SCHEMBL6079007

SCHEMBL6079007

O=[N+]([O-])c1cc([N+](=O)[O-])c2oc3c(cc([N+](=O)[O-])c4cc([N+](=O)[O-])[nH]c43)c2c1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.39
MEN1 O00255 6/20 0.39
KMT2A Q03164 6/20 0.39
MAPT P10636 6/20 0.39
RAB9A P51151 3/20 0.39
CYP1A2 P05177 2/20 0.39
CYP2C9 P11712 2/20 0.39
NPC1 O15118 2/20 0.39
NPSR1 Q6W5P4 2/20 0.39
LMNA P02545 1/20 0.39
HSP90AA1 P07900 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.39
TDP1 Q9NUW8 4/20 0.37
TSHR P16473 1/20 0.37
POLB P06746 1/20 0.34
GPR35 Q9HC97 4/20 0.33
KDM4E B2RXH2 3/20 0.33
HPGD P15428 2/20 0.33
ALOX15 P16050 2/20 0.33
ALOX12 P18054 2/20 0.33

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
SCHEMBL30424337 0.73 ALDH1A1 (0.49) ALDH1A1MEN1KMT2AMAPTRAB9A
SCHEMBL77405 0.73 ALDH1A1 (0.49) ALDH1A1MEN1KMT2AMAPTRAB9A
SCHEMBL29475172 0.67 ALDH1A1 (0.61) ALDH1A1MEN1KMT2AMAPTRAB9A
SCHEMBL56979 0.67 ALDH1A1 (0.61) ALDH1A1MEN1KMT2AMAPTRAB9A
SCHEMBL2338077 0.67 MEN1 (0.58) ALDH1A1MEN1KMT2AMAPTRAB9A
SCHEMBL11760932 0.64 ALDH1A1 (0.54) ALDH1A1MEN1KMT2AMAPTRAB9A
SCHEMBL1415118 0.64 HKDC1 (0.50) ALDH1A1MEN1KMT2AMAPTRAB9A
SCHEMBL11661116 0.62 ALDH1A1 (0.51) ALDH1A1MEN1KMT2AMAPTRAB9A
SCHEMBL9182503 0.61 CYP19A1 (0.56) ALDH1A1MEN1KMT2AMAPTRAB9A
SCHEMBL1951372 0.60 MAPT (0.56) ALDH1A1MEN1KMT2AMAPTRAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7015334-B2 A reactant/solvent dimethyl formamide is made slightly basic, heating the solution to reduce the water content, then cooling, adding the hexanitrostilbene, heating to a predetermined temperature, cooling and filtering to accumulate 2,4,7,9-tetranitro-10H-benzo[4,5]furo[3,2]indole product BWXT PANTEX, LLC (US) 2006-03-21 US claimed
US-20060025603-A1 A reactant/solvent dimethyl formamide is made slightly basic, heating the solution to reduce the water content, then cooling, adding the hexanitrostilbene, heating to a predetermined temperature, cooling and filtering to accumulate 2,4,7,9-tetranitro-10H-benzo[4,5]furo[3,2]indole product U.S. DEPARTMENT OF ENERGY 2006-02-02 US claimed