SCHEMBL4457331

SCHEMBL4457331

COc1cccc(-c2cnc(N)nc2N)c1

nearest known ligand 0.72

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ADORA2A P29274 1/20 0.72
ADORA1 P30542 1/20 0.72
DHFR P00374 6/20 0.61
FGFR1 P11362 2/20 0.56
TDO2 P48775 1/20 0.55
CLK1 P49759 4/20 0.55
CDK5 Q00535 2/20 0.55
CDK5R1 Q15078 2/20 0.55
PIK3CG P48736 1/20 0.53
PDGFRB P09619 1/20 0.52
SRC P12931 1/20 0.52
PDGFRA P16234 1/20 0.52
FYN P06241 1/20 0.51

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
SCHEMBL30488034 1.00 ADORA2A (0.72) ADORA2AADORA1DHFRFGFR1TDO2
SCHEMBL8132445 0.88 FGFR1 (0.76) ADORA2AADORA1FGFR1TDO2CLK1
SCHEMBL1388414 0.84 FGFR1 (0.75) ADORA2AADORA1DHFRFGFR1
SCHEMBL29655604 0.81 DHFR (0.59) ADORA2AADORA1DHFR
SCHEMBL1389085 0.81 DHFR (0.59) ADORA2AADORA1DHFR
SCHEMBL30488020 0.81 KMT2A (0.73) DHFRFGFR1
SCHEMBL264291 0.81 KMT2A (0.73) DHFRFGFR1
Hydrochloric Acid SCHEMBL6833029 0.80 DHFR (0.56) ADORA2AADORA1DHFR
SCHEMBL1388276 0.80 ADORA1 (0.70) ADORA2AADORA1DHFRFGFR1CDK5
SCHEMBL30488016 0.80 ADORA1 (0.70) ADORA2AADORA1DHFRFGFR1CDK5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111793035-B N4- (3-methoxyphenyl) -pyrimidinediamine targeted DDR1 inhibitor and preparation and application thereof 温州医科大学 2021-06-18 CN claimed
CN-111793035-A N4- (3-methoxyphenyl) -pyrimidinediamine targeted DDR1 inhibitor and preparation and application thereof 温州医科大学 2020-10-20 CN claimed
WO-2009017838-A2 COMBINATIONS OF JAK-2 INHIBITORS AND OTHER AGENTS EXELIXIS, INC. (US) 2009-02-05 WO claimed
CN-111793035-B N4- (3-methoxyphenyl) -pyrimidinediamine targeted DDR1 inhibitor and preparation and application thereof 温州医科大学 2021-06-18 CN disclosed
CN-111793035-B N4- (3-methoxyphenyl) -pyrimidinediamine targeted DDR1 inhibitor and preparation and application thereof 温州医科大学 2021-06-18 CN disclosed
CN-111793035-A N4- (3-methoxyphenyl) -pyrimidinediamine targeted DDR1 inhibitor and preparation and application thereof 温州医科大学 2020-10-20 CN disclosed
CN-111793035-A N4- (3-methoxyphenyl) -pyrimidinediamine targeted DDR1 inhibitor and preparation and application thereof 温州医科大学 2020-10-20 CN disclosed
CN-110325516-A HETEROARYL COMPOUNDS AND THEIR USE 米尼奥尔克斯治疗有限公司 2019-10-11 CN disclosed
CN-104844526-B A kind of 4,6- pyrimidinediamines class compound and its preparation method and application 温州医科大学 2018-08-31 CN disclosed
EP-0674627-A1 PYRIMIDINE, PYRIDINE, PTERIDINONE AND INDAZOLE DERIVATIVES AS ENZYME INHIBITORS THE WELLCOME FOUNDATION LIMITED (GB) 1995-10-04 EP disclosed