SCHEMBL127382

SCHEMBL127382

C=CC(=O)OCCN(C)C.COS(=O)(=O)O

nearest known ligand 0.44

Known targets — ChEMBL curated mechanism

ACHECHRM1CHRM3

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM1 known ✓ P11229 1/20 0.43
CHRM3 known ✓ P20309 1/20 0.43
TSHR P16473 6/20 0.44
HPGD P15428 1/20 0.44
ALDH1A1 P00352 6/20 0.44
TP53 P04637 3/20 0.44
HIF1A Q16665 3/20 0.44
CYP3A4 P08684 2/20 0.44
HSD17B10 Q99714 1/20 0.44
CHRM2 P08172 1/20 0.43
CHRM4 P08173 1/20 0.43
CHRM5 P08912 1/20 0.43
CHRNB2 P17787 1/20 0.43
CHRNA4 P43681 1/20 0.43
THRB P10828 2/20 0.38
DNM1 Q05193 1/20 0.36
CA12 O43570 1/20 0.34
CA1 P00915 1/20 0.34
CA2 P00918 1/20 0.34
CA9 Q16790 1/20 0.34

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
Water SCHEMBL28400901 0.98 TSHR (0.43) TSHRHPGDALDH1A1TP53HIF1A
Sulfuric Acid SCHEMBL128048 0.91 TSHR (0.48) TSHRHPGDALDH1A1TP53HIF1A
Sulfuric Acid SCHEMBL27667403 0.91 TSHR (0.48) TSHRHPGDALDH1A1TP53HIF1A
Sulfuric Acid Dimethyl Ester SCHEMBL2527183 0.90 TSHR (0.44) TSHRHPGDALDH1A1TP53HIF1A
Sulfuric Acid SCHEMBL28351009 0.90 TSHR (0.47) TSHRHPGDALDH1A1TP53HIF1A
Sulfuric Acid SCHEMBL28251440 0.90 TSHR (0.47) TSHRHPGDALDH1A1TP53HIF1A
SCHEMBL17003984 0.90 TSHR (0.47) TSHRHPGDALDH1A1TP53HIF1A
SCHEMBL28515730 0.88 TSHR (0.50) TSHRHPGDALDH1A1TP53HIF1A
SCHEMBL15115 0.88 TSHR (0.56) TSHRHPGDALDH1A1TP53HIF1A
SCHEMBL28802094 0.87 TSHR (0.46) TSHRHPGDALDH1A1TP53HIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122070397-A Use of fast reverse cationic emulsion polymers with polyvinylamines as retention and drainage aids 凯米拉公司 2026-05-19 CN claimed
EP-4739418-A2 ONE-PASS DEOXYGENATION METHOD FOR POLYACRYLAMIDE PRODUCTION KEMIRA OYJ (FI) 2026-05-13 EP claimed
EP-4728136-A1 STRENGTH SYNERGY BETWEEN POLYMER AND PAPERMAKING STRENGTH AID Ecolab USA, Inc. (US) 2026-04-22 EP claimed
EP-4716777-A2 USE OF AMPHOTERIC EMULSION POLYMERS WITH STRENGTH RESINS AS RETENTION AND DRAINAGE AIDS KEMIRA OYJ (FI) 2026-04-01 EP claimed
US-12553188-B2 GPAM compositions and methods KEMIRA OYJ (FI) 2026-02-17 US claimed
EP-4683950-A1 DUAL EMULSIFICATION OF ALKENYL SUCCINIC ANHYDRIDE TO IMPROVE SIZING PERFORMANCE AND STABILITY KEMIRA OYJ (FI) 2026-01-28 EP claimed
US-20250215649-A1 HIGH MOLECULAR WEIGHT GPAM WITH ANIONIC POLYSACCHARIDE PROMOTER KEMIRA OYJ (FI) 2025-07-03 US claimed
US-20250137200-A1 HIGH MOLECULAR WEIGHT GPAM WITH ANIONIC POLYMERIC PROMOTER KEMIRA OYJ (FI) 2025-05-01 US claimed
EP-4256009-B1 OIL-IN-WATER EMULSIONS QUADRISE INT LTD (GB) 2025-04-09 EP claimed
WO-2025072390-A1 USE OF QUICK INVERSION CATIONIC EMULSION POLYMERS WITH POLYVINYLAMINES AS RETENTION AND DRAINAGE AIDS KEMIRA OYJ (FI) 2025-04-03 WO claimed
US-20020198317-A1 Preparation of water soulble polymer dispersions from vinylamide monomers ECOLAB USA INC. 2002-12-26 US claimed
US-6344531-B1 Fluorescent water-soluble polymers NALCO CHEMICAL COMPANY 2002-02-05 US claimed
WO-2001081654-A1 FLUORESCENT MONOMERS AND TAGGED TREATMENT POLYMERS CONTAINING SAME FOR USE IN INDUSTRIAL WATER SYSTEMS ONDEO NALCO COMPANY (US) 2001-11-01 WO claimed
US-6177017-B1 COMPLEXING WITH 1,4-DIAZABICYCLO(2.2.2) OCTANE POLYMERS NALCO CHEMICAL COMPANY 2001-01-23 US claimed
US-6114484-A REMOVAL OF METAL CYANIDES OR OXOANIONS FROM AQUEOUS STREAMS SUCH AS WASTE WATER STREAMS WITH COMPOUNDS CONTAINING 1,4-DIAZABICYCLO(2.2.2)OCTANE NALCO CHEMICAL COMPANY (US) 2000-09-05 US claimed
EP-0984990-A1 PREPARATION OF WATER SOLUBLE POLYMER DISPERSIONS FROM VINYLAMIDE MONOMERS NALCO CHEMICAL COMPANY (US) 2000-03-15 EP claimed
EP-0970258-A1 POLYMERIC COMBINATIONS USED AS COPPER AND PRECIOUS METAL HEAP LEACHING AGGLOMERATION AIDS NALCO CHEMICAL COMPANY (US) 2000-01-12 EP claimed
WO-1999020803-A1 POLYMERIC COMBINATIONS USED AS COPPER AND PRECIOUS METAL HEAP LEACHING AGGLOMERATION AIDS NALCO CHEMICAL COMPANY (US) 1999-04-29 WO claimed
WO-1998054234-A1 PREPARATION OF WATER SOLUBLE POLYMER DISPERSIONS FROM VINYLAMIDE MONOMERS NALCO CHEMICAL COMPANY (US) 1998-12-03 WO claimed
US-5833937-A AGGLOMERATING BY SEQUENTIAL ADDITION OF FIRST WATER SOLUBLE ANIONIC OR NONIONIC POLYMER AND SECOND CATIONIC WATER SOLUBLE POLYMER NALCO CHEMICAL COMPANY (US) 1998-11-10 US claimed

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-12553188-B2 GPAM compositions and methods PGM2, SLC6A9, GNMT CHRM1 848/4885CHRM3 1722/4885TSHR 4437/4885

“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.