SCHEMBL1381928

SCHEMBL1381928

Cc1c(C(=O)Nc2ccc(S(C)(=O)=O)cc2)cn(CCCN(C)C)c1-c1ccccc1Oc1ccccc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NR3C2 P08235 2/20 0.55
PTGS2 P35354 1/20 0.41
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
LTA4H P09960 1/20 0.39
GAA P10253 2/20 0.38
ALDH1A1 P00352 1/20 0.38
POLB P06746 1/20 0.38
CRHBP P24387 1/20 0.38
FNTA P49354 1/20 0.38
FNTB P49356 1/20 0.38
CRHR2 Q13324 1/20 0.38
CACNA1B Q00975 4/20 0.38
CACNA1H O95180 2/20 0.38
MCHR1 Q99705 1/20 0.38
TOP2B Q02880 1/20 0.38
AVPR2 P30518 1/20 0.37
HTT P42858 1/20 0.36
BRD4 O60885 1/20 0.36
CNR1 P21554 1/20 0.36

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
SCHEMBL1381366 0.89 NR3C2 (0.69) NR3C2PTGS2MEN1KMT2AGAA
SCHEMBL1382588 0.89 NR3C2 (0.55) NR3C2PTGS2MEN1KMT2AGAA
SCHEMBL1381640 0.87 NR3C2 (0.61) NR3C2ALDH1A1TOP2BAVPR2
SCHEMBL1382032 0.85 NR3C2 (0.59) NR3C2MEN1KMT2AGAAALDH1A1
SCHEMBL1381755 0.85 NR3C2 (0.55) NR3C2PTGS2MEN1KMT2AGAA
SCHEMBL1381372 0.85 NR3C2 (0.53) NR3C2PTGS2MEN1KMT2AGAA
SCHEMBL1381035 0.85 NR3C2 (0.55) NR3C2PTGS2MEN1KMT2AGAA
SCHEMBL1383546 0.84 NR3C2 (0.56) NR3C2PTGS2KMT2AALDH1A1MCHR1
SCHEMBL2438460 0.83 NR3C2 (0.50) NR3C2LTA4HGAABRD4
SCHEMBL4638426 0.82 CACNA1H (0.40) LTA4HALDH1A1CACNA1BCACNA1HBRD4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8026237-B2 For modulating activity of one or more steroid nuclear receptors and for treatment, prevention, or amelioration of symptoms of disease or disorder related to the activity of receptors; 5-benzo[b]thiophen-2-yl-1,4-dimethyl-1H-pyrrole-3-carboxylic acid (4-methanesulfonyl-phenyl)-amide EXELIXIS, INC. (US) 2011-09-27 US claimed
JP-4703649-B2 2011-06-15 JP claimed
US-8026237-B2 For modulating activity of one or more steroid nuclear receptors and for treatment, prevention, or amelioration of symptoms of disease or disorder related to the activity of receptors; 5-benzo[b]thiophen-2-yl-1,4-dimethyl-1H-pyrrole-3-carboxylic acid (4-methanesulfonyl-phenyl)-amide EXELIXIS, INC. (US) 2011-09-27 US disclosed
US-8026237-B2 For modulating activity of one or more steroid nuclear receptors and for treatment, prevention, or amelioration of symptoms of disease or disorder related to the activity of receptors; 5-benzo[b]thiophen-2-yl-1,4-dimethyl-1H-pyrrole-3-carboxylic acid (4-methanesulfonyl-phenyl)-amide EXELIXIS, INC. (US) 2011-09-27 US disclosed
US-8026237-B2 For modulating activity of one or more steroid nuclear receptors and for treatment, prevention, or amelioration of symptoms of disease or disorder related to the activity of receptors; 5-benzo[b]thiophen-2-yl-1,4-dimethyl-1H-pyrrole-3-carboxylic acid (4-methanesulfonyl-phenyl)-amide EXELIXIS, INC. (US) 2011-09-27 US disclosed
US-20080234270-A1 Pyrrole Derivatives As Pharmaceutical Agents EXELIXIS, INC. (US) 2008-09-25 US disclosed
US-20080234270-A1 Pyrrole Derivatives As Pharmaceutical Agents EXELIXIS, INC. (US) 2008-09-25 US disclosed
US-20080234270-A1 Pyrrole Derivatives As Pharmaceutical Agents EXELIXIS, INC. (US) 2008-09-25 US 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 (1 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-20080234270-A1 Pyrrole Derivatives As Pharmaceutical Agents PRLHR, PTGDR, TACR1 NR3C2 119/4885PTGS2 275/4885MEN1 4434/4885

“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.