Everninic Acid

Everninic Acid

SCHEMBL609931

COc1cc(C)c(C(=O)O)c(O)c1

nearest known ligand 0.81

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 4/20 0.81
KMT2A Q03164 2/20 0.81
CYP3A4 P08684 7/20 0.71
HPGD P15428 3/20 0.71
MAPK1 P28482 3/20 0.66
KDM4E B2RXH2 2/20 0.66
MAPT P10636 2/20 0.66
RECQL P46063 2/20 0.66
GAA P10253 2/20 0.66
G6PD P11413 1/20 0.66
MCL1 Q07820 1/20 0.66
ACHE P22303 3/20 0.66
MEN1 O00255 1/20 0.63
ALDH1A1 P00352 1/20 0.63
ALOX15 P16050 1/20 0.63
HSD17B10 Q99714 1/20 0.63
USP2 O75604 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
ABL1 P00519 1/20 0.50
RIN1 Q13671 1/20 0.50

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
Evernic Acid SCHEMBL2552354 0.90 POLB (1.00) POLBKMT2ACYP3A4HPGDMAPK1
SCHEMBL484746 0.88 KMT2A (0.64) POLBKMT2ACYP3A4HPGDMAPK1
SCHEMBL2126879 0.88 POLB (0.64) POLBKMT2ACYP3A4HPGDMAPK1
Hydrochloric Acid SCHEMBL939484 0.86 KMT2A (0.62) POLBKMT2ACYP3A4HPGDMAPK1
SCHEMBL4263528 0.85 CYP3A4 (0.71) POLBKMT2ACYP3A4HPGDMAPK1
SCHEMBL30916607 0.85 CYP3A4 (0.71) POLBKMT2ACYP3A4HPGDMAPK1
SCHEMBL950536 0.83 CYP3A4 (1.00) POLBKMT2ACYP3A4HPGDMAPK1
SCHEMBL10187431 0.81 KMT2A (0.57) POLBKMT2ACYP3A4HPGDMAPK1
SCHEMBL28689599 0.81 CYP3A4 (0.61) POLBKMT2ACYP3A4HPGDMAPK1
SCHEMBL384123 0.81 POLB (0.57) POLBKMT2ACYP3A4HPGDMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260092029-A1 LIGAND-ENABLED SCALABLE C-H HYDROXYLATION OF BENZOIC AND PHENYLACETIC ACIDS AT ROOM TEMPERATURE SCRIPPS RESEARCH INST (US) 2026-04-02 US claimed
EP-4584236-A1 LIGAND-ENABLED SCALABLE C-H HYDROXYLATION OF BENZOIC AND PHENYLACETIC ACIDS AT ROOM TEMPERATURE The Scripps Research Institute (US) 2025-07-16 EP claimed
WO-2024054881-A1 LIGAND-ENABLED SCALABLE C-H HYDROXYLATION OF BENZOIC AND PHENYLACETIC ACIDS AT ROOM TEMPERATURE THE SCRIPPS RESEARCH INSTITUTE (US) 2024-03-14 WO claimed
CN-110554120-B Detection method of tree moss fragrant ester substance 云南中烟工业有限责任公司 2021-08-03 CN claimed
CN-110554120-A Detection method of tree moss aroma phenolic substances CHINA TOBACCO YUNNAN IND CO LTD 2019-12-10 CN claimed
CN-109541045-A The active components content assaying method such as a kind of halimasch and its product Asclerol 吉林农业大学 2019-03-29 CN claimed
CN-103052709-A Protoilludene synthase FRAUNHOFER INST FUER MOLEKULARBIOLOGIE UND ANGEWANDTE OEKOLOGIE 2013-04-17 CN claimed
US-20100048510-A1 DISSOLUTION OF AMYLOID FIBRILS BY FLAVONOIDS AND OTHER COMPOUNDS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2010-02-25 US claimed
WO-2008076351-A2 DISSOLUTION OF AMYLOID FIBRILS BY FLAVONOIDS AND OTHER COMPOUNDS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2008-06-26 WO claimed
US-20260092029-A1 LIGAND-ENABLED SCALABLE C-H HYDROXYLATION OF BENZOIC AND PHENYLACETIC ACIDS AT ROOM TEMPERATURE SCRIPPS RESEARCH INST (US) 2026-04-02 US disclosed
EP-4584236-A1 LIGAND-ENABLED SCALABLE C-H HYDROXYLATION OF BENZOIC AND PHENYLACETIC ACIDS AT ROOM TEMPERATURE The Scripps Research Institute (US) 2025-07-16 EP disclosed
CN-119604562-A Hydrophilic oil-repellent polymer 住友化学株式会社 2025-03-11 CN disclosed
CN-114994123-B Method and device for testing thermal stability of substance 江苏中烟工业有限责任公司 2024-11-19 CN disclosed
WO-2024054881-A1 LIGAND-ENABLED SCALABLE C-H HYDROXYLATION OF BENZOIC AND PHENYLACETIC ACIDS AT ROOM TEMPERATURE THE SCRIPPS RESEARCH INSTITUTE (US) 2024-03-14 WO disclosed
US-4431571-A ORGANOALUMINUM COMPOUND, REACTION PRODUCT OF TITANIUM HALIDE, ELEC STANDARD OIL COMPANY (INDIANA) (US) 1984-02-14 US disclosed
EP-0095290-A1 Retreating comminuted olefin polymerization catalyst with a titanium (IV) compound and an ester AMOCO CORPORATION (US) 1983-11-30 EP disclosed
US-4353813-A STEREOSPECIFIC COORDINATION CATALYST TREATED WIH HALOGENATED HYDROCARBON STANDARD OIL COMPANY (INDIANA) (US) 1982-10-12 US disclosed
US-4324690-A STEREOSPECIFIC;ORGANOALUMINUM COMPONENT AND COORDINATION CATALYST CONTAINING TITANIUM AND MAGNESIUM STANDARD OIL COMPANY (INDIANA) (US) 1982-04-13 US disclosed
US-4277370-A COORDINATION CATALYSTS STANDARD OIL COMPANY (INDIANA) (US) 1981-07-07 US disclosed
EP-0015645-A1 Alpha-olefin polymerization catalyst, process for producing catalyst component and process for polymerizing alpha-olefins Standard Oil Company (US) 1980-09-17 EP 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-20260092029-A1 LIGAND-ENABLED SCALABLE C-H HYDROXYLATION OF BENZOIC AND PHENYLACETIC ACIDS AT ROOM TEMPERATURE CYP2B6, CYP2A6, CYP1A1 POLB 1951/4885KMT2A 3199/4885CYP3A4 31/4885
US-20100048510-A1 DISSOLUTION OF AMYLOID FIBRILS BY FLAVONOIDS AND OTHER COMPOUNDS B2M, APP, BACE2 POLB 3980/4885KMT2A 4212/4885CYP3A4 658/4885

“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.