SCHEMBL3109160

SCHEMBL3109160

Cc1c(C)c2c(c(C)c1O)CCC(C)(CCCC(C)CCCC(C)C)O2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 3/20 1.00
▸ TTPA P49638 3/20 1.00
▸ MAPT P10636 2/20 1.00
▸ MEN1 O00255 2/20 1.00
▸ KMT2A Q03164 2/20 1.00
▸ GSTP1 P09211 1/20 1.00
▸ USP2 O75604 1/20 1.00
▸ THRB P10828 1/20 1.00
▸ CYP2C9 P11712 1/20 1.00
▸ CYP2C19 P33261 1/20 1.00
▸ NR1I2 O75469 2/20 0.85
▸ ALOX5 P09917 1/20 0.78
▸ PDE4A P27815 1/20 0.70
▸ PDE3A Q14432 1/20 0.70
▸ GSTO1 P78417 2/20 0.69
▸ PSEN1 P49768 2/20 0.67
▸ PTPN1 P18031 1/20 0.64
▸ AKT1 P31749 4/20 0.58
▸ PDPK1 O15530 1/20 0.58
▸ PHLPP1 O60346 1/20 0.58

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
Alpha-Tocopherol SCHEMBL14297170 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A
Alpha-Tocopherol SCHEMBL14167439 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A
Alpha-Tocopherol SCHEMBL13055549 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A
Alpha-Tocopherol SCHEMBL10295722 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A
Alpha-Tocopherol SCHEMBL8408151 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A
Alpha-Tochopherol SCHEMBL22303 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A
Alpha-Tocopherol SCHEMBL16430896 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A
SCHEMBL15441194 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A
Alpha-Tocopherol SCHEMBL20817063 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A
Alpha-Tochopherol SCHEMBL14315133 1.00 LMNA (1.00) LMNATTPAMAPTMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240209132-A1 COUPLING OF 2,3,5-TRIMETHYLHYDROQUINONE AND UNSATURATED ALCOHOLS DSM IP ASSETS B.V. (NL) 2024-06-27 — — US disclosed
US-20100273871-A1 ANTICANCER TOCOPHERYL SUCCINATE DERIVATIVES THE OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 2010-10-28 — — US disclosed
US-20100273871-A1 ANTICANCER TOCOPHERYL SUCCINATE DERIVATIVES THE OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 2010-10-28 — — US disclosed
US-7524836-B2 Nitrooxyderivative steroidal compounds NICOX S.A. (FR) 2009-04-28 — — US disclosed
EP-1986635-A4 ANTICANCER AGENTS UNIV OHIO STATE RES FOUND (US) 2009-04-22 — — EP disclosed
EP-1986635-A2 ANTICANCER AGENTS THE OHIO STATE RESEARCH FOUNDATION (US) 2008-11-05 — — EP disclosed
US-7378412-B2 Pharmaceutical compounds NICOX S.A. (FR) 2008-05-27 — — US disclosed
US-20080009545-A1 Anticancer agents THE OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 2008-01-10 — — US disclosed
WO-2007098139-A2 ANTICANCER AGENTS THE OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 2007-08-30 — — WO disclosed
US-20070142342-A1 Pharmaceutical compounds NICOX S.A. 2007-06-21 — — US disclosed
EP-0658552-B1 Process for the preparation of alpha-tocopherol derivatives EISAI CO LTD (JP) 1999-03-31 — — EP disclosed
US-5610113-A REACTION OF TRIMETHYLHYDROQUINONE AND ISOPHYTOL, CONDENSATION AND CYCLIZATION, SCANDIUM SAPONITE CATALYST EISAI CO., LTD. (JP) 1997-03-11 — — US disclosed
US-5536852-A ETHERIFICATION, CYCLIZATION EISAI CO., LTD. (JP) 1996-07-16 — — US disclosed
US-5532387-A CYCLIZATION OF TRIMETHYLHYDROQUINONE AND AN ALKENYL ALCOHOL, REUSABLE CATALYST, IIIB FLUOROSULFONATE, NITRATE, SULFATE, OR FLUOROALKYLSULFONATE EISAI CO., LTD. (JP) 1996-07-02 — — US disclosed
CN-1116203-A Process for the preparation of alpha-tocopherol derivatives, and catalyst EISAI CO LTD (JP) 1996-02-07 — — CN disclosed
EP-0677520-A1 Process for the preparation of alpha-tocopherol derivatives, and catalyst Eisai Co., Ltd. (JP) 1995-10-18 — — EP disclosed
CN-1108254-A Process for the preparation of alpha-tocopherol derivatives EISAI CO LTD (JP) 1995-09-13 — — CN disclosed
EP-0658552-A1 Process for the preparation of alpha-tocopherol derivatives Eisai Co., Ltd. (JP) 1995-06-21 — — EP disclosed
EP-0306904-B1 PHOSPHORIC ACID DIESTERS AND SALTS THEREOF Senju Pharmaceutical Co., Ltd. (JP) 1993-07-28 — — EP disclosed
EP-0306904-A2 Phosphoric acid diesters and salts thereof Senju Pharmaceutical Co., Ltd. (JP) 1989-03-15 — — 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 (3 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-20070142342-A1 Pharmaceutical compounds CYP11B2, CYP11B1, CYP2S1 LMNA 3381/4885TTPA 1068/4885MAPT 3031/4885
US-20100273871-A1 ANTICANCER TOCOPHERYL SUCCINATE DERIVATIVES SDHA, SDHB, SUCNR1 LMNA 1518/4885TTPA 8/4885MAPT 4728/4885
US-20080009545-A1 Anticancer agents SUCNR1, CPS1, HIF1AN LMNA 3247/4885TTPA 3406/4885MAPT 4790/4885

“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.

Send feedback