SCHEMBL488680

SCHEMBL488680

CC(O)c1c(Cl)ccc(F)c1Cl

nearest known ligand 0.44

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
MET P08581 12/20 0.44
SRC P12931 2/20 0.40
KDR P35968 2/20 0.40
KIT P10721 1/20 0.40
FGFR2 P21802 1/20 0.40
AXL P30530 1/20 0.40
FLT3 P36888 1/20 0.40
MST1R Q04912 1/20 0.40
INPPL1 O15357 7/20 0.39
NTRK1 P04629 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
SCHEMBL1581742 1.00 MET (0.44) METSRCKDRKITFGFR2
SCHEMBL2419732 1.00 MET (0.44) METSRCKDRKITFGFR2
SCHEMBL30236403 1.00 MET (0.44) METSRCKDRKITFGFR2
SCHEMBL30005568 1.00 MET (0.44) METSRCKDRKITFGFR2
SCHEMBL30005904 1.00 MET (0.44) METSRCKDRKITFGFR2
SCHEMBL30509670 1.00 MET (0.44) METSRCKDRKITFGFR2
SCHEMBL30765076 0.89 MET (0.36) METSRCKDRKITFGFR2
SCHEMBL1582536 0.89 MET (0.36) METSRCKDRKITFGFR2
SCHEMBL488432 0.89 MET (0.36) METSRCKDRKITFGFR2
SCHEMBL28018826 0.89 MET (0.36) METSRCKDRKITFGFR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116082110-B The method comprises the following steps of 11 C-labeled targeted anaplastic lymphoma kinase ALK mutant molecular probe and application thereof 北京肿瘤医院(北京大学肿瘤医院) 2024-04-12 CN claimed
CN-115448813-B Method for preparing (S) -2, 6-dichloro-3-fluorophenylethanol 中国科学院兰州化学物理研究所 2023-07-25 CN claimed
CN-116082110-A The method comprises the following steps of 11 C-labeled targeted anaplastic lymphoma kinase ALK mutant molecular probe and application thereof 北京肿瘤医院(北京大学肿瘤医院) 2023-05-09 CN claimed
CN-108285908-B Method for catalytic synthesis of (S) -1- (2, 6-dichloro-3-fluoro-phenyl) ethanol by using immobilized double enzymes 杭州师范大学 2021-02-09 CN claimed
CN-111118072-A Method for preparing enzatinib intermediate by enzyme method 长兴制药股份有限公司 2020-05-08 CN claimed
CN-109942485-A A kind of gram of azoles replaces the synthetic method of Buddhist nun's intermediate 青岛前线生物工程有限公司 2019-06-28 CN claimed
CN-109438180-A The preparation method of one kind (S) -1- (the chloro- 3- fluorophenyl of 2,6- bis-) ethyl alcohol 凯瑞斯德生化(苏州)有限公司 2019-03-08 CN claimed
CN-108285908-A A kind of method that immobilized bi-enzyme catalyzes and synthesizes (S) -1- (bis- chloro- 3- fluoro-phenyls of 2,6-) ethyl alcohol 杭州师范大学 2018-07-17 CN claimed
CN-107794282-A A kind of gram of azoles replaces the preparation method and bacterial strain of Buddhist nun's chiral intermediate 浙江工业大学 2018-03-13 CN claimed
CN-106047950-A Biological preparation method of (S)-1-(2,6-dichloro-3-fluorophenyl)ethanol 尚科生物医药(上海)有限公司 2016-10-26 CN claimed
CN-105906656-A Synthetic method of crizotinib intermediate 凯莱英医药集团(天津)股份有限公司 2016-08-31 CN claimed
EP-2198018-A2 KETOREDUCTASE POLYPEPTIDES FOR THE REDUCTION OF ACETOPHENONES Codexis, Inc. (US) 2010-06-23 EP claimed
WO-2009036404-A2 KETOREDUCTASE POLYPEPTIDES FOR THE REDUCTION OF ACETOPHENONES CODEXIS, INC. (US) 2009-03-19 WO claimed
EP-1791965-A1 ENANTIOSELECTIVE BIOTRANSFORMATION FOR PREPARATION OF PROTEIN TYROSINE KINASE INHIBITOR INTERMEDIATES Pfizer, Inc. (US) 2007-06-06 EP claimed
WO-2006021885-A1 ENANTIOSELECTIVE BIOTRANSFORMATION FOR PREPARATION OF PROTEIN TYROSINE KINASE INHIBITOR INTERMEDIATES PFIZER INC. (US) 2006-03-02 WO claimed
US-20060046287-A1 Enantioselective biotransformation for preparation of protein tyrosine kinase inhibitor intermediates AGOURON PHARMACEUTICALS, INC. 2006-03-02 US claimed
US-12415990-B2 Ketoreductase polypeptides for the reduction of acetophenones CODEXIS, INC. (US) 2025-09-16 US disclosed
CN-116496140-B Preparation method of tenidine drug intermediate 凯特立斯(深圳)科技有限公司 2025-03-04 CN disclosed
US-20050009840-A1 2-amino- pyridines and pyrazines additionally substituted witn one or more carbocyclic or heterocyclic groups, e.g., 4-[6-amino-5-(2,6-dichloro-benzyloxy)-pyridin-3-yl]-phenol, for treating many kinds of cancer SUGEN, INC. 2005-01-13 US disclosed
WO-2004076412-A2 AMINOHETEROARYL COMPOUNDS AS PROTEIN KINASE INHIBITORS SUGEN, INC. (US) 2004-09-10 WO 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-20050009840-A1 2-amino- pyridines and pyrazines additionally substituted witn one or more carbocyclic or heterocyclic groups, e.g., 4-[6-amino-5-(2,6-dichloro-benzyloxy)-pyridin-3-yl]-phenol, for treating many kinds of cancer MET, ERBB2, CDK4 MET 1/4885SRC 76/4885KDR 362/4885

“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.