Radotinib

Radotinib

SCHEMBL3359952

Cc1cn(-c2cc(NC(=O)c3ccc(C)c(Nc4nccc(-c5cnccn5)n4)c3)cc(C(F)(F)F)c2)cn1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1BCR

The experimentally established mechanism targets of Radotinib. 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
ABL1 known ✓ P00519 12/20 1.00
BCR known ✓ P11274 4/20 1.00
ADORA3 P0DMS8 2/20 1.00
NR1I2 O75469 1/20 1.00
PTGS1 P23219 1/20 1.00
KDR P35968 1/20 1.00
CHRNA4 P43681 1/20 1.00
PDE3A Q14432 1/20 1.00
KIT P10721 11/20 0.83
LDLR P01130 8/20 0.83
PCSK9 Q8NBP7 8/20 0.83
PDGFRB P09619 6/20 0.83
LCK P06239 4/20 0.83
LYN P07948 4/20 0.83
PDGFRA P16234 4/20 0.83
FLT3 P36888 4/20 0.83
DDR2 Q16832 4/20 0.83
EPHB2 P29323 2/20 0.83
SRC P12931 2/20 0.83
RAF1 P04049 2/20 0.83

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
Radotinib SCHEMBL29381661 1.00 ABL1 (1.00) ABL1BCRADORA3NR1I2PTGS1
Radotinib SCHEMBL29366343 1.00 ABL1 (1.00) ABL1BCRADORA3NR1I2PTGS1
Radotinib SCHEMBL30002961 0.99 ABL1 (0.99) ABL1BCRADORA3NR1I2PTGS1
Radotinib SCHEMBL15285797 0.99 ABL1 (0.99) ABL1BCRADORA3NR1I2PTGS1
Radotinib SCHEMBL15318848 0.99 ABL1 (0.97) ABL1BCRADORA3NR1I2PTGS1
SCHEMBL3945090 0.92 ABL1 (0.85) ABL1BCRADORA3NR1I2PTGS1
Nilotinib SCHEMBL29366964 0.91 ABL1 (1.00) ABL1BCRADORA3NR1I2PTGS1
Nilotinib SCHEMBL29580067 0.91 ABL1 (1.00) ABL1BCRADORA3NR1I2PTGS1
Nilotinib SCHEMBL7901 0.91 ABL1 (1.00) ABL1BCRADORA3NR1I2PTGS1
SCHEMBL20502603 0.91 KIT (0.85) ABL1BCRADORA3NR1I2PTGS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3875078-A1 COMPOUNDS FOR THE TREATMENT OF COVID-19 Dompe' Farmaceutici S.P.A. (IT) 2021-09-08 EP claimed
EP-1922309-B1 N-PHENYL-2-PYRIMIDINE-AMINE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF IL YANG PHARM CO LTD (KR) 2014-05-21 EP claimed
WO-2013147414-A1 PHARMACEUTICAL COMPOSITION AND PREPARATION METHOD THEREOF IL-YANG PHARM. CO., LTD (KR) 2013-10-03 WO claimed
US-7501424-B2 N-phenyl-2-pyrimidine-amine derivatives and process for the preparation thereof IL-YANG PHARM. CO., LTD. (KR) 2009-03-10 US claimed
US-20080096899-A1 N-Phenyl-2-Pyrimidine-Amine Derivatives and Process for the Preparation Thereof IL-YANG PHARM. CO., LTD. (KR) 2008-04-24 US claimed
EP-3875078-A1 COMPOUNDS FOR THE TREATMENT OF COVID-19 Dompe' Farmaceutici S.P.A. (IT) 2021-09-08 EP disclosed
EP-1922309-B1 N-PHENYL-2-PYRIMIDINE-AMINE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF IL YANG PHARM CO LTD (KR) 2014-05-21 EP disclosed
WO-2013147414-A1 PHARMACEUTICAL COMPOSITION AND PREPARATION METHOD THEREOF IL-YANG PHARM. CO., LTD (KR) 2013-10-03 WO disclosed
WO-2013147414-A1 PHARMACEUTICAL COMPOSITION AND PREPARATION METHOD THEREOF IL-YANG PHARM. CO., LTD (KR) 2013-10-03 WO disclosed
WO-2010018895-A1 PROCESS FOR THE PREPARATION OF N-PHENYL-2-PYRIMIDINE-AMINE DERIVATIVES IL-YANG PHARM. CO., LTD. (KR) 2010-02-18 WO disclosed
US-7501424-B2 N-phenyl-2-pyrimidine-amine derivatives and process for the preparation thereof IL-YANG PHARM. CO., LTD. (KR) 2009-03-10 US disclosed
US-20080096899-A1 N-Phenyl-2-Pyrimidine-Amine Derivatives and Process for the Preparation Thereof IL-YANG PHARM. CO., LTD. (KR) 2008-04-24 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 (1 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-20080096899-A1 N-Phenyl-2-Pyrimidine-Amine Derivatives and Process for the Preparation Thereof ITPA, TYMP, THPO ABL1 451/4885BCR 990/4885ADORA3 222/4885

“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.