SCHEMBL1427009

SCHEMBL1427009

CCOC(=O)C(C(=O)OCC)C(CC(C)C)C[N+](=O)[O-]

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CPA1 P15085 2/20 0.50
ALDH1A1 P00352 5/20 0.33
TP53 P04637 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
PPID Q08752 1/20 0.32
NPC1 O15118 1/20 0.31
MAPT P10636 3/20 0.31
LMNA P02545 1/20 0.31
HPGD P15428 1/20 0.31
RAB9A P51151 1/20 0.31
KMT2A Q03164 1/20 0.31
NPSR1 Q6W5P4 1/20 0.31
CRHBP P24387 1/20 0.31
CRHR2 Q13324 1/20 0.31
CA12 O43570 1/20 0.31
CA1 P00915 1/20 0.31
CA2 P00918 1/20 0.31
CA9 Q16790 1/20 0.31
CYP2C19 P33261 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.30

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
SCHEMBL5163506 1.00 CPA1 (0.50) CPA1ALDH1A1TP53SMN1; SMN2PPID
SCHEMBL4311206 0.92 CPA1 (0.54) CPA1ALDH1A1TP53SMN1; SMN2PPID
SCHEMBL18191192 0.92 CPA1 (0.46) CPA1ALDH1A1TP53SMN1; SMN2PPID
SCHEMBL4311209 0.92 CPA1 (0.54) CPA1ALDH1A1TP53SMN1; SMN2PPID
SCHEMBL18191197 0.92 CPA1 (0.46) CPA1ALDH1A1TP53SMN1; SMN2PPID
SCHEMBL6855469 0.87 CPA1 (0.50) CPA1ALDH1A1PPIDNPC1MAPT
SCHEMBL1116701 0.85 CPA1 (0.47) CPA1ALDH1A1SMN1; SMN2LMNACYP2C19
SCHEMBL14042757 0.85 CPA1 (0.47) CPA1ALDH1A1SMN1; SMN2LMNACYP2C19
SCHEMBL20659551 0.84 CPA1 (0.38) CPA1ALDH1A1MAPTLMNAHPGD
SCHEMBL13567330 0.79 CPA1 (0.52) CPA1

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3154930-B1 METHOD FOR THE PREPARATION OF BETA-SUBSTITUTED GAMMA-AMINO CARBOXYLIC ACIDS SIEGFRIED LTD (CH) 2018-04-18 EP disclosed
US-9745249-B2 Method for the preparation of beta-substituted gamma-amino carboxylic acids SIEGFRIED LTD. (CH) 2017-08-29 US disclosed
US-9745249-B2 Method for the preparation of beta-substituted gamma-amino carboxylic acids SIEGFRIED LTD. (CH) 2017-08-29 US disclosed
US-20170114003-A1 METHOD FOR THE PREPARATION OF BETA-SUBSTITUTED GAMMA-AMINO CARBOXYLIC ACIDS SIEGFRIED LTD. (CH) 2017-04-27 US disclosed
US-20170114003-A1 METHOD FOR THE PREPARATION OF BETA-SUBSTITUTED GAMMA-AMINO CARBOXYLIC ACIDS SIEGFRIED LTD. (CH) 2017-04-27 US disclosed
WO-2016173960-A1 OPTIMIZED SYNTHESIS OF PREGABALIN AND 4-AMINOBUTANE ACID USING AN IMPROVED METHOD FOR PRODUCING CONJUGATED NITROALKENES K.H.S. PHARMA HOLDING GMBH (DE) 2016-11-03 WO disclosed
WO-2015189068-A1 METHOD FOR THE PREPARATION OF BETA-SUBSTITUTED GAMMA-AMINO CARBOXYLIC ACIDS SIEGFRIED LTD. (CH) 2015-12-17 WO disclosed
US-8546112-B2 Process for the stereoselective enzymatic hydrolysis of 5-methyl-3-nitromethyl-hexanoic acid ester SANDOZ AG (CH) 2013-10-01 US disclosed
US-8546112-B2 Process for the stereoselective enzymatic hydrolysis of 5-methyl-3-nitromethyl-hexanoic acid ester SANDOZ AG (CH) 2013-10-01 US disclosed
EP-2294207-B1 Process for the stereoselective enzymatic hydrolysis of 5-methyl-3-nitromethyl-hexanoic acid ester SANDOZ AG (CH) 2012-09-26 EP disclosed
US-20120142949-A1 PROCESS FOR PREPARING PREGABALIN HELVETICA INDUSTRIES (P) LIMITED (IN) 2012-06-07 US disclosed
US-20110245508-A1 Processes For Making Pregabalin And Intermediates Therefor THIJS LAMBERTUS 2011-10-06 US disclosed
US-20110165636-A1 PROCESS FOR THE STEREOSELECTIVE ENZYMATIC HYDROLYSIS OF 5-METHYL-3-NITROMETHYL-HEXANOIC ACID ESTER SANDOZ AG (CH) 2011-07-07 US disclosed
US-20110165636-A1 PROCESS FOR THE STEREOSELECTIVE ENZYMATIC HYDROLYSIS OF 5-METHYL-3-NITROMETHYL-HEXANOIC ACID ESTER SANDOZ AG (CH) 2011-07-07 US disclosed
EP-2300416-A1 PROCESSES FOR MAKING PREGABALIN AND INTERMEDIATES THEREFOR Synthon B.V. (NL) 2011-03-30 EP disclosed
CN-1839116-B Asymmetric urea compound and process for producing asymmetric compound by asymmetric conjugate addition reaction with the same as catalyst SUMITOMO CHEMICAL CO 2010-05-26 CN disclosed
US-20090312560-A1 PROCESSES FOR MAKING PREGABALIN AND INTERMEDIATES THEREFOR SYNTHON BV (NL) 2009-12-17 US disclosed
WO-2009149928-A1 PROCESSES FOR MAKING PREGABALIN AND INTERMEDIATES THEREFOR SYNTHON B.V. (NL) 2009-12-17 WO disclosed
WO-2009141362-A2 PROCESS FOR THE STEREOSELECTIVE ENZYMATIC HYDROLYSIS OF 5-METHYL-3-NITROMETHYL-HEXANOIC ACID ESTER SANDOZ AG (CH) 2009-11-26 WO disclosed
CN-1839116-A Asymmetric urea compound and process for producing asymmetric compound by asymmetric conjugate addition reaction with the same as catalyst SUMITOMO CHEMICAL CO (JP) 2006-09-27 CN 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 (4 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-20120142949-A1 PROCESS FOR PREPARING PREGABALIN GRHPR, GABRG2, GABRG1 CPA1 2405/4885ALDH1A1 214/4885TP53 4881/4885
US-20170114003-A1 METHOD FOR THE PREPARATION OF BETA-SUBSTITUTED GAMMA-AMINO CARBOXYLIC ACIDS GLUL, GABRB2, GABRB1 CPA1 2759/4885ALDH1A1 513/4885TP53 4142/4885
US-20110245508-A1 Processes For Making Pregabalin And Intermediates Therefor GABRB2, GABRB1, GABRB3 CPA1 3552/4885ALDH1A1 510/4885TP53 4796/4885
US-20090312560-A1 PROCESSES FOR MAKING PREGABALIN AND INTERMEDIATES THEREFOR GABRB2, GABRB1, GABRB3 CPA1 3552/4885ALDH1A1 510/4885TP53 4796/4885

“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.