SCHEMBL6368985

SCHEMBL6368985

CN1CCN(C(=O)c2cc(N)cc3c2OCCCO3)CC1

nearest known ligand 0.54

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
HPGD P15428 2/20 0.46
SMN1; SMN2 Q16637 2/20 0.44
KMT2A Q03164 2/20 0.41
LMNA P02545 2/20 0.40
HSP90AA1 P07900 1/20 0.40
TP53 P04637 1/20 0.40
ALOX15 P16050 1/20 0.40
TSHR P16473 1/20 0.40
ALDH1A1 P00352 2/20 0.39
HRH4 Q9H3N8 4/20 0.38
KDM4E B2RXH2 2/20 0.38
RAB9A P51151 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
HCRTR1 O43613 1/20 0.38
HCRTR2 O43614 1/20 0.38
POLB P06746 1/20 0.37
CHEK1 O14757 1/20 0.37

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
SCHEMBL7260293 0.95 L3MBTL1 (0.43) HPGDSMN1; SMN2KMT2ALMNAHSP90AA1
SCHEMBL11269666 0.95 HPGD (0.51) HPGDSMN1; SMN2KMT2ALMNAHSP90AA1
SCHEMBL6368587 0.89 HPGD (0.55) HPGDSMN1; SMN2KMT2AHSP90AA1TSHR
SCHEMBL6368753 0.88 HPGD (0.57) HPGDSMN1; SMN2KMT2ALMNAHSP90AA1
SCHEMBL6369872 0.87 HPGD (0.46) HPGDSMN1; SMN2HSP90AA1TP53ALOX15
SCHEMBL6369845 0.85 HPGD (0.44) HPGDSMN1; SMN2KMT2ATP53ALOX15
SCHEMBL6374559 0.81 L3MBTL1 (0.54) HPGDSMN1; SMN2KMT2AALDH1A1HRH4
SCHEMBL6374998 0.81 HRH4 (0.38) HPGDKMT2ALMNAHSP90AA1TP53
SCHEMBL6368757 0.81 HCRTR1 (0.43) HPGDSMN1; SMN2TSHRKDM4EHCRTR1
SCHEMBL7261988 0.77 L3MBTL1 (0.50) HPGDSMN1; SMN2KMT2AALDH1A1HRH4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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 HPGD 1956/4885SMN1; SMN2 2393/4885KMT2A 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 HPGD 2567/4885SMN1; SMN2 3622/4885KMT2A 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.