Sugi Predict

Sugi Predict / Compounds / SCHEMBL6882235

SCHEMBL6882235

SCHEMBL6882235

CC1=CC[C@H](C(C)C)CC1

nearest known ligand 0.44

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 2/20 0.44
▸ PTPN1 P18031 1/20 0.35
▸ MEN1 O00255 2/20 0.33
▸ KMT2A Q03164 2/20 0.33
▸ CYP3A4 P08684 1/20 0.33
▸ ALOX15 P16050 1/20 0.33
▸ MAPK1 P28482 1/20 0.33
▸ CHRNA7 P36544 1/20 0.33
▸ STAT3 P40763 1/20 0.33
▸ MET P08581 1/20 0.31
▸ TAS2R46 P59540 4/20 0.31
▸ TAS2R31 P59538 2/20 0.31
▸ TAS2R10 Q9NYW0 2/20 0.31
▸ CNR2 P34972 1/20 0.30
▸ PPARA Q07869 1/20 0.30

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
SCHEMBL3851126 1.00 LMNA (0.44) LMNAPTPN1MEN1KMT2ACYP3A4
SCHEMBL5933973 1.00 LMNA (0.44) LMNAPTPN1MEN1KMT2ACYP3A4
SCHEMBL16796012 1.00 LMNA (0.44) LMNAPTPN1MEN1KMT2ACYP3A4
SCHEMBL736990 1.00 LMNA (0.44) LMNAPTPN1MEN1KMT2ACYP3A4
Bicarbonate SCHEMBL17847277 0.90 LMNA (0.42) LMNAPTPN1MEN1KMT2ACYP3A4
SCHEMBL8813386 0.89 LMNA (0.37) LMNAPTPN1TAS2R46TAS2R31TAS2R10
D-Limonene SCHEMBL4609927 0.83 LMNA (0.75) LMNAMEN1KMT2ACYP3A4ALOX15
SCHEMBL6402023 0.83 LMNA (0.46) LMNAPTPN1MEN1KMT2ACYP3A4
SCHEMBL1704609 0.83 LMNA (0.46) LMNAPTPN1MEN1KMT2ACYP3A4
SCHEMBL14764978 0.83 LMNA (0.41) LMNAPTPN1MEN1KMT2ACYP3A4

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 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040077063-A1 Process for the preparation of perillyl alcohol EIDGENOSSISCHE TECHNISCHE HOCHSCHULE ZURICH (CH) 2004-04-22 — — US claimed
EP-1364039-A1 PROCESS FOR THE PREPARATION OF PERILLYL ALCOHOL Eidgenössische Technische Hochschule Zürich (CH) 2003-11-26 — — EP claimed
EP-1236802-A1 Process for the preparation of perillyl alcohol AVENTIS ANIMAL NUTRITION S.A. (FR) 2002-09-04 — — EP claimed
WO-2002066662-A1 PROCESS FOR THE PREPARATION OF PERILLYL ALCOHOL Eidgenössische Technische Hochschule Zürich (CH) 2002-08-29 — — WO claimed
EP-3923917-B1 PROCESS FOR THE SYNTHESIS OF CANNABIDIOL AND INTERMEDIATES THEREOF COUNCIL OF SCIENT & INDUSTRIAL RESEARCH AN INDIAN REGISTERED BODY INCORPORATED UNDER THE REGISTRATIO (IN) 2026-03-04 — — EP disclosed
US-12545851-B2 Fragrances with note of lily of the valley SYMRISE AG (DE) 2026-02-10 — — US disclosed
CN-119822944-A Method for preparing solanone 上海致朴实业有限公司 2025-04-15 — — CN disclosed
WO-2025014885-A2 PINCER-LIGATED COBALT CATALYSTS AND METHODS OF MAKING AND USING THEREOF OHIO STATE INNOVATION FOUNDATION (US) 2025-01-16 — — WO disclosed
US-20240084216-A1 FRAGRANCES WITH NOTE OF LILY OF THE VALLEY SYMRISE AG (DE) 2024-03-14 — — US disclosed
CN-110191877-B Cleavable surfactants 弗门尼舍有限公司 2023-04-28 — — CN disclosed
CN-113167695-A Device for collecting volatile organic compounds 法国由内政部代表 2021-07-23 — — CN disclosed
CN-205844284-U For trapping the series connection cold solvent device of gaseous phase of main stream smoke of cigarette composition 中国烟草总公司郑州烟草研究院 2016-12-28 — — CN disclosed
US-9394325-B2 Enantiopure base-metal catalysts for asymmetric catalysis and bis(imino)pyridine iron alkyl complexes for catalysis THE TRUSTEES OF PRINCETON UNIVERSITY (US) 2016-07-19 — — US disclosed
US-20130281747-A1 COBALT PHOSPHINE ALKYL COMPLEXES FOR THE ASYMMETRIC HYDROGENATION OF ALKENES NATIONAL SCIENCE FOUNDATION 2013-10-24 — — US disclosed
US-20130079567-A1 ENANTIOPURE BASE-METAL CATALYSTS FOR ASYMMETRIC CATALYSIS AND BIS(IMINO)PYRIDINE IRON ALKYL COMPLEXES FOR CATALYSIS THE TRUSTEES OF PRINCETON UNIVERSITY (US) 2013-03-28 — — US disclosed
US-20040077063-A1 Process for the preparation of perillyl alcohol EIDGENOSSISCHE TECHNISCHE HOCHSCHULE ZURICH (CH) 2004-04-22 — — US disclosed
EP-1364039-A1 PROCESS FOR THE PREPARATION OF PERILLYL ALCOHOL Eidgenössische Technische Hochschule Zürich (CH) 2003-11-26 — — EP disclosed
EP-1236802-A1 Process for the preparation of perillyl alcohol AVENTIS ANIMAL NUTRITION S.A. (FR) 2002-09-04 — — EP disclosed
WO-2002066662-A1 PROCESS FOR THE PREPARATION OF PERILLYL ALCOHOL Eidgenössische Technische Hochschule Zürich (CH) 2002-08-29 — — 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 (4 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-20130079567-A1 ENANTIOPURE BASE-METAL CATALYSTS FOR ASYMMETRIC CATALYSIS AND BIS(IMINO)PYRIDINE IRON ALKYL COMPLEXES FOR CATALYSIS FECH, PARG, DOHH LMNA 2803/4885PTPN1 4700/4885MEN1 656/4885
US-20130281747-A1 COBALT PHOSPHINE ALKYL COMPLEXES FOR THE ASYMMETRIC HYDROGENATION OF ALKENES CPNE4, FTH1, HRH3 LMNA 4175/4885PTPN1 4336/4885MEN1 260/4885
US-12545851-B2 Fragrances with note of lily of the valley TRPA1, CDY1; CDY1B, TMEM109 LMNA 2825/4885PTPN1 254/4885MEN1 3646/4885
US-20240084216-A1 FRAGRANCES WITH NOTE OF LILY OF THE VALLEY DPM1, CD99, SUV39H2 LMNA 2052/4885PTPN1 1210/4885MEN1 3434/4885

“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.