SCHEMBL547153

SCHEMBL547153

C=CC(=O)c1ccc(OC)c(OC)c1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.63
CYP3A4 P08684 1/20 0.63
CYP2C9 P11712 1/20 0.63
TSHR P16473 1/20 0.63
CYP2C19 P33261 1/20 0.63
ABCG2 Q9UNQ0 6/20 0.63
CA12 O43570 1/20 0.61
CA1 P00915 1/20 0.61
CA2 P00918 1/20 0.61
CA4 P22748 1/20 0.61
CA6 P23280 1/20 0.61
CA7 P43166 1/20 0.61
TPMT P51580 1/20 0.61
CA9 Q16790 1/20 0.61
CA14 Q9ULX7 1/20 0.61
MAPT P10636 5/20 0.61
LMNA P02545 3/20 0.61
TNFRSF1A P19438 2/20 0.58
ABCB1 P08183 1/20 0.58
MEN1 O00255 3/20 0.55

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
SCHEMBL30307376 1.00 CYP1A2 (0.63) CYP1A2CYP3A4CYP2C9TSHRCYP2C19
SCHEMBL14903561 0.89 TSHR (0.67) CYP1A2CYP3A4CYP2C9TSHRCYP2C19
SCHEMBL12963322 0.87 TSHR (0.68) TSHRABCG2MAPTLMNAMEN1
SCHEMBL19632973 0.86 ABCG2 (0.47) CYP1A2CYP3A4CYP2C9TSHRCYP2C19
SCHEMBL3751049 0.86 SLC22A6 (0.66) CYP1A2ABCG2MEN1KMT2A
SCHEMBL28643734 0.86 TUBB1 (0.55) ABCG2MEN1KMT2AALDH1A1
SCHEMBL1824154 0.84 CYP1A2 (0.58) CYP1A2CYP3A4CYP2C9TSHRCYP2C19
SCHEMBL4895137 0.84 ALDH1A1 (0.49) CYP1A2CYP3A4CYP2C9TSHRCYP2C19
SCHEMBL20007220 0.84 ABCG2 (0.49) CYP1A2CYP3A4CYP2C19ABCG2MAPT
SCHEMBL20007006 0.84 HTT (0.65) CYP1A2CYP3A4CYP2C9TSHRCYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7875285-B1 n acrylic ester polymer including a drug having anovercoating of a different acrylic ester polymer having a glass transition temperature of 35-50 degrees C. to control elution of the drug; temperature change morphology of drug polymer to change and increase release; thrombolytic agents; restenosis ADVANCED CARDIOVASCULAR SYSTEMS, INC. (US) 2011-01-25 US claimed
CN-1376660-A Synthesis of substituted trans-cinnamic aldehyde-natural yellow dyestuff from phenylpropyl alkyl derivatives COUNCIL SCIENT IND RES (IN) 2002-10-30 CN claimed
CN-120005686-A Composition comprising lipase and sulfite 诺维信公司 2025-05-16 CN disclosed
CN-110651038-B Composition comprising lipase and sulfite 诺维信公司 2025-02-18 CN disclosed
US-11731953-B2 Methods and compounds for restoring mutant p53 function PMV PHARMACEUTICALS, INC. (US) 2023-08-22 US disclosed
US-11731953-B2 Methods and compounds for restoring mutant p53 function PMV PHARMACEUTICALS, INC. (US) 2023-08-22 US disclosed
US-11731953-B2 Methods and compounds for restoring mutant p53 function PMV PHARMACEUTICALS, INC. (US) 2023-08-22 US disclosed
EP-4168411-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT P53 FUNCTION PMV Pharmaceuticals, Inc. (US) 2023-04-26 EP disclosed
US-20230056253-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION PMV PHARMACEUTICALS, INC. 2023-02-23 US disclosed
US-20230056253-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION PMV PHARMACEUTICALS, INC. 2023-02-23 US disclosed
WO-2021262684-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION PMV PHARMACEUTICALS, INC. (US) 2021-12-30 WO disclosed
CN-1500769-A Process for the solid phase synthesis of aldehydes, ketones, oximes, amines and hydroxamic acid compounds ���µ�˹ҩ�﹫˾ 2004-06-02 CN disclosed
CN-1496999-A Solid phase synthesing method of aldehyde, ketonic, oxime amine and isohydroximic acid compound ���µ�˹ҩ�﹫˾ 2004-05-19 CN disclosed
CN-1132807-C Solid phase synthesis of aldehydes, ketones, oximes, amines and hydroxamic acid compounds RHONE POULENC RORER PHARMA (US) 2003-12-31 CN disclosed
CN-1429202-A Compounds for modulating cell proliferation HSC RES & DEV LTD PARTNERSHIP (CA) 2003-07-09 CN disclosed
CN-1376660-A Synthesis of substituted trans-cinnamic aldehyde-natural yellow dyestuff from phenylpropyl alkyl derivatives COUNCIL SCIENT IND RES (IN) 2002-10-30 CN disclosed
CN-1307553-A Solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and alpha, beta-unsaturated carboxylic acid and aldehyde compounds AVANTIES MEDICINE PRODUCT CO (US) 2001-08-08 CN disclosed
CN-1296493-A Aspartyl dipeptide ester derivatives and sweeteners AJINOMOTO KK (JP) 2001-05-23 CN disclosed
CN-1240418-A Solid phase synthesis of aldehydes, ketones, oximes, amines and hydroxamic acid compounds RHONE POULENC RORER PHARMA (US) 2000-01-05 CN disclosed
US-4788206-A CARDIOVASCULAR DISORDERS, PLATELETS HOFFMANN-LA ROCHE INC. (US) 1988-11-29 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-20230056253-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION TP53, TP53BP1, HRAS CYP1A2 4522/4885CYP3A4 4459/4885CYP2C9 4830/4885
US-11731953-B2 Methods and compounds for restoring mutant p53 function TP53, TP53BP1, HRAS CYP1A2 4522/4885CYP3A4 4459/4885CYP2C9 4830/4885

“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.