SCHEMBL4942296

SCHEMBL4942296

O=C(NNC(=O)c1sccc1Cl)c1ccc(Cl)cc1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 6/20 0.69
ALDH1A1 P00352 4/20 0.69
TDP1 Q9NUW8 2/20 0.69
MAPT P10636 1/20 0.69
AGTR1 P30556 1/20 0.69
RAB9A P51151 3/20 0.58
PKM P14618 1/20 0.56
KMT2A Q03164 2/20 0.55
NPC1 O15118 2/20 0.55
MEN1 O00255 1/20 0.55
POLB P06746 3/20 0.54
PTGS2 P35354 1/20 0.50
F10 P00742 1/20 0.49
MAPK1 P28482 1/20 0.49
ATM Q13315 1/20 0.49
KDM4E B2RXH2 3/20 0.49
TLR7 Q9NYK1 2/20 0.49
MAOA P21397 1/20 0.49
MAOB P27338 1/20 0.49
CYP2D6 P10635 1/20 0.47

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
SCHEMBL1859781 0.88 GAA (0.69) GAAALDH1A1TDP1MAPTAGTR1
SCHEMBL4947141 0.84 POLB (0.52) GAAALDH1A1TDP1MAPTAGTR1
SCHEMBL4947172 0.80 TDP1 (0.64) GAAALDH1A1TDP1MAPTAGTR1
SCHEMBL4952090 0.78 ALDH1A1 (0.55) GAAALDH1A1TDP1MAPTAGTR1
SCHEMBL4941117 0.78 ROCK2 (0.53) GAAALDH1A1TDP1MAPTAGTR1
SCHEMBL1863260 0.75 TP53 (0.63) GAAALDH1A1TDP1MAPTAGTR1
SCHEMBL13485774 0.74 GAA (0.57) GAAALDH1A1TDP1MAPTAGTR1
SCHEMBL1865862 0.74 GAA (0.54) GAAALDH1A1TDP1MAPTAGTR1
SCHEMBL7970243 0.73 GAA (0.56) GAAALDH1A1TDP1MAPTAGTR1
SCHEMBL4370162 0.73 ALDH1A1 (0.56) GAAALDH1A1TDP1MAPTAGTR1

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
US-7435750-B2 Method of using substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. (US) 2008-10-14 US disclosed
US-7041685-B2 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. (US) 2006-05-09 US disclosed
US-20050154012-A1 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2005-07-14 US disclosed
US-20030045546-A1 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2003-03-06 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-20030045546-A1 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CASP3, CASP1, API5 GAA 3175/4885ALDH1A1 136/4885TDP1 1636/4885
US-20050154012-A1 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CASP3, CASP1, CASP4 GAA 3337/4885ALDH1A1 229/4885TDP1 2188/4885

“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.