SCHEMBL14799290

SCHEMBL14799290

CCOC(=O)CS(=O)(=O)Nc1ccc(OC)c(OC)c1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SHMT2 P34897 1/20 0.54
MEN1 O00255 3/20 0.51
KMT2A Q03164 3/20 0.51
GAA P10253 1/20 0.51
MAPT P10636 1/20 0.51
SMN1; SMN2 Q16637 7/20 0.50
LMNA P02545 4/20 0.50
HTT P42858 2/20 0.50
MAPK1 P28482 2/20 0.49
ALOX15 P16050 1/20 0.49
HIF1A Q16665 1/20 0.47
HDAC8 Q9BY41 1/20 0.46
CA12 O43570 1/20 0.46
CA1 P00915 1/20 0.46
CA2 P00918 1/20 0.46
CA9 Q16790 1/20 0.46
HPGD P15428 2/20 0.46
HDAC4 P56524 1/20 0.46
HDAC1 Q13547 1/20 0.46
CYP1A2 P05177 1/20 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
SCHEMBL14799054 0.89 SMN1; SMN2 (0.55) SHMT2MEN1KMT2AGAASMN1; SMN2
SCHEMBL18437704 0.84 ALDH1A1 (0.64) MEN1KMT2AGAAMAPTLMNA
SCHEMBL2759559 0.81 SMN1; SMN2 (0.63) MEN1KMT2AMAPTSMN1; SMN2LMNA
SCHEMBL11225285 0.80 HPGD (0.48) KMT2AGAAMAPTSMN1; SMN2LMNA
SCHEMBL5864942 0.79 RORC (0.46) MEN1KMT2AGAAMAPTSMN1; SMN2
SCHEMBL8864726 0.78 ALDH1A1 (0.57) SHMT2MEN1KMT2AGAAMAPT
SCHEMBL6666950 0.77 HPGD (0.54) KMT2AGAASMN1; SMN2LMNAHTT
SCHEMBL9831200 0.75 MAPT (0.53) SHMT2MEN1KMT2AGAAMAPT
SCHEMBL28813545 0.75 SMN1; SMN2 (0.52) SHMT2MEN1KMT2ASMN1; SMN2LMNA
SCHEMBL960580 0.75 ALDH1A1 (0.55) MEN1KMT2AMAPTSMN1; SMN2LMNA

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-103827088-B It is used as the derivative of the pyridyl alkyl alcohol of 1 phenyl 2 of phosphodiesterase inhibitors 奇斯药制品公司 2017-10-13 CN disclosed
US-9265768-B2 Derivatives of 1-phenyl-2-pyridinyl alkyl alcohols as phosphodiesterase inhibitors CHIESI FARMACEUTICI S.P.A. (IT) 2016-02-23 US disclosed
EP-2760838-A1 DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS Chiesi Farmaceutici S.p.A. (IT) 2014-08-06 EP disclosed
US-20140142074-A1 DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2014-05-22 US disclosed
WO-2013045280-A1 DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2013-04-04 WO disclosed
US-20130079313-A1 DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2013-03-28 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-20130079313-A1 DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS PDE4A, PDE4B, PDE3A SHMT2 1363/4885MEN1 3052/4885KMT2A 2272/4885
US-20140142074-A1 DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS PDE4A, PDE4B, PDE3A SHMT2 1363/4885MEN1 3052/4885KMT2A 2272/4885

“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.