Cinnamic Alcohol

Cinnamic Alcohol

SCHEMBL5143596

O=C(O)c1ccccc1.OCC=Cc1ccccc1

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CACNA1CCACNA1DCACNA1FCACNA1SDPP4HTR1BHTR1D

The experimentally established mechanism targets of Cinnamic Alcohol. 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
PAM P19021 1/20 0.55
DAO P14920 1/20 0.54
TSHR P16473 1/20 0.54
NAPRT Q6XQN6 1/20 0.54
MAOB P27338 2/20 0.50
PLIN1 O60240 2/20 0.50
LMNA P02545 2/20 0.50
MAPT P10636 2/20 0.50
RECQL P46063 2/20 0.50
PLIN5 Q00G26 2/20 0.50
ABHD5 Q8WTS1 2/20 0.50
BCHE P06276 1/20 0.50
TNFRSF1A P19438 1/20 0.50
ACHE P22303 1/20 0.50
CYP1B1 Q16678 1/20 0.50
CES2 O00748 1/20 0.47
CES1 P23141 1/20 0.47
SRD5A2 P31213 1/20 0.47
TTR P02766 2/20 0.46
NPC1 O15118 2/20 0.46

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
Benzoic Acid SCHEMBL9838235 0.86 TSHR (0.67) DAOTSHRNAPRTMAPTCES2
Benzoic Acid SCHEMBL11652723 0.86 TSHR (0.67) DAOTSHRNAPRTMAPTCES2
Cinnamic Alcohol SCHEMBL27887623 0.85 PAM (0.58) PAMMAOBPLIN1LMNAMAPT
Cinnamic Alcohol SCHEMBL891462 0.85 PAM (0.58) PAMMAOBPLIN1LMNAMAPT
Cinnamic Alcohol SCHEMBL4175503 0.85 PAM (0.58) PAMMAOBPLIN1LMNAMAPT
Cinnamic Alcohol SCHEMBL39220 0.85 PAM (0.58) PAMMAOBPLIN1LMNAMAPT
Cinnamic Alcohol SCHEMBL39219 0.85 PAM (0.58) PAMMAOBPLIN1LMNAMAPT
Cinnamic Alcohol SCHEMBL28583889 0.85 PAM (0.58) PAMMAOBPLIN1LMNAMAPT
Cinnamic Alcohol SCHEMBL17812926 0.84 PAM (0.59) PAMMAOBPLIN1LMNAMAPT
(Z)-1,2-Diphenylethene SCHEMBL29118837 0.83 TSHR (0.70) DAOTSHRNAPRTMAOBPLIN1

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
US-10869474-B2 Fungicidal compositions UNIVERSITÄT BASEL (CH) 2020-12-22 US disclosed
US-20190200609-A1 FUNGICIDAL COMPOSITIONS UNIVERSITÄT BASEL (CH) 2019-07-04 US disclosed
EP-3471542-A1 FUNGICIDAL COMPOSITIONS Universität Basel (CH) 2019-04-24 EP disclosed
WO-2017220565-A1 FUNGICIDAL COMPOSITIONS UNIVERSITÄT BASEL (CH) 2017-12-28 WO disclosed
EP-3259991-A1 FUNGICIDAL COMPOSITIONS Universität Basel (CH) 2017-12-27 EP disclosed
US-7220529-B2 Photopolymerizable composition and recording material using the same FUJIFILM CORPORATION (JP) 2007-05-22 US disclosed
US-20050186504-A1 Photopolymerizable composition and recording material using the same FUJI PHOTO FILM CO., LTD. 2005-08-25 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 (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-20190200609-A1 FUNGICIDAL COMPOSITIONS CBR3, CYP1A1, CYP4F3 PAM 2192/4885DAO 821/4885TSHR 868/4885
US-10869474-B2 Fungicidal compositions CBR3, CYP3A7, CYP3A43 PAM 2217/4885DAO 931/4885TSHR 762/4885

“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.