SCHEMBL4175218

SCHEMBL4175218

C[C@H]1CCN1C(=O)OC(C)(C)C

nearest known ligand 0.49

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CHRM2 P08172 1/20 0.44
CHRM1 P11229 1/20 0.44
CHRM3 P20309 1/20 0.44
HSD17B10 Q99714 1/20 0.44
HPGD P15428 1/20 0.44
USP2 O75604 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
RECQL P46063 1/20 0.41
EPHX1 P07099 1/20 0.41
GPR119 Q8TDV5 1/20 0.40
PREP P48147 1/20 0.40
SETD7 Q8WTS6 1/20 0.39

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
SCHEMBL489126 1.00 CHRM2 (0.44) CHRM2CHRM1CHRM3HSD17B10HPGD
SCHEMBL489128 1.00 CHRM2 (0.44) CHRM2CHRM1CHRM3HSD17B10HPGD
SCHEMBL178721 0.89 HSD17B10 (0.52) CHRM2CHRM1CHRM3HSD17B10HPGD
SCHEMBL357042 0.89 HSD17B10 (0.52) CHRM2CHRM1CHRM3HSD17B10HPGD
SCHEMBL357043 0.89 HSD17B10 (0.52) CHRM2CHRM1CHRM3HSD17B10HPGD
Hydrochloric Acid SCHEMBL5783201 0.88 HSD17B10 (0.38) CHRM2CHRM1CHRM3HSD17B10HPGD
Hydrochloric Acid SCHEMBL5783202 0.88 HSD17B10 (0.38) CHRM2CHRM1CHRM3HSD17B10HPGD
SCHEMBL1202111 0.87 HPGD (0.49) HSD17B10HPGDSMN1; SMN2EPHX1PREP
SCHEMBL7005690 0.87 HPGD (0.49) HSD17B10HPGDSMN1; SMN2EPHX1PREP
SCHEMBL7002987 0.87 HPGD (0.49) HSD17B10HPGDSMN1; SMN2EPHX1PREP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230364070-A1 PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES USEFUL IN THE TREATMENT OF CANCER ANTARES THERAPEUTICS, INC. 2023-11-16 US disclosed
WO-2021252307-A1 RIPK1 INHIBITORS AND METHODS OF USE MERCK SHARP & DOHME CORP. (US) 2021-12-16 WO disclosed
US-11149035-B2 Chemical compounds as H—PGDS inhibitors GLAXOSMITHKLINE INTELLECTUAL PROPERTY DFVELOPMENT LIMITED (GB) 2021-10-19 US disclosed
US-11149035-B2 Chemical compounds as H—PGDS inhibitors GLAXOSMITHKLINE INTELLECTUAL PROPERTY DFVELOPMENT LIMITED (GB) 2021-10-19 US disclosed
EP-3390384-B1 QUINOLINE-3-CARBOXAMIDES AS H-PGDS INHIBITORS ASTEX THERAPEUTICS LTD (GB) 2021-09-15 EP disclosed
US-20210238162-A1 CHEMICAL COMPOUNDS GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED (GB) 2021-08-05 US disclosed
US-20210238162-A1 CHEMICAL COMPOUNDS GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED (GB) 2021-08-05 US disclosed
US-11053215-B2 Heterocyclic compounds useful as Pim kinase inhibitors INCYTE CORPORATION (US) 2021-07-06 US disclosed
US-20200123152-A1 Chemical Compounds as H-PGDS Inhibitors GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED (GB) 2020-04-23 US disclosed
US-20200123152-A1 Chemical Compounds as H-PGDS Inhibitors GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED (GB) 2020-04-23 US disclosed
EP-3390384-A1 QUINOLINE-3-CARBOXAMIDES AS H-PGDS INHIBITORS Astex Therapeutics Limited (GB) 2018-10-24 EP disclosed
US-9920032-B2 Heterocyclic compounds useful as pim kinase inhibitors INCYTE CORPORATION (US) 2018-03-20 US disclosed
US-9920032-B2 Heterocyclic compounds useful as pim kinase inhibitors INCYTE CORPORATION (US) 2018-03-20 US disclosed
WO-2017103851-A1 QUINOLINE-3-CARBOXAMIDES AS H-PGDS INHIBITORS ASTEX THERAPEUTICS LIMITED (GB) 2017-06-22 WO disclosed
US-20170096411-A1 HETEROCYCLIC COMPOUNDS USEFUL AS PIM KINASE INHIBITORS INCYTE CORPORATION 2017-04-06 US disclosed
US-20170096411-A1 HETEROCYCLIC COMPOUNDS USEFUL AS PIM KINASE INHIBITORS INCYTE CORPORATION 2017-04-06 US disclosed
US-20090186868-A1 Taxane Compound Having Azetidine Ring Structure DAIICHI SANKYO COMPANY LIMITED (JP) 2009-07-23 US disclosed
US-20090186868-A1 Taxane Compound Having Azetidine Ring Structure DAIICHI SANKYO COMPANY LIMITED (JP) 2009-07-23 US disclosed
US-20090186868-A1 Taxane Compound Having Azetidine Ring Structure DAIICHI SANKYO COMPANY LIMITED (JP) 2009-07-23 US disclosed
EP-1942109-A1 TAXANE COMPOUND WITH AZETIDINE RING STRUCTURE Daiichi Sankyo Company, Limited (JP) 2008-07-09 EP 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 (7 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-11149035-B2 Chemical compounds as H—PGDS inhibitors HPGDS, PTGS1, PTGIS CHRM2 2023/4885CHRM1 1441/4885CHRM3 2244/4885
US-20200123152-A1 Chemical Compounds as H-PGDS Inhibitors HPGDS, PTGS1, PTGIS CHRM2 2052/4885CHRM1 1476/4885CHRM3 2268/4885
US-20090186868-A1 Taxane Compound Having Azetidine Ring Structure ABCC1, AZI2, TPD52L2 CHRM2 2139/4885CHRM1 750/4885CHRM3 3337/4885
US-11053215-B2 Heterocyclic compounds useful as Pim kinase inhibitors PIM1, PIM2, PIM3 CHRM2 4853/4885CHRM1 4773/4885CHRM3 4768/4885
US-20230364070-A1 PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES USEFUL IN THE TREATMENT OF CANCER ERBB2, EGFR, ERBB3 CHRM2 1569/4885CHRM1 2149/4885CHRM3 2472/4885
US-20210238162-A1 CHEMICAL COMPOUNDS HPGDS, PTGS1, PTGIS CHRM2 1785/4885CHRM1 1661/4885CHRM3 2410/4885
US-20170096411-A1 HETEROCYCLIC COMPOUNDS USEFUL AS PIM KINASE INHIBITORS PIM1, PIM2, PIM3 CHRM2 4853/4885CHRM1 4773/4885CHRM3 4768/4885

“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.