SCHEMBL2515076

SCHEMBL2515076

CCOC(=O)CCC(O)c1cccs1

nearest known ligand 0.42

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 1/20 0.42
RAB9A P51151 1/20 0.42
KMT2A Q03164 1/20 0.42
ALDH1A1 P00352 1/20 0.41
CYP4F2 P78329 2/20 0.40
CYP4A11 Q02928 2/20 0.40
CES2 O00748 1/20 0.40
CES1 P23141 1/20 0.40
KEAP1 Q14145 1/20 0.40
SDHB P21912 1/20 0.39
HTR1A P08908 1/20 0.39
LMNA P02545 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38

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
SCHEMBL2859011 0.85 ALDH1A1 (0.43) RAB9AKMT2AALDH1A1CES2CES1
SCHEMBL2867866 0.85 ALDH1A1 (0.43) RAB9AKMT2AALDH1A1CES2CES1
SCHEMBL2859012 0.85 ALDH1A1 (0.43) RAB9AKMT2AALDH1A1CES2CES1
SCHEMBL11830228 0.81 CYP4F2 (0.40) KMT2AALDH1A1CYP4F2CYP4A11LMNA
SCHEMBL11095339 0.79 KMT2A (0.41) KMT2AALDH1A1CYP4F2CYP4A11L3MBTL1
SCHEMBL1946731 0.79 L3MBTL1 (0.41) NPC1RAB9AKMT2AALDH1A1CES2
SCHEMBL12546521 0.79 L3MBTL1 (0.41) NPC1RAB9AKMT2AALDH1A1CES2
SCHEMBL5915071 0.78 NPC1 (0.39) NPC1RAB9AKMT2AALDH1A1CES2
SCHEMBL5915046 0.78 NPC1 (0.39) NPC1RAB9AKMT2AALDH1A1CES2
SCHEMBL6382070 0.78 NPC1 (0.39) NPC1RAB9AKMT2AALDH1A1CES2

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-8034961-B2 Reduction of 4-aryl-4-ketobutanoic acid derivatives utilizing ruthenium containing catalysts LANXESS DEUTSCHLAND GMBH (US) 2011-10-11 US disclosed
US-20080103316-A1 Process for stereoselectively reducing 4-ARYL-4-oxobutanoic acid derivatives BAYER AKTIENGESELLSCHAFT (DE) 2008-05-01 US disclosed
US-7329766-B2 Process for stereoselectively reducing 4-aryl-4-oxobutanoic acid derivatives LANXESS DEUTSCHLAND GMBH (DE) 2008-02-12 US disclosed
US-20050245760-A1 Process for stereoselectively reducing 4-aryl-4-oxobutanoic acid derivatives BAYER AKTIENGESELLSCHAFT (DE) 2005-11-03 US disclosed
US-6921822-B2 Process for stereoselectively reducing 4-aryl-4-oxobutanoic acid derivatives BAYER AKTIENGESELLSCHAFT (DE) 2005-07-26 US disclosed
US-20040030181-A1 Process for stereoselectively reducing 4-aryl-4-oxobutanoic acid derivatives LANXESS DEUTSCHLAND GMBH (DE) 2004-02-12 US disclosed
EP-1369410-A1 Process for the stereoselective reduction of derivatives of 4-aryl-4-oxobutyric acid BAYER AG (DE) 2003-12-10 EP 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 (3 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-20080103316-A1 Process for stereoselectively reducing 4-ARYL-4-oxobutanoic acid derivatives HPD, GRHPR, CYP4B1 NPC1 3145/4885RAB9A 3582/4885KMT2A 692/4885
US-20040030181-A1 Process for stereoselectively reducing 4-aryl-4-oxobutanoic acid derivatives HPD, GRHPR, CYP4B1 NPC1 3145/4885RAB9A 3582/4885KMT2A 692/4885
US-20050245760-A1 Process for stereoselectively reducing 4-aryl-4-oxobutanoic acid derivatives HPD, GRHPR, CYP4B1 NPC1 3145/4885RAB9A 3582/4885KMT2A 692/4885

“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.