Crenolanib

Crenolanib

SCHEMBL2730601

CC1(COc2ccc3c(c2)ncn3-c2ccc3cccc(N4CCC(N)CC4)c3n2)COC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FLT3PDGFRAPDGFRB

The experimentally established mechanism targets of Crenolanib. 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
FLT3 known ✓ P36888 6/20 1.00
PDGFRB known ✓ P09619 1/20 1.00
PDGFRA known ✓ P16234 1/20 1.00
IRAK4 Q9NWZ3 2/20 1.00
GAK O14976 1/20 1.00
RIPK2 O43353 1/20 1.00
ULK1 O75385 1/20 1.00
STK10 O94804 1/20 1.00
PRKD3 O94806 1/20 1.00
MAP4K4 O95819 1/20 1.00
LATS1 O95835 1/20 1.00
PAK4 O96013 1/20 1.00
NTRK1 P04629 1/20 1.00
LCK P06239 1/20 1.00
CDK1 P06493 1/20 1.00
APRT P07741 1/20 1.00
RET P07949 1/20 1.00
PHKG2 P15735 1/20 1.00
NQO2 P16083 1/20 1.00
FECH P22830 1/20 1.00

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
Crenolanib SCHEMBL29350134 1.00 FLT3 (1.00) FLT3IRAK4GAKRIPK2ULK1
Crenolanib SCHEMBL29352568 1.00 FLT3 (1.00) FLT3IRAK4GAKRIPK2ULK1
Crenolanib SCHEMBL30002138 1.00 FLT3 (1.00) FLT3IRAK4GAKRIPK2ULK1
SCHEMBL22567082 0.93 IRAK4 (0.86) FLT3IRAK4GAKRIPK2ULK1
Crenolanib SCHEMBL29361948 0.92 FLT3 (0.85) FLT3IRAK4GAKRIPK2ULK1
Crenolanib SCHEMBL4681285 0.92 FLT3 (0.85) FLT3IRAK4GAKRIPK2ULK1
Crenolanib SCHEMBL29352554 0.92 FLT3 (0.85) FLT3IRAK4GAKRIPK2ULK1
SCHEMBL5662568 0.92 IRAK4 (0.85) FLT3IRAK4GAKRIPK2ULK1
SCHEMBL30775111 0.92 FLT3 (0.85) FLT3IRAK4GAKRIPK2ULK1
SCHEMBL27030604 0.92 FLT3 (0.85) FLT3IRAK4GAKRIPK2ULK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107382984-B Preparation method of medicine for treating leukemia 扬州市三药制药有限公司 2020-07-10 CN claimed
EP-1594858-B1 NOVEL BENZOIMIDAZOLE DERIVATIVES USEFUL AS ANTIPROLIFERATIVE AGENTS PFIZER PROD INC (US) 2009-10-14 EP claimed
EP-1641780-B1 PROCESSES FOR THE PREPARATION OF 1- [(BENZOIMIDAZOLE-1YL) QUINOLIN-8-YL] PIPERIDIN-4-YLAMINE DERIVATIVES PFIZER PROD INC (US) 2008-11-12 EP claimed
JP-2007516168-A 2007-06-21 JP claimed
US-7183414-B2 Processes for the preparation of benzoimidazole derivatives PFIZER INC (US) 2007-02-27 US claimed
US-7071337-B2 Benzoimidazole derivatives useful as antiproliferative agents PFIZER INC (US) 2006-07-04 US claimed
EP-1641780-A1 PROCESSES FOR THE PREPARATION OF 1- [(BENZOIMIDAZOLE-1YL) QUINOLIN-8-YL] PIPERIDIN-4-YLAMINE DERIVATIVES Pfizer Products Incorporated (US) 2006-04-05 EP claimed
EP-1594858-A2 NOVEL BENZOIMIDAZOLE DERIVATIVES USEFUL AS ANTIPROLIFERATIVE AGENTS Pfizer Products Inc. (US) 2005-11-16 EP claimed
US-20050124599-A1 Novel benzoimidazole derivatives useful as antiproliferative agents PFIZER INC. 2005-06-09 US claimed
US-20050020625-A1 Processes for the preparation of benzoimidazole derivatives PFIZER INC 2005-01-27 US claimed
WO-2004113322-A1 PROCESSES FOR THE PREPARATION OF 1-[(BENZOIMIDAZOLE-1YL) QUINOLIN-8-YL] PIPERIDIN-4-YLAMINE DERIVATIVES PFIZER PRODUCTS INC. (US) 2004-12-29 WO claimed
WO-2004020431-A2 NOVEL BENZOIMIDAZOLE DERIVATIVES USEFUL AS ANTIPROLIFERATIVE AGENTS PFIZER PRODUCTS INC. (US) 2004-03-11 WO claimed
US-20250223630-A1 IDENTIFYING DISEASE-CAUSING HUMAN DDX41 GENETIC VARIANTS WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2025-07-10 US disclosed
US-20240277636-A1 COMBINATION COMPRISING AT LEAST ONE SEROTONIN REUPTAKE INHIBITOR AND AT LEAST ONE STIMULATOR OF POTASSIUM-CHLORIDE COTRANSPORTER TYPE 2 AND ITS MEDICAL USE UNIVERSITé LAVAL (CA) 2024-08-22 US disclosed
CN-117897147-A Combination comprising at least one serotonin reuptake inhibitor and at least one potassium chloride type 2 cotransporter stimulator and medical use thereof 波尔多大学 2024-04-16 CN disclosed
US-20240102081-A1 IDENTIFYING DISEASE-CAUSING HUMAN DDX41 GENETIC VARIANTS WISCONSIN ALUMNI RESEARCH FOUNDATION 2024-03-28 US disclosed
US-20050124599-A1 Novel benzoimidazole derivatives useful as antiproliferative agents PFIZER INC. 2005-06-09 US disclosed
US-20050020625-A1 Processes for the preparation of benzoimidazole derivatives PFIZER INC 2005-01-27 US disclosed
WO-2004113322-A1 PROCESSES FOR THE PREPARATION OF 1-[(BENZOIMIDAZOLE-1YL) QUINOLIN-8-YL] PIPERIDIN-4-YLAMINE DERIVATIVES PFIZER PRODUCTS INC. (US) 2004-12-29 WO disclosed
WO-2004020431-A2 NOVEL BENZOIMIDAZOLE DERIVATIVES USEFUL AS ANTIPROLIFERATIVE AGENTS PFIZER PRODUCTS INC. (US) 2004-03-11 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 (2 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-20050124599-A1 Novel benzoimidazole derivatives useful as antiproliferative agents CCNI, CCNT1, CCNA1 FLT3 297/4885PDGFRB 1621/4885PDGFRA 1234/4885
US-20050020625-A1 Processes for the preparation of benzoimidazole derivatives CCNI, CCNT1, CCNE1 FLT3 567/4885PDGFRB 1909/4885PDGFRA 1486/4885

“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.