SCHEMBL11894467

SCHEMBL11894467

O=[N+]([O-])c1ccccc1C1=C2C=CC(=N2)C=C2C=CC(=N2)C(c2ccccc2[N+](=O)[O-])=C2C=CC(=N2)C=C2C=CC1=N2

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 3/20 0.39
▸ TDP1 Q9NUW8 1/20 0.39
▸ PTPN1 P18031 1/20 0.36
▸ MAOB P27338 1/20 0.36
▸ S100A4 P26447 2/20 0.35
▸ PTPRC P08575 1/20 0.35
▸ MGAM O43451 1/20 0.35
▸ GAA P10253 1/20 0.35
▸ SI P14410 1/20 0.35
▸ MGAM2 Q2M2H8 1/20 0.35
▸ L3MBTL1 Q9Y468 1/20 0.35
▸ SOS1 Q07889 1/20 0.33
▸ GSK3B P49841 1/20 0.32
▸ HSD11B1 P28845 1/20 0.32
▸ MEN1 O00255 2/20 0.32
▸ KMT2A Q03164 2/20 0.32
▸ GUSB P08236 1/20 0.32
▸ F2 P00734 1/20 0.32
▸ C1R P00736 1/20 0.32
▸ MAPT P10636 1/20 0.32

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
SCHEMBL2536323 0.85 ALDH1A1 (0.49) ALDH1A1TDP1PTPN1MAOBS100A4
SCHEMBL28548550 0.80 ALDH1A1 (0.56) ALDH1A1TDP1PTPN1MAOBS100A4
SCHEMBL28277294 0.79 — —
SCHEMBL28665179 0.78 MAPK1 (0.37) ALDH1A1L3MBTL1MEN1KMT2AMAPT
SCHEMBL6033614 0.78 PTPN1 (0.43) ALDH1A1TDP1PTPN1MAOBS100A4
SCHEMBL8689824 0.77 NPC1 (0.31) RAB9ASMN1; SMN2
SCHEMBL27122607 0.77 ALDH1A1 (0.34) ALDH1A1L3MBTL1
SCHEMBL28898189 0.77 ALDH1A1 (0.36) ALDH1A1TDP1PTPN1MAOBS100A4
Hydrochloric Acid SCHEMBL28455293 0.76 ALDH1A1 (0.35) ALDH1A1TDP1PTPN1MAOBS100A4
SCHEMBL28554886 0.74 MAPK1 (0.34) ALDH1A1GAAL3MBTL1MEN1KMT2A

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-8431117-B2 Sickled erythrocytes with anti-tumor agents induce tumor vaso-occlusion and tumoricidal effects TERMAN DAVID S (US) 2013-04-30 — — US disclosed
US-20120195869-A1 Sickled Erythrocytes with Anti-tumor Agents Induce Tumor Vaso-occlusion and Tumoricidal Effects TERMAN DAVID S (US) 2012-08-02 — — US disclosed
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