SCHEMBL31317570

SCHEMBL31317570

O=C(c1ccccc1)c1nc2cc(Cl)ccc2c(=O)[nH]1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TOP2A P11388 1/20 0.56
▸ TOP2B Q02880 1/20 0.56
▸ BRD4 O60885 1/20 0.56
▸ HPGD P15428 2/20 0.56
▸ MEN1 O00255 2/20 0.56
▸ KMT2A Q03164 2/20 0.56
▸ KDM4E B2RXH2 2/20 0.56
▸ MAPT P10636 1/20 0.56
▸ HTT P42858 1/20 0.56
▸ TUBB4A P04350 1/20 0.54
▸ TUBB P07437 1/20 0.54
▸ TUBA3C P0DPH7 1/20 0.54
▸ TUBA1B P68363 1/20 0.54
▸ TUBA4A P68366 1/20 0.54
▸ TUBB4B P68371 1/20 0.54
▸ TUBB3 Q13509 1/20 0.54
▸ TUBB2A Q13885 1/20 0.54
▸ TUBB8 Q3ZCM7 1/20 0.54
▸ TUBA3E Q6PEY2 1/20 0.54
▸ TUBA1A Q71U36 1/20 0.54

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
SCHEMBL31317497 0.90 TOP2A (0.54) TOP2ATOP2BBRD4HPGDMEN1
SCHEMBL13343606 0.84 KDM4E (0.59) HPGDMEN1KMT2AKDM4EMAPT
SCHEMBL27334538 0.84 BRD4 (0.74) TOP2ATOP2BBRD4HPGDMEN1
SCHEMBL28738679 0.77 TOP2A (0.54) TOP2ATOP2BBRD4HPGDMEN1
SCHEMBL31317513 0.77 TOP2A (0.54) TOP2ATOP2BBRD4HPGDMEN1
SCHEMBL400070 0.74 TNKS (0.73) HPGDMEN1KMT2AKDM4EMAPT
SCHEMBL29764046 0.74 TNKS (0.73) HPGDMEN1KMT2AKDM4EMAPT
SCHEMBL31317501 0.74 TOP2A (0.72) TOP2ATOP2BBRD4HPGDMEN1
SCHEMBL13343598 0.74 KDM4E (0.57) HPGDMEN1KMT2AKDM4EMAPT
SCHEMBL31317586 0.74 BRD4 (0.75) TOP2ATOP2BBRD4MEN1KMT2A

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-119462527-A Visible light promotion I2Catalytic C (sp)3) Method for synthesizing 2-benzoyl quinazoline-4 (3H) -ketone by virtue of amination reaction of (E) -H 桂林理工大学 2025-02-18 — — CN disclosed
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