SCHEMBL954461

SCHEMBL954461

C[C@@H](N)c1cc(F)c(NS(C)(=O)=O)c(F)c1

nearest known ligand 0.45

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
ADRA2C P18825 1/20 0.38
ADRA1A P35348 1/20 0.38
ADRA1B P35368 1/20 0.38
TRPV1 Q8NER1 2/20 0.35

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
SCHEMBL1987964 1.00 ADRA2C (0.38) ADRA2CADRA1AADRA1BTRPV1
SCHEMBL954462 1.00 ADRA2C (0.38) ADRA2CADRA1AADRA1BTRPV1
Hydrochloric Acid SCHEMBL18784069 0.98 ADRA2C (0.37) ADRA2CADRA1AADRA1BTRPV1
Hydrochloric Acid SCHEMBL953690 0.98 ADRA2C (0.37) ADRA2CADRA1AADRA1BTRPV1
SCHEMBL2345703 0.90 ADRA2C (0.35) ADRA2CADRA1AADRA1B
SCHEMBL16472958 0.85 L3MBTL1 (0.38) ADRA2CADRA1AADRA1BTRPV1
SCHEMBL2957662 0.85 ADRA2C (0.35) ADRA2CADRA1AADRA1BTRPV1
SCHEMBL2953335 0.85 ADRA2C (0.35) ADRA2CADRA1AADRA1BTRPV1
SCHEMBL953544 0.83 ADRA2C (0.39) ADRA2CADRA1AADRA1BTRPV1
SCHEMBL957268 0.83 ADRA2C (0.39) ADRA2CADRA1AADRA1BTRPV1

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
US-10858315-B2 Method for preparing (R)-N-[4-(1-amino-ethyl)-2,6-difluoro-phenyl]-methanesulfonamide AMOREPACIFIC CORPORATION (KR) 2020-12-08 US claimed
CN-106660949-B Chiral resolution method of N- [4- (1-aminoethyl) -phenyl ] -sulfamide derivative 株式会社爱茉莉太平洋 2020-11-13 CN claimed
US-20200031766-A1 METHOD FOR PREPARING (R)-N-[4-(1-AMINO-ETHYL)-2,6-DIFLUORO-PHENYL]-METHANESULFONAMIDE AMOREPACIFIC CORPORATION (KR) 2020-01-30 US claimed
US-10479763-B2 Chiral resolution method of N-[4-(1-aminoethyl)-phenyl]-sulfonamide derivatives AMOREPACIFIC CORPORATION (KR) 2019-11-19 US claimed
CN-110023282-A The method for being used to prepare (R)-N- [4- (1- amine ethyl) -2,6- difluorophenyl] Methanesulfonamide 株式会社爱茉莉太平洋 2019-07-16 CN claimed
EP-3162793-B1 CHIRAL RESOLUTION METHOD OF N-[4-(1-AMINOETHYL)-PHENYL]-SULFONAMIDE DERIVATIVES AMOREPACIFIC CORP (KR) 2019-04-10 EP claimed
US-20170342027-A1 CHIRAL RESOLUTION METHOD OF N-[4-(1-AMINOETHYL)-PHENYL]-SULFONAMIDE DERIVATIVES AMOREPACIFIC CORPORATION (KR) 2017-11-30 US claimed
EP-3162793-A1 CHIRAL RESOLUTION METHOD OF N-[4-(1-AMINOETHYL)-PHENYL]-SULFONAMIDE DERIVATIVES Amorepacific Corporation (KR) 2017-05-03 EP claimed
EP-1861359-B1 N-(N-SULFONYLAMINOMETHYL)CYCLOPROPANECARBOXAMIDE DERIVATIVES USEFUL FOR THE TREATMENT OF PAIN PFIZER (US) 2012-11-14 EP claimed
EP-2024272-A2 AMIDE DERIVATIVES AS ION-CHANNEL LIGANDS AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME Renovis, Inc. (US) 2009-02-18 EP claimed
WO-2007133637-A2 AMIDE DERIVATIVES AS ION-CHANNEL LIGANDS AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME RENOVIS, INC. (US) 2007-11-22 WO claimed
CN-109608368-B Synthesis and resolution method of N- [4- (1-aminoethyl) -2, 6-difluorophenyl ] methanesulfonamide 常州市阳光药业有限公司 2021-03-09 CN disclosed
US-10858315-B2 Method for preparing (R)-N-[4-(1-amino-ethyl)-2,6-difluoro-phenyl]-methanesulfonamide AMOREPACIFIC CORPORATION (KR) 2020-12-08 US disclosed
US-10858315-B2 Method for preparing (R)-N-[4-(1-amino-ethyl)-2,6-difluoro-phenyl]-methanesulfonamide AMOREPACIFIC CORPORATION (KR) 2020-12-08 US disclosed
CN-106660949-B Chiral resolution method of N- [4- (1-aminoethyl) -phenyl ] -sulfamide derivative 株式会社爱茉莉太平洋 2020-11-13 CN disclosed
US-20080312234-A1 NOVEL COMPOUNDS, ISOMER THEREOF, OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF AS VANILLOID RECEPTOR ANTAGONIST; AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AMOREPACIFIC CORPORATION (KR) 2008-12-18 US disclosed
US-20080312234-A1 NOVEL COMPOUNDS, ISOMER THEREOF, OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF AS VANILLOID RECEPTOR ANTAGONIST; AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AMOREPACIFIC CORPORATION (KR) 2008-12-18 US disclosed
WO-2008013414-A1 NOVEL COMPOUNDS, ISOMER THEREOF, OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF AS VANILLOID RECEPTOR ANTAGONIST; AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AMOREPACIFIC CORPORATION (KR) 2008-01-31 WO disclosed
WO-2007133637-A2 AMIDE DERIVATIVES AS ION-CHANNEL LIGANDS AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME RENOVIS, INC. (US) 2007-11-22 WO disclosed
WO-2007133637-A2 AMIDE DERIVATIVES AS ION-CHANNEL LIGANDS AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME RENOVIS, INC. (US) 2007-11-22 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 (3 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-20080312234-A1 NOVEL COMPOUNDS, ISOMER THEREOF, OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF AS VANILLOID RECEPTOR ANTAGONIST; AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME TRPV1, TRPA1, TRPV2 ADRA2C 448/4885ADRA1A 370/4885ADRA1B 495/4885
US-10479763-B2 Chiral resolution method of N-[4-(1-aminoethyl)-phenyl]-sulfonamide derivatives DHCR24, SRR, ACMSD ADRA2C 1709/4885ADRA1A 1488/4885ADRA1B 2568/4885
US-20170342027-A1 CHIRAL RESOLUTION METHOD OF N-[4-(1-AMINOETHYL)-PHENYL]-SULFONAMIDE DERIVATIVES DHCR24, SRR, ACMSD ADRA2C 1709/4885ADRA1A 1488/4885ADRA1B 2568/4885

“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.