SCHEMBL6368673

SCHEMBL6368673

CCOC(=O)CN1CCCOc2ccc(N)cc21

nearest known ligand 0.44

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
HTT P42858 3/20 0.44
USP2 O75604 1/20 0.44
MAPT P10636 4/20 0.41
ALDH1A1 P00352 4/20 0.40
NPC1 O15118 1/20 0.40
TP53 P04637 1/20 0.40
GLA P06280 1/20 0.40
RAB9A P51151 1/20 0.40
TSHR P16473 1/20 0.38
KMT2A Q03164 4/20 0.38
POLB P06746 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
CNR2 P34972 1/20 0.38
TNF P01375 2/20 0.37
MEN1 O00255 2/20 0.37
LMNA P02545 2/20 0.36
THRB P10828 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
SCHEMBL6368485 0.82 SMN1; SMN2 (0.43) HTTUSP2MAPTALDH1A1NPC1
SCHEMBL2062027 0.82 MAPT (0.49) HTTMAPTALDH1A1KMT2APOLB
SCHEMBL2061505 0.80 GAA (0.39) MAPTALDH1A1KMT2ASMN1; SMN2MEN1
SCHEMBL6376509 0.80 KMT2A (0.60) MAPTTSHRKMT2APOLBSMN1; SMN2
SCHEMBL6373833 0.79 KMT2A (0.58) MAPTTSHRKMT2APOLBSMN1; SMN2
SCHEMBL6369714 0.78 KMT2A (0.49) MAPTALDH1A1TSHRKMT2APOLB
SCHEMBL6376953 0.78 KMT2A (0.51) MAPTALDH1A1TP53TSHRKMT2A
SCHEMBL25804434 0.77 CHRM2 (0.50) HTTMAPTALDH1A1TP53KMT2A
SCHEMBL6369066 0.76 KMT2A (0.46) MAPTALDH1A1NPC1RAB9ATSHR
SCHEMBL6369111 0.76 TSHR (0.46) MAPTALDH1A1NPC1RAB9ATSHR

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 HTT 1710/4885USP2 4806/4885MAPT 2550/4885
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 HTT 2257/4885USP2 3598/4885MAPT 1817/4885

“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.