SCHEMBL3324155

SCHEMBL3324155

CC(=O)Oc1cc(C)ccc1C

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 2/20 0.62
LMNA P02545 3/20 0.52
TSHR P16473 3/20 0.51
SMN1; SMN2 Q16637 4/20 0.50
TDP1 Q9NUW8 2/20 0.49
GAA P10253 2/20 0.49
HTT P42858 2/20 0.49
CYP2C9 P11712 2/20 0.49
ALDH1A1 P00352 2/20 0.47
RAB9A P51151 2/20 0.47
NPC1 O15118 1/20 0.47
KDM4E B2RXH2 2/20 0.46
TTR P02766 1/20 0.45
CYP1A2 P05177 1/20 0.45
CYP2C8 P10632 1/20 0.45
CHRM1 P11229 1/20 0.45
ADRA1A P35348 1/20 0.45
PPARG P37231 1/20 0.45
HTR2B P41595 1/20 0.45
PPARA Q07869 1/20 0.45

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
SCHEMBL8350024 0.85 TSHR (0.60) ACHELMNATSHRSMN1; SMN2GAA
SCHEMBL10931521 0.85 TSHR (0.53) ACHELMNATSHRSMN1; SMN2TDP1
SCHEMBL21551646 0.85 TSHR (0.53) ACHELMNATSHRSMN1; SMN2TDP1
SCHEMBL12755255 0.83 ACHE (0.62) ACHELMNATSHRTDP1GAA
SCHEMBL21991761 0.83 TSHR (0.56) ACHELMNATSHRSMN1; SMN2TDP1
SCHEMBL1799618 0.83 LMNA (0.52) ACHELMNATSHRSMN1; SMN2GAA
SCHEMBL1317441 0.82 KDM4E (0.69) ACHELMNATSHRSMN1; SMN2TDP1
SCHEMBL4884127 0.82 TSHR (0.47) ACHELMNATSHRSMN1; SMN2TDP1
SCHEMBL18697274 0.82 TSHR (0.50) ACHELMNATSHRSMN1; SMN2TDP1
SCHEMBL13176949 0.82 ACHE (0.61) ACHETSHRSMN1; SMN2GAAHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115872849-A Method for preparing 2, 5-dimethylphenylacetic acid 阜新睿光氟化学有限公司 2023-03-31 CN claimed
CN-110305010-B Preparation method of 2, 5-dimethylphenylacetic acid 江苏中旗科技股份有限公司 2022-05-13 CN claimed
CN-111170851-A Preparation of acetic acid-2, 5-dimethylphenyl ester and 2, 5-dimethylnitrobenzene by one-pot method 蚌埠学院 2020-05-19 CN claimed
CN-110357774-A A method of 2,5- dimethyl phenyl acetic acid is prepared by raw material of 2,5- dimethyl halobenzene 江苏中旗科技股份有限公司 2019-10-22 CN claimed
CN-110305009-A A method of 2,5- dimethyl phenyl acetic acid is synthesized by 2,5- dimethylbenzyl halogen 江苏中旗科技股份有限公司 2019-10-08 CN claimed
US-20250229198-A1 COMPOUNDS FOR SEPARATION OF RARE EARTH ELEMENTS AND S-, P-, D- METALS, METHOD OF SEPARATION, AND USE THEREOF USTAV ORGANICKE CHEMIE A BIOCHEMIE AV CR, V.V.I (CZ) 2025-07-17 US disclosed
US-12268977-B2 Compounds for separation of rare earth elements and s-, p-, d-metals, method of separation, and use thereof USTAV ORGANICKE CHEMIE A BIOCHEMIE AV CR. V.V.I. (CZ) 2025-04-08 US disclosed
CN-111511728-B Compound for separating rare earth elements and s, p, d metals, separation method and use thereof 有机生物化学公司 2023-12-08 CN disclosed
CN-114409664-B Spiro heterocyclic tetrahydropyran compound and preparation method and application thereof 河北威远生物化工有限公司 2023-07-18 CN disclosed
CN-115872849-A Method for preparing 2, 5-dimethylphenylacetic acid 阜新睿光氟化学有限公司 2023-03-31 CN disclosed
CN-110305010-B Preparation method of 2, 5-dimethylphenylacetic acid 江苏中旗科技股份有限公司 2022-05-13 CN disclosed
CN-110305010-B Preparation method of 2, 5-dimethylphenylacetic acid 江苏中旗科技股份有限公司 2022-05-13 CN disclosed
US-6270843-B1 REACTING A SALT COMPRISING ANIONIC FORM OF SUBSTITUENT WITH AN ELECTROPHILIC FLUORINATION AGENT TO PROVIDE AN ELECTROPHILE COMPRISING CATIONIC FORM OF SUBSTITUENT; ELECTROPHILICALLY SUBSTITUTING ELECTROPHILE ON SUBSTRATE AIR PRODUCTS AND CHEMICALS, INC. 2001-08-07 US disclosed
CN-1032134-C Process for preparing 2,2-dimethyl-5-(2,5-dimethyl phenoxy) pentanoic acid GYOGYSZERKUTATO INTEZET (HU) 1996-06-26 CN disclosed
US-5235097-A Reacting halogen terminated diester with alkali salt of 2,5-dimethylphenol EGIS GYOGYSZERGYAR (HU) 1993-08-10 US disclosed
US-5155260-A PROCESS FOR THE PREPARATION OF 2,2-DIMETHYL-5-(2,5-DIMETHYL-PHENOXY)-PENTANOIC ACID, INTERMEDIATES FOR PREPARING THIS COMPOUND AND PROCESS FOR PREPARING THE INTERMEDIATES EGIS GYOGYSZERGYAR (HU) 1992-10-13 US disclosed
CN-1056487-A 2, the preparation method of 2-dimethyl-5-(2, the 5-xylyloxy) valeric acid GYOGYSZERKUTATO INTEZET (HU) 1991-11-27 CN disclosed
EP-0342943-A1 Thermosetting resin composition MITSUI TOATSU CHEMICALS, Inc. (JP) 1989-11-23 EP disclosed
US-4544450-A Electrochemical process for the synthesis of organic compounds ANIC S.P.A. (IT) 1985-10-01 US disclosed
US-4056572-A Method for the manufacture of phenols BASHKIROV ANDREI NIKOLAEVICH 1977-11-01 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-20250229198-A1 COMPOUNDS FOR SEPARATION OF RARE EARTH ELEMENTS AND S-, P-, D- METALS, METHOD OF SEPARATION, AND USE THEREOF SCO2, SOD3, SLC39A3 ACHE 4654/4885LMNA 593/4885TSHR 711/4885
US-12268977-B2 Compounds for separation of rare earth elements and s-, p-, d-metals, method of separation, and use thereof SCLY, SFXN1, PTCD3 ACHE 3623/4885LMNA 2040/4885TSHR 3902/4885

“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.