SCHEMBL68692

SCHEMBL68692

CCCCCCCCc1cc(O)cc(O)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PTGS2 P35354 5/20 1.00
▸ CYP3A4 P08684 2/20 0.95
▸ ESR1 P03372 2/20 0.63
▸ ADRA2A P08913 2/20 0.63
▸ ADORA3 P0DMS8 2/20 0.63
▸ TACR2 P21452 2/20 0.63
▸ SLC6A2 P23975 2/20 0.63
▸ SLC6A4 P31645 2/20 0.63
▸ SLC6A3 Q01959 2/20 0.63
▸ KDM4E B2RXH2 1/20 0.63
▸ ALDH1A1 P00352 1/20 0.63
▸ LMNA P02545 1/20 0.63
▸ SHBG P04278 1/20 0.63
▸ TP53 P04637 1/20 0.63
▸ HSPD1 P10809 1/20 0.63
▸ ADRB3 P13945 1/20 0.63
▸ HTR2C P28335 1/20 0.63
▸ HSPE1 P61604 1/20 0.63
▸ HIF1A Q16665 1/20 0.63
▸ TST Q16762 1/20 0.63

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
SCHEMBL2468227 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3
SCHEMBL16432840 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3
SCHEMBL70443 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3
Cardol SCHEMBL406402 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3
SCHEMBL4448056 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3
SCHEMBL70292 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3
SCHEMBL70057 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3
SCHEMBL11737365 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3
SCHEMBL4444098 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3
SCHEMBL17201654 1.00 PTGS2 (1.00) PTGS2CYP3A4ESR1ADRA2AADORA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101522738-A Modified alkylresorcinol resins and applications thereof INDSPEC CHEMICAL CORP (US) 2009-09-02 — — CN claimed
EP-2087022-A1 MODIFIED ALKYLRESORCINOL RESINS AND APPLICATIONS THEREOF INDSPEC CHEMICAL CORPORATION (US) 2009-08-12 — — EP claimed
WO-2008048839-A1 MODIFIED ALKYLRESORCINOL RESINS AND APPLICATIONS THEREOF INDSPEC CHEMICAL CORPORATION (US) 2008-04-24 — — WO claimed
EP-4714444-A1 PREPARATION FOR AND USE OF CANNABIDIOL DERIVATIVE DRUGS Changchun Institute Of Applied Chemistry Chinese Academy Of Sciences (CN) 2026-03-25 — — EP disclosed
WO-2024239921-A1 PREPARATION FOR AND USE OF CANNABIDIOL DERIVATIVE DRUGS 中国科学院长春应用化学研究所 2024-11-28 — — WO disclosed
US-20240117388-A1 ACYL ACTIVATING ENZYMES FOR PREPARATION OF CANNABINOIDS BAYMEDICA, INC. 2024-04-11 — — US disclosed
EP-4281553-A1 ACYL ACTIVATING ENZYMES FOR PREPARATION OF CANNABINOIDS BayMedica, Inc. (US) 2023-11-29 — — EP disclosed
US-20230063396-A1 GENETICALLY MODIFIED YEAST FOR THE PRODUCTION OF CANNABIGEROLIC ACID, CANNABICHROMENIC ACID AND RELATED CANNABINOIDS BAYMEDICA, INC. 2023-03-02 — — US disclosed
US-11555211-B2 Recombinant production systems for prenylated polyketides of the cannabinoid family BAYMEDICA, INC. (US) 2023-01-17 — — US disclosed
CN-115552010-A Genetically modified yeast for production of cannabigerolic acid, cannabichromenic acid and related cannabinoids 海湾医学公司 2022-12-30 — — CN disclosed
EP-4093874-A1 GENETICALLY MODIFIED YEAST FOR THE PRODUCTION OF CANNABIGEROLIC ACID, CANNABICHROMENIC ACID AND RELATED CANNABINOIDS BayMedica, Inc. (US) 2022-11-30 — — EP disclosed
EP-0811619-A1 Novel ester compound and thermosetting resin composition using the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1997-12-10 — — EP disclosed
CN-1125218-A Novel aryl ester compound, process for producing the same, epoxy resin composition using the same, and copper-clad laminate using the same SUMITOMO CHEMICAL CO (JP) 1996-06-26 — — CN disclosed
EP-0699670-A2 Aryl ester compound, its production process, epoxy resin composition using said compound, and copper-clad laminate using the epoxy resin composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1996-03-06 — — EP disclosed
EP-0004753-B1 PREPARATION OF TETRAHYDROBENZOXOCINS AND CIS-HEXAHYDRODIBENZOPYRANONES ELI LILLY AND COMPANY (US) 1982-05-26 — — EP disclosed
EP-0004753-A1 Preparation of tetrahydrobenzoxocins and cis-hexahydrodibenzopyranones ELI LILLY AND COMPANY (US) 1979-10-17 — — EP disclosed
US-4171315-A Preparation of cis-hexahydrodibenzopyranones ELI LILLY AND COMPANY (US) 1979-10-16 — — US disclosed
US-4131614-A Process for preparing cis-hexahydrodibenzopyranones ELI LILLY AND COMPANY (US) 1978-12-26 — — US disclosed
US-4075230-A Preparation of optically active trans-hexahydrodibenzopyranones ELI LILLY AND COMPANY (US) 1978-02-21 — — US disclosed
US-4054582-A Process for converting cis-hexahydrodibenzo[b,d]pyran-9-ones to trans-hexahydrodibenzo[b,d]-pyran-9-ones ELI LILLY AND COMPANY (US) 1977-10-18 — — US disclosed
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