SCHEMBL4783944

SCHEMBL4783944

CCC(C)(CC(C)=O)CC(=O)O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HMGCR P04035 1/20 0.44
CHRM1 P11229 1/20 0.44
TBXA2R P21731 1/20 0.44
ADRA1A P35348 1/20 0.44
ALDH1A1 P00352 4/20 0.42
CYP2C19 P33261 2/20 0.42
HIF1A Q16665 2/20 0.42
CYP2D6 P10635 1/20 0.42
TSHR P16473 1/20 0.42
TDP1 Q9NUW8 2/20 0.38
KDM4E B2RXH2 1/20 0.38
FFAR1 O14842 1/20 0.38
CPT2 P23786 1/20 0.38
FFAR3 O14843 2/20 0.35
LMNA P02545 1/20 0.35
SLC15A2 Q16348 1/20 0.35
TET2 Q6N021 1/20 0.31
HSPD1 P10809 1/20 0.31
BLM P54132 1/20 0.31
HSPE1 P61604 1/20 0.31

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
SCHEMBL16587771 1.00 HMGCR (0.44) HMGCRCHRM1TBXA2RADRA1AALDH1A1
SCHEMBL2612031 0.90 ALDH1A1 (0.42) HMGCRCHRM1TBXA2RADRA1AALDH1A1
SCHEMBL1335602 0.90 HMGCR (0.52) HMGCRCHRM1TBXA2RADRA1AALDH1A1
SCHEMBL14109353 0.87 HMGCR (0.50) HMGCRCHRM1TBXA2RADRA1AALDH1A1
SCHEMBL17933420 0.85 ALDH1A1 (0.42) HMGCRCHRM1TBXA2RADRA1AALDH1A1
SCHEMBL1419066 0.85 HMGCR (0.52) HMGCRCHRM1TBXA2RADRA1AALDH1A1
SCHEMBL3495260 0.81 HMGCR (0.44) HMGCRCHRM1TBXA2RADRA1AALDH1A1
Adipic Acid SCHEMBL20592369 0.79 AKR1B1 (0.52) ALDH1A1TSHRTDP1FFAR1LMNA
SCHEMBL193895 0.77 HMGCR (0.41) HMGCRCHRM1TBXA2RADRA1AALDH1A1
SCHEMBL11922837 0.76 HMGCR (0.44) HMGCRCHRM1TBXA2RADRA1AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170096446-A1 Extended Triterpene Derivatives MYREXIS, INC. (US) 2017-04-06 US disclosed
US-9505800-B2 Extended triterpene derivatives MYREXIS, INC. (US) 2016-11-29 US disclosed
WO-2013148067-A1 3,28-DISUBSTITUTED BETULINIC ACID DERIVATIVES AS ANTI-HIV AGENTS THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2013-10-03 WO disclosed
US-8318425-B2 Inhibition of HIV-1 replication by disruption of the processing of the viral capsid-spacer peptide 1 protein The United States of America, as represented by the Secretary, Department & Human Services (US) 2012-11-27 US disclosed
WO-2010132334-A1 3,28-DISUBSTITUTED BETULINIC ACID DERIVATIVES AS ANTI-HIV AGENTS THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2010-11-18 WO disclosed
US-20100240630-A1 COMPOUNDS AND THERAPEUTIC USES THEREOF Myriad Pharmaceuticals, Inc.. (US) 2010-09-23 US disclosed
US-20100221264-A1 Inhibition of HIV-1 Replication by Disruption of the Processing of the Viral Capsid-Spacer Peptide 1 Protein PANACOS PHARMACEUTICALS, INC. (US) 2010-09-02 US disclosed
US-7537765-B2 Inhibition of HIV-1 replication by disruption of the processing of the viral capsid-spacer peptide 1 protein PANACOS PHARMACEUTICALS, INC. (US) 2009-05-26 US disclosed
WO-2008099019-A1 6-HYDROXY-DIBENZODIAZEPINONES USEFUL AS HEPATITIS C VIRUS INHIBITORS TIBOTEC PHARMACEUTICALS LTD. (IE) 2008-08-21 WO disclosed
WO-2008099019-A1 6-HYDROXY-DIBENZODIAZEPINONES USEFUL AS HEPATITIS C VIRUS INHIBITORS TIBOTEC PHARMACEUTICALS LTD. (IE) 2008-08-21 WO disclosed
US-20060014826-A1 Dioxocyclohexane carboxylic acid phenyl amide derivatives for modulating voltage-gated potassium channels and pharmaceutical compositions containing the same WYETH (US) 2006-01-19 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 (4 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-20060014826-A1 Dioxocyclohexane carboxylic acid phenyl amide derivatives for modulating voltage-gated potassium channels and pharmaceutical compositions containing the same KCNC1, KCNA1, KCNH2 HMGCR 4018/4885CHRM1 1187/4885TBXA2R 691/4885
US-20170096446-A1 Extended Triterpene Derivatives BET1, PGGT1B, TMPO HMGCR 254/4885CHRM1 3305/4885TBXA2R 403/4885
US-20100240630-A1 COMPOUNDS AND THERAPEUTIC USES THEREOF HAVCR2, FURIN, SARS1 HMGCR 132/4885CHRM1 3870/4885TBXA2R 1139/4885
US-20100221264-A1 Inhibition of HIV-1 Replication by Disruption of the Processing of the Viral Capsid-Spacer Peptide 1 Protein SP1, CPSF1, BET1 HMGCR 4652/4885CHRM1 2076/4885TBXA2R 4161/4885

“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.