SCHEMBL28849432

SCHEMBL28849432

O=C(CCCC/C=C\c1ccncc1)c1ccccc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TBXAS1 P24557 3/20 0.53
▸ HDAC1 Q13547 7/20 0.53
▸ HDAC8 Q9BY41 7/20 0.53
▸ HDAC3 O15379 2/20 0.53
▸ HDAC4 P56524 2/20 0.53
▸ HDAC7 Q8WUI4 2/20 0.53
▸ HDAC2 Q92769 2/20 0.53
▸ HDAC10 Q969S8 2/20 0.53
▸ HDAC11 Q96DB2 2/20 0.53
▸ HDAC6 Q9UBN7 2/20 0.53
▸ HDAC9 Q9UKV0 2/20 0.53
▸ HDAC5 Q9UQL6 2/20 0.53
▸ L3MBTL1 Q9Y468 3/20 0.53
▸ TDP1 Q9NUW8 2/20 0.53
▸ LMNA P02545 1/20 0.53
▸ MAPT P10636 1/20 0.53
▸ CYP1A2 P05177 2/20 0.49
▸ CYP2C19 P33261 2/20 0.49
▸ PLOD2 O00469 1/20 0.49
▸ PLOD3 O60568 1/20 0.49

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
SCHEMBL28849439 0.85 TBXAS1 (0.76) TBXAS1L3MBTL1TDP1LMNAMAPT
SCHEMBL29950720 0.85 TBXAS1 (0.76) TBXAS1L3MBTL1TDP1LMNAMAPT
SCHEMBL28454162 0.85 L3MBTL1 (0.58) TBXAS1HDAC1HDAC8HDAC3HDAC4
SCHEMBL4412682 0.82 TBXAS1 (0.67) TBXAS1HDAC1HDAC8HDAC3HDAC4
SCHEMBL28849443 0.80 CYP1A2 (0.55) HDAC1HDAC8HDAC3HDAC4HDAC7
SCHEMBL11831935 0.80 NPC1 (0.56) TBXAS1HDAC1HDAC8HDAC3HDAC4
SCHEMBL28618838 0.78 PAM (0.53) HDAC1HDAC8HDAC3HDAC4HDAC7
SCHEMBL25871487 0.78 PAM (0.53) HDAC1HDAC8HDAC3HDAC4HDAC7
SCHEMBL850920 0.75 TBXAS1 (0.69) TBXAS1HDAC1HDAC8HDAC3HDAC4
SCHEMBL850919 0.75 TBXAS1 (0.69) TBXAS1HDAC1HDAC8HDAC3HDAC4

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
CN-115108875-B Nitrogen-containing heteroarene chiral cyclic alcohol constructed by asymmetric catalysis of visible light, and preparation method and application thereof 河南师范大学 2023-07-04 — — CN disclosed
CN-115108875-A Nitrogen-containing heteroarene chiral cyclic alcohol constructed by visible light asymmetric catalysis, and preparation method and application thereof 河南师范大学 2022-09-27 — — CN disclosed
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