SCHEMBL1502275

SCHEMBL1502275

O=C(O)C=CCN1CCOCC1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 2/20 0.48
GLA P06280 1/20 0.46
KDM4E B2RXH2 2/20 0.44
TSHR P16473 2/20 0.42
ALOX15 P16050 1/20 0.42
ALDH1A1 P00352 3/20 0.42
SMN1; SMN2 Q16637 1/20 0.40
HSP90AA1 P07900 1/20 0.39
MAPT P10636 2/20 0.38
KMT2A Q03164 2/20 0.38
USP2 O75604 1/20 0.38
HRH3 Q9Y5N1 1/20 0.37
GABRR1 P24046 2/20 0.37
GABRR2 P28476 2/20 0.37
BLM P54132 2/20 0.37
GABRR3 A8MPY1 1/20 0.37
LMNA P02545 1/20 0.37
APEX1 P27695 1/20 0.37
NPSR1 Q6W5P4 1/20 0.37
TDP1 Q9NUW8 1/20 0.37

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
SCHEMBL2978048 1.00 HSD17B10 (0.48) HSD17B10GLAKDM4ETSHRALOX15
Hydrochloric Acid SCHEMBL20839693 0.98 GLA (0.48) HSD17B10GLAKDM4ETSHRALOX15
Hydrochloric Acid SCHEMBL27001777 0.98 GLA (0.48) HSD17B10GLAKDM4ETSHRALOX15
SCHEMBL2840849 0.98 HSD17B10 (0.52) HSD17B10GLAKDM4ETSHRALOX15
SCHEMBL2840850 0.98 HSD17B10 (0.52) HSD17B10GLAKDM4ETSHRALOX15
SCHEMBL23074882 0.82 KDM4E (0.52) HSD17B10GLAKDM4ETSHRALOX15
SCHEMBL2228548 0.82 KDM4E (0.42) HSD17B10GLAKDM4ETSHRALOX15
SCHEMBL14165795 0.82 KDM4E (0.42) HSD17B10GLAKDM4ETSHRALOX15
SCHEMBL2228544 0.82 KDM4E (0.42) HSD17B10GLAKDM4ETSHRALOX15
SCHEMBL14165793 0.82 KDM4E (0.42) HSD17B10GLAKDM4ETSHRALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7772243-B2 4-phenylamino-quinazolin-6-yl-amides WARNER-LAMBERT COMPANY LLC (US) 2010-08-10 US claimed
JP-4205757-B2 2009-01-07 JP claimed
JP-2007536368-A 2007-12-13 JP claimed
EP-1746999-A1 4-PHENYLAMINO-QUINAZOLIN-6-YL-AMIDES Warner-Lambert Company LLC (US) 2007-01-31 EP claimed
WO-2005107758-A1 4-PHENYLAMINO-QUINAZOLIN-6-YL-AMIDES WARNER-LAMBERT COMPANY LLC (US) 2005-11-17 WO claimed
US-20050250761-A1 such as -Piperidin-1-yl-but-2-enoic acid [4(3-chloro-4-fluoro-phenylamino)-7-methoxy-quinazolin-6-yl]-amide, used as tyrosine kinase inhibitors, for the prevention of proliferative diseases, including cancer, atherosclerosis, restenosis, endometriosis and psoriasis PFIZER INC 2005-11-10 US claimed
EP-1263503-B1 USE OF CYANOQUINOLINES FOR TREATING OR INHIBITING COLONIC POLYPS WYETH CORP (US) 2005-11-02 EP claimed
EP-1549297-A2 STABILIZED PHARMACEUTICAL COMPOSITION CONTAINING BASIC EXCIPIENTS Wyeth Holdings Corporation (US) 2005-07-06 EP claimed
US-20040122048-A1 Stabilized pharmaceutical composition containing basic excipients WYETH HOLDINGS CORPORATION 2004-06-24 US claimed
WO-2004032909-A2 STABILIZED PHARMACEUTICAL COMPOSITION CONTAINING BASIC EXCIPIENTS WYETH HOLDINGS CORPORATION (US) 2004-04-22 WO claimed
EP-0973746-B1 SUBSTITUTED 3-CYANO QUINOLINES WYETH CORP (US) 2003-09-24 EP claimed
JP-2003526686-A 2003-09-09 JP claimed
EP-1263503-A2 USE OF CYANOQUINOLINES FOR TREATING OR INHIBITING COLONIC POLYPS AMERICAN CYANAMID COMPANY (US) 2002-12-11 EP claimed
US-6384051-B1 ANTITUMOR AGENTS AMERICAN CYANAMID COMPANY 2002-05-07 US claimed
WO-2001068186-A2 USE OF CYANOQUINOLINES FOR TREATING OR INHIBITING COLONIC POLYPS AMERICAN CYANAMID COMPANY (US) 2001-09-20 WO claimed
EP-0973746-A1 SUBSTITUTED 3-CYANO QUINOLINES American Cyanamid Company (US) 2000-01-26 EP claimed
US-6002008-A Substituted 3-cyano quinolines AMERICAN CYANAMID COMPANY 1999-12-14 US claimed
WO-1998043960-A1 SUBSTITUTED 3-CYANO QUINOLINES AMERICAN CYANAMID COMPANY (US) 1998-10-08 WO claimed
CN-122079960-A Alkynyl quinazoline compounds 2026-05-26 CN disclosed
US-6002008-A Substituted 3-cyano quinolines AMERICAN CYANAMID COMPANY 1999-12-14 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-20050250761-A1 such as -Piperidin-1-yl-but-2-enoic acid [4(3-chloro-4-fluoro-phenylamino)-7-methoxy-quinazolin-6-yl]-amide, used as tyrosine kinase inhibitors, for the prevention of proliferative diseases, including cancer, atherosclerosis, restenosis, endometriosis and psoriasis JAK1, JAK2, EDNRA HSD17B10 3078/4885GLA 4405/4885KDM4E 632/4885
US-20040122048-A1 Stabilized pharmaceutical composition containing basic excipients F7, H1-10, F12 HSD17B10 2458/4885GLA 1196/4885KDM4E 774/4885

“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.