SCHEMBL6368353

SCHEMBL6368353

O=C(CC1(CNC(=O)c2ccccc2)CCCCC1)OCc1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.50
GLA P06280 1/20 0.46
KMT2A Q03164 3/20 0.46
MEN1 O00255 2/20 0.46
MAPT P10636 2/20 0.46
SLC6A5 Q9Y345 3/20 0.45
RAB9A P51151 3/20 0.43
SMN1; SMN2 Q16637 3/20 0.43
TP53 P04637 1/20 0.43
HPGD P15428 1/20 0.43
ALDH1A1 P00352 3/20 0.43
MAPK1 P28482 2/20 0.43
L3MBTL1 Q9Y468 2/20 0.43
ADRB2 P07550 1/20 0.43
POLB P06746 1/20 0.43
NPC1 O15118 1/20 0.43
CTSL P07711 1/20 0.42
CTSB P07858 1/20 0.42
CTSS P25774 1/20 0.42
SLC6A2 P23975 1/20 0.42

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
SCHEMBL6101144 0.86 LMNA (0.51) LMNAKMT2AMEN1SLC6A5SMN1; SMN2
SCHEMBL6368371 0.85 ALDH1A1 (0.49) LMNAKMT2AMEN1MAPTRAB9A
SCHEMBL6368219 0.83 CTSS (0.43) ALDH1A1MAPK1L3MBTL1POLBCTSL
SCHEMBL6367586 0.82 LMNA (0.52) LMNAKMT2AMEN1SLC6A5RAB9A
SCHEMBL4580794 0.82 SYK (0.49) KMT2AMEN1MAPTALDH1A1MAPK1
SCHEMBL6367594 0.82 LMNA (0.60) LMNASMN1; SMN2HPGDALDH1A1MAPK1
SCHEMBL19209664 0.81 CTSL (0.43) LMNAKMT2AMEN1MAPTSMN1; SMN2
SCHEMBL6368418 0.81 LMNA (0.50) LMNAKMT2AMEN1RAB9ASMN1; SMN2
SCHEMBL2861616 0.80 LMNA (0.58) LMNARAB9ASMN1; SMN2TP53ALDH1A1
SCHEMBL394093 0.80 ALDH1A1 (0.50) LMNAKMT2ASMN1; SMN2HPGDALDH1A1

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-20050059735-A1 Cyclic amino acid derivatives useful as pharmaceutical agents BRYANS JUSTIN STEPHEN (GB) 2005-03-17 US claimed
US-20030216469-A1 Cyclic amino acid derivatives useful as pharmaceutical agents BRYANS JUSTIN STEPHEN (GB) 2003-11-20 US claimed
EP-1284960-A1 CYCLIC AMINO ACID DERIVATIVES USEFUL AS PHARMACEUTICAL AGENTS WARNER-LAMBERT COMPANY (US) 2003-02-26 EP claimed
WO-2001090052-A1 CYCLIC AMINO ACID DERIVATIVES USEFUL AS PHARMACEUTICAL AGENTS WARNER-LAMBERT COMPANY (US) 2001-11-29 WO claimed
US-20050059735-A1 Cyclic amino acid derivatives useful as pharmaceutical agents BRYANS JUSTIN STEPHEN (GB) 2005-03-17 US disclosed
US-20030216469-A1 Cyclic amino acid derivatives useful as pharmaceutical agents BRYANS JUSTIN STEPHEN (GB) 2003-11-20 US disclosed
EP-1284960-A1 CYCLIC AMINO ACID DERIVATIVES USEFUL AS PHARMACEUTICAL AGENTS WARNER-LAMBERT COMPANY (US) 2003-02-26 EP disclosed
WO-2001090052-A1 CYCLIC AMINO ACID DERIVATIVES USEFUL AS PHARMACEUTICAL AGENTS WARNER-LAMBERT COMPANY (US) 2001-11-29 WO 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-20050059735-A1 Cyclic amino acid derivatives useful as pharmaceutical agents QPCT, ARGLU1, PNISR LMNA 783/4885GLA 3726/4885KMT2A 3098/4885
US-20030216469-A1 Cyclic amino acid derivatives useful as pharmaceutical agents QPCT, ARGLU1, QPCTL LMNA 653/4885GLA 3410/4885KMT2A 3288/4885

“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.