SCHEMBL2550259

SCHEMBL2550259

CC(C)Oc1ccc(C(=O)O)cc1[N+](=O)[O-]

nearest known ligand 0.72

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
PDK1 Q15118 1/20 0.72
CASP6 P55212 1/20 0.58
TSHR P16473 3/20 0.58
HCAR3 P49019 8/20 0.57
LMNA P02545 1/20 0.54
TTR P02766 1/20 0.53
XDH P47989 1/20 0.53
EP300 Q09472 1/20 0.53
HIF1A Q16665 1/20 0.53
ALDH1A1 P00352 1/20 0.51
CYP3A4 P08684 1/20 0.51
TDP1 Q9NUW8 1/20 0.51
MAPT P10636 2/20 0.50
MEN1 O00255 1/20 0.50
HPGD P15428 1/20 0.50
KMT2A Q03164 1/20 0.50

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
SCHEMBL31439475 0.88 PDK1 (0.69) PDK1CASP6TSHRHCAR3LMNA
SCHEMBL30658490 0.88 EP300 (0.61) PDK1CASP6TSHRHCAR3LMNA
SCHEMBL8800296 0.88 PDK1 (0.72) PDK1TSHRLMNAXDHALDH1A1
SCHEMBL528040 0.88 EP300 (0.61) PDK1CASP6TSHRHCAR3LMNA
SCHEMBL28748723 0.87 PDK1 (0.75) PDK1TSHRHCAR3LMNAXDH
SCHEMBL6112853 0.87 PDK1 (0.71) PDK1TSHRLMNAALDH1A1CYP3A4
SCHEMBL16956345 0.86 PDK1 (0.70) PDK1TSHRHCAR3LMNAXDH
SCHEMBL28316244 0.86 HCAR3 (0.59) PDK1CASP6TSHRHCAR3LMNA
SCHEMBL6113956 0.85 PDK1 (0.69) PDK1TSHRLMNAXDHALDH1A1
SCHEMBL28317018 0.85 PDK1 (0.69) PDK1TSHRLMNAALDH1A1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110183348-B N- (3-nitro-4-alkoxy benzoyl) amino acid compound, preparation method and application thereof 中国医科大学 2022-06-03 CN disclosed
CN-110183348-A N- (3- nitro -4- alkoxybenzoyl) amino acids, preparation method and its usage 中国医科大学 2019-08-30 CN disclosed
EP-2563783-B1 3-(4-((1H-IMIDAZOL-1-YL)METHYL)PHENYL)-5-ARYL-1,2,4-OXADIAZOLE DERIVATIVES AS SPHINGOSINE-1 PHOSPHATE RECEPTORS MODULATORS ALLERGAN INC (US) 2014-07-23 EP disclosed
US-8440698-B2 3-(4-((1H-imidazol-1-yl)methyl)phenyl)-5-aryl-1,2,4-oxadiazole derivatives as sphingosine-1 phosphate receptors modulators ALLERGAN, INC. (US) 2013-05-14 US disclosed
EP-2563783-A1 3-(4-((1H-IMIDAZOL-1-YL)METHYL)PHENYL)-5-ARYL-1,2,4-OXADIAZOLE DERIVATIVES AS SPHINGOSINE-1 PHOSPHATE RECEPTORS MODULATORS Allergan, Inc. (US) 2013-03-06 EP disclosed
US-20120302606-A1 3-(4-((1H-IMIDAZOL-1-YL)METHYL)PHENYL)-5-ARYL-1,2,4-OXADIAZOLE DERIVATIVES AS SPHINGOSINE-1 PHOSPHATE RECEPTORS MODULATORS ALLERGAN, INC. (US) 2012-11-29 US disclosed
US-8318783-B2 3-(4-((1H-imidazol-1-yl)methyl)phenyl)-5-aryl-1,2,4-oxadiazole derivatives as sphingosine-1 phosphate receptors modulators ALLERGAN, INC. (US) 2012-11-27 US disclosed
WO-2011136927-A1 3-(4-((1H-IMIDAZOL-1-YL)METHYL)PHENYL)-5-ARYL-1,2,4-OXADIAZOLE DERIVATIVES AS SPHINGOSINE-1 PHOSPHATE RECEPTORS MODULATORS ALLERGAN, INC. (US) 2011-11-03 WO disclosed
US-20110263661-A1 3-(4-((1H-IMIDAZOL-1-YL)METHYL)PHENYL)-5-ARYL-1,2,4-OXADIAZOLE DERIVATIVES AS SPHINGOSINE-1 PHOSPHATE RECEPTORS MODULATORS ALLERGAN, INC. (US) 2011-10-27 US disclosed
US-20070043235-A1 Process for preparing 3-nitro-4-alkoxybenzoic acid KABUSHIKI KAISHA UENO SEIYAKU OYO KENKYUJO (JP) 2007-02-22 US disclosed
US-20060223826-A1 Indole derivatives as somatostatin agonists or antagonists TAKEDA PHARMACEUTICAL COMPANY LIMITED INTELLECTUAL PROPERTY DEPARTMENT (JP) 2006-10-05 US disclosed
CN-1809525-A Process for producing 3-nitro-4-alkoxybenzoic acid UENO SEIYAKU OYO KENKYUJO KK (JP) 2006-07-26 CN disclosed
EP-1621528-A1 PROCESS FOR PRODUCING 3-NITRO-4-ALKOXYBENZOIC ACID KABUSHIKI KAISHA UENO SEIYAKU OYO KENKYUJO (JP) 2006-02-01 EP disclosed
EP-1562898-A1 INDOLE DERIVATIVES AS SOMATOSTATIN AGONISTS OR ANTAGONISTS Takeda Pharmaceutical Company Limited (JP) 2005-08-17 EP disclosed
WO-2004046107-A1 INDOLE DERIVATIVES AS SOMATOSTATIN AGONISTS OR ANTAGONISTS TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2004-06-03 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-20060223826-A1 Indole derivatives as somatostatin agonists or antagonists SSTR1, SSTR3, NPY1R PDK1 1879/4885CASP6 2428/4885TSHR 22/4885
US-20110263661-A1 3-(4-((1H-IMIDAZOL-1-YL)METHYL)PHENYL)-5-ARYL-1,2,4-OXADIAZOLE DERIVATIVES AS SPHINGOSINE-1 PHOSPHATE RECEPTORS MODULATORS S1PR3, S1PR1, S1PR4 PDK1 1491/4885CASP6 4576/4885TSHR 239/4885
US-20120302606-A1 3-(4-((1H-IMIDAZOL-1-YL)METHYL)PHENYL)-5-ARYL-1,2,4-OXADIAZOLE DERIVATIVES AS SPHINGOSINE-1 PHOSPHATE RECEPTORS MODULATORS S1PR3, S1PR1, S1PR4 PDK1 1491/4885CASP6 4576/4885TSHR 239/4885
US-20070043235-A1 Process for preparing 3-nitro-4-alkoxybenzoic acid NOS3, NOS1, NOS2 PDK1 2200/4885CASP6 941/4885TSHR 4228/4885

“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.