Glasdegib

Glasdegib

SCHEMBL2068016

CN1CC[C@@H](NC(=O)Nc2ccc(C#N)cc2)C[C@@H]1c1nc2ccccc2[nH]1.Cl

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SMO

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

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 1/20 0.44
USP30 Q70CQ3 1/20 0.44
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
POLB P06746 1/20 0.43
MAPT P10636 1/20 0.43
KCNH2 Q12809 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
EPHX2 P34913 1/20 0.42
PDPK1 O15530 1/20 0.40

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
Glasdegib SCHEMBL29362720 1.00 EPHX1 (0.44) EPHX1USP30NPC1RAB9APOLB
Glasdegib SCHEMBL22104131 0.99 EPHX1 (0.45) EPHX1USP30NPC1RAB9APOLB
Glasdegib SCHEMBL27100349 0.99 EPHX1 (0.45) EPHX1USP30NPC1RAB9APOLB
Glasdegib SCHEMBL18184932 0.99 EPHX1 (0.45) EPHX1USP30NPC1RAB9APOLB
Glasdegib SCHEMBL2068480 0.99 EPHX1 (0.45) EPHX1USP30NPC1RAB9APOLB
Glasdegib SCHEMBL24503991 0.99 EPHX1 (0.45) EPHX1USP30NPC1RAB9APOLB
Glasdegib SCHEMBL29359708 0.99 EPHX1 (0.45) EPHX1USP30NPC1RAB9APOLB
Glasdegib SCHEMBL18171549 0.94 USP30 (0.41) EPHX1USP30NPC1RAB9APOLB
Glasdegib SCHEMBL29359798 0.94 USP30 (0.41) EPHX1USP30NPC1RAB9APOLB
Glasdegib SCHEMBL18171548 0.94 USP30 (0.41) EPHX1USP30NPC1RAB9APOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023017541-A1 IMPROVED PROCESS FOR THE PREPARATION OF 1-((2R,4R)-2-(1H-BENZO[D]IMIDAZOL-2-YL)-1-METHYL PIPERIDIN-4-YL)-3-(4-CYANOPHENYL)UREA MALEATE MSN LABORATORIES PRIVATE LIMITED, R&D CENTER (IN) 2023-02-16 WO disclosed
EP-2170860-B9 BENZIMIDAZOLE DERIVATIVES PFIZER (US) 2017-02-22 EP disclosed
EP-2170860-B1 BENZIMIDAZOLE DERIVATIVES PFIZER (US) 2016-11-02 EP disclosed
US-8431597-B2 Benzimidazole derivatives PFIZER INC. (US) 2013-04-30 US disclosed
US-20120157495-A1 BENZIMIDAZOLE DERIVATIVES PFIZER INC. 2012-06-21 US disclosed
US-8148401-B2 Benzimidazole derivatives PFIZER INC. (US) 2012-04-03 US disclosed
US-20090005416-A1 BENZIMIDAZOLE DERIVATIVES PFIZER INC. 2009-01-01 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 (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-20090005416-A1 BENZIMIDAZOLE DERIVATIVES BOD1L1, H1-3, BRIX1 EPHX1 4079/4885USP30 4188/4885NPC1 2444/4885
US-20120157495-A1 BENZIMIDAZOLE DERIVATIVES BOD1L1, H1-3, BRIX1 EPHX1 4079/4885USP30 4188/4885NPC1 2444/4885

“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.