P-Cresol

P-Cresol

SCHEMBL9107906

Cc1ccc(O)cc1.O=C(O)Cc1cccc(Cl)c1

nearest known ligand 0.56

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CTBP2 P56545 2/20 0.51
CA2 P00918 2/20 0.49
CAMK2A Q9UQM7 1/20 0.49
PIK3CA P42336 1/20 0.48
FFAR1 O14842 1/20 0.45
FFAR4 Q5NUL3 1/20 0.45
HTR3E A5X5Y0 1/20 0.45
HTR3B O95264 1/20 0.45
HTR3A P46098 1/20 0.45
HTR3D Q70Z44 1/20 0.45
HTR3C Q8WXA8 1/20 0.45
CSNK1D P48730 2/20 0.44
THRA P10827 1/20 0.44
THRB P10828 1/20 0.44
PTGDR2 Q9Y5Y4 1/20 0.44
ALDH1A1 P00352 2/20 0.43
MEN1 O00255 1/20 0.43
HPGD P15428 1/20 0.43
KMT2A Q03164 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43

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
Parachlorophenol SCHEMBL9108351 0.89 CTBP2 (0.55) CTBP2CA2CAMK2APIK3CAHTR3E
SCHEMBL467923 0.85 CTBP2 (0.66) CTBP2CA2PIK3CAHTR3EHTR3B
Ammonia Solution, Strong SCHEMBL28761900 0.84 CTBP2 (0.64) CTBP2CA2PIK3CAHTR3EHTR3B
Hydrochloric Acid SCHEMBL2531827 0.84 CTBP2 (0.64) CTBP2CA2PIK3CAHTR3EHTR3B
Ammonia Solution, Strong SCHEMBL5702482 0.84 CTBP2 (0.64) CTBP2CA2PIK3CAHTR3EHTR3B
Phenylacetic Acid SCHEMBL8319811 0.82 CA2 (0.67) CA2CAMK2AFFAR1KMT2ASMN1; SMN2
SCHEMBL11774837 0.79 CTBP2 (0.58) CTBP2CA2PIK3CAHTR3EHTR3B
3-Hydroxyphenylacetate SCHEMBL28209149 0.78 AKR1B1 (0.53) CTBP2CA2CAMK2AFFAR1MEN1
SCHEMBL4208044 0.76 GRIN2D (0.55) CTBP2CA2LMNA
Toluene SCHEMBL28858324 0.75 CA2 (0.73) CTBP2CA2CAMK2AFFAR1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2646026-B1 NOVEL OXADIAZOLE DERIVATIVES AS SPHINGOSINE 1-PHOSPHATE (S1P) RECEPTOR MODULATORS ALLERGAN INC (US) 2014-10-15 EP disclosed
US-20140057952-A1 NOVEL OXADIAZOLE DERIVATIVES AS SPHINGOSINE 1-PHOSPHATE (S1P) RECEPTOR MODULATORS ALLERGAN, INC. (US) 2014-02-27 US disclosed
US-8618139-B2 Oxadiazole derivatives as sphingosine 1-phosphate (S1P) receptor modulators ALLERGAN, INC. (US) 2013-12-31 US disclosed
US-20120142739-A1 NOVEL OXADIAZOLE DERIVATIVES AS SPHINGOSINE 1-PHOSPHATE (S1P) RECEPTOR MODULATORS ALLERGAN, INC. (US) 2012-06-07 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-20140057952-A1 NOVEL OXADIAZOLE DERIVATIVES AS SPHINGOSINE 1-PHOSPHATE (S1P) RECEPTOR MODULATORS S1PR3, S1PR1, S1PR2 CTBP2 3215/4885CA2 3682/4885CAMK2A 901/4885
US-20120142739-A1 NOVEL OXADIAZOLE DERIVATIVES AS SPHINGOSINE 1-PHOSPHATE (S1P) RECEPTOR MODULATORS S1PR3, S1PR1, S1PR2 CTBP2 3215/4885CA2 3682/4885CAMK2A 901/4885

“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.