SCHEMBL6368987

SCHEMBL6368987

O=C(Nc1cc2c(c(C(=O)O)c1)OCCCO2)c1cc2cc(Cl)ccc2[nH]1

nearest known ligand 0.56

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
NHERF1 O14745 5/20 0.56
MEN1 O00255 1/20 0.52
KMT2A Q03164 1/20 0.52
RXFP1 Q9HBX9 1/20 0.52
PYGL P06737 13/20 0.50
F7 P08709 1/20 0.47
F3 P13726 1/20 0.47
APP P05067 1/20 0.45

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
SCHEMBL6368672 0.90 PYGL (0.51) NHERF1MEN1KMT2ARXFP1PYGL
SCHEMBL6369217 0.86 NHERF1 (0.53) NHERF1MEN1KMT2ARXFP1PYGL
SCHEMBL6373769 0.85 HRH4 (0.58) NHERF1MEN1KMT2ARXFP1PYGL
SCHEMBL6376602 0.82 NHERF1 (0.62) NHERF1MEN1KMT2ARXFP1PYGL
SCHEMBL6369723 0.78 PYGL (0.52) NHERF1MEN1KMT2ARXFP1PYGL
SCHEMBL6369118 0.76 KMT2A (0.47) NHERF1MEN1KMT2ARXFP1PYGL
SCHEMBL5405858 0.75 NHERF1 (0.67) NHERF1MEN1KMT2ARXFP1PYGL
SCHEMBL6772117 0.75 NPC1 (0.71) NHERF1MEN1KMT2ARXFP1PYGL
SCHEMBL6369837 0.74 NHERF1 (0.51) NHERF1MEN1KMT2ARXFP1PYGL
SCHEMBL31058769 0.73 NHERF1 (0.78) NHERF1MEN1KMT2ARXFP1PYGL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050020661-A1 Substituted 1H-indole-2- carboxamides and 6H-thieno(2,3-b)pyrrole-5-carboxamides useful for inhibiting glycogen phosphorylase in a mammal GAMMILL RONALD B (US) 2005-01-27 US claimed
US-6821977-B2 SUBSTITUTED 1H-(INDOLE-2- CARBOXAMIDES AND 6H-THIENO(2,3-B)PYRROLE-5-CARBOXAMIDES USEFUL FOR INHIBITING GLYCOGEN PHOSPHORYLASE IN A MAMMAL PFIZER, INC. 2004-11-23 US claimed
US-20030199553-A1 Antidiabetic agents GAMMILL RONALD B (US) 2003-10-23 US claimed
WO-2003072570-A1 ANTIDIABETIC AGENTS PFIZER PRODUCTS INC. (US) 2003-09-04 WO claimed
EP-1340500-A1 Antidiabetic agents Pfizer Products Inc. (US) 2003-09-03 EP claimed
US-20050020661-A1 Substituted 1H-indole-2- carboxamides and 6H-thieno(2,3-b)pyrrole-5-carboxamides useful for inhibiting glycogen phosphorylase in a mammal GAMMILL RONALD B (US) 2005-01-27 US disclosed
US-6821977-B2 SUBSTITUTED 1H-(INDOLE-2- CARBOXAMIDES AND 6H-THIENO(2,3-B)PYRROLE-5-CARBOXAMIDES USEFUL FOR INHIBITING GLYCOGEN PHOSPHORYLASE IN A MAMMAL PFIZER, INC. 2004-11-23 US disclosed
US-20030199553-A1 Antidiabetic agents GAMMILL RONALD B (US) 2003-10-23 US disclosed
WO-2003072570-A1 ANTIDIABETIC AGENTS PFIZER PRODUCTS INC. (US) 2003-09-04 WO disclosed
EP-1340500-A1 Antidiabetic agents Pfizer Products Inc. (US) 2003-09-03 EP 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-20030199553-A1 Antidiabetic agents GPR119, IRS1, INSR NHERF1 101/4885MEN1 1828/4885KMT2A 4151/4885
US-20050020661-A1 Substituted 1H-indole-2- carboxamides and 6H-thieno(2,3-b)pyrrole-5-carboxamides useful for inhibiting glycogen phosphorylase in a mammal PYGM, PYGL, IRS1 NHERF1 2862/4885MEN1 3460/4885KMT2A 2347/4885

“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.