SCHEMBL4314801

SCHEMBL4314801

CCCC(OCc1ccccc1)N1CCC1=O

nearest known ligand 0.43

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.43
MEN1 O00255 4/20 0.43
KMT2A Q03164 4/20 0.43
ALDH1A1 P00352 3/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
SLC6A2 P23975 1/20 0.39
CACNA2D1 P54289 1/20 0.39
APOBEC3A P31941 1/20 0.39
RECQL P46063 1/20 0.39
APOBEC3G Q9HC16 1/20 0.39
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
SCHEMBL131141 0.92 POLB (0.42) POLBMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL6135690 0.72 CYP3A4 (0.43) POLBMEN1KMT2AALDH1A1SLC6A2
SCHEMBL7229504 0.71 DPP4 (0.39) SLC6A2
SCHEMBL7049996 0.71 CTSL (0.41) MEN1KMT2AALDH1A1
SCHEMBL11010892 0.70 CYP3A4 (0.46) POLBMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL4314794 0.69 PKM (0.44) POLBMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL4317705 0.69 PKM (0.44) POLBMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL6098576 0.69 SLC1A3 (0.42) POLBMEN1KMT2AALDH1A1L3MBTL1
SCHEMBL7407155 0.69 APOBEC3A (0.46) POLBMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL13672306 0.68 TSHR (0.44) POLBMEN1KMT2AALDH1A1SLC6A2

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-20090131707-A1 CHEMICAL PROCESS FOR THE PREPARATION OF INTERMEDIATES TO OBTAIN N-FORMYL HYDROXYLAMINE COMPOUNDS NOVARTIS AG (CH) 2009-05-21 US disclosed
US-7452999-B2 Chemical process for the preparation of intermediates to obtain N-formyl hydroxy-lamine compounds NOVARTIS AG (CH) 2008-11-18 US disclosed
CN-101092342-A Chemical process for the preparation of intermediates to obtain n-formyl hydroxy-lamine compounds NOVARTIS AG (CH) 2007-12-26 CN disclosed
US-20070179298-A1 Chemical process for the preparation of intermediates to obtain n-formyl hydroxy-lamine compounds NOVARTIS AG (CH) 2007-08-02 US disclosed
CN-1759097-A Chemical process for preparing intermediates for obtaining N-formyl hydroxylamines NOVARTIS AG (CH) 2006-04-12 CN disclosed
EP-1599440-A2 CHEMICAL PROCESS FOR THE PREPARATION OF INTERMEDIATES TO OBTAIN N-FORMYL HYDROXYLAMINE COMPOUNDS Novartis AG (CH) 2005-11-30 EP disclosed
WO-2004076053-A2 CHEMICAL PROCESS FOR THE PREPARATION OF INTERMEDIATES TO OBTAIN N-FORMYL HYDROXYLAMINE COMPOUNDS NOVARTIS AG (CH) 2004-09-10 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 (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-20090131707-A1 CHEMICAL PROCESS FOR THE PREPARATION OF INTERMEDIATES TO OBTAIN N-FORMYL HYDROXYLAMINE COMPOUNDS HAO2, HAO1, HAAO POLB 287/4885MEN1 3891/4885KMT2A 3306/4885
US-20070179298-A1 Chemical process for the preparation of intermediates to obtain n-formyl hydroxy-lamine compounds HAO1, LMNA, HAO2 POLB 150/4885MEN1 3412/4885KMT2A 3919/4885

“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.