SCHEMBL4412147

SCHEMBL4412147

O=CC=C(c1ccccc1)C(F)(F)F

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CES1 P23141 4/20 0.48
▸ ALDH1A1 P00352 3/20 0.40
▸ TDP1 Q9NUW8 2/20 0.40
▸ MAPK1 P28482 1/20 0.40
▸ CES2 O00748 2/20 0.36
▸ TSHR P16473 2/20 0.36
▸ DAO P14920 1/20 0.36
▸ NAPRT Q6XQN6 1/20 0.36
▸ AKT1 P31749 1/20 0.34
▸ NPC1 O15118 1/20 0.34
▸ RAB9A P51151 1/20 0.34
▸ NFE2L2 Q16236 1/20 0.33
▸ PTPN1 P18031 1/20 0.33
▸ PREP P48147 1/20 0.33
▸ POLB P06746 1/20 0.33
▸ CYP3A4 P08684 1/20 0.33
▸ PARP1 P09874 1/20 0.33
▸ MAPT P10636 1/20 0.33
▸ CYP2C19 P33261 1/20 0.33
▸ RECQL P46063 1/20 0.33

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
SCHEMBL27919056 0.81 ALDH1A1 (0.41) CES1ALDH1A1TDP1MAPK1CES2
SCHEMBL7810264 0.80 CES2 (0.40) CES1ALDH1A1MAPK1CES2TSHR
SCHEMBL7810262 0.80 CES2 (0.40) CES1ALDH1A1MAPK1CES2TSHR
SCHEMBL29117952 0.79 CES1 (0.43) CES1ALDH1A1TDP1MAPK1CES2
SCHEMBL11043913 0.78 CES1 (0.42) CES1ALDH1A1CES2NPC1RAB9A
SCHEMBL11043916 0.78 CES1 (0.42) CES1ALDH1A1CES2NPC1RAB9A
SCHEMBL20919883 0.76 CES1 (0.48) CES1ALDH1A1TDP1MAPK1CES2
SCHEMBL28269583 0.76 CES1 (0.48) CES1ALDH1A1TDP1MAPK1CES2
SCHEMBL3731523 0.76 CES1 (0.48) CES1ALDH1A1TDP1MAPK1CES2
SCHEMBL9575084 0.75 CES1 (0.54) CES1ALDH1A1TDP1MAPK1CES2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115010753-A Method for preparing phosphorylated gem-difluorodiene compound in aqueous phase 南京工业大学 2022-09-06 — — CN disclosed
CN-105130726-A Method for preparing cinnamyl aldehyde compounds UNIV HUNAN 2015-12-09 — — CN disclosed
CN-104844422-A Preparation method of substituted cinnamyl alcohol compound UNIV DALIAN TECH 2015-08-19 — — CN disclosed
CN-104592037-A Synthesis method of cinacalcet UNIV ZHEJIANG 2015-05-06 — — CN disclosed
US-20090082362-A1 Use of capsaicin receptor antagonists to treat symptoms of tear gas exposure BAKTHAVATCHALAM RAJAGOPAL 2009-03-26 — — US disclosed
US-6723730-B2 DIARYL PIPERAZINES AND RELATED COMPOUNDS USEFUL IN THE TREATMENT OF A CHRONIC AND ACUTE PAIN CONDITIONS, ITCH AND URINARY INCONTINENCE. NEUROGEN CORPORATION 2004-04-20 — — US 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-20090082362-A1 Use of capsaicin receptor antagonists to treat symptoms of tear gas exposure TRPV1, TRPA1, TRPV5 CES1 2842/4885ALDH1A1 1282/4885TDP1 3155/4885

“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.

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