SCHEMBL24049840

SCHEMBL24049840

C=c1c(=C)n(CC)c2ccccc12

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 8/20 0.60
▸ KDM4E B2RXH2 6/20 0.50
▸ PGR P06401 2/20 0.47
▸ RCE1 Q9Y256 1/20 0.47
▸ MAPT P10636 6/20 0.47
▸ HTT P42858 4/20 0.47
▸ MEN1 O00255 4/20 0.47
▸ KMT2A Q03164 4/20 0.47
▸ HSD17B10 Q99714 3/20 0.47
▸ HPGD P15428 3/20 0.47
▸ TDP1 Q9NUW8 2/20 0.47
▸ MAPK1 P28482 2/20 0.47
▸ NPSR1 Q6W5P4 2/20 0.47
▸ NSD2 O96028 1/20 0.47
▸ RXFP1 Q9HBX9 1/20 0.47
▸ HBB P68871 1/20 0.47
▸ NPC1 O15118 2/20 0.46
▸ HCRTR1 O43613 1/20 0.46
▸ USP2 O75604 1/20 0.46
▸ TP53 P04637 1/20 0.46

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
Ethylene SCHEMBL28271437 0.79 ALDH1A1 (0.69) ALDH1A1KDM4EPGRRCE1MAPT
SCHEMBL151563 0.78 ALDH1A1 (0.75) ALDH1A1KDM4ERCE1MAPTHTT
SCHEMBL29360167 0.78 ALDH1A1 (0.75) ALDH1A1KDM4ERCE1MAPTHTT
SCHEMBL29963695 0.78 ALDH1A1 (0.75) ALDH1A1KDM4ERCE1MAPTHTT
Formaldehyde SCHEMBL27505377 0.77 ALDH1A1 (0.73) ALDH1A1KDM4EPGRRCE1MAPT
SCHEMBL13247889 0.77 ALDH1A1 (0.40) ALDH1A1KDM4EPGRHTTMEN1
SCHEMBL12498669 0.76 ALDH1A1 (0.72) ALDH1A1KDM4ERCE1MAPTHTT
SCHEMBL31676670 0.76 ALDH1A1 (0.72) ALDH1A1KDM4ERCE1MAPTHTT
SCHEMBL28676971 0.76 ALDH1A1 (0.72) ALDH1A1KDM4ERCE1MAPTHTT
SCHEMBL18565498 0.75 ALDH1A1 (0.46) ALDH1A1KDM4EPGRRCE1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230183391-A1 BIOMASS DERIVED DIKETONES AS EFFICIENT VISIBLE LIGHT PHOTOINITIATORS BOWLING GREEN STATE UNIVERSITY (US) 2023-06-15 — — US disclosed
WO-2023067628-A1 A METHOD FOR THE PREPARATION OF INDOLE-3-CARBOXYLIC ACID DERIVATIVES COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH AN INDIAN REGISTERED BODY INCORPORATED UNDER THE REGN. OF SOC. ACT (ACT XXI OF 1860) (IN) 2023-04-27 — — WO disclosed
WO-2021236489-A1 BIOMASS DERIVED DIKETONES AS EFFICIENT VISIBLE LIGHT PHOTOINITIATORS BOWLING GREEN STATE UNIVERSITY (US) 2021-11-25 — — WO disclosed
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