SCHEMBL976391

SCHEMBL976391

CCCCCCCC(C)C[O]

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACE2 Q9BYF1 1/20 0.54
OPRM1 P35372 1/20 0.46
ADH1B P00325 1/20 0.45
ADH1C P00326 1/20 0.45
ADH1A P07327 1/20 0.45
ADH4 P08319 1/20 0.45
ADH7 P40394 1/20 0.45
GPR84 Q9NQS5 3/20 0.43
FDPS P14324 3/20 0.43
SPHK1 Q9NYA1 1/20 0.43
FFAR1 O14842 1/20 0.43
CA1 P00915 1/20 0.43
LMNA P02545 1/20 0.42
TSHR P16473 1/20 0.42
THRB P10828 1/20 0.42
DNM1 Q05193 1/20 0.42
MAPT P10636 1/20 0.41
TP53 P04637 1/20 0.41
LCK P06239 1/20 0.41
PPARD Q03181 1/20 0.41

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
SCHEMBL5684054 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A
SCHEMBL354924 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A
SCHEMBL28621809 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A
SCHEMBL3726879 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A
SCHEMBL1021842 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A
SCHEMBL5683929 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A
SCHEMBL29242009 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A
SCHEMBL3742493 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A
SCHEMBL3726882 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A
SCHEMBL3739044 1.00 ACE2 (0.54) ACE2OPRM1ADH1BADH1CADH1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023223888-A1 METHOD FOR PRODUCING POLYCARBONATE RESIN, AND ALICYCLIC POLYCARBONATE RESIN 旭化成株式会社 2023-11-23 WO disclosed
CN-109721723-B Surfactant, method for producing the same, and solution containing the same 中日合成化学股份有限公司 2021-07-06 CN disclosed
EP-2132167-B1 METHOD FOR THE PRODUCTION OF beta-KETONITRILES BASF SE (DE) 2013-12-25 EP disclosed
US-8501748-B2 Method for the production of β-ketonitriles BASF SE (DE) 2013-08-06 US disclosed
US-20130005970-A1 Method for the production of beta-ketonitriles BASF SE (DE) 2013-01-03 US disclosed
US-8309751-B2 Method for the production of β-ketonitriles BASF SE (DE) 2012-11-13 US disclosed
US-20110001221-A1 DIELECTRIC LAYER INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2011-01-06 US disclosed
US-7829137-B2 Fabricating dielectric layer INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2010-11-09 US disclosed
US-20100279963-A1 DICARBONYL DERIVATIVES AND METHODS OF USE ABRAXIS BIOSCIENCE, LLC (US) 2010-11-04 US disclosed
US-7799954-B2 Dicarbonyl derivatives and methods of use ABRAXIS BIOSCIENCE, LLC (US) 2010-09-21 US disclosed
US-5369106-A N-acryloylpiperazine derivatives, their preparation and their use of PAF antagonists SANKYO COMPANY, LIMITED (JP) 1994-11-29 US disclosed
EP-0591699-A1 N-hydroxy-N-phenylcarboxamides, processes for their production and agents containing them for the controlling of harmful fungi BASF Aktiengesellschaft (DE) 1994-04-13 EP disclosed
EP-0589301-A1 Carboxynilides derivatives, process for their preparation and fungicidal compositions containing them BASF Aktiengesellschaft (DE) 1994-03-30 EP disclosed
EP-0589313-A1 Cyclohex(en)ylcarboxamides, process for their preparation and anti-fungal agents containing them BASF Aktiengesellschaft (DE) 1994-03-30 EP disclosed
US-5192766-A Platelet activating factor antagonist SANKYO COMPANY, LIMITED (JP) 1993-03-09 US disclosed
WO-1991018905-A1 RADICICOL DERIVATIVES, THEIR PREPARATION AND THEIR ANTI-TUMOR ACTIVITY SANKYO COMPANY LIMITED (JP) 1991-12-12 WO disclosed
EP-0460950-A1 Radicicol derivatives, their preparation and their anti-tumour activity Sankyo Company Limited (JP) 1991-12-11 EP disclosed
EP-0395446-A2 N-acryloylpiperazine derivatives, their preparation and their use as paf antagonists Sankyo Company Limited (JP) 1990-10-31 EP disclosed
US-4818429-A FERROELECTRIC LIQUID CRYSTAL DISPLAY ELEMENTS; GOOD RESPONSE CHISSO CORPORATION (JP) 1989-04-04 US disclosed
EP-0260153-A2 Cyclohexylphenylpyridazines Chisso Corporation (JP) 1988-03-16 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-20130005970-A1 Method for the production of beta-ketonitriles AKR1C3, AKR1C4, AKR1C1 ACE2 1552/4885OPRM1 3316/4885ADH1B 723/4885
US-20100279963-A1 DICARBONYL DERIVATIVES AND METHODS OF USE AADAC, DCK, MLYCD ACE2 3329/4885OPRM1 4442/4885ADH1B 2650/4885

“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.