Sugi Predict

Sugi Predict / Compounds / SCHEMBL1401422

SCHEMBL1401422

SCHEMBL1401422

COC(C)=Cc1ccc(O)cc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ESR1 P03372 3/20 0.54
▸ ESR2 Q92731 3/20 0.54
▸ KDM4E B2RXH2 3/20 0.52
▸ ALDH1A1 P00352 2/20 0.52
▸ NQO2 P16083 4/20 0.48
▸ PTGS1 P23219 4/20 0.48
▸ PTGS2 P35354 4/20 0.48
▸ CA12 O43570 2/20 0.47
▸ CA1 P00915 2/20 0.47
▸ CA2 P00918 2/20 0.47
▸ CA7 P43166 2/20 0.47
▸ CA9 Q16790 2/20 0.47
▸ CA14 Q9ULX7 2/20 0.47
▸ TYR P14679 1/20 0.47
▸ ABCG2 Q9UNQ0 3/20 0.46
▸ MEN1 O00255 3/20 0.43
▸ KMT2A Q03164 3/20 0.43
▸ THRB P10828 1/20 0.43
▸ CISD1 Q9NZ45 1/20 0.43
▸ MIF P14174 1/20 0.43

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
SCHEMBL29137843 0.80 ALDH1A1 (0.59) KDM4EALDH1A1NQO2PTGS1PTGS2
SCHEMBL14006881 0.80 TRPA1 (0.50) ALDH1A1PTGS1PTGS2MEN1KMT2A
SCHEMBL7990626 0.79 ALDH1A1 (0.50) ALDH1A1MEN1KMT2AMAPTNPC1
SCHEMBL9464901 0.79 ESR1 (0.50) ESR1ESR2KDM4EALDH1A1NQO2
SCHEMBL8225802 0.79 ALDH1A1 (0.50) ALDH1A1MEN1KMT2AMAPTNPC1
SCHEMBL28565029 0.77 CA12 (0.51) ESR1ESR2KDM4EALDH1A1NQO2
SCHEMBL11570212 0.77 CA12 (0.51) ESR1ESR2KDM4EALDH1A1NQO2
SCHEMBL1682626 0.77 ABL1 (0.49) KDM4EALDH1A1PTGS1CA12CA2
SCHEMBL276966 0.75 ESR1 (0.62) ESR1ESR2KDM4EALDH1A1NQO2
SCHEMBL9335450 0.75 KDM4E (0.55) ESR1ESR2KDM4EALDH1A1CA12

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
CN-113150287-A Preparation method of cross-linkable fluorine-containing polyphosphazene 北京化工大学 2021-07-23 — — CN claimed
CN-119751221-A A process for preparing high-value chemicals from bamboo 大连龙缘化学有限公司 2025-04-04 — — CN disclosed
CN-116840198-A Eugenol time-resolved fluorescence immunochromatography test strip and preparation method thereof 浙江工商大学 2023-10-03 — — CN disclosed
CN-113150287-B Preparation method of crosslinkable fluorine-containing polyphosphazene 山东玥能新材料科技有限公司 2023-04-21 — — CN disclosed
CN-113150287-A Preparation method of cross-linkable fluorine-containing polyphosphazene 北京化工大学 2021-07-23 — — CN disclosed
US-9585826-B2 Triggerable compositions for two-stage, controlled release of active chemistry KIMBERLY-CLARK WORLDWIDE, INC. (US) 2017-03-07 — — US disclosed
US-20140128827-A1 TRIGGERABLE COMPOSITIONS FOR TWO-STAGE, CONTROLLED RELEASE OF ACTIVE CHEMISTRY KIMBERLY-CLARK WORLDWIDE, INC. (US) 2014-05-08 — — US disclosed
US-20130252292-A1 BIOMASS EXTRACTION PROCESS LIGNOL INNOVATIONS LTD. (CA) 2013-09-26 — — US disclosed
WO-2011101181-A1 PERFUME COMPOSITIONS HENKEL AG & CO. KGAA (DE) 2011-08-25 — — WO disclosed
EP-1661978-B1 Detergent compositions PROCTER & GAMBLE (US) 2011-03-02 — — EP disclosed
EP-1781239-A2 COMPOSITIONS EFFECTIVE IN ALTERING THE PERCEPTION OF MALODOR Patus Ltd (IL) 2007-05-09 — — EP disclosed
US-20070065394-A1 Compositions effective in altering the perception of malodor PATUS LTD. (IL) 2007-03-22 — — US disclosed
EP-1661978-A1 Detergent compositions The Procter and Gamble Company (US) 2006-05-31 — — EP disclosed
EP-1652834-A1 Process for producing salicylic esters KAO CORPORATION (JP) 2006-05-03 — — EP disclosed
WO-2005046632-A9 COMPOSITIONS EFFECTIVE IN ALTERING THE PERCEPTION OF MALODOR PATUS LTD (IL) 2005-09-22 — — WO disclosed
WO-2005046632-A2 COMPOSITIONS EFFECTIVE IN ALTERING THE PERCEPTION OF MALODOR PATUS LTD. (IL) 2005-05-26 — — WO disclosed
US-6660288-B1 Particularly for mosquitoes; tricyclodecenyl allyl ether perfume (Fleuroxene\"); hydrophobicity such that the common logarithm of the octanol-water partition coefficient, log P, of the perfume ingredient is in the range 1.0 to 6.0 QUEST INTERNATIONAL B.V. (NL) 2003-12-09 — — US disclosed
EP-0321155-A2 Ethylenically-unsaturated ethers of alkenyl phenols as reactive diluents for bismaleimides AMOCO CORPORATION (US) 1989-06-21 — — EP disclosed
US-4812511-A FIBER REINFORCED COMPOSITES AMOCO CORPORATION (US) 1989-03-14 — — US disclosed
US-4154769-A Process for the production of 2-alkoxy-4-propen-1-yl-phenols HAARMANN & REIMER GMBH (DE) 1979-05-15 — — 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 (1 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-20140128827-A1 TRIGGERABLE COMPOSITIONS FOR TWO-STAGE, CONTROLLED RELEASE OF ACTIVE CHEMISTRY BCHE, CEL, ACHE ESR1 1869/4885ESR2 1714/4885KDM4E 3072/4885

“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.