SCHEMBL3448389

SCHEMBL3448389

CCN(C)C(=O)N(C)CC

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM1 P11229 3/20 0.36
CHRM2 P08172 2/20 0.36
CHRM4 P08173 2/20 0.36
CHRM5 P08912 2/20 0.36
CHRM3 P20309 2/20 0.36
ALDH1A1 P00352 5/20 0.35
TSHR P16473 3/20 0.35
NFKB1 P19838 1/20 0.35
THPO P40225 1/20 0.35
HSD17B10 Q99714 1/20 0.35
MAPT P10636 1/20 0.35
APEX1 P27695 1/20 0.35
PMP22 Q01453 1/20 0.35
LMNA P02545 1/20 0.35
TDP1 Q9NUW8 2/20 0.33
FFAR3 O14843 1/20 0.33
MMP1 P03956 1/20 0.33
MMP2 P08253 1/20 0.33
MMP3 P08254 1/20 0.33
MMP8 P22894 1/20 0.33

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
SCHEMBL14674 0.87
SCHEMBL19288013 0.86 EPHX2 (0.38) CHRM1CHRM2CHRM4CHRM5CHRM3
SCHEMBL8902429 0.84 LMNA (0.42) CHRM1CHRM2CHRM4CHRM5CHRM3
SCHEMBL1617287 0.84
SCHEMBL25473017 0.82
SCHEMBL20388653 0.82
SCHEMBL16986039 0.80 MLYCD (0.31)
SCHEMBL5837521 0.80 ALDH1A1 (0.33) CHRM1CHRM2CHRM4CHRM5CHRM3
SCHEMBL17704771 0.79 CHRM1 (0.36) CHRM1ALDH1A1TSHRNFKB1THPO
SCHEMBL9074850 0.78

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5618951-A REACTING A CHLORODIFLUOROACETATE WITH A HALOSILANE USING AN UREA SILVENT AND A REDUCING AGENT ELI LILLY AND COMPANY (US) 1997-04-08 US claimed
US-20230340018-A1 MPRO CYSTEINE PROTEASE INHIBITORS ANIXA BIOSCIENCES, INC. 2023-10-26 US disclosed
EP-4183807-A1 COPOLYMER AND HOT MELT COMPOSITIONS COMPRISING SAID COPOLYMER Henkel AG & Co. KGaA (DE) 2023-05-24 EP disclosed
WO-2021113679-A1 DIMERIC COMPOUNDS AS STING AGONISTS MERSANA THERAPEUTICS, INC. (US) 2021-06-10 WO disclosed
US-9856349-B2 Catalysts and methods for polymer synthesis SAUDI ARAMCO TECHNOLOGIES COMPANY (SA) 2018-01-02 US disclosed
US-20170349762-A1 WATER-BASED COATING AGENT COMPOSITION, WATER-BASED LUBRICATING FILM PAINT COMPOSITION COMPRISING SAME, AND MEMBER DUPONT TORAY SPECIALTY MATERIALS KABUSHIKI KAISHA (JP) 2017-12-07 US disclosed
US-20170073463-A1 CATALYTIC CARBONYLATION CATALYSTS AND METHODS NOVOMER, INC. (US) 2017-03-16 US disclosed
US-9505878-B2 Catalysts and methods for polymer synthesis NOVOMER, INC. (US) 2016-11-29 US disclosed
US-9327280-B2 Catalytic carbonylation catalysts and methods NOVOMER, INC. (US) 2016-05-03 US disclosed
WO-2016025865-A1 METHODS OF PRODUCING ALKYLFURANS MICROMIDAS, INC. (US) 2016-02-18 WO disclosed
EP-0584043-B1 Process for the preparation of substituted benzenes and benzene sulfonic acid and derivatives thereof and a process for the preparation of N'N-substituted ureas CIBA GEIGY AG (CH) 1996-10-30 EP disclosed
US-5508402-A Process for the preparation of N,N'-substituted ureas CIBA-GEIGY CORPORATION (US) 1996-04-16 US disclosed
US-5464697-A Substituted tetracyanoquinodimethanes, processes for their preparation and their use CIBA-GEIGY CORPORATION (US) 1995-11-07 US disclosed
EP-0552586-B1 Process for the production of cyclopropylmethylketone CIBA GEIGY AG (CH) 1995-09-20 EP disclosed
US-5426232-A Substituted tetracyanoquinodimethanes, processes for their preparation and their use CIBA-GEIGY CORPORATION (US) 1995-06-20 US disclosed
US-5349062-A Charge tranfer compounds CIBA-GEIGY CORPORATION (US) 1994-09-20 US disclosed
EP-0584043-A1 Process for the preparation of substituted benzenes and benzene sulfonic acid and derivatives thereof and a process for the preparation of N'N-substituted ureas CIBA-GEIGY AG (CH) 1994-02-23 EP disclosed
US-5281730-A Substituted tetracyanoquinodimethanes, processes for their preparation and their use CIBA-GEIGY CORPORATION (US) 1994-01-25 US disclosed
US-5254739-A Heating a-acetylbutyrolactone in presence of a halide CIBA-GEIGY CORPORATION (US) 1993-10-19 US disclosed
EP-0552586-A1 Process for the production of cyclopropylmethylketone CIBA-GEIGY AG (CH) 1993-07-28 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-20230340018-A1 MPRO CYSTEINE PROTEASE INHIBITORS SERPINB1, PREP, PRCP CHRM1 4869/4885CHRM2 4856/4885CHRM4 4833/4885
US-20170073463-A1 CATALYTIC CARBONYLATION CATALYSTS AND METHODS CBR3, CBR1, EPHX2 CHRM1 1818/4885CHRM2 2539/4885CHRM4 1046/4885

“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.