Rabusertib

Rabusertib

SCHEMBL304748

Cc1cnc(NC(=O)Nc2cc(Br)c(C)cc2OCC2CNCCO2)cn1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHEK1

The experimentally established mechanism targets of Rabusertib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHEK1 known ✓ O14757 10/20 1.00
FECH P22830 1/20 1.00
KCNH2 Q12809 1/20 1.00
RPS6KA3 P51812 3/20 0.42
SRPK1 Q96SB4 3/20 0.42
MAP4K4 O95819 2/20 0.42
RET P07949 2/20 0.42
FLT4 P35916 2/20 0.42
CLK2 P49760 2/20 0.42
GSK3B P49841 2/20 0.42
IRAK1 P51617 2/20 0.42
BRSK1 Q8TDC3 2/20 0.42
MAP4K5 Q9Y4K4 2/20 0.42
IKBKB O14920 1/20 0.42
AURKA O14965 1/20 0.42
DCLK1 O15075 1/20 0.42
RPS6KA5 O75582 1/20 0.42
PRKD3 O94806 1/20 0.42
PHKG2 P15735 1/20 0.42
CDK2 P24941 1/20 0.42

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
Rabusertib SCHEMBL304747 1.00 CHEK1 (1.00) CHEK1FECHKCNH2RPS6KA3SRPK1
Rabusertib SCHEMBL30403507 1.00 CHEK1 (1.00) CHEK1FECHKCNH2RPS6KA3SRPK1
SCHEMBL14189549 0.93 CHEK1 (0.86) CHEK1FECHKCNH2RPS6KA3SRPK1
SCHEMBL305203 0.93 CHEK1 (0.86) CHEK1FECHKCNH2RPS6KA3SRPK1
SCHEMBL306054 0.90 CHEK1 (0.82) CHEK1FECHKCNH2RPS6KA3SRPK1
SCHEMBL305673 0.90 CHEK1 (0.82) CHEK1FECHKCNH2RPS6KA3SRPK1
SCHEMBL306053 0.90 CHEK1 (0.82) CHEK1FECHKCNH2RPS6KA3SRPK1
SCHEMBL305395 0.89 CHEK1 (0.79) CHEK1FECHKCNH2EPHA2ADRB2
SCHEMBL305112 0.89 CHEK1 (0.79) CHEK1FECHKCNH2EPHA2ADRB2
SCHEMBL305113 0.89 CHEK1 (0.79) CHEK1FECHKCNH2EPHA2ADRB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10744141-B2 Compositions and methods for treating cancer CASE WESTERN RESERVE UNIVERSITY (US) 2020-08-18 US claimed
US-20180185382-A1 COMPOSITIONS AND METHODS FOR TREATING CANCER CASE WESTERN RESERVE UNIVERSITY 2018-07-05 US claimed
EP-3313819-A1 COMPOSITIONS AND METHODS FOR TREATING CANCER Case Western Reserve University (US) 2018-05-02 EP claimed
WO-2016210134-A1 COMPOSITIONS AND METHODS FOR TREATING CANCER CASE WESTERN RESERVE UNIVERSITY (US) 2016-12-29 WO claimed
US-8093244-B2 Heteroaryl urea derivatives useful for inhibiting CHK1 ICOS CORPORATION (US) 2012-01-10 US claimed
EP-1869020-B1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHK1 ICOS CORP (US) 2010-12-01 EP claimed
US-20090143357-A1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHK1 ICOS CORPORATION (US) 2009-06-04 US claimed
US-20260076968-A1 AZA-QUINOLINE COMPOUNDS AND USES THEREOF NOVARTIS AG (CH) 2026-03-19 US disclosed
US-12570625-B2 3-(5-hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof NOVARTIS AG (CH) 2026-03-10 US disclosed
EP-4034535-B1 AZA-QUINOLINE COMPOUNDS AND USES THEREOF NOVARTIS AG (CH) 2026-03-04 EP disclosed
US-12544374-B2 AZA-quinoline compounds and uses thereof NOVARTIS AG (CH) 2026-02-10 US disclosed
EP-4541381-B1 STABLE, CONCENTRATED RADIONUCLIDE COMPLEX SOLUTIONS ADVANCED ACCELERATOR APPLICATIONS S A (FR) 2026-02-04 EP disclosed
EP-4541380-B1 STABLE, CONCENTRATED RADIONUCLIDE COMPLEX SOLUTIONS ADVANCED ACCELERATOR APPLICATIONS S A (FR) 2025-12-10 EP disclosed
EP-1869020-B1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHK1 ICOS CORP (US) 2010-12-01 EP disclosed
EP-1869020-B1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHK1 ICOS CORP (US) 2010-12-01 EP disclosed
US-20090143357-A1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHK1 ICOS CORPORATION (US) 2009-06-04 US disclosed
US-20090143357-A1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHK1 ICOS CORPORATION (US) 2009-06-04 US disclosed
US-20090143357-A1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHK1 ICOS CORPORATION (US) 2009-06-04 US disclosed
EP-1869020-A1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHKl ICOS Corporation (US) 2007-12-26 EP disclosed
WO-2006105262-A1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHKl ICOS CORPORATION (US) 2006-10-05 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 (6 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-12570625-B2 3-(5-hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof IKZF1, IKZF2, BCL6 CHEK1 2505/4885FECH 4884/4885KCNH2 583/4885
US-20180185382-A1 COMPOSITIONS AND METHODS FOR TREATING CANCER PPP2CA, PPP3CA, PPP4C CHEK1 178/4885FECH 3200/4885KCNH2 4752/4885
US-20260076968-A1 AZA-QUINOLINE COMPOUNDS AND USES THEREOF EZH2, SUZ12, NR3C1 CHEK1 3282/4885FECH 2641/4885KCNH2 2430/4885
US-10744141-B2 Compositions and methods for treating cancer PPP2CA, PPP3CA, PPP4C CHEK1 178/4885FECH 3200/4885KCNH2 4752/4885
US-12544374-B2 AZA-quinoline compounds and uses thereof EZH2, NR3C1, SUZ12 CHEK1 3267/4885FECH 3303/4885KCNH2 1579/4885
US-20090143357-A1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHK1 CHEK1, CHEK2, PCNA CHEK1 1/4885FECH 2006/4885KCNH2 3943/4885

“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.