SCHEMBL987970

SCHEMBL987970

COCC(=O)Nc1ccc2c(c1)CCC2

nearest known ligand 0.71

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ATM Q13315 1/20 0.68
SMN1; SMN2 Q16637 4/20 0.64
MAPT P10636 3/20 0.64
ALDH1A1 P00352 3/20 0.64
L3MBTL1 Q9Y468 1/20 0.64
LMNA P02545 3/20 0.61
HTT P42858 1/20 0.61
NPSR1 Q6W5P4 1/20 0.61
POLB P06746 2/20 0.60
RAB9A P51151 5/20 0.59
NPC1 O15118 4/20 0.59
CYP1A2 P05177 1/20 0.59
CYP3A4 P08684 1/20 0.59
CYP2D6 P10635 1/20 0.59
HPGD P15428 1/20 0.59
CYP2C19 P33261 1/20 0.59
MAPK1 P28482 1/20 0.59

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
SCHEMBL14279905 0.81 NPC1 (0.62) SMN1; SMN2MAPTALDH1A1L3MBTL1POLB
SCHEMBL30493983 0.81 ALDH1A1 (0.58) ATMSMN1; SMN2MAPTALDH1A1L3MBTL1
SCHEMBL11657482 0.81 NPC1 (0.66) SMN1; SMN2MAPTALDH1A1HTTPOLB
SCHEMBL13336896 0.81 ITGB3 (0.56) SMN1; SMN2MAPTALDH1A1L3MBTL1HTT
SCHEMBL7937669 0.80 NPC1 (0.64) SMN1; SMN2ALDH1A1LMNAHTTPOLB
SCHEMBL28366098 0.80 NPC1 (0.64) SMN1; SMN2ALDH1A1HTTPOLBRAB9A
SCHEMBL4866115 0.80 NPC1 (0.64) SMN1; SMN2ALDH1A1LMNAHTTPOLB
SCHEMBL29975245 0.80 NPC1 (0.64) SMN1; SMN2ALDH1A1HTTPOLBRAB9A
SCHEMBL22639891 0.79 KDM4E (0.65) ATMSMN1; SMN2MAPTALDH1A1L3MBTL1
SCHEMBL28255419 0.78 LMNA (0.74) ATMSMN1; SMN2MAPTALDH1A1L3MBTL1

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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2213664-B1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG INT LTD (GB) 2014-04-30 EP disclosed
EP-2213664-B1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG INT LTD (GB) 2014-04-30 EP disclosed
US-8552016-B2 Anti-cancer cyclopenta(g)quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2013-10-08 US disclosed
US-8486955-B2 Anti-cancer cyclopenta [g] quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2013-07-16 US disclosed
US-8063056-B2 Anti-cancer cyclopenta [g]quinazonline compounds BTG INTERNATIONAL LIMITED (GB) 2011-11-22 US disclosed
EP-1421069-B1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG INT LTD (GB) 2011-08-10 EP disclosed
EP-2332962-A1 Cyclopenta[g]quinazoline compounds for use in the treatment of inflammatory or allergic conditions BTG International Limited (GB) 2011-06-15 EP disclosed
EP-2311850-A1 Anti-cancer cyclopenta[g]quinazoline compounds BTG International Limited (GB) 2011-04-20 EP disclosed
US-7863284-B2 Anti-cancer cyclopenta[G]quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2011-01-04 US disclosed
US-20100273817-A1 Anti-cancer cyclopenta(g)quinazoline compounds BGT International Limited (GB) 2010-10-28 US disclosed
US-7297701-B2 Anti-cancer cyclopenta [G]quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2007-11-20 US disclosed
US-7250511-B2 Process for the preparation of cyclopenta[g]quinazoline derivatives BTG INTERNATIONAL LIMITED (GB) 2007-07-31 US disclosed
US-7250511-B2 Process for the preparation of cyclopenta[g]quinazoline derivatives BTG INTERNATIONAL LIMITED (GB) 2007-07-31 US disclosed
US-7250511-B2 Process for the preparation of cyclopenta[g]quinazoline derivatives BTG INTERNATIONAL LIMITED (GB) 2007-07-31 US disclosed
US-20040266798-A1 Process for the preparation of cyclopenta[g]quinazoline derivatives BTG INTERNATIONAL LIMITED (GB) 2004-12-30 US disclosed
US-20040242606-A1 Anti-cancer cyclopenta (g)quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2004-12-02 US disclosed
EP-1421105-A1 ANTI-CANCER CYCLOPENTA[G]QUINAZOLINE COMPOUNDS BTG INTERNATIONAL LIMITED (GB) 2004-05-26 EP disclosed
EP-1421069-A1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG International Limited (GB) 2004-05-26 EP disclosed
WO-2003020748-A1 ANTI-CANCER CYCLOPENTA[G]QUINAZOLINE COMPOUNDS BTG INTERNATIONAL LIMITED (GB) 2003-03-13 WO disclosed
WO-2003020706-A1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[g]QUINAZOLINE DERIVATIVES BTG INTERNATIONAL LIMITED (GB) 2003-03-13 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 (3 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-20100273817-A1 Anti-cancer cyclopenta(g)quinazoline compounds H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CNR1, NR0B1 ATM 3007/4885SMN1; SMN2 3828/4885MAPT 4843/4885
US-20040266798-A1 Process for the preparation of cyclopenta[g]quinazoline derivatives COX6A1, MT-ND6, CYP2D6 ATM 3727/4885SMN1; SMN2 4026/4885MAPT 3724/4885
US-20040242606-A1 Anti-cancer cyclopenta (g)quinazoline compounds H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CBR1, NR4A1 ATM 2098/4885SMN1; SMN2 2994/4885MAPT 4820/4885

“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.