SCHEMBL24673209

SCHEMBL24673209

O=P(O)(O)Cc1ccc(CN2CCN([C@H](CO)[C@H](O)CO)CCN([C@H](CO)[C@H](O)CO)CC2)cc1

nearest known ligand 0.41

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
PGK1 P00558 3/20 0.41
PGK2 P07205 3/20 0.41
HDAC1 Q13547 4/20 0.38
HDAC4 P56524 3/20 0.38
KCNH2 Q12809 3/20 0.38
APOBEC3A P31941 1/20 0.38
RECQL P46063 1/20 0.38
APOBEC3G Q9HC16 1/20 0.38
ATM Q13315 2/20 0.37
MEN1 O00255 1/20 0.36
KMT2A Q03164 1/20 0.36
ALDH1A1 P00352 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
CACNA1G O43497 1/20 0.35
HRH3 Q9Y5N1 2/20 0.35
HDAC6 Q9UBN7 2/20 0.35
LMNA P02545 1/20 0.34
HDAC8 Q9BY41 1/20 0.34
KDM4E B2RXH2 1/20 0.34

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
SCHEMBL24672262 0.87 POLB (0.38) HDAC1HDAC4KCNH2APOBEC3ARECQL
SCHEMBL24672263 0.81 LMNA (0.38) HDAC1HDAC4KCNH2APOBEC3ARECQL
SCHEMBL24673327 0.81 POLB (0.53) ATMMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL24673250 0.80 SIGMAR1 (0.56) APOBEC3ARECQLAPOBEC3GATMMEN1
SCHEMBL24672858 0.80 HDAC4 (0.46) HDAC1HDAC4KCNH2APOBEC3ARECQL
SCHEMBL24673197 0.78 KDM4E (0.45) MEN1KMT2AALDH1A1KDM4E
SCHEMBL24673258 0.75 MAPT (0.33) ALDH1A1KDM4E
SCHEMBL24673213 0.75 PGK1 (0.45) PGK1PGK2HDAC1HDAC4KCNH2
SCHEMBL24673260 0.74 APOBEC3A (0.51) APOBEC3ARECQLAPOBEC3GATMMEN1
SCHEMBL24672258 0.73 KDM4E (0.51) HDAC1HDAC4APOBEC3ARECQLAPOBEC3G

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
WO-2022204065-A1 IRON(III) MACROCYCLIC COMPLEXES WITH MIXED HYROXYL PENDANTS AS MRI CONTRAST AGENTS THE RESEARCH FOUNDATION FOR THE STATE UNIVERSITY OF NEW YORK (US) 2022-09-29 WO disclosed