SCHEMBL21479334

SCHEMBL21479334

CCc1ccc(NC(=O)c2cccc(C(F)(F)F)c2)cc1C

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MEN1 O00255 1/20 0.67
▸ HTT P42858 1/20 0.67
▸ RAB9A P51151 1/20 0.67
▸ KMT2A Q03164 1/20 0.67
▸ KCNK3 O14649 2/20 0.65
▸ KCNK9 Q9NPC2 1/20 0.65
▸ MAPT P10636 1/20 0.63
▸ P2RX1 P51575 1/20 0.61
▸ LMNA P02545 1/20 0.61
▸ PTGS1 P23219 2/20 0.61
▸ BRAF P15056 6/20 0.60
▸ GAA P10253 1/20 0.60
▸ LCK P06239 2/20 0.59
▸ KIT P10721 2/20 0.59
▸ ABL1 P00519 1/20 0.59
▸ SRC P12931 1/20 0.59
▸ MAPK14 Q16539 1/20 0.59
▸ BTK Q06187 1/20 0.59
▸ CSF1R P07333 3/20 0.58
▸ ALDH1A1 P00352 1/20 0.57

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
SCHEMBL24737179 0.90 MEN1 (0.67) MEN1HTTRAB9AKMT2AKCNK3
SCHEMBL22088439 0.90 MEN1 (0.70) MEN1HTTRAB9AKMT2AKCNK3
SCHEMBL12858422 0.87 MEN1 (0.73) MEN1HTTRAB9AKMT2AKCNK3
SCHEMBL1264161 0.85 MEN1 (0.70) MEN1HTTRAB9AKMT2AKCNK3
SCHEMBL21479330 0.84 MEN1 (0.59) MEN1HTTRAB9AKMT2AKCNK3
SCHEMBL22337424 0.84 MEN1 (0.59) MEN1HTTRAB9AKMT2AKCNK3
SCHEMBL2974812 0.84 MEN1 (0.68) MEN1HTTRAB9AKMT2AKCNK3
SCHEMBL30822434 0.84 PTGS1 (0.70) MEN1HTTRAB9AKMT2AKCNK3
SCHEMBL22025296 0.84 PTGS1 (0.70) MEN1HTTRAB9AKMT2AKCNK3
SCHEMBL14468045 0.84 MEN1 (0.68) MEN1HTTRAB9AKMT2AKCNK3

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 10 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-20230234959-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF THE BROAD INSTITUTE, INC. (US) 2023-07-27 — — 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-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 (10 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-20200253981-A1 USES OF PYRIMIDOPYRIMIDINONES AS SIK INHIBITORS SIK2, SIK1, SIK3 MEN1 4515/4885HTT 4191/4885RAB9A 2153/4885
US-20210147425-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF SIK1, SIK2, SIK3 MEN1 4510/4885HTT 1967/4885RAB9A 2401/4885
US-20200179387-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS FOR TREATING OSTEOPOROSIS SOST, SIK2, SIK1 MEN1 3184/4885HTT 3638/4885RAB9A 1608/4885
US-20220305016-A1 USES OF SALT-INDUCIBLE KINASE (SIK) INHIBITORS FOR TREATING OSTEOPOROSIS SOST, SIK2, SIK1 MEN1 3184/4885HTT 3638/4885RAB9A 1608/4885
US-20200317675-A9 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF SIK1, SIK2, SIK3 MEN1 4493/4885HTT 1748/4885RAB9A 2462/4885
US-20190315752-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF SIK1, SIK2, SIK3 MEN1 4493/4885HTT 1748/4885RAB9A 2462/4885
US-11241435-B2 Uses of salt-inducible kinase (SIK) inhibitors for treating osteoporosis SOST, SIK2, SIK1 MEN1 3184/4885HTT 3638/4885RAB9A 1608/4885
US-20230234959-A1 BICYCLIC UREA KINASE INHIBITORS AND USES THEREOF SIK1, SIK2, SIK3 MEN1 4493/4885HTT 1748/4885RAB9A 2462/4885
US-11725011-B2 Bicyclic urea kinase inhibitors and uses thereof SIK1, SIK2, SIK3 MEN1 4493/4885HTT 1748/4885RAB9A 2462/4885
US-10954242-B2 Bicyclic urea kinase inhibitors and uses thereof SIK1, SIK2, SIK3 MEN1 4493/4885HTT 1748/4885RAB9A 2462/4885

“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.

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