Cinnamic Acid

Cinnamic Acid

SCHEMBL669104

CCCC[P+](CCCC)(CCCC)CCCC.O=C(O)C=Cc1ccccc1.O=C([O-])c1ccccc1O

nearest known ligand 0.48

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHE

The experimentally established mechanism targets of Cinnamic Acid. 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
MAPT P10636 6/20 0.48
CYP2C19 P33261 2/20 0.48
BCHE P06276 1/20 0.48
KDM4E B2RXH2 4/20 0.46
RAB9A P51151 2/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
TDP1 Q9NUW8 2/20 0.46
KCNH2 Q12809 1/20 0.46
NPC1 O15118 1/20 0.46
HDAC3 O15379 2/20 0.45
TNKS O95271 1/20 0.45
HDAC4 P56524 1/20 0.45
HDAC1 Q13547 1/20 0.45
HCAR2 Q8TDS4 1/20 0.45
HDAC7 Q8WUI4 1/20 0.45
HDAC2 Q92769 1/20 0.45
HDAC10 Q969S8 1/20 0.45
HDAC11 Q96DB2 1/20 0.45
HDAC8 Q9BY41 1/20 0.45

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
Salicylic Acid SCHEMBL666959 0.86 KDM4E (0.59) MAPTKDM4ERAB9AKMT2ATDP1
Salicylic Acid SCHEMBL668244 0.83 KDM4E (0.53) KDM4EMEN1KMT2AALDH1A1HPGD
Salicylic Acid SCHEMBL3468302 0.81 ALDH1A1 (0.50) MAPTKDM4EMEN1KMT2AALDH1A1
Salicylic Acid SCHEMBL17710452 0.79 ALDH1A1 (0.54) MAPTKDM4EMEN1KMT2AALDH1A1
SCHEMBL669103 0.79 KMT2A (0.47) MAPTBCHEKDM4ERAB9AMEN1
Phthalic Acid SCHEMBL5048545 0.77 ALDH1A1 (0.47) MAPTCYP2C19KDM4EMEN1KMT2A
Cinnamic Acid SCHEMBL8407378 0.75 MAPT (0.63) MAPTCYP2C19BCHEKDM4ERAB9A
Cinnamic Acid SCHEMBL8407375 0.75 MAPT (0.63) MAPTCYP2C19BCHEKDM4ERAB9A
Cetylpyridinium SCHEMBL2369770 0.74 MAPT (0.43) MAPTCYP2C19BCHEKDM4ERAB9A
Cinnamic Acid SCHEMBL28752126 0.74 HDAC3 (0.70) MAPTKDM4ERAB9AKMT2ATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9278134-B2 Dual functioning ionic liquids and salts thereof THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ALABAMA (US) 2016-03-08 US disclosed
US-20130203602-A1 SUPPORTED BIOLOGICALLY ACTIVE COMPOUNDS DANMARKS TEKNISKE UNIVERSITET (DK) 2013-08-08 US disclosed
US-20120046244-A1 DUAL FUNCTIONING IONIC LIQUIDS AND SALTS THEREOF THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ALABAMA (US) 2012-02-23 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-20130203602-A1 SUPPORTED BIOLOGICALLY ACTIVE COMPOUNDS MIF, BMP2, BMP4 MAPT 3938/4885CYP2C19 1830/4885BCHE 974/4885
US-20120046244-A1 DUAL FUNCTIONING IONIC LIQUIDS AND SALTS THEREOF SLC6A6, SLC10A2, CLK2 MAPT 833/4885CYP2C19 805/4885BCHE 1459/4885

“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.