SCHEMBL3179065

SCHEMBL3179065

O=c1cnc2ccccc2c2ccccc12

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ GPR3 P46089 3/20 0.56
▸ KDM4E B2RXH2 3/20 0.56
▸ SMN1; SMN2 Q16637 2/20 0.45
▸ PDPK1 O15530 1/20 0.45
▸ CA12 O43570 1/20 0.45
▸ PARP1 P09874 1/20 0.45
▸ ALOX15 P16050 1/20 0.45
▸ CA9 Q16790 1/20 0.45
▸ TNKS2 Q9H2K2 1/20 0.45
▸ ERN1 O75460 1/20 0.44
▸ PAX8 Q06710 1/20 0.41
▸ MAPT P10636 2/20 0.41
▸ TOP2A P11388 1/20 0.40
▸ GABRA1 P14867 1/20 0.39
▸ GABRG2 P18507 1/20 0.39
▸ GABRB3 P28472 1/20 0.39
▸ GABRA5 P31644 1/20 0.39
▸ GABRA3 P34903 1/20 0.39
▸ GABRA2 P47869 1/20 0.39
▸ GABRA6 Q16445 1/20 0.39

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
SCHEMBL19020845 0.78 GPR3 (0.68) GPR3KDM4ESMN1; SMN2PDPK1CA12
SCHEMBL29421129 0.72 PARP1 (0.55) GPR3KDM4ESMN1; SMN2PDPK1CA12
Phenanthridine SCHEMBL30823553 0.71 GPR3 (1.00) GPR3KDM4ESMN1; SMN2PDPK1ERN1
Phenanthridine SCHEMBL9106884 0.71 GPR3 (1.00) GPR3KDM4ESMN1; SMN2PDPK1ERN1
Phenanthridine SCHEMBL30914262 0.71 GPR3 (1.00) GPR3KDM4ESMN1; SMN2PDPK1ERN1
Phenanthridine SCHEMBL8666 0.71 GPR3 (1.00) GPR3KDM4ESMN1; SMN2PDPK1ERN1
SCHEMBL17498089 0.71 MAPT (0.50) KDM4ESMN1; SMN2ALOX15PAX8MAPT
SCHEMBL8525477 0.71 PARP1 (0.46) GPR3KDM4ESMN1; SMN2PDPK1CA12
Phenanthridine SCHEMBL23003530 0.70 GPR3 (0.95) GPR3KDM4ESMN1; SMN2PDPK1ERN1
SCHEMBL2231455 0.70 KDM4E (0.68) GPR3KDM4EERN1MAPTNCF1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112375038-A Preparation method of dibenzozepine 山东嘉成医药科技有限公司 2021-02-19 — — CN claimed
EP-2164830-B1 PROCESS FOR THE PREPARATION OF DIBENZO [B,D]AZEPIN-6-ONE DERIVATIVE HOFFMANN LA ROCHE (CH) 2013-05-29 — — EP claimed
US-7579464-B2 Process for preparation of enantiomerically pure compounds HOFFMANN-LA ROCHE INC. (US) 2009-08-25 — — US claimed
US-20080293933-A1 PROCESS FOR PREPARATION OF ENANTIOMERICALLY PURE COMPOUNDS HOFFMANN-LA ROCHE, INC. 2008-11-27 — — US claimed
EP-1633348-B1 4- BROMO - 5 - (2- CHLORO - BENZOYLAMINO) - 1H - PYRAZOLE - 3 - CARBOXYLIC ACID AMIDE DERIVATIVES AND RELATED COMPOUNDS AS BRADYKININ B sb 1 /sb RECEPTOR ANTAGONISTS FOR THE TREATMENT OF INFLAMMATORY DISEASES ELAN PHARM INC (US) 2008-10-08 — — EP claimed
US-20060281733-A1 4-Bromo-5-(2-chloro-benzoylamino)-1h-pyrazole-3-carvoxylic acid amide derivatives and related compounds as bradykinin b1 receptor antagonists for the treatment of inflammatory diseases ELAN PHARMACEUTICALS, INC. 2006-12-14 — — US claimed
EP-1633348-A1 4- BROMO - 5 - (2- CHLORO - BENZOYLAMINO) - 1H - PYRAZOLE - 3 - CARBOXYLIC ACID AMIDE DERIVATIVES AND RELATED COMPOUNDS AS BRADYKININ B sb 1 /sb RECEPTOR ANTAGONISTS FOR THE TREATMENT OF INFLAMMATORY DISEASES Elan Pharmaceuticals, Inc. (US) 2006-03-15 — — EP claimed
US-20050020659-A1 Substituted pyrazole derivatives and related compounds as bradykinin B1 receptor antagonists ELAN PHARMACEUTICALS, INC. 2005-01-27 — — US claimed
