SCHEMBL163312

SCHEMBL163312

Oc1ncc2ccccc2n1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.46
GPR3 P46089 1/20 0.46
EGFR P00533 1/20 0.46
ALDH1A1 P00352 3/20 0.44
HPGD P15428 2/20 0.44
MAPT P10636 2/20 0.44
GLA P06280 1/20 0.44
ACHE P22303 1/20 0.44
CYP1A2 P05177 4/20 0.43
GAA P10253 1/20 0.42
STAT3 P40763 1/20 0.42
HTR3A P46098 1/20 0.42
HRH4 Q9H3N8 1/20 0.42
AR P10275 1/20 0.39
MGAM O43451 2/20 0.38
BCHE P06276 1/20 0.38
NCF1 P14598 1/20 0.38
NOS2 P35228 1/20 0.38
BACE1 P56817 1/20 0.38
CA12 O43570 1/20 0.38

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
SCHEMBL31235102 1.00 KDM4E (0.46) KDM4EGPR3EGFRALDH1A1HPGD
SCHEMBL28762595 0.98 KDM4E (0.45) KDM4EGPR3EGFRALDH1A1HPGD
Hydrochloric Acid SCHEMBL27927852 0.98 KDM4E (0.45) KDM4EGPR3EGFRALDH1A1HPGD
Hypophosphorous Acid SCHEMBL1654733 0.90 KDM4E (0.39) KDM4EGPR3EGFRALDH1A1HPGD
Phosphonic Acid SCHEMBL4070174 0.90 KDM4E (0.39) KDM4EGPR3EGFRALDH1A1HPGD
Trifluoroacetic Acid SCHEMBL6614032 0.84 PAX8 (0.44) KDM4EALDH1A1HPGDMAPTMGAM
SCHEMBL6830494 0.78 MAPT (0.36) KDM4EALDH1A1HPGDMAPTCYP1A2
SCHEMBL30198446 0.75 CYP1A2 (0.60) KDM4EGPR3EGFRALDH1A1HPGD
SCHEMBL1672650 0.75 CYP1A2 (0.60) KDM4EGPR3EGFRALDH1A1HPGD
SCHEMBL30527184 0.75 CYP1A2 (0.60) KDM4EGPR3EGFRALDH1A1HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108117649-B Organic porous material based on butterfly tricyclic quinazoline unit and synthetic method thereof 中国科学院大连化学物理研究所 2020-05-19 CN claimed
US-20200101057-A1 COMBINATION THERAPY AGAINST CHEMORESISTANCE IN LEUKEMIA THE GENERAL HOSPITAL CORPORATION 2020-04-02 US claimed
CN-110218193-A 3- hydroxyquinazoline -2,4 (1H, 3H)-diketone derivative and the preparation method and application thereof 山东大学 2019-09-10 CN claimed
WO-2018183559-A1 COMBINATION THERAPY AGAINST CHEMORESISTANCE IN LEUKEMIA THE GENERAL HOSPITAL CORPORATION (US) 2018-10-04 WO claimed
WO-2016154694-A1 N-ACYLHYDRAZONE COMPOUNDS INHIBITING HISTONE DESACETYLASE ENZYMES, PHARMACEUTICAL COMPOSITIONS CONTAINING SAME, AND METHOD FOR PRODUCING SAME UNIVERSIDADE FEDERAL DO RIO DE JANEIRO-UFRJ (BR) 2016-10-06 WO claimed
CN-102850397-B Multi-target antitumor compounds and preparation method and application thereof UNIV BEIJING 2015-02-18 CN claimed
CN-103910688-A 2-propyl-4-chloroquinazoline derivative, its preparation method thereof and its application thereof CHUNLIN CHEN 2014-07-09 CN claimed
EP-0407237-B1 Indolino-spiro-oxazine photochromic compounds, process for their preparation and photochromic compositions and materials containing them ESSILOR INT (FR) 1995-11-29 EP claimed
EP-0387119-B1 Process for the condensation of at least one epoxide with at least one cyclic anhydride in the presence of a catalyst based on at least one nitrogen containing titanium complex INST FRANCAIS DU PETROLE (FR) 1993-11-18 EP claimed
US-5030711-A Process for condensing at least one epoxide on at least one cyclic anhydride in the presence of a catalyst consisting of at least one titanium nitrogenous complex INSTITUT FRANCAIS DU PETROLE (FR) 1991-07-09 US claimed
US-4997910-A Polyesters INSTITUT FRANCAIS DU PETROLE (FR) 1991-03-05 US claimed
EP-0407237-A2 Indolino-spiro-oxazine photochromic compounds, process for their preparation and photochromic compositions and materials containing them ESSILOR INTERNATIONAL (Compagnie Générale d'Optique) (FR) 1991-01-09 EP claimed
EP-0031237-B1 QUINAZOLINE DERIVATIVES, PROCESSES FOR THEIR PREPARATION, COMPOSITIONS CONTAINING THEM AND THEIR USE AS ANTI-CANCER AGENTS NATIONAL RESEARCH DEVELOPMENT CORPORATION (GB) 1984-10-17 EP claimed
JP-53044597-A None JP disclosed
EP-4676600-A1 PROTEIN KINASE INHIBITORS AND USES THEREOF Deliver Therapeutics, Inc. (US) 2026-01-14 EP disclosed
US-20250289830-A1 KRAS INHIBITORS ELI LILLY AND COMPANY 2025-09-18 US disclosed
US-4141895-A Hydroxyquinazolines and their use as intermediates for pharmaceutical agents E. I. DU PONT DE NEMOURS AND COMPANY (US) 1979-02-27 US disclosed
US-4141895-A Hydroxyquinazolines and their use as intermediates for pharmaceutical agents E. I. DU PONT DE NEMOURS AND COMPANY (US) 1979-02-27 US disclosed
JP-S5344597-A CONDENSED QUINAZOLINOL DERIVATIVE DAI ICHI SEIYAKU CO LTD 1978-04-21 JP disclosed
US-4038240-A PROCESS FOR DYEING POLYURETHANE RESINS BAYER AKTIENGESELLSCHAFT (DT) 1977-07-26 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-20250289830-A1 KRAS INHIBITORS KRAS, NRAS, HRAS KDM4E 2640/4885GPR3 745/4885EGFR 26/4885

“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.