N-(4-Methoxyphenyl)Cinnamamide

N-(4-Methoxyphenyl)Cinnamamide

SCHEMBL4131114

COc1ccc(NC(=O)C=Cc2ccccc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MMP1 P03956 10/20 1.00
MMP2 P08253 10/20 1.00
MMP9 P14780 10/20 1.00
EGFR P00533 6/20 1.00
MAPT P10636 4/20 0.76
SMN1; SMN2 Q16637 4/20 0.76
TP53 P04637 2/20 0.76
THRB P10828 1/20 0.76
KMT2A Q03164 3/20 0.76
NPC1 O15118 3/20 0.74
RAB9A P51151 3/20 0.74
MEN1 O00255 2/20 0.74
CYP3A4 P08684 1/20 0.74
CYP2D6 P10635 1/20 0.74
PKM P14618 1/20 0.74
TSHR P16473 1/20 0.74
NFKB1 P19838 1/20 0.74
MAPK1 P28482 1/20 0.74
CYP2C19 P33261 1/20 0.74
THPO P40225 1/20 0.74

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
N-(4-Methoxyphenyl)Cinnamamide SCHEMBL4131112 1.00 MMP1 (1.00) MMP1MMP2MMP9EGFRMAPT
N-(4-Methoxyphenyl)Cinnamamide SCHEMBL9094893 1.00 MMP1 (1.00) MMP1MMP2MMP9EGFRMAPT
SCHEMBL11299307 0.96 MMP1 (0.92) MMP1MMP2MMP9EGFRMAPT
4-Methoxy-Cinnamanilide SCHEMBL14375152 0.94 MMP1 (0.89) MMP1MMP2MMP9EGFRMAPT
SCHEMBL17693073 0.92 MAPT (0.88) MMP1MMP2MMP9EGFRMAPT
SCHEMBL8751515 0.87 MAPT (0.77) MMP1MMP2MMP9EGFRMAPT
SCHEMBL8751492 0.87 MAPT (0.77) MMP1MMP2MMP9EGFRMAPT
SCHEMBL11590995 0.87 EGFR (0.92) MMP1MMP2MMP9EGFRKMT2A
SCHEMBL8751550 0.87 MMP1 (0.76) MMP1MMP2MMP9EGFRMAPT
SCHEMBL8751546 0.87 MMP1 (0.76) MMP1MMP2MMP9EGFRMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111217694-B Method for selectively reducing carbon-carbon double bond in alpha, beta-unsaturated carbonyl compound 五邑大学 2022-09-30 CN disclosed
CN-111217694-A method for selectively reducing carbon-carbon double bond in α, beta-unsaturated carbonyl compound 五邑大学 2020-06-02 CN disclosed
US-20090247579-A1 2-[3H-THIAZOL-2-YLIDINEMETHYL]PYRIDINES AND RELATED COMPOUNDS AND THEIR USE CANCER RESEARCH TECHNOLOGY LIMITED 2009-10-01 US disclosed
US-7102046-B2 By reaction of haloaromatics or arylsulfonates with olefins in presence of palladium catalyst, bulky nitrogen base and salt BAYER AKTIENGESELLSCHAFT (DE) 2006-09-05 US disclosed
US-20030105353-A1 Process for the arylation of olefins LANXESS DEUTSCHLAND GMBH (DE) 2003-06-05 US disclosed
US-5576324-A Quinoline derivatives or salt thereof and remedy for cardiac diseases containing the same KOWA CO., LTD. (JP) 1996-11-19 US disclosed
EP-0638571-A1 QUINOLINE DERIVATIVE OR SALT THEREOF AND REMEDY FOR CARDIAC DISEASES CONTAINING THE SAME KOWA CO. LTD. (JP) 1995-02-15 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 (2 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-20030105353-A1 Process for the arylation of olefins NEK6, JUN, AOC2 MMP1 4607/4885MMP2 4852/4885MMP9 4783/4885
US-20090247579-A1 2-[3H-THIAZOL-2-YLIDINEMETHYL]PYRIDINES AND RELATED COMPOUNDS AND THEIR USE RB1, RBBP5, RRM2B MMP1 3817/4885MMP2 4170/4885MMP9 3904/4885

“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.