SCHEMBL72924

SCHEMBL72924

CC(C)(C)c1cc(NC(=O)Nc2ccc(-c3cn4c(n3)sc3ccc(OCCN5CCOCC5)cc34)cc2)no1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FLT3 P36888 20/20 1.00
KDR P35968 2/20 0.91
BMPR1B O00238 1/20 0.91
MUSK O15146 1/20 0.91
EPHB6 O15197 1/20 0.91
MAP3K7 O43318 1/20 0.91
RIPK2 O43353 1/20 0.91
PAK3 O75914 1/20 0.91
STK10 O94804 1/20 0.91
MAP4K4 O95819 1/20 0.91
ABL1 P00519 1/20 0.91
NTRK1 P04629 1/20 0.91
LCK P06239 1/20 0.91
CSF1R P07333 1/20 0.91
YES1 P07947 1/20 0.91
LYN P07948 1/20 0.91
RET P07949 1/20 0.91
PDGFRB P09619 1/20 0.91
KIT P10721 1/20 0.91
PDGFRA P16234 1/20 0.91

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
Hydrochloric Acid SCHEMBL74122 0.99 FLT3 (0.99) FLT3KDRBMPR1BMUSKEPHB6
Hydrochloric Acid SCHEMBL742748 0.99 FLT3 (0.99) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL72923 0.95 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL29349937 0.95 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL74121 0.94 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL742377 0.94 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL29435035 0.94 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
SCHEMBL1759073 0.93 FLT3 (0.87) FLT3KDRBMPR1BMUSKEPHB6
SCHEMBL1759300 0.93 FLT3 (0.87) FLT3KDRBMPR1BMUSKEPHB6
SCHEMBL74274 0.93 FLT3 (0.86) FLT3KDRBMPR1BMUSKEPHB6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3260119-B1 COMBINATION METHOD FOR TREATING CANCER DAIICHI SANKYO CO LTD (JP) 2023-11-15 EP claimed
US-10716790-B2 Method for treating cancer by combined use DAIICHI SANKYO COMPANY, LIMITED (JP) 2020-07-21 US claimed
EP-2521782-B1 FLT3 RECEPTOR ANTAGONISTS FOR THE TREATMENT OR THE PREVENTION OF PAIN DISORDERS INST NAT SANTE RECH MED (FR) 2019-04-10 EP claimed
EP-2903593-B1 TABLET CONTAINING COMPOSITE WITH CYCLODEXTRIN AMBIT BIOSCIENCES CORP (US) 2018-03-21 EP claimed
EP-3260119-A1 COMBINATION METHOD FOR TREATING CANCER DAIICHI SANKYO COMPANY, LIMITED (JP) 2017-12-27 EP claimed
US-20170348320-A1 IMIDAZOLOTHIAZOLE COMPOUNDS FOR THE TREATMENT OF DISEASE AMBIT BIOSCIENCES CORP (US) 2017-12-07 US claimed
US-20170216302-A1 METHOD FOR TREATING CANCER BY COMBINED USE DAIICHI SANKYO COMPANY, LIMITED (JP) 2017-08-03 US claimed
US-9675549-B2 Tablet containing composite with cyclodextrin AMBIT BIOSCIENCES CORPORATION (US) 2017-06-13 US claimed
EP-2496584-B1 PROCESS FOR THE PREPARATION OF IMIDAZO[2,1-B][1,3]BENZOTHIAZOLE DERIVATIVES AMBIT BIOSCIENCES CORP (US) 2016-09-21 EP claimed
US-9284332-B2 Process for the preparation of imidazo[2,1-B][1,3]benzothiazole derivatives AMBIT BIOSCIENCES CORPORATION (US) 2016-03-15 US claimed
EP-2001892-B1 IMIDAZOLOTHIAZOLE COMPOUNDS FOR THE TREATMENT OF PROLIFERATIVE DISEASES AMBIT BIOSCIENCES CORP (US) 2013-04-24 EP claimed
