Erlotinib

Erlotinib

SCHEMBL3826918

C#Cc1cccc(Nc2ncnc3cc(OCCOC)c(OCCOC)cc23)c1.Cl.O

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

EGFR

The experimentally established mechanism targets of Erlotinib. 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
EGFR known ✓ P00533 16/20 0.98
ERBB2 P04626 5/20 0.98
GAK O14976 3/20 0.96
ILK Q13418 3/20 0.96
KDR P35968 2/20 0.96
PLK4 O00444 1/20 0.96
CIT O14578 1/20 0.96
AURKA O14965 1/20 0.96
EPHB6 O15197 1/20 0.96
SLC22A1 O15245 1/20 0.96
DAPK3 O43293 1/20 0.96
RIPK2 O43353 1/20 0.96
BUB1 O43683 1/20 0.96
KDM1A O60341 1/20 0.96
JAK2 O60674 1/20 0.96
RPS6KA4 O75676 1/20 0.96
STK17B O94768 1/20 0.96
STK10 O94804 1/20 0.96
SLCO2B1 O94956 1/20 0.96
ABCB11 O95342 1/20 0.96

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
Erlotinib SCHEMBL1759094 1.00 EGFR (0.98) EGFRERBB2GAKILKKDR
Erlotinib SCHEMBL417841 0.99 EGFR (0.98) EGFRERBB2GAKILKKDR
Erlotinib SCHEMBL29460839 0.99 EGFR (1.00) EGFRERBB2GAKILKKDR
Erlotinib SCHEMBL18563 0.99 EGFR (1.00) EGFRERBB2GAKILKKDR
Erlotinib SCHEMBL21176918 0.99 EGFR (1.00) EGFRERBB2GAKILKKDR
Erlotinib SCHEMBL16767632 0.99 EGFR (1.00) EGFRERBB2GAKILKKDR
Erlotinib SCHEMBL29351329 0.98 EGFR (1.00) EGFRERBB2GAKILKKDR
Erlotinib SCHEMBL30362833 0.98 EGFR (1.00) EGFRERBB2GAKILKKDR
Erlotinib SCHEMBL3667407 0.98 EGFR (1.00) EGFRERBB2GAKILKKDR
Erlotinib SCHEMBL8413 0.98 EGFR (1.00) EGFRERBB2GAKILKKDR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106749048-A A kind of Eriotinib Hydrochloride form compound and preparation method thereof 山东裕欣药业有限公司 2017-05-31 CN claimed
US-8372856-B2 Crystalline, formed by crystallizing from an aqueous solution without agitation; treating cancer SYNTHON BV (NL) 2013-02-12 US claimed
EP-2099772-A2 HYDRATES OF ERLOTINIB HYDROCHLORIDE Synthon B.V. (NL) 2009-09-16 EP claimed
US-20080167327-A1 Crystalline, formed by crystallizing from an aqueous solution without agitation; treating cancer SYNTHON BV (NL) 2008-07-10 US claimed
WO-2008049645-A2 HYDRATES OF ERLOTINIB HYDROCHLORIDE SYNTHON B.V. (NL) 2008-05-02 WO claimed
CN-106749048-B Erlotinib hydrochloride crystal form compound and preparation method thereof 山东裕欣药业有限公司 2020-03-20 CN disclosed
CN-106749048-A A kind of Eriotinib Hydrochloride form compound and preparation method thereof 山东裕欣药业有限公司 2017-05-31 CN disclosed
CN-103124557-A Pure erlotinib GENERICS UK LTD 2013-05-29 CN disclosed
US-8372856-B2 Crystalline, formed by crystallizing from an aqueous solution without agitation; treating cancer SYNTHON BV (NL) 2013-02-12 US disclosed
US-8372856-B2 Crystalline, formed by crystallizing from an aqueous solution without agitation; treating cancer SYNTHON BV (NL) 2013-02-12 US disclosed
US-7625911-B2 Amorphous form of erlotinib hydrochloride and its solid amorphous dispersion MAI DE LTD. (US) 2009-12-01 US disclosed
EP-2099772-A2 HYDRATES OF ERLOTINIB HYDROCHLORIDE Synthon B.V. (NL) 2009-09-16 EP disclosed
EP-2099772-A2 HYDRATES OF ERLOTINIB HYDROCHLORIDE Synthon B.V. (NL) 2009-09-16 EP disclosed
WO-2008049645-A3 HYDRATES OF ERLOTINIB HYDROCHLORIDE SYNTHON BV (NL) 2008-07-31 WO disclosed
US-20080167327-A1 Crystalline, formed by crystallizing from an aqueous solution without agitation; treating cancer SYNTHON BV (NL) 2008-07-10 US disclosed
US-20080167327-A1 Crystalline, formed by crystallizing from an aqueous solution without agitation; treating cancer SYNTHON BV (NL) 2008-07-10 US disclosed
WO-2008049645-A2 HYDRATES OF ERLOTINIB HYDROCHLORIDE SYNTHON B.V. (NL) 2008-05-02 WO disclosed
WO-2008049645-A2 HYDRATES OF ERLOTINIB HYDROCHLORIDE SYNTHON B.V. (NL) 2008-05-02 WO disclosed
CN-101016266-A Novel amorphous form of erlotinib hydrochloride and its solid amorphous dispersion MAI DE LTD (CN) 2007-08-15 CN disclosed
US-20060154941-A1 Novel amorphous form of erlotinib hydrochloride and its solid amorphous dispersion MAI DE LTD. 2006-07-13 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-20080167327-A1 Crystalline, formed by crystallizing from an aqueous solution without agitation; treating cancer TP53, KRAS, HRAS EGFR 6/4885ERBB2 91/4885GAK 316/4885
US-20060154941-A1 Novel amorphous form of erlotinib hydrochloride and its solid amorphous dispersion EGFR, EPS15, KRAS EGFR 1/4885ERBB2 4/4885GAK 667/4885

“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.