SCHEMBL68851

SCHEMBL68851

CCOC(=O)Cc1ccc(CC(=O)OCC)cc1

nearest known ligand 0.75

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP4Z1 Q86W10 1/20 0.62
▸ MAPT P10636 2/20 0.58
▸ LMNA P02545 3/20 0.55
▸ SMN1; SMN2 Q16637 2/20 0.55
▸ CYP4F2 P78329 2/20 0.55
▸ CYP4A11 Q02928 2/20 0.55
▸ ALDH1A1 P00352 2/20 0.52
▸ L3MBTL1 Q9Y468 2/20 0.52
▸ MAPK1 P28482 1/20 0.52
▸ KDM4E B2RXH2 1/20 0.51
▸ TSHR P16473 1/20 0.51
▸ HSD17B10 Q99714 1/20 0.51
▸ TBXAS1 P24557 1/20 0.50
▸ MGAM O43451 1/20 0.50
▸ GAA P10253 1/20 0.50
▸ SI P14410 1/20 0.50
▸ MGAM2 Q2M2H8 1/20 0.50
▸ LIPE Q05469 1/20 0.50
▸ PAM P19021 1/20 0.50
▸ MEN1 O00255 2/20 0.49

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
SCHEMBL68930 0.94 CYP4Z1 (0.57) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2
SCHEMBL1107146 0.94 CYP4Z1 (0.57) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2
SCHEMBL10299459 0.94 CYP4Z1 (0.57) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2
SCHEMBL6057577 0.94 CYP4F2 (0.59) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2
SCHEMBL5034285 0.92 CYP4Z1 (0.59) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2
SCHEMBL18932531 0.92 CYP4Z1 (0.55) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2
SCHEMBL6207253 0.92 CYP4Z1 (0.55) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2
SCHEMBL1179218 0.92 CYP4Z1 (0.55) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2
SCHEMBL5545889 0.92 CYP4Z1 (0.55) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2
SCHEMBL85523 0.90 PPID (0.58) CYP4Z1MAPTLMNASMN1; SMN2CYP4F2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118007442-B Unidirectional moisture-conducting fabric and preparation method thereof 广东云蝶园内衣科技有限公司 2024-07-12 — — CN claimed
CN-118007442-A Unidirectional moisture-conducting fabric and preparation method thereof 广东云蝶园内衣科技有限公司 2024-05-10 — — CN claimed
CN-118007442-B Unidirectional moisture-conducting fabric and preparation method thereof 广东云蝶园内衣科技有限公司 2024-07-12 — — CN disclosed
CN-118007442-A Unidirectional moisture-conducting fabric and preparation method thereof 广东云蝶园内衣科技有限公司 2024-05-10 — — CN disclosed
CN-115739054-A Preparation and application of carboxylic acid column [5] arene modified attapulgite 兰州城市学院 2023-03-07 — — CN disclosed
EP-3939974-A1 MODULATORS OF ROR-GAMMA Vitae Pharmaceuticals, LLC (US) 2022-01-19 — — EP disclosed
EP-3939974-A1 MODULATORS OF ROR-GAMMA Vitae Pharmaceuticals, LLC (US) 2022-01-19 — — EP disclosed
CN-113549010-A Preparation and application of compound with AMPK agonistic activity and prodrug thereof 中国科学院上海药物研究所 2021-10-26 — — CN disclosed
EP-3408268-B1 BENZIMIDAZOLE DERIVATIVES AS MODULATORS OF ROR-GAMMA VITAE PHARMACEUTICALS LLC (US) 2021-08-04 — — EP disclosed
EP-3408268-B1 BENZIMIDAZOLE DERIVATIVES AS MODULATORS OF ROR-GAMMA VITAE PHARMACEUTICALS LLC (US) 2021-08-04 — — EP disclosed
US-20210094940-A1 MODULATORS OF ROR-GAMMA VITAE PHARMACEUTICALS, LLC 2021-04-01 — — US disclosed
US-20050171147-A1 Sulfonamide derivatives for the treatment of diseases PFIZER INC. 2005-08-04 — — US disclosed
US-6573384-B1 1,4-substituted cyclic amine compound which is useful as a pharmaceutical, and an intermediate for the process EISAI CO., LTD. (JP) 2003-06-03 — — US disclosed
EP-1179532-A1 PROCESS FOR THE PRODUCTION OF INDOLE DERIVATIVES AND INTERMEDIATES THEREFOR Eisai Co., Ltd. (JP) 2002-02-13 — — EP disclosed
EP-0618899-B1 AROMATIC ESTERS OF PHENYLENEDIALKANOATES AS INHIBITORS OF HUMAN NEUTROPHIL ELASTASE CORTECH INC (US) 1996-03-13 — — EP disclosed
EP-0618899-A4 AROMATIC ESTERS OF PHENYLENEDIALKANOATES AS INHIBITORS OF HUMAN NEUTROPHIL ELASTASE. CORTECH INC (US) 1994-11-02 — — EP disclosed
EP-0618899-A1 AROMATIC ESTERS OF PHENYLENEDIALKANOATES AS INHIBITORS OF HUMAN NEUTROPHIL ELASTASE. CORTECH INC (US) 1994-10-12 — — EP disclosed
WO-1993011760-A1 AROMATIC ESTERS OF PHENYLENEDIALKANOATES AS INHIBITORS OF HUMAN NEUTROPHIL ELASTASE CORTECH, INC. (US) 1993-06-24 — — WO disclosed
US-5216022-A Antiischemic agents CORTECH, INC. (US) 1993-06-01 — — US disclosed
US-4016194-A CATALYTIC CARBONYLATION TEXACO INC. (US) 1977-04-05 — — 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 (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-20050171147-A1 Sulfonamide derivatives for the treatment of diseases SULT2A1, STS, SULT1A1 CYP4Z1 1316/4885MAPT 3819/4885LMNA 2902/4885
US-20210094940-A1 MODULATORS OF ROR-GAMMA RORC, RORB, RORA CYP4Z1 569/4885MAPT 3475/4885LMNA 4554/4885

“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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