SCHEMBL9544504

SCHEMBL9544504

C1CCN(CCOCCOCCN2CCCC2)C1

nearest known ligand 0.55

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
HRH3 Q9Y5N1 4/20 0.52
KDM4E B2RXH2 6/20 0.49
HTT P42858 3/20 0.49
LTA4H P09960 1/20 0.46
ALDH1A1 P00352 4/20 0.45
SMN1; SMN2 Q16637 2/20 0.45
CHRM2 P08172 1/20 0.43
ADRA2C P18825 1/20 0.43
SLC6A2 P23975 1/20 0.43
SLC6A4 P31645 1/20 0.43
HRH1 P35367 1/20 0.43
SLC6A3 Q01959 1/20 0.43
KCNH2 Q12809 1/20 0.43
CACNA1C Q13936 1/20 0.43
SCN5A Q14524 1/20 0.43
KMT2A Q03164 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
SCHEMBL9542003 1.00 HRH3 (0.52) HRH3KDM4EHTTLTA4HALDH1A1
SCHEMBL10914988 1.00 HRH3 (0.52) HRH3KDM4EHTTLTA4HALDH1A1
SCHEMBL9541684 0.97 HRH3 (0.57) HRH3KDM4EHTTLTA4HALDH1A1
SCHEMBL9542084 0.97 HRH3 (0.57) HRH3KDM4EHTTLTA4HALDH1A1
SCHEMBL9544441 0.97 HRH3 (0.57) HRH3KDM4EHTTLTA4HALDH1A1
SCHEMBL7110089 0.97 HRH3 (0.55) HRH3KDM4EHTTLTA4HALDH1A1
SCHEMBL24059343 0.94 HRH3 (0.60) HRH3KDM4EHTTLTA4HSMN1; SMN2
SCHEMBL7887990 0.94 HRH3 (0.60) HRH3KDM4EHTTLTA4HSMN1; SMN2
SCHEMBL8361918 0.94 HRH3 (0.60) HRH3KDM4EHTTLTA4HSMN1; SMN2
SCHEMBL28656506 0.91 HRH3 (0.48) HRH3KDM4EHTTLTA4HALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117244422-A Preparation method of anion exchange membrane 天府新能源研究院 2023-12-19 CN claimed
US-11136434-B2 Polyamines, synthesis method thereof and use thereof for the selective elimination of H2S from a gaseous effluent comprising CO2 IFP Energies Nouvelles (FR) 2021-10-05 US claimed
US-10710021-B2 Polyamines, synthesis process thereof and use of same for the selective elimination of H2S from a gaseous effluent comprising CO2 IFP Energies Nouvelles (FR) 2020-07-14 US claimed
US-20200148824-A1 NOVEL POLYAMINES, SYNTHESIS METHOD THEREOF AND USE THEREOF FOR THE SELECTIVE ELIMINATION OF H2S FROM A GASEOUS EFFLUENT COMPRISING CO2 IFP Energies Nouvelles (FR) 2020-05-14 US claimed
EP-3397671-B1 NOVEL POLYAMINES, SYNTHESIS PROCESS THEREOF AND USE OF SAME FOR THE SELECTIVE ELIMINATION OF H2S FROM A GASEOUS EFFLUENT COMPRISING CO2 IFP ENERGIES NOW (FR) 2020-02-12 EP claimed
US-20180369743-A1 NOVEL POLYAMINES, SYNTHESIS PROCESS THEREOF AND USE OF SAME FOR THE SELECTIVE ELIMINATION OF H2S FROM A GASEOUS EFFLUENT COMPRISING CO2 IFP Energies Nouvelles (FR) 2018-12-27 US claimed
US-4405582-A Process for selective removal of H2 S from mixtures containing H22 using diaminoether solutions EXXON RESEARCH AND ENGINEERING CO. (US) 1983-09-20 US claimed
CN-117244422-A Preparation method of anion exchange membrane 天府新能源研究院 2023-12-19 CN disclosed
EP-3713915-B1 METHOD FOR PRODUCING BISPYRROLIDINE COMPOUNDS BASF SE (DE) 2022-10-19 EP disclosed
US-11345680-B2 Method for producing bispyrrolidine compounds BASF SE (DE) 2022-05-31 US disclosed
US-11136434-B2 Polyamines, synthesis method thereof and use thereof for the selective elimination of H2S from a gaseous effluent comprising CO2 IFP Energies Nouvelles (FR) 2021-10-05 US disclosed
CN-109153933-B Carbon dioxide co-fluid 艾默生环境优化技术有限公司 2021-09-03 CN disclosed
CN-108778467-B Absorbent solution based on hydroxy derivatives of 1, 6-hexanediamine and process for eliminating acidic compounds from gaseous effluents IFP 新能源公司 2021-05-04 CN disclosed
EP-2540376-A1 Method for deacidifying a gas with a plurality of steps of placing in co-current contact with an absorbent solution IFP Energies nouvelles (FR) 2013-01-02 EP disclosed
US-20110202328-A1 System for the determination of selective absorbent molecules through predictive correlations EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2011-08-18 US disclosed
US-20110202328-A1 System for the determination of selective absorbent molecules through predictive correlations EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2011-08-18 US disclosed
WO-1993010883-A1 LEAN ACID GAS ENRICHMENT WITH SELECTIVE HINDERED AMINES EXXON RESEARCH AND ENGINEERING COMPANY (US) 1993-06-10 WO disclosed
EP-0087856-B1 A PROCESS FOR THE REMOVAL OF H2S FROM GASEOUS MIXTURES USING DIAMINOETHERS EXXON RESEARCH AND ENGINEERING COMPANY (US) 1986-02-26 EP disclosed
US-4405582-A Process for selective removal of H2 S from mixtures containing H22 using diaminoether solutions EXXON RESEARCH AND ENGINEERING CO. (US) 1983-09-20 US disclosed
EP-0087856-A1 A process for the removal of H2S from gaseous mixtures using diaminoethers EXXON RESEARCH AND ENGINEERING COMPANY (US) 1983-09-07 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 (1 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-11345680-B2 Method for producing bispyrrolidine compounds BCKDK, BBOX1, DHPS HRH3 306/4885KDM4E 1969/4885HTT 2512/4885

“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.