SCHEMBL18561982

SCHEMBL18561982

CNC(=O)c1ccnc(Cl)c1N

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CASP1 P29466 1/20 0.43
GAA P10253 1/20 0.41
PIK3C3 Q8NEB9 1/20 0.40
PTPN11 Q06124 1/20 0.40
JAK2 O60674 1/20 0.39
NUDT1 P36639 1/20 0.38
LMNA P02545 2/20 0.38
SMN1; SMN2 Q16637 2/20 0.38
ALDH1A1 P00352 1/20 0.38
HPGD P15428 1/20 0.38
ATR Q13535 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
MTOR P42345 5/20 0.37
SLC40A1 Q9NP59 1/20 0.36
GRM5 P41594 1/20 0.35
ADORA3 P0DMS8 1/20 0.35
ADORA2A P29274 1/20 0.35
ADORA2B P29275 1/20 0.35
ADORA1 P30542 1/20 0.35
ALOX5AP P20292 1/20 0.35

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
SCHEMBL24311969 0.83 GAA (0.44) CASP1GAANUDT1LMNASMN1; SMN2
SCHEMBL6180683 0.82 CASP1 (0.45) CASP1GAAPIK3C3PTPN11NUDT1
SCHEMBL5743790 0.81 CASP1 (0.44) CASP1GAAJAK2NUDT1LMNA
SCHEMBL17619241 0.80 LMNA (0.40) GAAJAK2LMNASMN1; SMN2ALDH1A1
SCHEMBL29472130 0.80 LMNA (0.40) GAAJAK2LMNASMN1; SMN2ALDH1A1
SCHEMBL3943083 0.79 ATR (0.54) CASP1GAAALDH1A1HPGDATR
SCHEMBL18754294 0.79 ATR (0.43) CASP1GAAPIK3C3NUDT1LMNA
SCHEMBL3667384 0.78 SMN1; SMN2 (0.55) CASP1LMNASMN1; SMN2ALDH1A1L3MBTL1
SCHEMBL15645010 0.78 KDM4E (0.42) CASP1GAALMNASMN1; SMN2ALDH1A1
SCHEMBL29439594 0.78 SMN1; SMN2 (0.55) CASP1LMNASMN1; SMN2ALDH1A1L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10662204-B2 Substituted quinazoline and pyridopyrimidine derivatives useful as anticancer agents PFIZER INC. (US) 2020-05-26 US disclosed
US-20190233440-A1 Substituted Quinazoline and Pyridopyrimidine Derivatives Useful as Anticancer Agents PFIZER INC. (US) 2019-08-01 US disclosed
US-20170057955-A1 Pyridopyrimidinone Compounds for Modulating the Catalytic Activity of Histone Lysine Demethylases (KDMs) DONG-A ST CO., LTD. (KR) 2017-03-02 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 (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-10662204-B2 Substituted quinazoline and pyridopyrimidine derivatives useful as anticancer agents DPYD, PDXK, TYMP CASP1 882/4885GAA 841/4885PIK3C3 1609/4885
US-20190233440-A1 Substituted Quinazoline and Pyridopyrimidine Derivatives Useful as Anticancer Agents DPYD, TYMP, TOP2A CASP1 1227/4885GAA 763/4885PIK3C3 1147/4885
US-20170057955-A1 Pyridopyrimidinone Compounds for Modulating the Catalytic Activity of Histone Lysine Demethylases (KDMs) KDM1B, KDM1A, KDM3B CASP1 2484/4885GAA 1574/4885PIK3C3 2661/4885

“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.