Pki-166

Pki-166

SCHEMBL209560

CC(Nc1ncnc2[nH]c(-c3ccc(O)cc3)cc12)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

EGFR

The experimentally established mechanism targets of Pki-166. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
EGFR known ✓ P00533 19/20 1.00
CSF1R P07333 1/20 0.78
HDAC3 O15379 1/20 0.74
KDR P35968 1/20 0.74
HDAC4 P56524 1/20 0.74
HDAC1 Q13547 1/20 0.74
HDAC7 Q8WUI4 1/20 0.74
HDAC2 Q92769 1/20 0.74
HDAC10 Q969S8 1/20 0.74
HDAC11 Q96DB2 1/20 0.74
HDAC8 Q9BY41 1/20 0.74
HDAC6 Q9UBN7 1/20 0.74
HDAC9 Q9UKV0 1/20 0.74
HDAC5 Q9UQL6 1/20 0.74

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
Pki-166 SCHEMBL185822 1.00 EGFR (1.00) EGFRCSF1RHDAC3KDRHDAC4
Pki-166 SCHEMBL30883827 1.00 EGFR (1.00) EGFRCSF1RHDAC3KDRHDAC4
Pki-166 SCHEMBL29352405 1.00 EGFR (1.00) EGFRCSF1RHDAC3KDRHDAC4
Pki-166 SCHEMBL9973098 1.00 EGFR (1.00) EGFRCSF1RHDAC3KDRHDAC4
Pki-166 SCHEMBL29409570 0.99 EGFR (0.98) EGFRCSF1RHDAC3KDRHDAC4
SCHEMBL12308303 0.89 EGFR (0.86) EGFRCSF1RHDAC3KDRHDAC4
SCHEMBL4766235 0.89 EGFR (0.86) EGFRCSF1RHDAC3KDRHDAC4
SCHEMBL4766237 0.89 EGFR (0.86) EGFRCSF1RHDAC3KDRHDAC4
SCHEMBL7499430 0.89 EGFR (0.86) EGFRCSF1RHDAC3KDRHDAC4
SCHEMBL4901987 0.89 EGFR (1.00) EGFRHDAC3KDRHDAC4HDAC1

