SCHEMBL17509525

SCHEMBL17509525

Cc1cccc(C)c1NC(=O)N(C)c1cc(Nc2ccc(N3CCN(C)CC3)cc2)ncn1

nearest known ligand 0.88

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LCK P06239 13/20 0.88
FGFR3 P22607 7/20 0.70
SIK1 P57059 1/20 0.69
MELK Q14680 1/20 0.69
SIK2 Q9H0K1 1/20 0.69
SIK3 Q9Y2K2 1/20 0.69
CYP3A4 P08684 2/20 0.63
CYP2C19 P33261 2/20 0.63
CYP2C9 P11712 1/20 0.63
JAK2 O60674 2/20 0.59
ABL1 P00519 2/20 0.59
INSR P06213 2/20 0.59
FYN P06241 2/20 0.59
YES1 P07947 2/20 0.59
LYN P07948 2/20 0.59
RET P07949 2/20 0.59
MET P08581 2/20 0.59
ROS1 P08922 2/20 0.59
KIT P10721 2/20 0.59
FGFR1 P11362 2/20 0.59

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
SCHEMBL17537436 0.94 LCK (1.00) LCKFGFR3SIK1MELKSIK2
SCHEMBL583166 0.83 FGFR3 (0.86) LCKFGFR3CYP3A4CYP2C19CYP2C9
SCHEMBL374214 0.83 FGFR3 (1.00) LCKFGFR3SIK1MELKSIK2
SCHEMBL23771703 0.82 FGFR3 (0.85) LCKFGFR3SIK1MELKSIK2
SCHEMBL19224079 0.82 LCK (0.81) LCKFGFR3CYP3A4CYP2C19CYP2C9
SCHEMBL29440265 0.82 SIK1 (1.00) LCKFGFR3SIK1MELKSIK2
SCHEMBL15271960 0.82 SIK1 (1.00) LCKFGFR3SIK1MELKSIK2
SCHEMBL374547 0.81 FGFR3 (1.00) LCKFGFR3SIK1MELKSIK2
SCHEMBL374685 0.81 LCK (1.00) LCKFGFR3CYP3A4CYP2C19CYP2C9
SCHEMBL17537383 0.80 LCK (0.80) LCKFGFR3CYP3A4CYP2C19CYP2C9

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
US-20220305016-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS FOR TREATING OSTEOPOROSIS THE GENERAL HOSPITAL CORPORATION (US) 2022-09-29 US disclosed
US-11241435-B2 Uses of salt-inducible kinase (SIK) inhibitors for treating osteoporosis THE GENERAL HOSPITAL CORPORATION (US) 2022-02-08 US disclosed
US-20200338087-A9 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2020-10-29 US disclosed
US-20200338087-A9 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2020-10-29 US disclosed
US-20200179387-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS FOR TREATING OSTEOPOROSIS THE GENERAL HOSPITAL CORPORATION (US) 2020-06-11 US disclosed
US-20190343842-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2019-11-14 US disclosed
US-20190343842-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2019-11-14 US disclosed
EP-3536323-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS Dana Farber Cancer Institute, Inc. (US) 2019-09-11 EP disclosed
EP-3536323-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS Dana Farber Cancer Institute, Inc. (US) 2019-09-11 EP disclosed
US-10265321-B2 Uses of salt-inducible kinase (SIK) inhibitors DANA-FARBER CANCER INSTITUTE, INC. (US) 2019-04-23 US disclosed
US-10265321-B2 Uses of salt-inducible kinase (SIK) inhibitors DANA-FARBER CANCER INSTITUTE, INC. (US) 2019-04-23 US disclosed
US-20180221379-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2018-08-09 US disclosed
US-20180221379-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2018-08-09 US disclosed
US-20180221379-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2018-08-09 US disclosed
US-20170224700-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2017-08-10 US disclosed
US-20170224700-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2017-08-10 US disclosed
US-20170224700-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2017-08-10 US disclosed
EP-3177295-A2 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS Dana Farber Cancer Institute, Inc. (US) 2017-06-14 EP disclosed
WO-2016023014-A2 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2016-02-11 WO disclosed
WO-2016023014-A2 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2016-02-11 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 (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-20190343842-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS SIK1, SIK3, SIK2 LCK 215/4885FGFR3 1863/4885SIK1 1/4885
US-20200179387-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS FOR TREATING OSTEOPOROSIS SOST, SIK2, SIK1 LCK 308/4885FGFR3 710/4885SIK1 3/4885
US-20220305016-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS FOR TREATING OSTEOPOROSIS SOST, SIK2, SIK1 LCK 308/4885FGFR3 710/4885SIK1 3/4885
US-10265321-B2 Uses of salt-inducible kinase (SIK) inhibitors SIK1, SIK2, SIK3 LCK 239/4885FGFR3 1974/4885SIK1 1/4885
US-20170224700-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS SIK1, SIK2, SIK3 LCK 239/4885FGFR3 1974/4885SIK1 1/4885
US-11241435-B2 Uses of salt-inducible kinase (SIK) inhibitors for treating osteoporosis SOST, SIK2, SIK1 LCK 308/4885FGFR3 710/4885SIK1 3/4885
US-20200338087-A9 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS SIK1, SIK3, SIK2 LCK 215/4885FGFR3 1863/4885SIK1 1/4885
US-20180221379-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS SIK1, SIK2, SIK3 LCK 239/4885FGFR3 1974/4885SIK1 1/4885

“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.