SCHEMBL6705382

SCHEMBL6705382

CC(C)(C)[Si](C)(C)OCCCOc1ccc(C(O)(c2ccccc2)c2ccc(OCCCO[Si](C)(C)C(C)(C)C)cc2)cc1

nearest known ligand 0.44

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.44
KDM4E B2RXH2 9/20 0.44
ALDH1A1 P00352 6/20 0.44
MEN1 O00255 6/20 0.44
KMT2A Q03164 6/20 0.44
HTT P42858 1/20 0.44
POLB P06746 2/20 0.42
LMNA P02545 2/20 0.41
TDP1 Q9NUW8 1/20 0.41
ACSS2 Q9NR19 2/20 0.41
GAA P10253 2/20 0.39
MITF O75030 1/20 0.39
PPARA Q07869 1/20 0.39

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
SCHEMBL13681654 0.95 AHR (0.42) SMN1; SMN2KDM4EALDH1A1MEN1KMT2A
SCHEMBL13681661 0.82 DRD2 (0.42) SMN1; SMN2KDM4EALDH1A1MEN1KMT2A
SCHEMBL25369942 0.79 LTA4H (0.50) LMNA
SCHEMBL5854524 0.77 PLA2G4B (0.57) ALDH1A1HTTPOLBTDP1
SCHEMBL1629693 0.77 HRH3 (0.43) SMN1; SMN2KDM4EALDH1A1MEN1KMT2A
SCHEMBL20204806 0.76 MAPT (0.47) KDM4EALDH1A1MEN1KMT2ATDP1
SCHEMBL578484 0.76 KDM4E (0.53) KDM4EALDH1A1TDP1
SCHEMBL20568979 0.76 APP (0.41) SMN1; SMN2KDM4EALDH1A1
SCHEMBL17589883 0.76 PPARA (0.60) KDM4EALDH1A1LMNAGAAPPARA
SCHEMBL17589885 0.76 PPARA (0.44) HTTPOLBTDP1GAAPPARA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040116685-A1 Method for solution phase synthesis of oligonucleotides PROLIGO LLC 2004-06-17 US disclosed
US-6262251-B1 PRODUCT ANCHORED SEQUENCIAL SYNTHESIS (PASS); AN ANCHOR GROUP ATTACHED TO THE 5' END OF THE GROWING OLIGONUCLEOTIDE PRODUCT ALLOWS THE COUPLED PRODUCT TO BE SEPARATED FROM UNREACTED STARTING MATERIALS PROLIGO LLC 2001-07-17 US disclosed
EP-0979233-A4 METHOD FOR SOLUTION PHASE SYNTHESIS OF OLIGONUCLEOTIDES PROLIGO L L C (US) 2001-03-21 EP disclosed
EP-0979233-A1 METHOD FOR SOLUTION PHASE SYNTHESIS OF OLIGONUCLEOTIDES NeXstar Pharmaceuticals, Inc. (US) 2000-02-16 EP disclosed
US-6001966-A REACTING N-TERMINAL PROTECTED AMINO ACID WITH PEPTIDE STARTING MATERIAL FORMING A PEPTIDE PRODUCT, PARTITIONING FROM UNREACTED MATERIAL AND REAGENTS BASED ON PRESENCE OF N-TERMINAL BLOCKING/ANCHORING GROUP PROLIGO LLC (US) 1999-12-14 US disclosed
US-5874532-A USING A N-TERMINAL PROTECTED AMINO ACID MONOMER NEXSTAR PHARMACEUTICALS, INC. (US) 1999-02-23 US disclosed
WO-1998047910-A1 METHOD FOR SOLUTION PHASE SYNTHESIS OF OLIGONUCLEOTIDES PROLIGO LLC (US) 1998-10-29 WO disclosed