SCHEMBL2343009

SCHEMBL2343009

O=C(NCCO)c1ccc(Cl)c([N+](=O)[O-])c1

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.70
HPGD P15428 2/20 0.70
HSP90AA1 P07900 1/20 0.70
SMN1; SMN2 Q16637 1/20 0.70
MAPT P10636 6/20 0.66
MAPK1 P28482 4/20 0.66
MEN1 O00255 4/20 0.66
KMT2A Q03164 4/20 0.66
HTT P42858 2/20 0.66
POLB P06746 1/20 0.66
VCAM1 P19320 2/20 0.60
PKM P14618 1/20 0.57
KDM4E B2RXH2 1/20 0.56
LMNA P02545 2/20 0.55
GAA P10253 1/20 0.55
CYP1A2 P05177 1/20 0.53
CYP3A4 P08684 1/20 0.53
CYP2D6 P10635 1/20 0.53
CYP2C9 P11712 1/20 0.53
CYP2C19 P33261 1/20 0.53

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
SCHEMBL10541320 0.89 ALDH1A1 (0.70) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT
SCHEMBL7491797 0.87 ALDH1A1 (0.73) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT
SCHEMBL3406144 0.85 ALDH1A1 (0.70) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT
SCHEMBL22382437 0.85 ALDH1A1 (0.70) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT
SCHEMBL4497059 0.84 ALDH1A1 (0.68) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT
SCHEMBL2336351 0.84 ALDH1A1 (0.68) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT
SCHEMBL10390221 0.84 ALDH1A1 (0.65) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT
Dinitrochlorobenzene SCHEMBL27642052 0.83 SMN1; SMN2 (0.61) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT
SCHEMBL1569717 0.83 SMN1; SMN2 (0.82) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT
SCHEMBL5666032 0.82 SMN1; SMN2 (0.65) ALDH1A1HPGDHSP90AA1SMN1; SMN2MAPT

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1465882-B1 HETROCYCLIC MODULATORS OF NUCLEAR RECEPTORS X CEPTOR THERAPEUTICS INC (US) 2011-08-24 EP disclosed
US-7115640-B2 Heterocyclic modulators of nuclear receptors X-CEPTOR THERAPEUTICS, INC. (US) 2006-10-03 US disclosed
EP-1465882-A4 HETROCYCLIC MODULATORS OF NUCLEAR RECEPTORS X CEPTOR THERAPEUTICS INC (US) 2005-04-06 EP disclosed
EP-1465882-A2 HETROCYCLIC MODULATORS OF NUCLEAR RECEPTORS X-Ceptor Therapeutics, Inc. (US) 2004-10-13 EP disclosed
US-20040180942-A1 Heterocyclic modulators of nuclear receptors X-CEPTOR THERAPEUTICS, INC. 2004-09-16 US disclosed
US-6696473-B2 THIAZOLIDINONE DERIVATIVES; MODULATING CHOLESTEROL METABOLISM X-CEPTOR THERAPEUTICS, INC. 2004-02-24 US disclosed
WO-2003060078-A9 HETEROCYCLIC MODULATORS OF NUCLEAR RECEPTORS X CEPTOR THERAPEUTICS INC (US) 2004-02-19 WO disclosed
US-20030212111-A1 Heterocyclic modulators of nuclear receptors AKARNA THERAPEUTICS, LTD. (GB) 2003-11-13 US disclosed
WO-2003060078-A2 HETEROCYCLIC MODULATORS OF NUCLEAR RECEPTORS X-CEPTOR THERAPEUTICS, INC. (US) 2003-07-24 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-20040180942-A1 Heterocyclic modulators of nuclear receptors NR1H2, NR1H3, NR1H4 ALDH1A1 2884/4885HPGD 482/4885HSP90AA1 1586/4885
US-20030212111-A1 Heterocyclic modulators of nuclear receptors NR1H2, NR1H3, NR1H4 ALDH1A1 2884/4885HPGD 482/4885HSP90AA1 1586/4885

“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.