SCHEMBL584148

SCHEMBL584148

CC(=O)c1c(N2CCOCC2)nc2c(-c3cnc4ccccc4c3)cnn2c1N

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AKR1C3 P42330 1/20 0.43
NPSR1 Q6W5P4 1/20 0.43
NPC1 O15118 3/20 0.43
KDM4E B2RXH2 3/20 0.43
RAB9A P51151 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
MAPT P10636 1/20 0.43
HDAC1 Q13547 1/20 0.42
PIK3CA P42336 6/20 0.41
ERAP1 Q9NZ08 1/20 0.41
HSP90AA1 P07900 1/20 0.41
MEN1 O00255 1/20 0.40
ALDH1A1 P00352 1/20 0.40
KMT2A Q03164 1/20 0.40
ATM Q13315 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
LCK P06239 1/20 0.40
KDR P35968 1/20 0.40
HSD17B10 Q99714 1/20 0.40
PIK3CD O00329 1/20 0.40

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
SCHEMBL6893608 0.89 MAP4K4 (0.38) AKR1C3NPC1HDAC1PIK3CAMEN1
SCHEMBL6893430 0.84 NPC1 (0.44) AKR1C3NPC1KDM4ERAB9ASMN1; SMN2
SCHEMBL10234722 0.83 PIK3CA (0.36) AKR1C3PIK3CALCKKDRPIK3CD
SCHEMBL7883140 0.82 SIGMAR1 (0.42) NPSR1NPC1KDM4ERAB9ASMN1; SMN2
SCHEMBL7882692 0.82 PIK3CA (0.34) NPC1PIK3CAHSP90AA1MEN1KMT2A
SCHEMBL585053 0.82 ADORA2A (0.45) NPC1KDM4ERAB9ASMN1; SMN2MAPT
SCHEMBL10234729 0.82 NPC1 (0.42) AKR1C3NPC1KDM4ERAB9ASMN1; SMN2
SCHEMBL584149 0.81 NPC1 (0.43) AKR1C3NPC1KDM4ERAB9ASMN1; SMN2
SCHEMBL6894323 0.81 NPC1 (0.41) AKR1C3NPC1KDM4ERAB9ASMN1; SMN2
SCHEMBL7885236 0.81 PIK3CA (0.36) AKR1C3PIK3CAMTORMAP4K4CSNK1G2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8591943-B2 Pyrazolo[1,5-a]pyrimidine derivatives as mTOR inhibitors MERCK SHARP & DOHME CORP. (US) 2013-11-26 US disclosed
US-20120114739-A1 PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS MERCK SHARP & DOHME LLC 2012-05-10 US disclosed
US-20120114739-A1 PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS MERCK SHARP & DOHME LLC 2012-05-10 US disclosed
US-20120114739-A1 PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS MERCK SHARP & DOHME LLC 2012-05-10 US disclosed
EP-2417138-A1 PYRAZOLO [1, 5-A] PYRIMIDINE DERIVATIVES AS MTOR INHIBITORS Schering Corporation (US) 2012-02-15 EP disclosed
WO-2010118207-A1 PYRAZOLO [1, 5-A] PYRIMIDINE DERIVATIVES AS MTOR INHIBITORS SCHERING CORPORATION (US) 2010-10-14 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 (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-20120114739-A1 PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS MTOR, RICTOR, RPTOR AKR1C3 3323/4885NPSR1 4243/4885NPC1 348/4885

“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.