SCHEMBL1970528

SCHEMBL1970528

[CH2]CC(CC)C(C)CCCC

nearest known ligand 0.34

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.34
TDP1 Q9NUW8 1/20 0.34
TSHR P16473 2/20 0.33
DNM1 Q05193 2/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
CYP3A4 P08684 1/20 0.33
CA2 P00918 3/20 0.32
MAPK1 P28482 1/20 0.32
OPRM1 P35372 1/20 0.32
CA1 P00915 1/20 0.31

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
SCHEMBL1971315 0.93 OPRM1 (0.41) DNM1OPRM1CA1
SCHEMBL7057450 0.91 OPRM1 (0.39) TSHRDNM1OPRM1
SCHEMBL1970569 0.87 LMNA (0.37) TSHR
SCHEMBL8969121 0.84 ALDH1A1 (0.33) ALDH1A1TDP1TSHRDNM1SMN1; SMN2
SCHEMBL7099297 0.82 DNM1 (0.41) TSHRDNM1CA2OPRM1
SCHEMBL5985716 0.82
SCHEMBL17607505 0.81 ALDH1A1 (0.34) ALDH1A1TDP1TSHRDNM1SMN1; SMN2
SCHEMBL3358967 0.81 ALDH1A1 (0.34) ALDH1A1TDP1TSHRDNM1SMN1; SMN2
SCHEMBL3438064 0.80 ALDH1A1 (0.37) ALDH1A1TDP1TSHRDNM1SMN1; SMN2
SCHEMBL5985809 0.80

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11578031-B2 Dissymmetric N,N-dialkylamides used particularly for separating uranium(VI) from plutonium(IV), synthesis thereof and uses of same COMMISSARIAT À L'ÉNERGIE ATOMIQUE ET AUX ÊNERGIES ALTERNATIVES (FR) 2023-02-14 US disclosed
CN-110312702-B Asymmetric N, N-dialkylamides, in particular for separating uranium (VI) and plutonium (IV), their synthesis and use 原子能和替代能源委员会 2022-10-14 CN disclosed
US-20210332002-A1 DISSYMMETRIC N,N-DIALKYLAMIDES USED PARTICULARLY FOR SEPARATING URANIUM(VI) FROM PLUTONIUM(IV), SYNTHESIS THEREOF AND USES OF SAME ORANO CYCLE (FR) 2021-10-28 US disclosed
EP-3194371-B1 ANTIMICROBIAL IMIDAZOLIUM COMPOUNDS AGENCY SCIENCE TECH & RES (SG) 2020-09-02 EP disclosed
CN-107108518-B Antibacterial imidazolium compounds 新加坡科技研究局 2020-08-11 CN disclosed
CN-107922314-B Novel asymmetric N, N-dialkyl amide and synthetic method and application thereof 欧安诺循环 2020-07-07 CN disclosed
US-10570097-B2 Antimicrobial imidazolium compounds AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2020-02-25 US disclosed
CN-110312702-A Particularly for the asymmetric N of SEPARATION OF URANIUM (VI) and plutonium (IV), N- dialkyl amide, synthesis and purposes 原子能和替代能源委员会 2019-10-08 CN disclosed
US-10252983-B2 Dissymmetric N,N-dialkylamides, the synthesis thereof and uses of same COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2019-04-09 US disclosed
US-20190016684-A1 ANTIMICROBIAL IMIDAZOLIUM COMPOUNDS AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2019-01-17 US disclosed
EP-3194371-A1 ANTIMICROBIAL IMIDAZOLIUM COMPOUNDS Agency for Science, Technology and Research (SG) 2017-07-26 EP disclosed
WO-2017017193-A1 NOVEL DISSYMMETRIC N,N-DIALKYLAMIDES, THE SNYTHESIS THEREOF AND USES OF SAME AREVA NC (FR) 2017-02-02 WO disclosed
US-9469662-B2 Process for preparing optically active biophosphinylalkanes BASF SE (DE) 2016-10-18 US disclosed
WO-2016043660-A1 ANTIMICROBIAL IMIDAZOLIUM COMPOUNDS AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2016-03-24 WO disclosed
CN-101253183-B Process for preparing optically active diphosphanes BASF SE 2013-07-10 CN disclosed
EP-1913007-B1 PROCESS FOR PREPARING OPTICALLY ACTIVE DIPHOSPHANES BASF SE (DE) 2011-06-22 EP disclosed
US-20080242893-A1 Process for Preparing Optically Active Diphosphanes BASF AKTIENGESELLSCHAFT (DE) 2008-10-02 US disclosed
CN-101253183-A Process for preparing optically active diphosphanes BASF SE (DE) 2008-08-27 CN disclosed
EP-1913007-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE DIPHOSPHANES BASF SE (DE) 2008-04-23 EP disclosed
WO-2007012655-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE DIPHOSPHANES BASF SE (DE) 2007-02-01 WO 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 (6 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-10570097-B2 Antimicrobial imidazolium compounds CCNI, MACF1, ECI1 ALDH1A1 3371/4885TDP1 4399/4885TSHR 3989/4885
US-10252983-B2 Dissymmetric N,N-dialkylamides, the synthesis thereof and uses of same SMOX, DUOX2, NOS2 ALDH1A1 1648/4885TDP1 1120/4885TSHR 4037/4885
US-11578031-B2 Dissymmetric N,N-dialkylamides used particularly for separating uranium(VI) from plutonium(IV), synthesis thereof and uses of same NOS2, NOS1, NOS3 ALDH1A1 1859/4885TDP1 841/4885TSHR 2439/4885
US-20210332002-A1 DISSYMMETRIC N,N-DIALKYLAMIDES USED PARTICULARLY FOR SEPARATING URANIUM(VI) FROM PLUTONIUM(IV), SYNTHESIS THEREOF AND USES OF SAME NOS2, NOS1, NOS3 ALDH1A1 1859/4885TDP1 841/4885TSHR 2439/4885
US-20190016684-A1 ANTIMICROBIAL IMIDAZOLIUM COMPOUNDS CCNI, MACF1, ECI1 ALDH1A1 3371/4885TDP1 4399/4885TSHR 3989/4885
US-20080242893-A1 Process for Preparing Optically Active Diphosphanes PHOSPHO1, DCTPP1, DCPS ALDH1A1 899/4885TDP1 4215/4885TSHR 4357/4885

“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.