SCHEMBL2805987

SCHEMBL2805987

CCOC(=O)C(C)Oc1ccccc1

nearest known ligand 0.72

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.72
L3MBTL1 Q9Y468 1/20 0.72
ALDH1A1 P00352 2/20 0.57
TDP1 Q9NUW8 2/20 0.57
TSHR P16473 2/20 0.57
MAPK1 P28482 1/20 0.57
KMT2A Q03164 3/20 0.57
MEN1 O00255 2/20 0.57
SMN1; SMN2 Q16637 1/20 0.57
MAPT P10636 2/20 0.56
CYP1A2 P05177 1/20 0.51
GAA P10253 1/20 0.51
CYP2C9 P11712 1/20 0.51
PKM P14618 1/20 0.51
CYP2C19 P33261 1/20 0.51
MTNR1A P48039 1/20 0.51
MTNR1B P49286 1/20 0.51
PIN1 Q13526 1/20 0.50
TP53 P04637 2/20 0.49
ALOX15 P16050 1/20 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
SCHEMBL17901029 1.00 LMNA (0.72) LMNAL3MBTL1ALDH1A1TDP1TSHR
SCHEMBL16673235 0.86 LMNA (0.56) LMNAL3MBTL1ALDH1A1TDP1TSHR
SCHEMBL11548487 0.85 L3MBTL1 (0.63) LMNAL3MBTL1ALDH1A1TDP1TSHR
SCHEMBL18562096 0.85 LMNA (0.63) LMNAL3MBTL1ALDH1A1TDP1TSHR
SCHEMBL5205374 0.85 LMNA (0.63) LMNAL3MBTL1ALDH1A1TDP1TSHR
SCHEMBL9857703 0.85 LMNA (0.63) LMNAL3MBTL1ALDH1A1TDP1TSHR
SCHEMBL9063261 0.85 LMNA (0.63) LMNAL3MBTL1ALDH1A1TDP1TSHR
SCHEMBL25437242 0.85 LMNA (0.55) LMNAL3MBTL1ALDH1A1TDP1TSHR
SCHEMBL9367416 0.85 LMNA (1.00) LMNAL3MBTL1ALDH1A1MAPT
SCHEMBL9621415 0.85 LMNA (1.00) LMNAL3MBTL1ALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109362781-B Bactericide for net cage culture of whitmania pigra 浙江海洋大学 2020-10-16 CN claimed
CN-102558087-A Method for combining high quality fenoxaprop-p-ethyl JIANGSU TIANRONG GROUP CO LTD 2012-07-11 CN claimed
CN-119684070-A HFIP power assisting C (sp3) Direct methylation method of-H bond and application thereof 西南大学 2025-03-25 CN disclosed
CN-117645540-A Preparation method of chlorophenoxycarboxylate 山东润博生物科技有限公司 2024-03-05 CN disclosed
CN-117362166-A Preparation method of R- (+) -2- (4-hydroxyphenoxy) propionic acid 上海筑裕新材料科技有限公司 2024-01-09 CN disclosed
EP-3490705-B1 CATALYSTS FOR MAKING ACRYLIC ACID FROM LACTIC ACID OR ITS DERIVATIVES IN LIQUID PHASE PROCTER & GAMBLE (US) 2023-08-30 EP disclosed
US-20220204455-A1 A PROCESS FOR THE SYNTHESIS OF LOFEXIDINE PROCOS S.P.A. (IT) 2022-06-30 US disclosed
CN-109415290-B Method for producing acrylic acid from lactic acid or derivatives thereof in liquid phase 宝洁公司 2022-03-08 CN disclosed
CN-109475848-B Catalyst for preparing acrylic acid from lactic acid or its derivative in liquid phase 宝洁公司 2021-11-19 CN disclosed
US-11078150-B2 Preparation method for chlorophenoxycarboxylate SHANDONG RAINBOW BIOTECH CO., LTD. (CN) 2021-08-03 US disclosed
US-11034641-B2 Methods of making acrylic acid from lactic acid or its derivatives in liquid phase THE PROCTER & GAMBLE COMPANY (US) 2021-06-15 US disclosed
EP-1026149-A1 AMIDOCARBOXYLIC ACID DERIVATIVES Sankyo Company Limited (JP) 2000-08-09 EP disclosed
US-5900485-A Methods for the manufacture of neofazodone APOTEX, INC. (CA) 1999-05-04 US disclosed
EP-0712388-A1 USE OF PHENOLS AND PHENOL DERIVATES AS MEDICAMENTS WITH FIBRINOGEN-REDUCING EFFECT Roche Diagnostics GmbH (DE) 1996-05-22 EP disclosed
WO-1995005358-A1 USE OF PHENOLS AND PHENOL DERIVATES AS MEDICAMENTS WITH FIBRINOGEN-REDUCING EFFECT BOEHRINGER MANNHEIM GMBH (DE) 1995-02-23 WO disclosed
CN-1017428-B HETEROCYCLIC COMPOUNDS ICI PLC (GB) 1992-07-15 CN disclosed
EP-0077662-B1 PREPARATION OF NITROARYLACETIC ACID ESTERS AND DERIVATIVES THEREOF ETHYL CORPORATION (US) 1985-10-02 EP disclosed
EP-0077662-A1 Preparation of nitroarylacetic acid esters and derivatives thereof ETHYL CORPORATION (US) 1983-04-27 EP disclosed
US-4169720-A 2-[4-(4-Chlorophenoxymethyl)-phenoxy]-propionic acid compounds as herbicides CELAMERCK GMBH & CO. KG (DE) 1979-10-02 US disclosed
US-4105790-A ANTICOAGULANTS IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1978-08-08 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-11078150-B2 Preparation method for chlorophenoxycarboxylate CBLB, CBL, CBLC LMNA 2077/4885L3MBTL1 754/4885ALDH1A1 1381/4885
US-20220204455-A1 A PROCESS FOR THE SYNTHESIS OF LOFEXIDINE LOX, SLC6A9, CYP2C9 LMNA 3061/4885L3MBTL1 3689/4885ALDH1A1 1927/4885

“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.