US-20130005966-A1 PROCESS FOR THE PREPARATION OF IMIDAZO[2,1-B][1,3]BENZOTHIAZOLE DERIVATIVES AMBIT BIOSCIENCES CORP. (US) 2013-01-03 US claimed
US-20120129850-A1 IMIDAZOLOTHIAZOLE COMPOUNDS FOR THE TREATMENT OF DISEASE AMBIT BIOSCIENCES CORPORATION 2012-05-24 US claimed
US-20120070410-A1 IMIDAZOLOTHIAZOLE COMPOUNDS AND METHODS OF USE THEREOF AMBIT BIOSCIENCES CORPORATION 2012-03-22 US claimed
US-8129374-B2 Method of using imidazolothiazole compounds for the treatment of disease AMBIT BIOSCIENCE CORPORATION (US) 2012-03-06 US claimed
US-20100298313-A1 METHOD OF USING IMIDAZOLOTHIAZOLE COMPOUNDS FOR THE TREATMENT OF DISEASE AMBIT BIOSCIENCES CORPORATION 2010-11-25 US claimed
US-7820657-B2 receptor kinase inhibitors such as 3-(2-{4-[3-(5-tert-Butyl-isoxazol-3-yl)-ureido]-phenyl}-benzo[d]imidazo[2,1-b]thiazol-7-yl)-N-(2-morpholin-4-yl-ethyl)-propionamide; flk inhibitors AMBIT BIOSCIENCES CORPORATION (US) 2010-10-26 US claimed
EP-2001892-A2 IMIDAZOLOTHIAZOLE COMPOUNDS FOR THE TREATMENT OF DISEASE Ambit Biosciences Corporation (US) 2008-12-17 EP claimed
US-20070232604-A1 receptor kinase inhibitors such as 3-(2-{4-[3-(5-tert-Butyl-isoxazol-3-yl)-ureido]-phenyl}-benzo[d]imidazo[2,1-b]thiazol-7-yl)-N-(2-morpholin-4-yl-ethyl)-propionamide; flk inhibitors AMBIT BIOSCIENCES CORPORATION 2007-10-04 US claimed
WO-2007109120-A2 IMIDAZOLOTHIAZOLE COMPOUNDS FOR THE TREATMENT OF DISEASE AMBIT BIOSCIENCES CORPORATION (US) 2007-09-27 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 (8 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-20120129850-A1 IMIDAZOLOTHIAZOLE COMPOUNDS FOR THE TREATMENT OF DISEASE GRK2, GRK4, GRK3 FLT3 210/4885KDR 540/4885BMPR1B 2351/4885
US-20100298313-A1 METHOD OF USING IMIDAZOLOTHIAZOLE COMPOUNDS FOR THE TREATMENT OF DISEASE GRK2, GRK4, GRK5 FLT3 363/4885KDR 675/4885BMPR1B 2817/4885
US-20170216302-A1 METHOD FOR TREATING CANCER BY COMBINED USE FLT3, MDM2, TP53 FLT3 1/4885KDR 281/4885BMPR1B 3374/4885
US-20170348320-A1 IMIDAZOLOTHIAZOLE COMPOUNDS FOR THE TREATMENT OF DISEASE GRK2, GRK4, GRK3 FLT3 210/4885KDR 540/4885BMPR1B 2351/4885
US-20130005966-A1 PROCESS FOR THE PREPARATION OF IMIDAZO[2,1-B][1,3]BENZOTHIAZOLE DERIVATIVES FLT4, FLT1, FLT3 FLT3 3/4885KDR 13/4885BMPR1B 1133/4885
US-20070232604-A1 receptor kinase inhibitors such as 3-(2-{4-[3-(5-tert-Butyl-isoxazol-3-yl)-ureido]-phenyl}-benzo[d]imidazo[2,1-b]thiazol-7-yl)-N-(2-morpholin-4-yl-ethyl)-propionamide; flk inhibitors GRK2, GRK3, BLK FLT3 128/4885KDR 279/4885BMPR1B 2105/4885
US-20120070410-A1 IMIDAZOLOTHIAZOLE COMPOUNDS AND METHODS OF USE THEREOF GRK2, GRK3, GRK4 FLT3 189/4885KDR 448/4885BMPR1B 3045/4885
US-10716790-B2 Method for treating cancer by combined use FLT3, MDM2, TP53 FLT3 1/4885KDR 281/4885BMPR1B 3374/4885

“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.