SCHEMBL2035570

SCHEMBL2035570

OCCc1ccc2c(c1)CCO2

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PRKCI P41743 1/20 0.49
RAB9A P51151 2/20 0.48
POLB P06746 2/20 0.48
NPC1 O15118 1/20 0.48
ALDH1A1 P00352 1/20 0.45
KDM1A O60341 1/20 0.45
MAOA P21397 1/20 0.45
MAOB P27338 1/20 0.45
CHRM1 P11229 4/20 0.43
CHRM5 P08912 3/20 0.43
CHRM2 P08172 3/20 0.43
CHRM3 P20309 3/20 0.43
CHRM4 P08173 2/20 0.43
ADRB2 P07550 1/20 0.43
ADRB1 P08588 1/20 0.43
ADRA2A P08913 1/20 0.43
DRD2 P14416 1/20 0.43
KCNE1 P15382 1/20 0.43
ADRA2B P18089 1/20 0.43
ADRA2C P18825 1/20 0.43

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
SCHEMBL29791018 1.00 PRKCI (0.49) PRKCIRAB9APOLBNPC1ALDH1A1
SCHEMBL2140286 0.90 CTNNB1 (0.47) PRKCIRAB9APOLBNPC1ALDH1A1
SCHEMBL80222 0.90 PRKCI (0.46) PRKCIRAB9APOLBNPC1ALDH1A1
SCHEMBL13945187 0.86 PRKCI (0.46) PRKCIRAB9APOLBNPC1ALDH1A1
SCHEMBL17726436 0.86 CHRM2 (0.55) PRKCIRAB9APOLBNPC1ALDH1A1
SCHEMBL30922323 0.85 PRKCI (0.51) PRKCIRAB9APOLBNPC1ALDH1A1
SCHEMBL317341 0.85 PRKCI (0.51) PRKCIRAB9APOLBNPC1ALDH1A1
SCHEMBL8938493 0.83 ALDH1A1 (0.39) PRKCIRAB9APOLBNPC1ALDH1A1
SCHEMBL292900 0.82 RAB9A (0.45) PRKCIRAB9APOLBNPC1KDM1A
SCHEMBL1276487 0.82 RAB9A (0.46) PRKCIRAB9APOLBNPC1KDM1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113122061-A Quantum dot ink and preparation method of quantum dot film TCL集团股份有限公司 2021-07-16 CN claimed
US-20080269505-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICALS USA, INC. FOR BARBADOS 2008-10-30 US claimed
EP-1877393-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE Teva Pharmaceutical Fine Chemicals S.R.L. (IT) 2008-01-16 EP claimed
US-20070203221-A1 (S)-2-{1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]-3-pyrrolidinyl}-2,2-diphenylacetamide, selective muscarinic acetylcholine receptor antagonists, used for treating urogenital disorders such as incontinence TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-08-30 US claimed
WO-2007076158-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-07-05 WO claimed
CN-118922418-A Tetrahydroisoquinoline derivatives serving as pan-KRAS inhibitor as well as preparation method and application thereof 思路迪生物医药(上海)有限公司 2024-11-08 CN disclosed
WO-2023169481-A1 TETRAHYDROISOQUINOLINE DERIVATIVE AS PAN-KRAS INHIBITOR, PREPARATION METHOD THEREFOR AND USE THEREOF 思路迪生物医药(上海)有限公司 2023-09-14 WO disclosed
CN-114874201-B Pan-KRAS inhibitor and preparation and application thereof 思路迪生物医药(上海)有限公司 2023-01-20 CN disclosed
CN-114907389-A Boronic acid derivatives 首药控股(北京)股份有限公司 2022-08-16 CN disclosed
CN-114874201-A Pan-KRAS inhibitor and preparation and application thereof 思路迪生物医药(上海)有限公司 2022-08-09 CN disclosed
CN-113122061-A Quantum dot ink and preparation method of quantum dot film TCL集团股份有限公司 2021-07-16 CN disclosed
CN-107721954-B Novel preparation method of darifenacin intermediate 2, 3-dihydro-5-benzofuran acetic acid 内蒙古京东药业有限公司 2020-02-14 CN disclosed
EP-0388054-A1 Pyrrolidine derivatives Pfizer Limited (GB) 1990-09-19 EP disclosed
EP-0376358-A1 Muscarinic receptor antagonists PFIZER INC. (US) 1990-07-04 EP disclosed
WO-1990005133-A1 MUSCARINIC RECEPTOR ANTAGONISTS PFIZER LIMITED (GB) 1990-05-17 WO disclosed
WO-1990004583-A1 MUSCARINIC RECEPTOR ANTAGONISTS PFIZER LIMITED (GB) 1990-05-03 WO disclosed
EP-0365093-A1 Muscarinic receptor antagonists PFIZER INC. (US) 1990-04-25 EP disclosed
EP-0364123-A1 Muscarinic receptor antagonists Pfizer Limited (GB) 1990-04-18 EP disclosed
CN-1039415-A New 1, the preparation method of 3-3-disubstituted piperidine derivatives PFIZER (GB) 1990-02-07 CN disclosed
EP-0350309-A1 Piperidine derivatives Pfizer Limited (GB) 1990-01-10 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 (2 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-20070203221-A1 (S)-2-{1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]-3-pyrrolidinyl}-2,2-diphenylacetamide, selective muscarinic acetylcholine receptor antagonists, used for treating urogenital disorders such as incontinence CHRNE, CHRM3, CHRM2 PRKCI 3442/4885RAB9A 3273/4885POLB 2444/4885
US-20080269505-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B PRKCI 4076/4885RAB9A 956/4885POLB 587/4885

“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.