SCHEMBL1228652

SCHEMBL1228652

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

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CPA1 P15085 1/20 0.45
KDM4E B2RXH2 1/20 0.37
LMNA P02545 1/20 0.37
MAPT P10636 1/20 0.37
MGAM O43451 1/20 0.35
GAA P10253 1/20 0.35
SI P14410 1/20 0.35
MGAM2 Q2M2H8 1/20 0.35
ALDH1A1 P00352 3/20 0.33
TRPA1 O75762 1/20 0.33
CYP3A4 P08684 2/20 0.33
ALOX15 P16050 2/20 0.33
TSHR P16473 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
CACNA2D1 P54289 2/20 0.33
CACNB3 P54284 1/20 0.33
CACNA1C Q13936 1/20 0.33
PGR P06401 1/20 0.33
ADRA1A P35348 1/20 0.33
HTR2B P41595 1/20 0.33

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
SCHEMBL2912395 1.00 CPA1 (0.45) CPA1KDM4ELMNAMAPTMGAM
SCHEMBL1410099 1.00 CPA1 (0.45) CPA1KDM4ELMNAMAPTMGAM
SCHEMBL3121387 0.88 KDM4E (0.39) CPA1KDM4ELMNAMAPTMGAM
SCHEMBL29021009 0.87 MAPT (0.37) CPA1KDM4ELMNAMAPTMGAM
SCHEMBL29021054 0.84 KDM4E (0.36) CPA1KDM4ELMNAMAPTMGAM
SCHEMBL3867987 0.84 CPA1 (0.42) CPA1KDM4ELMNAMAPTMGAM
SCHEMBL17748406 0.83 CPA1 (0.47) CPA1LMNAMAPTALDH1A1TSHR
SCHEMBL234997 0.82 MGAM (0.46) LMNAMGAMGAASIMGAM2
SCHEMBL1664773 0.82 MAPT (0.38) CPA1KDM4ELMNAMAPTMGAM
SCHEMBL4302076 0.82 MAPT (0.38) CPA1KDM4ELMNAMAPTMGAM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108997128-B Preparation method of pregabalin intermediate 3-nitromethyl-5-ethyl methylhexanoate 浙江工业大学 2021-02-02 CN claimed
CN-108997128-B Preparation method of pregabalin intermediate 3-nitromethyl-5-ethyl methylhexanoate 浙江工业大学 2021-02-02 CN disclosed
CN-106488906-B β -SUBSTITUTED GAMMA-AMINOCARBOXYLIC ACIDS AND THEIR USE AS ANTHROMATIC AGENTS 斯福瑞有限公司 2018-10-26 CN disclosed
EP-3154930-B1 METHOD FOR THE PREPARATION OF BETA-SUBSTITUTED GAMMA-AMINO CARBOXYLIC ACIDS SIEGFRIED LTD (CH) 2018-04-18 EP disclosed
EP-3210667-A1 MODULAR CONTINUOUS FLOW DEVICE Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2017-08-30 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-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
US-20070197827-A1 Novel asymmetric synthesis of (S)-(+)-3-(aminomethyl)-5-methylhexanoic acid TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-08-23 US disclosed
US-20070191636-A1 Chiral 3-carbamoylmethyl-5-methyl hexanoic acids, key intermediates for the synthesis of (S)-Pregabalin TEVA PHARMACEUTICAL USA, INC. 2007-08-16 US disclosed
US-20070191636-A1 Chiral 3-carbamoylmethyl-5-methyl hexanoic acids, key intermediates for the synthesis of (S)-Pregabalin TEVA PHARMACEUTICAL USA, INC. 2007-08-16 US disclosed
EP-1768950-A2 PROCESS FOR MAKING (S)-PREGABALIN TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-04-04 EP disclosed
EP-1768973-A1 SUBSTITUTED QUINOLONES AiCuris GmbH & Co. KG (DE) 2007-04-04 EP disclosed
WO-2007035890-A1 AN ASYMMETRIC SYNTHESIS OF ( S ) - ( + ) -3- (AMINOMETHYL) -5-METHYLHEXANOIC ACID TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-03-29 WO disclosed
WO-2007035789-A1 CHIRAL 3-CARBAMOYLMETHYL-5-METHYL HEXANOIC ACIDS, KEY INTERMEDIATES FOR THE NEW SYNTHESIS OF (S)-PREGABALIN TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-03-29 WO disclosed
US-20070066846-A1 Process for making (S)-Pregabalin TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-03-22 US disclosed
WO-2006110783-A2 PROCESS FOR MAKING (S)-PREGABALIN TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2006-10-19 WO disclosed
WO-2006008046-A1 SUBSTITUTED QUINOLONES AICURIS GMBH & CO. KG (DE) 2006-01-26 WO 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-20070197827-A1 Novel asymmetric synthesis of (S)-(+)-3-(aminomethyl)-5-methylhexanoic acid RIMKLA, COASY, GABRE CPA1 3694/4885KDM4E 1334/4885LMNA 4205/4885
US-20170114003-A1 METHOD FOR THE PREPARATION OF BETA-SUBSTITUTED GAMMA-AMINO CARBOXYLIC ACIDS GLUL, GABRB2, GABRB1 CPA1 2759/4885KDM4E 2153/4885LMNA 1678/4885
US-20070066846-A1 Process for making (S)-Pregabalin GABRE, GABRA6, GABRA5 CPA1 3500/4885KDM4E 1059/4885LMNA 3151/4885
US-20070191636-A1 Chiral 3-carbamoylmethyl-5-methyl hexanoic acids, key intermediates for the synthesis of (S)-Pregabalin GABRE, GABRA5, GABRA6 CPA1 2816/4885KDM4E 434/4885LMNA 4132/4885

“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.