SCHEMBL6368672

SCHEMBL6368672

COC(=O)c1cc(NC(=O)c2cc3cc(Cl)ccc3[nH]2)cc2c1OCCCO2

nearest known ligand 0.51

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
PYGL P06737 11/20 0.51
KMT2A Q03164 2/20 0.49
MEN1 O00255 1/20 0.49
RXFP1 Q9HBX9 1/20 0.49
NHERF1 O14745 5/20 0.48
POLB P06746 1/20 0.48
KDM4E B2RXH2 2/20 0.47
NPC1 O15118 2/20 0.47
MAPT P10636 2/20 0.47
RAB9A P51151 1/20 0.47

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
SCHEMBL6368987 0.90 NHERF1 (0.56) PYGLKMT2AMEN1RXFP1NHERF1
SCHEMBL6369118 0.86 KMT2A (0.47) PYGLKMT2AMEN1RXFP1NHERF1
SCHEMBL6373769 0.84 HRH4 (0.58) PYGLKMT2AMEN1RXFP1NHERF1
SCHEMBL6369837 0.83 NHERF1 (0.51) PYGLKMT2AMEN1RXFP1NHERF1
SCHEMBL6369723 0.80 PYGL (0.52) PYGLKMT2AMEN1RXFP1NHERF1
SCHEMBL6369217 0.76 NHERF1 (0.53) PYGLKMT2AMEN1RXFP1NHERF1
SCHEMBL6376602 0.74 NHERF1 (0.62) PYGLKMT2AMEN1RXFP1NHERF1
SCHEMBL6369645 0.73 POLB (0.55) PYGLKMT2AMEN1RXFP1NHERF1
SCHEMBL6369643 0.73 POLB (0.55) PYGLKMT2AMEN1RXFP1NHERF1
SCHEMBL6772117 0.73 NPC1 (0.71) PYGLKMT2AMEN1RXFP1NHERF1

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 5 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 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 PYGL 75/4885KMT2A 4151/4885MEN1 1828/4885
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 PYGL 2/4885KMT2A 2347/4885MEN1 3460/4885

“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.