SCHEMBL571508

SCHEMBL571508

C=C(C)CCc1c(O)cc(O)c2c1OC(c1ccc(O)cc1)CC2=O

nearest known ligand 0.76

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ESR1 P03372 13/20 0.76
▸ ESR2 Q92731 12/20 0.76
▸ ABCG2 Q9UNQ0 3/20 0.68
▸ AKR1B10 O60218 2/20 0.68
▸ AKR1B1 P15121 2/20 0.68
▸ CACNA1G O43497 1/20 0.68
▸ CACNA1H O95180 1/20 0.68
▸ MAOA P21397 1/20 0.68
▸ PDE5A O76074 1/20 0.68
▸ CYP19A1 P11511 2/20 0.61
▸ CYP3A4 P08684 1/20 0.56
▸ CYP2D6 P10635 1/20 0.56
▸ CYP2C9 P11712 1/20 0.56
▸ ACHE P22303 1/20 0.56
▸ CYP2C19 P33261 1/20 0.56
▸ PDPK1 O15530 1/20 0.56
▸ PRKCA P17252 1/20 0.56
▸ BACE1 P56817 1/20 0.56
▸ PRKCQ Q04759 1/20 0.56
▸ MEN1 O00255 1/20 0.53

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
SCHEMBL31187090 0.90 ESR1 (0.61) ESR1ESR2ABCG2AKR1B10AKR1B1
SCHEMBL28485097 0.90 ESR1 (0.71) ESR1ESR2ABCG2AKR1B10AKR1B1
SCHEMBL31517131 0.87 MAPT (0.65) ESR1ESR2ABCG2AKR1B10AKR1B1
SCHEMBL17387053 0.86 ESR1 (1.00) ESR1ESR2ABCG2AKR1B10AKR1B1
SCHEMBL3965403 0.85 CACNA1H (0.72) ESR1ESR2AKR1B1CACNA1GCACNA1H
SCHEMBL13893460 0.83 ESR1 (0.82) ESR1ESR2ABCG2AKR1B10AKR1B1
SCHEMBL5313882 0.83 ESR1 (1.00) ESR1ESR2ABCG2AKR1B10AKR1B1
SCHEMBL1931876 0.83 ESR1 (1.00) ESR1ESR2ABCG2AKR1B10AKR1B1
Sophoraflavanone B SCHEMBL14304885 0.81 ESR1 (1.00) ESR1ESR2ABCG2AKR1B10AKR1B1
Sophoraflavanone B SCHEMBL29396586 0.81 ESR1 (1.00) ESR1ESR2ABCG2AKR1B10AKR1B1

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 52 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024087261-A1 METHOD FOR EXTRACTING, SEPARATING, AND PURIFYING 8-PRENYLNARINGENIN FROM HOPS 长沙市惠瑞生物科技有限公司 2024-05-02 — — WO claimed
CN-115650942-A Method for extracting, separating and purifying 8-isopentenyl naringenin from hops 长沙市惠瑞生物科技有限公司 2023-01-31 — — CN claimed
CN-115364144-A Yuqing lobular Kuding tea extract and preparation method and application thereof 贵州省中国科学院天然产物化学重点实验室(贵州医科大学天然产物化学重点实验室) 2022-11-22 — — CN claimed
CN-114146083-A Sophora flower extract and active component and application thereof in preparation of product for treating glycolipid metabolic syndrome 天津科技大学 2022-03-08 — — CN claimed
US-10512667-B2 Compositions and methods for treating conditions related to adrenocortical activity and/or excessive steroid production THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2019-12-24 — — US claimed
US-20180369321-A1 COMPOSITIONS AND METHODS FOR TREATING CONDITIONS RELATED TO ADRENOCORTICAL ACTIVITY AND/OR EXCESSIVE STEROID PRODUCTION THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2018-12-27 — — US claimed
WO-2024212685-A1 USE OF INTEGRIN Α5Β1 AS TARGET IN SCREENING OF DRUGS FOR PREVENTING AND/OR TREATING BONE LOSS 香港理工大学 2024-10-17 — — WO disclosed
EP-4393488-A1 COMPOSITION COMPRISING AT LEAST ONE NATURAL OR SYNTHETIC N-ALKYLAMIDE AS ACTIVE SUBSTANCE AND METHOD FOR MANUFACTURING SAME Eleonor (BE) 2024-07-03 — — EP disclosed
US-20240207205-A1 COMPOSITION COMPRISING AT LEAST ONE NATURAL OR SYNTHETIC N-ALKYLAMIDE AS ACTIVE SUBSTANCE AND ITS MANUFACTURING PROCESS ELEONOR SPRL (BE) 2024-06-27 — — US disclosed
WO-2024087261-A1 METHOD FOR EXTRACTING, SEPARATING, AND PURIFYING 8-PRENYLNARINGENIN FROM HOPS 长沙市惠瑞生物科技有限公司 2024-05-02 — — WO disclosed
US-20230381135-A1 COMPOSITION COMPRISING AT LEAST ONE LABDANE DITERPENE AND METHOD FOR MANUFACTURING SAME ELEONOR (BE) 2023-11-30 — — US disclosed
EP-4228604-A1 COMPOSITION COMPRISING AT LEAST ONE LABDANE DITERPENE AND METHOD FOR MANUFACTURING SAME Tilman (BE) 2023-08-23 — — EP disclosed
EP-4135666-A1 COMPOSITION COMPRISING AT LEAST ONE PROTOBERBERINE ALKALOID AND METHOD FOR MANUFACTURING SAME Eleonor (BE) 2023-02-22 — — EP disclosed
CN-101871924-A Method for synchronous detection of xanthohumol, isoxanthohumol and 8-isopentenylnaringenin in lupulus UNIV ZHEJIANG 2010-10-27 — — CN disclosed
CN-101871924-A Method for synchronous detection of xanthohumol, isoxanthohumol and 8-isopentenylnaringenin in lupulus UNIV ZHEJIANG 2010-10-27 — — CN disclosed
WO-2010039679-A1 COMPOSITIONS FOR PROLIFERATION OF CELLS AND RELATED METHODS THE HOSPITAL FOR SICK CHILDREN (CA) 2010-04-08 — — WO disclosed
WO-2008003774-A1 METHOD FOR PRODUCING ENANTIOPURE FLAVANONES Technische Universität Dresden (DE) 2008-01-10 — — WO disclosed
US-20050019438-A1 Hop extracts and use thereof in the production of a medicament having estrogenic properties BOURGES-SEVENIER CEDRIC (FR) 2005-01-27 — — US disclosed
EP-1381379-A1 HOP EXTRACTS AND USE THEREOF IN THE PRODUCTION OF A MEDICAMENT HAVING ESTROGENIC PROPERTIES BERKEM (FR) 2004-01-21 — — EP disclosed
WO-2002085393-A1 HOP EXTRACTS AND USE THEREOF IN THE PRODUCTION OF A MEDICAMENT HAVING ESTROGENIC PROPERTIES BERKEM (FR) 2002-10-31 — — 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 (1 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-20240207205-A1 COMPOSITION COMPRISING AT LEAST ONE NATURAL OR SYNTHETIC N-ALKYLAMIDE AS ACTIVE SUBSTANCE AND ITS MANUFACTURING PROCESS NPPA, PIGS, IAPP ESR1 4706/4885ESR2 4093/4885ABCG2 1192/4885

“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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