SCHEMBL24345232

SCHEMBL24345232

CCCCCCCCCCCC#CC(=O)c1ccc(OC)cc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC1 Q13547 3/20 0.47
HDAC3 O15379 2/20 0.47
HDAC2 Q92769 2/20 0.47
APP P05067 1/20 0.47
MMP2 P08253 1/20 0.46
MMP12 P39900 1/20 0.46
HDAC8 Q9BY41 3/20 0.45
GSK3B P49841 1/20 0.45
HDAC4 P56524 1/20 0.45
HDAC7 Q8WUI4 1/20 0.45
HDAC10 Q969S8 1/20 0.45
HDAC11 Q96DB2 1/20 0.45
HDAC6 Q9UBN7 1/20 0.45
HDAC9 Q9UKV0 1/20 0.45
HDAC5 Q9UQL6 1/20 0.45
CNR1 P21554 2/20 0.45
CNR2 P34972 1/20 0.45
NPC1 O15118 1/20 0.44
RAB9A P51151 1/20 0.44
TP53 P04637 1/20 0.44

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
SCHEMBL12003540 0.94 HDAC3 (0.49) HDAC1HDAC3HDAC2APPHDAC8
SCHEMBL17494710 0.83 ALDH1A1 (0.47) NPC1RAB9ATSHR
SCHEMBL28647964 0.82 NR1I2 (0.41) HDAC1HDAC3HDAC2MMP2MMP12
SCHEMBL28408619 0.81 CES1 (0.50) MMP2MMP12
SCHEMBL24345107 0.81 MMP2 (0.47) MMP2MMP12
SCHEMBL31614581 0.81 ESR1 (0.49) MMP2MMP12NPC1RAB9ATSHR
SCHEMBL31595927 0.81 NR1I2 (0.42) HDAC1HDAC3HDAC2MMP2MMP12
SCHEMBL25749243 0.81 MMP2 (0.47) MMP2MMP12
SCHEMBL9241002 0.80 CES2 (0.49) MMP2MMP12
SCHEMBL1315161 0.79 MMP2 (0.52) MMP2MMP12GSK3BRAB9ATSHR

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-11691135-B2 Synthesis of alkynones via carbonylative Sonogashira coupling reactions catalyzed by Pd(II)-N-Heterocyclic carbene-pyridine complexes KING FAHD UNIVERSITY OF PETROLEUM & MINERALS (SA) 2023-07-04 US disclosed
US-20220118435-A1 SYNTHESIS OF ALKYNONES VIA CARBONYLATIVE SONOGASHIRA COUPLING REACTIONS CATALYZED BY PD(II)-N-HETEROCYCLIC CARBENE-PYRIDINE COMPLEXES KING FAHD UNIVERSITY OF PETROLEUM & MINERALS (SA) 2022-04-21 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11691135-B2 Synthesis of alkynones via carbonylative Sonogashira coupling reactions catalyzed by Pd(II)-N-Heterocyclic carbene-pyridine complexes PDK2, SNCA, YAP1 HDAC1 2261/4885HDAC3 2504/4885HDAC2 931/4885
US-20220118435-A1 SYNTHESIS OF ALKYNONES VIA CARBONYLATIVE SONOGASHIRA COUPLING REACTIONS CATALYZED BY PD(II)-N-HETEROCYCLIC CARBENE-PYRIDINE COMPLEXES PDK2, SNCA, YAP1 HDAC1 2261/4885HDAC3 2504/4885HDAC2 931/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.