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 1310 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2207805-B1 NLRR-1 ANTAGONISTS AND USES THEREOF GENENTECH INC (US) 2014-07-09 EP claimed
US-20100310477-A1 Pharmaceutical compositions based on anticholingerics and additional active ingredients BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG. (DE) 2010-12-09 US claimed
US-20100144639-A1 USE OF INHIBITORS OF THE EGFR-MEDIATED SIGNAL TRANSDUCTION FOR THE TREATMENT OF BENIGN PROSTATIC HYPERPLASIA (BPH) / PROSTATIC HYPERTROPHY BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2010-06-10 US claimed
US-20090306072-A1 USE OF TYROSINE KINASE INHIBITORS FOR THE TREATMENT OF INFLAMMATORY PROCESSES BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2009-12-10 US claimed
EP-2116245-A2 EGFR kinase inhibitor combinations for treating respiratory and gastrointestinal disorders Boehringer Ingelheim International GmbH (DE) 2009-11-11 EP claimed
US-20090221519-A1 COMBINATIONS OF RECEPTOR TYROSINE KINASE INHIBITOR WITH AN A1-ACIDIC GLYCOPROTEIN BINDING COMPOUND NOVARTIS AG (CH) 2009-09-03 US claimed
US-20090017036-A1 PHARMACEUTICAL COMPOSITIONS FOR TREATMENT OF RESPIRATORY AND GASTROINTESTINAL DISORDERS JUNG BIRGIT 2009-01-15 US claimed
CN-101035540-A Pharmaceutical combinations containing benzoxazine for treating respiratory diseases BOEHRINGER INGELHEIM INT (DE) 2007-09-12 CN claimed
EP-1553950-B1 THERAPEUTIC TREATMENT ASTRAZENECA AB (SE) 2007-08-08 EP claimed
US-20070099918-A1 Use of inhibitors of the EGFR-mediated signal transduction for the treatment of benign prostatic hyperplasia (BPH) / prostatic hypertrophy BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2007-05-03 US claimed
US-20030125343-A1 Combinations of receptor tyrosine kinase inhibitor with an a1-acidic glycoprotein binding compound GAMBACORTI-PASSERINI CARLO (IT) 2003-07-03 US claimed
WO-2003037897-A2 USE OF 7H-PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES IN THE TREATMENT OF SOLID TUMOR DISEASES NOVARTIS AG (CH) 2003-05-08 WO claimed
US-20030065000-A1 Method of treating cancer COHEN PAMELA SARAH (US) 2003-04-03 US claimed
EP-1250140-A2 COMBINATIONS OF A RECEPTOR TYROSINE KINASE INHIBITOR WITH ALPHA1-ACIDIC GLYCOPROTEIN BINDING COMPOUND Novartis AG (CH) 2002-10-23 EP claimed
WO-2002050306-A1 PROCESSES FOR DETERMINING THE BIOLOGICAL ACTIVITY OF EPIDERMAL GROWTH FACTOR RECEPTOR TYROSINE KINASE INHIBITORS NOVARTIS AG (CH) 2002-06-27 WO claimed
EP-0836605-B1 PYRROLOPYRIMIDINES AND PROCESSES FOR THE PREPARATION THEREOF NOVARTIS AG (CH) 2002-02-06 EP claimed
WO-2001047507-A2 COMBINATIONS OF RECEPTOR TYROSINE KINASE INHIBITOR WITH AN A1-ACIDIC GLYCOPROTEIN BINDING COMPOUND NOVARTIS AG (CH) 2001-07-05 WO claimed
US-6140332-A Pyrrolopyrimidines and processes for the preparation thereof NOVARTIS AG (CH) 2000-10-31 US claimed
EP-0836605-A1 PYRROLOPYRIMIDINES AND PROCESSES FOR THE PREPARATION THEREOF Novartis AG (CH) 1998-04-22 EP claimed
WO-1997002266-A1 PYRROLOPYRIMIDINES AND PROCESSES FOR THE PREPARATION THEREOF NOVARTIS AG (CH) 1997-01-23 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (7 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-20090221519-A1 COMBINATIONS OF RECEPTOR TYROSINE KINASE INHIBITOR WITH AN A1-ACIDIC GLYCOPROTEIN BINDING COMPOUND PDGFRA, PDGFRB, TEK EGFR 22/4885CSF1R 57/4885HDAC3 4594/4885
US-20090306072-A1 USE OF TYROSINE KINASE INHIBITORS FOR THE TREATMENT OF INFLAMMATORY PROCESSES ERBB2, EGFR, ERBB4 EGFR 2/4885CSF1R 645/4885HDAC3 3897/4885
US-20070099918-A1 Use of inhibitors of the EGFR-mediated signal transduction for the treatment of benign prostatic hyperplasia (BPH) / prostatic hypertrophy BPHL, EGFR, ERBB3 EGFR 2/4885CSF1R 350/4885HDAC3 1941/4885
US-20090017036-A1 PHARMACEUTICAL COMPOSITIONS FOR TREATMENT OF RESPIRATORY AND GASTROINTESTINAL DISORDERS BDKRB2, EDNRB, GRK5 EGFR 53/4885CSF1R 2553/4885HDAC3 3882/4885
US-20100144639-A1 USE OF INHIBITORS OF THE EGFR-MEDIATED SIGNAL TRANSDUCTION FOR THE TREATMENT OF BENIGN PROSTATIC HYPERPLASIA (BPH) / PROSTATIC HYPERTROPHY BPHL, EGFR, ERBB3 EGFR 2/4885CSF1R 350/4885HDAC3 1941/4885
US-20100310477-A1 Pharmaceutical compositions based on anticholingerics and additional active ingredients PDE4B, CHRM3, ADRA2C EGFR 43/4885CSF1R 2574/4885HDAC3 3515/4885
US-20030125343-A1 Combinations of receptor tyrosine kinase inhibitor with an a1-acidic glycoprotein binding compound PDGFRA, PDGFRB, TEK EGFR 23/4885CSF1R 58/4885HDAC3 4667/4885

“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.