SCHEMBL21479239

SCHEMBL21479239

COc1ccc(N2C(=O)N(c3c(C)cccc3Cl)Cc3cnc(Nc4ccc(C5CCN(C)CC5)cc4OC)nc32)nc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
SIK2 Q9H0K1 2/20 1.00
CSF1R P07333 1/20 1.00
SIK1 P57059 1/20 1.00
SIK3 Q9Y2K2 1/20 1.00
TNK2 Q07912 3/20 0.48
MAPK7 Q13164 1/20 0.48
ALK Q9UM73 5/20 0.47
EGFR P00533 5/20 0.47
INSR P06213 1/20 0.47
IGF1R P08069 1/20 0.47
TTK P33981 2/20 0.46
PTK2 Q05397 1/20 0.46
BRD4 O60885 3/20 0.44
PLK1 P53350 3/20 0.44
FGFR1 P11362 1/20 0.44

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
SCHEMBL29450843 1.00 SIK2 (1.00) SIK2CSF1RSIK1SIK3TNK2
SCHEMBL30309489 1.00 SIK2 (1.00) SIK2CSF1RSIK1SIK3TNK2
SCHEMBL21479301 0.96 SIK2 (0.92) SIK2CSF1RSIK1SIK3TNK2
SCHEMBL25882204 0.95 SIK2 (0.91) SIK2CSF1RSIK1SIK3TNK2
SCHEMBL21479278 0.95 SIK2 (0.91) SIK2CSF1RSIK1SIK3TNK2
SCHEMBL21479253 0.94 SIK2 (0.88) SIK2CSF1RSIK1SIK3TNK2
SCHEMBL22337166 0.93 SIK2 (0.86) SIK2CSF1RSIK1SIK3TNK2
SCHEMBL25315123 0.92 SIK2 (0.85) SIK2CSF1RSIK1SIK3TNK2
SCHEMBL30439431 0.92 SIK2 (0.85) SIK2CSF1RSIK1SIK3TNK2
SCHEMBL25972187 0.92 SIK2 (0.85) SIK2CSF1RSIK1SIK3TNK2

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11725011-B2 Bicyclic urea kinase inhibitors and uses thereof THE GENERAL HOSPITAL CORPORATION (US) 2023-08-15 US disclosed
US-11725011-B2 Bicyclic urea kinase inhibitors and uses thereof THE GENERAL HOSPITAL CORPORATION (US) 2023-08-15 US disclosed
US-20230234959-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF THE BROAD INSTITUTE, INC. (US) 2023-07-27 US disclosed
US-20230234959-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF THE BROAD INSTITUTE, INC. (US) 2023-07-27 US disclosed
US-20230192701-A1 BICYCLIC KINASE INHIBITORS AND USES THEREOF IOMX THERAPEUTICS AG (DE) 2023-06-22 US disclosed
US-20230192701-A1 BICYCLIC KINASE INHIBITORS AND USES THEREOF IOMX THERAPEUTICS AG (DE) 2023-06-22 US disclosed
US-20220305016-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS FOR TREATING OSTEOPOROSIS THE GENERAL HOSPITAL CORPORATION (US) 2022-09-29 US disclosed
US-20220133736-A1 USES OF PYRIMIDOPYRIMIDINONES AS SIK INHIBITORS THE GENERAL HOSPITAL CORPORATION (US) 2022-05-05 US disclosed
EP-3481830-B1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF BROAD INST INC (US) 2022-02-16 EP 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-20210147425-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF THE BROAD INSTITUTE, INC. (US) 2021-05-20 US disclosed
US-10954242-B2 Bicyclic urea kinase inhibitors and uses thereof THE BROAD INSTITUTE, INC. (US) 2021-03-23 US disclosed
US-20200317675-A9 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF THE BROAD INSTITUTE, INC. (US) 2020-10-08 US disclosed
US-20200253981-A1 USES OF PYRIMIDOPYRIMIDINONES AS SIK INHIBITORS THE GENERAL HOSPITAL CORPORATION (US) 2020-08-13 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-20190315752-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF THE BROAD INSTITUTE, INC. (US) 2019-10-17 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 (12 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-20220133736-A1 USES OF PYRIMIDOPYRIMIDINONES AS SIK INHIBITORS SIK2, SIK1, SIK3 SIK2 1/4885CSF1R 3749/4885SIK1 2/4885
US-20200253981-A1 USES OF PYRIMIDOPYRIMIDINONES AS SIK INHIBITORS SIK2, SIK1, SIK3 SIK2 1/4885CSF1R 3749/4885SIK1 2/4885
US-20210147425-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF SIK1, SIK2, SIK3 SIK2 2/4885CSF1R 4501/4885SIK1 1/4885
US-20200179387-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS FOR TREATING OSTEOPOROSIS SOST, SIK2, SIK1 SIK2 2/4885CSF1R 6/4885SIK1 3/4885
US-20220305016-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS FOR TREATING OSTEOPOROSIS SOST, SIK2, SIK1 SIK2 2/4885CSF1R 6/4885SIK1 3/4885
US-20200317675-A9 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF SIK1, SIK2, SIK3 SIK2 2/4885CSF1R 4476/4885SIK1 1/4885
US-20190315752-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF SIK1, SIK2, SIK3 SIK2 2/4885CSF1R 4476/4885SIK1 1/4885
US-20230192701-A1 BICYCLIC KINASE INHIBITORS AND USES THEREOF MITF, PRKDC, PRKACA SIK2 116/4885CSF1R 28/4885SIK1 97/4885
US-11241435-B2 Uses of salt-inducible kinase (SIK) inhibitors for treating osteoporosis SOST, SIK2, SIK1 SIK2 2/4885CSF1R 6/4885SIK1 3/4885
US-20230234959-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF SIK1, SIK2, SIK3 SIK2 2/4885CSF1R 4476/4885SIK1 1/4885
US-11725011-B2 Bicyclic urea kinase inhibitors and uses thereof SIK1, SIK2, SIK3 SIK2 2/4885CSF1R 4476/4885SIK1 1/4885
US-10954242-B2 Bicyclic urea kinase inhibitors and uses thereof SIK1, SIK2, SIK3 SIK2 2/4885CSF1R 4476/4885SIK1 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.