SCHEMBL10165334

SCHEMBL10165334

COC(=O)[C@@H]1CC[C@H]1C(=O)O

nearest known ligand 0.46

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CHRM2 P08172 1/20 0.46
CHRM4 P08173 1/20 0.46
CHRM3 P20309 1/20 0.46
PPM1B O75688 1/20 0.45
PTPN1 P18031 1/20 0.45
PPP1CC P36873 1/20 0.45
CYP3A4 P08684 1/20 0.42
CYP1A2 P05177 1/20 0.42
CYP2D6 P10635 1/20 0.42
TSHR P16473 1/20 0.42
MAPK1 P28482 1/20 0.42
HSD17B10 Q99714 1/20 0.42

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
SCHEMBL17887005 1.00 CHRM2 (0.46) CHRM2CHRM4CHRM3PPM1BPTPN1
SCHEMBL2500766 1.00 CHRM2 (0.46) CHRM2CHRM4CHRM3PPM1BPTPN1
SCHEMBL13560693 1.00 CHRM2 (0.46) CHRM2CHRM4CHRM3PPM1BPTPN1
SCHEMBL15057681 1.00 CHRM2 (0.46) CHRM2CHRM4CHRM3PPM1BPTPN1
SCHEMBL2965076 1.00 CHRM2 (0.46) CHRM2CHRM4CHRM3PPM1BPTPN1
SCHEMBL17816439 0.91 CHRM2 (0.47) CHRM2CHRM4CHRM3PPM1BPTPN1
SCHEMBL15590800 0.91 SLC6A2 (0.46) CHRM2CHRM4CHRM3PPM1BPTPN1
SCHEMBL596153 0.91 CHRM2 (0.47) CHRM2CHRM4CHRM3PPM1BPTPN1
SCHEMBL3944070 0.91 SLC6A2 (0.46) CHRM2CHRM4CHRM3PPM1BPTPN1
SCHEMBL4444010 0.91 CHRM2 (0.47) CHRM2CHRM4CHRM3PPM1BPTPN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3986553-B1 CYCLOBUTYL CARBOXYLIC ACIDS AS LPA ANTAGONISTS BRISTOL MYERS SQUIBB CO (US) 2026-03-25 EP disclosed
US-20260015350-A1 AZAQUINAZOLINE PAN-KRAS INHIBITORS MIRATI THERAPEUTICS INC (US) 2026-01-15 US disclosed
US-12466804-B2 Cyclobutyl carboxylic acids as LPA antagonists BRISTOL-MYERS SQUIBB COMPANY (US) 2025-11-11 US disclosed
CN-119677749-A Azaquinazoline pan KRAS inhibitors 米拉蒂治疗股份有限公司 2025-03-21 CN disclosed
US-11760736-B2 Processes and intermediates for preparing MCL1 inhibitors GILEAD SCIENCES, INC. (US) 2023-09-19 US disclosed
US-20220235027-A1 CYCLOBUTYL CARBOXYLIC ACIDS AS LPA ANTAGONISTS BRISTOL-MYERS SQUIBB COMPANY 2022-07-28 US disclosed
CN-114599641-A Cyclobutylcarboxylic acids as LPA antagonists 百时美施贵宝公司 2022-06-07 CN disclosed
EP-3986553-A1 CYCLOBUTYL CARBOXYLIC ACIDS AS LPA ANTAGONISTS Bristol-Myers Squibb Company (US) 2022-04-27 EP disclosed
WO-2020257139-A1 CYCLOBUTYL CARBOXYLIC ACIDS AS LPA ANTAGONISTS BRISTOL-MYERS SQUIBB COMPANY (US) 2020-12-24 WO disclosed
US-20120015920-A1 HETEROBICYCLIC METALLOPROTEASE INHIBITORS ALANTOS PHARMACEUTICALS HOLDING, INC. (US) 2012-01-19 US disclosed
US-20090137547-A1 Heterobicyclic metalloprotease inhibitors ALANTOS PHARMACEUTICALS HOLDING, INC. 2009-05-28 US disclosed
US-20090137547-A1 Heterobicyclic metalloprotease inhibitors ALANTOS PHARMACEUTICALS HOLDING, INC. 2009-05-28 US disclosed
US-7521445-B2 Heterocyclic substituted carbonyl derivatives and their use as dopamine D3 receptor ligands AVENTIS PHARMACEUTICALS INC. (US) 2009-04-21 US disclosed
US-7521445-B2 Heterocyclic substituted carbonyl derivatives and their use as dopamine D3 receptor ligands AVENTIS PHARMACEUTICALS INC. (US) 2009-04-21 US disclosed
US-20070161641-A1 Novel heterocyclic substituted carbonyl derivatives and their use as dopamine D3 receptor ligands AVENTIS PHARMACEUTICALS INC. (US) 2007-07-12 US disclosed
US-20070161641-A1 Novel heterocyclic substituted carbonyl derivatives and their use as dopamine D3 receptor ligands AVENTIS PHARMACEUTICALS INC. (US) 2007-07-12 US disclosed
US-20070155738-A1 Heterobicyclic metalloprotease inhibitors ALANTOS PHARMACEUTICALS, INC. 2007-07-05 US disclosed
US-20070155738-A1 Heterobicyclic metalloprotease inhibitors ALANTOS PHARMACEUTICALS, INC. 2007-07-05 US disclosed
US-7186724-B2 Heterocyclic substituted carbonyl derivatives and their use as dopamine D3 receptor ligands AVENTIS PHARMACEUTICALS INC. (US) 2007-03-06 US disclosed
US-7186724-B2 Heterocyclic substituted carbonyl derivatives and their use as dopamine D3 receptor ligands AVENTIS PHARMACEUTICALS INC. (US) 2007-03-06 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 (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-11760736-B2 Processes and intermediates for preparing MCL1 inhibitors MCL1, BAK1, BCL3 CHRM2 4881/4885CHRM4 4872/4885CHRM3 4876/4885
US-20120015920-A1 HETEROBICYCLIC METALLOPROTEASE INHIBITORS MMP13, TIMP3, MMP3 CHRM2 4781/4885CHRM4 4874/4885CHRM3 4323/4885
US-20090137547-A1 Heterobicyclic metalloprotease inhibitors MMP13, TIMP3, MMP3 CHRM2 4781/4885CHRM4 4874/4885CHRM3 4323/4885
US-20220235027-A1 CYCLOBUTYL CARBOXYLIC ACIDS AS LPA ANTAGONISTS LPAR1, LPAR3, LPAR2 CHRM2 650/4885CHRM4 517/4885CHRM3 271/4885
US-20070161641-A1 Novel heterocyclic substituted carbonyl derivatives and their use as dopamine D3 receptor ligands DRD3, DRD2, HTR3C CHRM2 350/4885CHRM4 322/4885CHRM3 139/4885
US-20260015350-A1 AZAQUINAZOLINE PAN-KRAS INHIBITORS KRAS, NRAS, HRAS CHRM2 3537/4885CHRM4 3866/4885CHRM3 3807/4885
US-20070155738-A1 Heterobicyclic metalloprotease inhibitors MMP13, TIMP3, MMP3 CHRM2 4781/4885CHRM4 4874/4885CHRM3 4323/4885
US-12466804-B2 Cyclobutyl carboxylic acids as LPA antagonists LPAR1, LPAR3, LPAR2 CHRM2 650/4885CHRM4 517/4885CHRM3 271/4885

“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.