WO-2004098589-A1 4- BROMO - 5 - (2- CHLORO - BENZOYLAMINO) - 1H - PYRAZOLE - 3 - CARBOXYLIC ACID AMIDE DERIVATIVES AND RELATED COMPOUNDS AS BRADYKININ B1 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF INFLAMMATORY DISEASES ELAN PHARMACEUTICALS, INC. (US) 2004-11-18 — — WO claimed
EP-1093372-A4 CYCLIC AMINO ACID COMPOUNDS, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, AND METHODS FOR INHIBITING $g(b)-AMYLOID PEPTIDE RELEASE AND/OR ITS SYNTHESIS BY USE OF SUCH COMPOUNDS ELAN PHARM INC (US) 2004-09-29 — — EP claimed
EP-0713093-B1 Improved methodology for colorimetrically determining the concentration of white blood cells in a biological fluid BAYER AG (US) 2001-10-10 — — EP claimed
EP-1093372-A1 CYCLIC AMINO ACID COMPOUNDS, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, AND METHODS FOR INHIBITING $g(b)-AMYLOID PEPTIDE RELEASE AND/OR ITS SYNTHESIS BY USE OF SUCH COMPOUNDS Elan Pharmaceuticals, Inc. (US) 2001-04-25 — — EP claimed
WO-1999066934-A1 CYCLIC AMINO ACID COMPOUNDS, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, AND METHODS FOR INHIBITING β-AMYLOID PEPTIDE RELEASE AND/OR ITS SYNTHESIS BY USE OF SUCH COMPOUNDS ELAN PHARMACEUTICALS, INC. (US) 1999-12-29 — — WO claimed
EP-0698600-B1 Composition, method and test device for determining the presence of leukocyte cells, esterase or protease in a test sample BAYER AG (US) 1999-11-10 — — EP claimed
CN-122036610-A Synthesis method of central chiral aza seven-membered bridged aromatic compound containing chiral axis 浙江大学 2026-05-15 — — CN disclosed
US-20260097047-A1 Small molecule inhibitors of the ribosome biogenesis factor NVL2 BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2026-04-09 — — US disclosed
US-20260097047-A1 Small molecule inhibitors of the ribosome biogenesis factor NVL2 BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2026-04-09 — — US disclosed
US-4434100-A TRANQUILIZING, ANTICONVULSANTS, ANXIOLYTIC CIBA-GEIGY CORPORATION (US) 1984-02-28 — — US disclosed
US-4356176-A TRANQUILIZERS, ANTICONVULSANT CIBA-GEIGY CORPORATION (US) 1982-10-26 — — US disclosed
US-4315926-A ANXIOLYTIC AGENTS CIBA-GEIGY CORPORATION (US) 1982-02-16 — — 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 (4 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-20050020659-A1 Substituted pyrazole derivatives and related compounds as bradykinin B1 receptor antagonists BDKRB1, BDKRB2, BRS3 GPR3 197/4885KDM4E 4503/4885SMN1; SMN2 3553/4885
US-20080293933-A1 PROCESS FOR PREPARATION OF ENANTIOMERICALLY PURE COMPOUNDS BACE1, BACE2, BCHE GPR3 1558/4885KDM4E 477/4885SMN1; SMN2 2294/4885
US-20260097047-A1 Small molecule inhibitors of the ribosome biogenesis factor NVL2 NOC2L, RPS6, RPS3A GPR3 2998/4885KDM4E 2720/4885SMN1; SMN2 2686/4885
US-20060281733-A1 4-Bromo-5-(2-chloro-benzoylamino)-1h-pyrazole-3-carvoxylic acid amide derivatives and related compounds as bradykinin b1 receptor antagonists for the treatment of inflammatory diseases BDKRB1, BDKRB2, CNR1 GPR3 76/4885KDM4E 2152/4885SMN1; SMN2 3662/4885

“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.

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