SCHEMBL19639618

SCHEMBL19639618

CN(C)C(=O)C12CC(C(=O)O)(C1)C2

nearest known ligand 0.37

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
GRM1 Q13255 2/20 0.37
MEN1 O00255 1/20 0.33
KMT2A Q03164 1/20 0.33
FFAR3 O14843 1/20 0.31

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
SCHEMBL14075738 0.89 MEN1 (0.37) MEN1KMT2A
SCHEMBL1648486 0.78 GRM1 (0.50) GRM1FFAR3
SCHEMBL6058438 0.78 KMT2A (0.54) MEN1KMT2A
SCHEMBL9142496 0.78 GRM1 (0.50) GRM1FFAR3
SCHEMBL19766525 0.77 MEN1 (0.34) MEN1KMT2A
SCHEMBL30937226 0.77 MEN1 (0.34) MEN1KMT2A
SCHEMBL19639655 0.76 MEN1 (0.32) MEN1KMT2A
Hydrochloric Acid SCHEMBL27190969 0.75 MEN1 (0.33) MEN1KMT2A
SCHEMBL12858008 0.75 PKM (0.52) MEN1KMT2A
SCHEMBL19639616 0.75 SMN1; SMN2 (0.33) MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3661941-B1 THIAZOLOPYRIDINE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS MERCK PATENT GMBH (DE) 2022-12-14 EP claimed
US-11186592-B2 Thiazolopyridine derivatives as adenosine receptor antagonists MERCK PATENT GMBH (DE) 2021-11-30 US claimed
US-20200181171-A1 THIAZOLOPYRIDINE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS MERCK PATENT GMBH (DE) 2020-06-11 US claimed
US-12049460-B2 EGFR inhibitor compounds RECURIUM IP HOLDINGS, LLC (US) 2024-07-30 US disclosed
EP-3464275-B1 EGFR INHIBITOR COMPOUNDS RECURIUM IP HOLDINGS LLC (US) 2024-05-08 EP disclosed
EP-3661941-B1 THIAZOLOPYRIDINE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS MERCK PATENT GMBH (DE) 2022-12-14 EP disclosed
US-20210395230-A1 EGFR INHIBITOR COMPOUNDS RECURIUM IP HOLDINGS, LLC (US) 2021-12-23 US disclosed
US-11186592-B2 Thiazolopyridine derivatives as adenosine receptor antagonists MERCK PATENT GMBH (DE) 2021-11-30 US disclosed
US-20200181120-A1 EGFR INHIBITOR COMPOUNDS KALYRA PHARMACEUTICALS, INC. 2020-06-11 US disclosed
US-20200181171-A1 THIAZOLOPYRIDINE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS MERCK PATENT GMBH (DE) 2020-06-11 US disclosed
US-20170342055-A1 EGFR INHIBITOR COMPOUNDS RECURIUM IP HOLDINGS, LLC 2017-11-30 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 (6 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-20200181120-A1 EGFR INHIBITOR COMPOUNDS EGFR, ERBB2, ERBB3 GRM1 2187/4885MEN1 2877/4885KMT2A 3296/4885
US-11186592-B2 Thiazolopyridine derivatives as adenosine receptor antagonists ADORA1, ADORA2A, AMPD2 GRM1 1666/4885MEN1 2653/4885KMT2A 3978/4885
US-20170342055-A1 EGFR INHIBITOR COMPOUNDS EGFR, ERBB2, ERBB3 GRM1 2187/4885MEN1 2877/4885KMT2A 3296/4885
US-12049460-B2 EGFR inhibitor compounds EGFR, ERBB2, ERBB3 GRM1 1989/4885MEN1 1932/4885KMT2A 3178/4885
US-20210395230-A1 EGFR INHIBITOR COMPOUNDS EGFR, ERBB2, ERBB3 GRM1 2187/4885MEN1 2877/4885KMT2A 3296/4885
US-20200181171-A1 THIAZOLOPYRIDINE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS ADORA1, ADORA2A, AMPD2 GRM1 1666/4885MEN1 2653/4885KMT2A 3978/4885

“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.