SCHEMBL1059941

SCHEMBL1059941

CC(C)(C)c1ccc(OC[C]=O)cc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.55
APP P05067 1/20 0.47
NR4A2 P43354 1/20 0.46
RXRA P19793 1/20 0.46
RXRB P28702 1/20 0.46
KDM4E B2RXH2 1/20 0.45
CA1 P00915 1/20 0.44
CA2 P00918 1/20 0.44
CA9 Q16790 1/20 0.44
LMNA P02545 4/20 0.43
RAB9A P51151 3/20 0.43
NPC1 O15118 2/20 0.43
MITF O75030 1/20 0.43
TP53 P04637 1/20 0.43
POLB P06746 1/20 0.42
ATM Q13315 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
MAOB P27338 1/20 0.42
AOC3 Q16853 1/20 0.42
HRH3 Q9Y5N1 1/20 0.42

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
SCHEMBL2170360 0.82 CA12 (0.42) KDM4ECA1CA2CA9LMNA
SCHEMBL15845321 0.82 CYP3A4 (0.58) SMN1; SMN2LMNATP53HRH3ALDH1A1
SCHEMBL9501750 0.80 GABRA1 (0.37) SMN1; SMN2RXRARXRBPOLB
SCHEMBL513003 0.80 ALDH1A1 (0.49) CA1CA2CA9MAOBAOC3
SCHEMBL10707563 0.80 ACACB (0.39) SMN1; SMN2KDM4ECA1CA2CA9
SCHEMBL15604421 0.80 SMN1; SMN2 (0.50) SMN1; SMN2APPNR4A2RXRARXRB
SCHEMBL5104116 0.80 SMN1; SMN2 (0.50) SMN1; SMN2APPNR4A2RXRARXRB
SCHEMBL7909459 0.79 SMN1; SMN2 (0.47) SMN1; SMN2APPNR4A2RXRARXRB
SCHEMBL23911695 0.77 SMN1; SMN2 (0.47) SMN1; SMN2APPNR4A2RXRARXRB
SCHEMBL514644 0.77 L3MBTL1 (0.47) LMNANPC1L3MBTL1MAOBMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117924393-A Monomer of 3' -mercapto nucleoside analogue and its synthesis process 天津兴博润生物制药有限公司 2024-04-26 CN claimed
US-20230014840-A1 METHOD FOR PRODUCING OLIGONUCLEIC ACID COMPOUND NIPPON SHINYAKU CO., LTD. (JP) 2023-01-19 US claimed
US-20230018780-A1 METHOD FOR PRODUCING OLIGONUCLEIC ACID COMPOUND NIPPON SHINYAKU CO., LTD. (JP) 2023-01-19 US claimed
CN-115397831-A Compositions comprising nucleic acid oligomers 住友化学株式会社 2022-11-25 CN claimed
CN-114981280-A Method for producing oligonucleotide compound 日本新药株式会社 2022-08-30 CN claimed
CN-114981281-A Method for producing oligonucleotide compound 日本新药株式会社 2022-08-30 CN claimed
US-20210206809-A1 PEPTIDE NUCLEIC ACID (PNA) MONOMERS WITH AN ORTHOGONALLY PROTECTED ESTER MOIETY VERA THERAPEUTICS INC (US) 2021-07-08 US claimed
WO-2021095875-A1 METHOD FOR PRODUCING OLIGONUCLEIC ACID COMPOUND 日本新薬株式会社 2021-05-20 WO claimed
WO-2021095874-A1 METHOD FOR PRODUCING OLIGONUCLEIC ACID COMPOUND 日本新薬株式会社 2021-05-20 WO claimed
US-20200318109-A1 LNA-G Process F. HOFFMANN-LA ROCHE AG (CH) 2020-10-08 US claimed
US-6750335-B2 NUCLEOSIDE FOR USE IN THE GENERATION OF PREFERENTIAL OLIGONUCEOTIDES NIGU CHEMIE GMBH (DE) 2004-06-15 US claimed
EP-1006121-B1 A universal polymer support for the synthesis of oligonucleotides COUNCIL SCIENT IND RES (IN) 2003-05-02 EP claimed
EP-1224198-B1 NUCLEOSIDE DERIVATIVES WITH PHOTOLABILE PROTECTING GROUPS NIGU CHEMIE GMBH (DE) 2003-04-23 EP claimed
US-6541626-B2 Protecting/blocking the exocyclic amino function of purine nucleosides without effecting hydroxyl groups of sugar moieties via forming activated ester ISIS PHARMACEUTICALS, INC. 2003-04-01 US claimed
US-20030022862-A1 Process for selective N-acylation of purine nucleosides ALLAHABAD, UNIVERSITY OF (IN) 2003-01-30 US claimed
WO-2002083702-A1 PROCESS FOR SELECTIVE N-ACYLATION OF PURINE NUCLEOSIDES ISIS PHARMACEUTICALS, INC. (US) 2002-10-24 WO claimed
US-6075143-A USEFUL FOR FORMING PEPTIDE NUCLEIC ACIDS OR HYBRID OF PEPTIDE NUCLEIC ACIDS AND DEOXYNUCLEIC ACID HOECHST AKTIENGESELLSCHAFT (DE) 2000-06-13 US claimed
EP-1006121-A1 A universal polymer support for the synthesis of oligonucleotides Council of Scientific and Industrial Research (IN) 2000-06-07 EP claimed
US-5817811-A AMIDATION OF THE CORRESPOND ESTERIFIED AMINE COMPOUND WITH A CARBOXYLATED NUCLEOTIDE BASE HOECHST AKTIENGESELLSCHAFT (DE) 1998-10-06 US claimed
EP-0672661-A1 Substituted N-ethyl-glycinderivatives for the preparation of PNA and PNA-/DNA hybrides HOECHST AKTIENGESELLSCHAFT (DE) 1995-09-20 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 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-20200318109-A1 LNA-G Process OGG1, DUT, FBL SMN1; SMN2 606/4885APP 2843/4885NR4A2 2722/4885
US-20230018780-A1 METHOD FOR PRODUCING OLIGONUCLEIC ACID COMPOUND POLRMT, POLR2H, POLM SMN1; SMN2 1263/4885APP 2814/4885NR4A2 4469/4885
US-20030022862-A1 Process for selective N-acylation of purine nucleosides PNP, NUDT1, ADAR SMN1; SMN2 1207/4885APP 4466/4885NR4A2 3268/4885
US-20210206809-A1 PEPTIDE NUCLEIC ACID (PNA) MONOMERS WITH AN ORTHOGONALLY PROTECTED ESTER MOIETY AGO2, TARBP1, TPR SMN1; SMN2 840/4885APP 1769/4885NR4A2 2464/4885
US-20230014840-A1 METHOD FOR PRODUCING OLIGONUCLEIC ACID COMPOUND DNASE1, XRN2, FBL SMN1; SMN2 1489/4885APP 2036/4885NR4A2 3618/4885

“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.