SCHEMBL3336558

SCHEMBL3336558

COCCOc1nc(N)nc2ccc(-c3cccc(C#N)c3)cc12

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADORA2A P29274 2/20 0.50
MAP4K4 O95819 1/20 0.50
ADORA1 P30542 1/20 0.46
CYP1A2 P05177 10/20 0.45
CYP3A4 P08684 9/20 0.45
ALDH1A1 P00352 8/20 0.45
CLK4 Q9HAZ1 6/20 0.45
SQOR Q9Y6N5 1/20 0.43
HSD17B10 Q99714 7/20 0.43
CYP2C9 P11712 5/20 0.43
USP2 O75604 3/20 0.43
HIF1A Q16665 3/20 0.43
LMNA P02545 3/20 0.43
TSHR P16473 3/20 0.43
MAPK1 P28482 3/20 0.43
CYP2D6 P10635 3/20 0.43
TP53 P04637 2/20 0.43
RECQL P46063 1/20 0.43
CYP2C19 P33261 2/20 0.43
MEN1 O00255 1/20 0.41

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
SCHEMBL3337685 0.88 ADORA2A (0.53) ADORA2AMAP4K4ADORA1CYP1A2CYP3A4
SCHEMBL3337841 0.81 DHFR (0.44) ADORA2AMAP4K4CYP1A2CYP3A4ALDH1A1
SCHEMBL3341682 0.81 ADORA2A (0.53) ADORA2AMAP4K4ADORA1CYP1A2CYP3A4
SCHEMBL3336480 0.81 TRIM58 (0.48) ADORA2AMAP4K4ADORA1CYP1A2CYP3A4
SCHEMBL3333821 0.80 HSP90AB1 (0.47) ADORA2AMAP4K4ADORA1CYP1A2CYP3A4
SCHEMBL3336135 0.79 SQOR (0.46) ADORA2AMAP4K4SQORTSHR
SCHEMBL3340872 0.79 PIK3CA (0.40) ADORA2AMAP4K4TSHR
SCHEMBL3337376 0.78 DHFR (0.46) ADORA1HSD17B10RECQLKDM4E
SCHEMBL3335310 0.78 PIK3CA (0.39) ADORA2AMAP4K4CYP1A2CYP3A4SQOR
SCHEMBL3335044 0.76 PIM1 (0.44) AKT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100143299-A1 4,6-DI- AND 2,4,6-TRISUBSTITUTED QUINAZOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS USEFUL FOR TREATING VIRAL INFECTIONS GILEAD SCIENCES, INC. (US) 2010-06-10 US claimed
WO-2008009077-A2 4,6-DL- AND 2,4,6-TRISUBSTITUTED QUINAZOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS USEFUL FOR TREATING VIRAL INFECTIONS GILEAD SCIENCES, INC. (US) 2008-01-24 WO claimed
US-8673929-B2 4,6-di- and 2,4,6-trisubstituted quinazoline derivatives and pharmaceutical compositions useful for treating viral infections GILEAD SCIENCES, INC. (US) 2014-03-18 US disclosed
US-20100143299-A1 4,6-DI- AND 2,4,6-TRISUBSTITUTED QUINAZOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS USEFUL FOR TREATING VIRAL INFECTIONS GILEAD SCIENCES, INC. (US) 2010-06-10 US 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 (1 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-20100143299-A1 4,6-DI- AND 2,4,6-TRISUBSTITUTED QUINAZOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS USEFUL FOR TREATING VIRAL INFECTIONS OPRD1, IFNAR1, NR4A1 ADORA2A 1968/4885MAP4K4 2433/4885ADORA1 870/4885

“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.