SCHEMBL2840285

SCHEMBL2840285

CCCCCCCC(=O)C=Cc1ccc(O)c(OC)c1

nearest known ligand 0.82

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HTR1A P08908 1/20 0.82
▸ APP P05067 5/20 0.73
▸ CYP2D6 P10635 3/20 0.72
▸ ALOX5 P09917 3/20 0.72
▸ MAPT P10636 3/20 0.72
▸ MAOB P27338 3/20 0.72
▸ BACE1 P56817 3/20 0.72
▸ CYP2C9 P11712 2/20 0.72
▸ TSHR P16473 2/20 0.72
▸ HSD17B10 Q99714 2/20 0.72
▸ TOP2A P11388 2/20 0.72
▸ ABCB1 P08183 2/20 0.72
▸ AKR1B1 P15121 2/20 0.72
▸ MAOA P21397 2/20 0.72
▸ CYP1A2 P05177 2/20 0.72
▸ NFKB1 P19838 2/20 0.72
▸ HSD11B1 P28845 2/20 0.72
▸ STAT3 P40763 2/20 0.72
▸ NFKB2 Q00653 2/20 0.72
▸ RELA Q04206 2/20 0.72

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
SCHEMBL2840282 1.00 HTR1A (0.82) HTR1AAPPCYP2D6ALOX5MAPT
SCHEMBL20668211 1.00 HTR1A (0.82) HTR1AAPPCYP2D6ALOX5MAPT
SCHEMBL30240113 1.00 HTR1A (0.82) HTR1AAPPCYP2D6ALOX5MAPT
SCHEMBL27927798 0.95 HTR1A (0.77) HTR1AAPPCYP2D6ALOX5MAPT
Curcumin SCHEMBL28117506 0.93 APP (0.84) HTR1AAPPCYP2D6ALOX5MAPT
Curcumin SCHEMBL25240986 0.92 HTR1A (0.73) HTR1AAPPCYP2D6ALOX5MAPT
Curcumin SCHEMBL25245838 0.92 HTR1A (0.73) HTR1AAPPCYP2D6ALOX5MAPT
Curcumin SCHEMBL25247326 0.92 HTR1A (0.73) HTR1AAPPCYP2D6ALOX5MAPT
Curcumin SCHEMBL25287577 0.92 HTR1A (0.73) HTR1AAPPCYP2D6ALOX5MAPT
Curcumin SCHEMBL25285963 0.92 HTR1A (0.73) HTR1AAPPCYP2D6ALOX5MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11964935-B2 Gingerol derivative having inhibitory activity against biofilm formation and pharmaceutical composition comprising same as effective ingredient for preventing or treating biofilm-caused infection symptom KOREA UNIVERSITY RESEARCH AND BUSINESS FOUNDATION, SEJONG CAMPUS (KR) 2024-04-23 — — US disclosed
CN-112457192-B Synthetic method of paradol 桂林理工大学 2023-03-14 — — CN disclosed
CN-112457192-A Synthetic method of paradol 桂林理工大学 2021-03-09 — — CN disclosed
US-20200283364-A1 GINGEROL DERIVATIVE HAVING INHIBITORY ACTIVITY AGAINST BIOFILM FORMATION AND PHARMACEUTICAL COMPOSITION COMPRISING SAME AS EFFECTIVE INGREDIENT FOR PREVENTING OR TREATING BIOFILM-CAUSED INFECTION SYMPTOM KOREA UNIVERSITY RESEARCH AND BUSINESS FOUNDATION, SEJONG CAMPUS (KR) 2020-09-10 — — US disclosed
EP-2488257-B1 FORMULATION WITH IRRITATION REDUCING ACTION COMPRISING BISABOLOL AND [6]-PARADOL SYMRISE AG (DE) 2018-05-02 — — EP disclosed
US-9549911-B2 Ginger metabolites and uses thereof NORTH CAROLINA A&T STATE UNIVERSITY (US) 2017-01-24 — — US disclosed
US-20160235697-A1 GINGER METABOLITES AND USES THEREOF NORTH CAROLINA A&T STATE UNIVERSITY (US) 2016-08-18 — — US disclosed
US-9272994-B1 Ginger metabolites and uses thereof NORTH CAROLINA A&T STATE UNIVERSITY (US) 2016-03-01 — — US disclosed
US-8951507-B2 Formulation with irritation reducing action comprising bisabolol and [6]-paradol SYMRISE AG (DE) 2015-02-10 — — US disclosed
US-20120258058-A1 FORMULATION WITH IRRITATION REDUCING ACTION COMPRISING BISABOLOL AND [6]-PARADOL SYMRISE AG (DE) 2012-10-11 — — US disclosed
EP-2488257-A2 FORMULATION WITH IRRITATION REDUCING ACTION COMPRISING BISABOLOL AND [6]-PARADOL Symrise AG (DE) 2012-08-22 — — EP disclosed
WO-2010000877-A2 FORMULATION WITH IRRITATION REDUCING ACTION COMPRISING BISABOLOL AND [6]-PARADOL SYMRISE GMBH & CO. KG (DE) 2010-01-07 — — WO 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-20120258058-A1 FORMULATION WITH IRRITATION REDUCING ACTION COMPRISING BISABOLOL AND [6]-PARADOL FHIT, DAGLA, TRPV1 HTR1A 116/4885APP 1202/4885CYP2D6 83/4885
US-20160235697-A1 GINGER METABOLITES AND USES THEREOF GNMT, GSTM2, GSTM1 HTR1A 2873/4885APP 2419/4885CYP2D6 577/4885
US-20200283364-A1 GINGEROL DERIVATIVE HAVING INHIBITORY ACTIVITY AGAINST BIOFILM FORMATION AND PHARMACEUTICAL COMPOSITION COMPRISING SAME AS EFFECTIVE INGREDIENT FOR PREVENTING OR TREATING BIOFILM-CAUSED INFECTION SYMPTOM LSS, F2R, CFTR HTR1A 1415/4885APP 1017/4885CYP2D6 1825/4885
US-11964935-B2 Gingerol derivative having inhibitory activity against biofilm formation and pharmaceutical composition comprising same as effective ingredient for preventing or treating biofilm-caused infection symptom LSS, F2R, CFTR HTR1A 1415/4885APP 1017/4885CYP2D6 1825/4885

“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.

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