SCHEMBL3848321

SCHEMBL3848321

C[C@H](Oc1ccc(O)cc1)C(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.67
GAA P10253 1/20 0.67
CYP2C9 P11712 1/20 0.67
PKM P14618 1/20 0.67
CYP2C19 P33261 1/20 0.67
TDP1 Q9NUW8 1/20 0.61
ALDH2 P05091 1/20 0.52
PPARG P37231 2/20 0.51
PPARA Q07869 2/20 0.51
SMN1; SMN2 Q16637 1/20 0.50
NPSR1 Q6W5P4 1/20 0.50
TBXAS1 P24557 2/20 0.48
KMT2A Q03164 2/20 0.47
TAS1R3 Q7RTX0 1/20 0.47
TAS1R1 Q7RTX1 1/20 0.47
TAS1R2 Q8TE23 1/20 0.47
KDM4E B2RXH2 1/20 0.46
ALDH1A1 P00352 1/20 0.46
HPGD P15428 1/20 0.46
ADRB3 P13945 3/20 0.44

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
SCHEMBL637870 1.00 CYP1A2 (0.67) CYP1A2GAACYP2C9PKMCYP2C19
SCHEMBL502837 1.00 CYP1A2 (0.67) CYP1A2GAACYP2C9PKMCYP2C19
SCHEMBL28971374 0.98 CYP1A2 (0.65) CYP1A2GAACYP2C9PKMCYP2C19
SCHEMBL28971376 0.98 CYP1A2 (0.65) CYP1A2GAACYP2C9PKMCYP2C19
SCHEMBL30301175 0.98 CYP1A2 (0.65) CYP1A2GAACYP2C9PKMCYP2C19
SCHEMBL5597362 0.98 CYP1A2 (0.65) CYP1A2GAACYP2C9PKMCYP2C19
SCHEMBL10706539 0.98 CYP1A2 (0.65) CYP1A2GAACYP2C9PKMCYP2C19
SCHEMBL1984871 0.98 CYP1A2 (0.65) CYP1A2GAACYP2C9PKMCYP2C19
Hydrochloric Acid SCHEMBL3128493 0.98 CYP1A2 (0.65) CYP1A2GAACYP2C9PKMCYP2C19
Hydrochloric Acid SCHEMBL3128499 0.98 CYP1A2 (0.65) CYP1A2GAACYP2C9PKMCYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109929822-B Aspergillus oryzae lipase mutant and application thereof 浙江工业大学 2021-04-06 CN claimed
CN-106187678-B The preparation method of one kind chloro- 1,2- propylene glycol of (R) -3- 上海科利生物医药有限公司 2019-03-08 CN claimed
CN-108821962-A A method of synthesis herbicide clodinafop-propargyl key intermediate 浙江工业大学 2018-11-16 CN claimed
CN-106187678-A A kind of preparation method of (R) 3 chlorine 1,2 propylene glycol 上海科利生物医药有限公司 2016-12-07 CN claimed
US-20090326258-A1 PROCESS FOR THE PREPARATION OF SUBSTITUTED TETRALIN AND SUBSTITUTED INDANE DERIVATIVES ZHAN-PLASKET FAN 2009-12-31 US claimed
US-20080096962-A1 Process for the Preparation of Substituted Tetralin and Substituted Indane Derivatives JANSSEN PHARMACEUTICA N.V. (BE) 2008-04-24 US claimed
CN-101018766-A Process for preparing substituted tetralin and substituted indane derivatives JANSSEN PHARMACEUTICA NV (BE) 2007-08-15 CN claimed
EP-1745016-A1 PROCESS FOR THE PREPARATION OF SUBSTITUTED TETRALIN AND SUBSTITUTED INDANE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 2007-01-24 EP claimed
WO-2005105737-A1 PROCESS FOR THE PREPARATION OF SUBSTITUTED TETRALIN AND SUBSTITUTED INDANE DERIVATIVES JANSSEN PHARMACEUTICA, N.V. (BE) 2005-11-10 WO claimed
US-20050240049-A1 Process for the preparation of substituted tetralin and substituted indane derivatives JANSSEN PHARMACEUTICA N.V. (BE) 2005-10-27 US claimed
CN-1179937-C Process for prep. of (R)-and (S)-2-(4-hydroxy-pheneyloxy) propionic acid and/or its alkyl ester mixture �����ɷ� 2004-12-15 CN claimed
CN-1332147-A Process for prep. of (R)-and (S)-2-(4-hydroxy-pheneyloxy) propionic acid and/or its alkyl ester mixture BASF AG (DE) 2002-01-23 CN claimed
EP-0701547-B1 THE PREPARATION OF MIXTURES OF (R)- AND (S)-2-(4-ALKANOYLPHENOXY)- OR (R)- AND (S)-2-(4-AROYLPHENOXY)PROPIONIC ESTERS BASF AG (DE) 1998-07-29 EP claimed
CN-1124954-A Process for preparing -and- (S) -2- (4-alkanoylphenoxy) -or -and- (S) -2- (4-aroylphenoxy) propionate mixture BASF AG (DE) 1996-06-19 CN claimed
EP-0701547-A1 THE PREPARATION OF MIXTURES OF (R)- AND (S)-2-(4-ALKANOYLPHENOXY)- OR (R)- AND (S)-2-(4-AROYLPHENOXY)PROPIONIC ESTERS BASF AKTIENGESELLSCHAFT (DE) 1996-03-20 EP claimed
WO-1994027950-A1 THE PREPARATION OF MIXTURES OF (R)- AND (S)-2-(4-ALKANOYLPHENOXY)- OR (R)- AND (S)-2-(4-AROYLPHENOXY)PROPIONIC ESTERS BASF AKTIENGESELLSCHAFT (DE) 1994-12-08 WO claimed
CN-112812002-B Preparation method of (R) - (+) -2- (4-hydroxyphenoxy) propionic acid 锦州三丰科技有限公司 2022-12-09 CN disclosed
CN-112812002-A Preparation method of (R) - (+) -2- (4-hydroxyphenoxy) propionic acid 锦州三丰科技有限公司 2021-05-18 CN disclosed
US-5296363-A Oxidizing 2-phenoxypropionic acid under aerobic conditions in presence of soil inhabiting Streptomycetes bacteria or fungus BASE AKTIENGESELLSCHAFT (DE) 1994-03-22 US disclosed
US-4760172-A Process for the preparation of optically active 2-(4-methoxyphenoxy) propionic acid THE DOW CHEMICAL COMPANY (US) 1988-07-26 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 (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-20090326258-A1 PROCESS FOR THE PREPARATION OF SUBSTITUTED TETRALIN AND SUBSTITUTED INDANE DERIVATIVES TDO2, ITPA, TTI2 CYP1A2 59/4885GAA 2523/4885CYP2C9 199/4885
US-20080096962-A1 Process for the Preparation of Substituted Tetralin and Substituted Indane Derivatives TDO2, ITPA, TTI2 CYP1A2 59/4885GAA 2523/4885CYP2C9 199/4885
US-20050240049-A1 Process for the preparation of substituted tetralin and substituted indane derivatives TDO2, TTI2, ITPA CYP1A2 54/4885GAA 2579/4885CYP2C9 183/4885

“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.