Acrylamide

Acrylamide

SCHEMBL29250079

C=CC(N)=O.CC(C)S(=O)(=O)[O-].[Li+]

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GSK3AGSK3BIMPA1

The experimentally established mechanism targets of Acrylamide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.50
ALDH1A1 P00352 2/20 0.50
FGFR4 P22455 1/20 0.50

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
Acrylamide SCHEMBL29249980 0.95 TSHR (0.50) TSHRALDH1A1FGFR4
Acrylamide SCHEMBL19665935 0.95 TSHR (0.50) TSHRALDH1A1FGFR4
Acrylamide SCHEMBL2099063 0.81 TSHR (0.55) TSHRALDH1A1FGFR4
Acrylamide SCHEMBL23607544 0.79 ALDH1A1 (0.52) TSHRALDH1A1FGFR4
Acrylamide SCHEMBL29249902 0.79 TSHR (0.52) TSHRALDH1A1FGFR4
Acrylamide SCHEMBL2196034 0.78 TSHR (0.58) TSHRALDH1A1FGFR4
Acrylamide SCHEMBL7059174 0.78 ALDH1A1 (0.58) TSHRALDH1A1FGFR4
Acrylamide SCHEMBL4669815 0.78 ALDH1A1 (0.41) TSHRALDH1A1FGFR4
Acrylamide SCHEMBL14118868 0.78 ALDH1A1 (0.65) TSHRALDH1A1FGFR4
Acrylamide SCHEMBL14118871 0.78 ALDH1A1 (0.65) TSHRALDH1A1FGFR4

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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118324995-A Modified binder for lithium battery and preparation method and application thereof 杭州辛想科技有限公司 2024-07-12 CN disclosed