SCHEMBL19986218

SCHEMBL19986218

Cc1csc2c1C(c1ccc(Cl)cc1)=NCC(=O)N2

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CDK2 P24941 1/20 0.44
GSK3A P49840 1/20 0.44
GSK3B P49841 1/20 0.44
ROCK1 Q13464 1/20 0.44
CAMK2B Q13554 1/20 0.44
DYRK1A Q13627 1/20 0.44
PGR P06401 2/20 0.44
HTR1A P08908 1/20 0.44
ADRA2A P08913 1/20 0.44
ADORA3 P0DMS8 1/20 0.44
AR P10275 1/20 0.44
PDE4A P27815 1/20 0.44
ADRA1A P35348 1/20 0.44
CNR1 P21554 1/20 0.41
NTSR1 P30989 1/20 0.41
OPRK1 P41145 1/20 0.41
PDE4D Q08499 1/20 0.41
ALDH1A1 P00352 2/20 0.39
HPGD P15428 2/20 0.39
MEN1 O00255 2/20 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
SCHEMBL7479638 0.80 CDK2 (0.47) CDK2GSK3AGSK3BROCK1CAMK2B
SCHEMBL19986220 0.78 CDK2 (0.45) CDK2GSK3AGSK3BROCK1CAMK2B
SCHEMBL19986215 0.76 RECQL (0.36) ALDH1A1MEN1KMT2ANPSR1GABRA1
SCHEMBL20456616 0.76 RECQL (0.36) ALDH1A1MEN1KMT2ANPSR1GABRA1
SCHEMBL22370118 0.70 BRD4 (0.46) ADORA3BRD4TSPO
SCHEMBL22370120 0.70 BRD4 (0.46) ADORA3BRD4TSPO
SCHEMBL12228130 0.68 PGR (0.48) CDK2GSK3AGSK3BROCK1CAMK2B
SCHEMBL13113703 0.67 BRD4 (0.56) ADRA1ACNR1OPRK1PDE4DALDH1A1
SCHEMBL29424164 0.66 BRD4 (0.53) ADORA3BRD4TSPO
SCHEMBL31736768 0.66 CDK2 (0.65) CDK2GSK3AGSK3BROCK1CAMK2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220356192-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS UNIV MICHIGAN REGENTS (US) 2022-11-10 US disclosed
EP-3858837-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS The Regents of The University of Michigan (US) 2021-08-04 EP disclosed
US-11046709-B2 Fused 1,4-diazepines as BET bromodomain inhibitors THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2021-06-29 US disclosed
US-10975093-B2 Fused 1,4-diazepines as BET protein degraders THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2021-04-13 US disclosed
EP-3512853-B1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS UNIV MICHIGAN REGENTS (US) 2020-12-23 EP disclosed
US-20190263827-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS UNIV MICHIGAN REGENTS (US) 2019-08-29 US disclosed
WO-2018144789-A1 FUSED 1,4-DIAZEPINES AS BET BROMODOMAIN INHIBITORS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2018-08-09 WO disclosed
WO-2018052949-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2018-03-22 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 (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-20190263827-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS BRD4, BRD1, BET1 CDK2 491/4885GSK3A 2304/4885GSK3B 1856/4885
US-11046709-B2 Fused 1,4-diazepines as BET bromodomain inhibitors BRD4, BRD3, BRD1 CDK2 391/4885GSK3A 2512/4885GSK3B 1943/4885
US-10975093-B2 Fused 1,4-diazepines as BET protein degraders BRD4, BRD1, BET1 CDK2 491/4885GSK3A 2304/4885GSK3B 1856/4885
US-20220356192-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS BRD4, BRD1, BET1 CDK2 491/4885GSK3A 2304/4885GSK3B 1856/4885

“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.