polyheterocyclic compounds as METTL3 inhibitors STORM THERAPEUTICS LIMITED (GB) 2025-01-14 US disclosed
US-20250002475-A1 PIPERIDINE DERIVATIVES AS METTL3 INHIBITORS EPICS THERAPEUTICS (BE) 2025-01-02 US disclosed
US-20240374588-A1 IRAK4 PROTACS ASTRAZENECA AB (SE) 2024-11-14 US disclosed
WO-2024209044-A1 IRAK4 PROTACS ASTRAZENECA AB (SE) 2024-10-10 WO disclosed
US-12091400-B2 Piperidine derivatives as METTL3 inhibitors EPICS THERAPEUTICS (BE) 2024-09-17 US disclosed
WO-2010138589-A1 BICYCLIC PYRIMIDINE PI3K INHIBITOR COMPOUNDS SELECTIVE FOR P110 DELTA, AND METHODS OF USE GENENTECH, INC. (US) 2010-12-02 WO disclosed
US-7803810-B2 Inhibitors PROBIODRUG AG (DE) 2010-09-28 US disclosed
US-7803810-B2 Inhibitors PROBIODRUG AG (DE) 2010-09-28 US disclosed
US-7803810-B2 Inhibitors PROBIODRUG AG (DE) 2010-09-28 US disclosed
EP-2118101-A1 IMIDAZO [1,5-A] PYRIDINE DERIVATIVES AS INHIBITORS OF GLUTAMINYL CYCLASE Probiodrug AG (DE) 2009-11-18 EP disclosed
US-20080234313-A1 NOVEL INHIBITORS PROBIODRUG AG (DE) 2008-09-25 US disclosed
US-20080234313-A1 NOVEL INHIBITORS PROBIODRUG AG (DE) 2008-09-25 US disclosed
US-20080234313-A1 NOVEL INHIBITORS PROBIODRUG AG (DE) 2008-09-25 US disclosed
WO-2008110523-A1 IMIDAZO [1,5-A] PYRIDINE DERIVATIVES AS INHIBITORS OF GLUTAMINYL CYCLASE PROBIODRUG AG (DE) 2008-09-18 WO disclosed
WO-2008110523-A1 IMIDAZO [1,5-A] PYRIDINE DERIVATIVES AS INHIBITORS OF GLUTAMINYL CYCLASE PROBIODRUG AG (DE) 2008-09-18 WO 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 (8 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-20250122195-A1 POLYHETEROCYCLIC COMPOUNDS AS METTL3 INHIBITORS METTL3, DIMT1, TPMT IDO1 906/4885QPCT 756/4885QPCTL 524/4885
US-12331039-B2 Inhibitors of fibroblast growth factor receptor kinases FGFR1, FGFR2, FGFR3 IDO1 3517/4885QPCT 3277/4885QPCTL 4457/4885
US-20250002475-A1 PIPERIDINE DERIVATIVES AS METTL3 INHIBITORS METTL3, METTL16, DIMT1 IDO1 1091/4885QPCT 2344/4885QPCTL 712/4885
US-20250333399-A1 INHIBITORS OF FIBROBLAST GROWTH FACTOR RECEPTOR KINASES FGFR1, FGFR2, FGFR3 IDO1 3517/4885QPCT 3277/4885QPCTL 4457/4885
US-20240374588-A1 IRAK4 PROTACS IRAK4, IRAK2, IRAK3 IDO1 3091/4885QPCT 4838/4885QPCTL 2788/4885
US-12195458-B2 Polyheterocyclic compounds as METTL3 inhibitors METTL3, DIMT1, TPMT IDO1 906/4885QPCT 756/4885QPCTL 524/4885
US-12091400-B2 Piperidine derivatives as METTL3 inhibitors METTL3, METTL16, DIMT1 IDO1 1091/4885QPCT 2344/4885QPCTL 712/4885
US-20080234313-A1 NOVEL INHIBITORS SF3A1, HBS1L, SF3A3 IDO1 808/4885QPCT 4475/4885QPCTL 4381/4885

“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.