Pyrimidine

Pyrimidine

SCHEMBL27818758

Clc1ncnc2nc[nH]c12.c1cncnc1

nearest known ligand 0.47

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PI4KA P42356 2/20 0.47
▸ PI4K2B Q8TCG2 2/20 0.47
▸ PI4K2A Q9BTU6 2/20 0.47
▸ PI4KB Q9UBF8 2/20 0.47
▸ LRRK2 Q5S007 2/20 0.47
▸ LMNA P02545 2/20 0.47
▸ DRD3 P35462 1/20 0.47
▸ XDH P47989 1/20 0.47
▸ G6PD P11413 1/20 0.46
▸ CYP1A2 P05177 2/20 0.43
▸ CYP3A4 P08684 2/20 0.43
▸ PDPK1 O15530 2/20 0.43
▸ TP53 P04637 2/20 0.43
▸ CHEK1 O14757 1/20 0.43
▸ AURKA O14965 1/20 0.43
▸ CHEK2 O96017 1/20 0.43
▸ HSP90AA1 P07900 1/20 0.43
▸ HSP90AB1 P08238 1/20 0.43
▸ PRKACA P17612 1/20 0.43
▸ CCNE1 P24864 1/20 0.43

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
SCHEMBL29559610 0.89 LMNA (0.57) PI4KAPI4K2BPI4K2API4KBLRRK2
SCHEMBL9082 0.89 LMNA (0.57) PI4KAPI4K2BPI4K2API4KBLRRK2
Hydrochloric Acid SCHEMBL11162217 0.87 PI4KA (0.59) PI4KAPI4K2BPI4K2API4KBLRRK2
Water SCHEMBL27775008 0.87 LMNA (0.55) PI4KAPI4K2BPI4K2API4KBLRRK2
SCHEMBL8716028 0.87 LMNA (0.55) PI4KAPI4K2BPI4K2API4KBLRRK2
SCHEMBL30834859 0.87 LMNA (0.55) PI4KAPI4K2BPI4K2API4KBLRRK2
SCHEMBL9798930 0.87 LMNA (0.55) PI4KAPI4K2BPI4K2API4KBLRRK2
Iodomethane SCHEMBL27477608 0.83 LRRK2 (0.52) PI4KAPI4K2BPI4K2API4KBLRRK2
Furan SCHEMBL28132991 0.81 PI4KA (0.46) PI4KAPI4K2BPI4K2API4KBLRRK2
Hypoxanthine SCHEMBL11439075 0.80 ALDH1A1 (0.67) PI4KAPI4K2BPI4K2API4KBLRRK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101848891-A Preparation of synthetic nucleosides by pi-allyl transition metal complex formation UNIV EMORY 2010-09-29 — — CN disclosed
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