SCHEMBL17090793

SCHEMBL17090793

CCCCCCCCCCCCCCCCC[SiH](CCCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCCC

nearest known ligand 0.57

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.57
THRB P10828 1/20 0.57
ALDH1A1 P00352 3/20 0.50
LMNA P02545 2/20 0.50
MEN1 O00255 2/20 0.50
KMT2A Q03164 2/20 0.50
HSD17B10 Q99714 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.44
DNM1 Q05193 6/20 0.42
SLC22A1 O15245 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
SCHEMBL17090805 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1
SCHEMBL17090787 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1
SCHEMBL1033088 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1
SCHEMBL367967 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1
SCHEMBL17090806 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1
SCHEMBL10416490 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1
SCHEMBL10416460 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1
SCHEMBL17090779 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1
SCHEMBL17090843 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1
SCHEMBL475823 1.00 TSHR (0.57) TSHRTHRBALDH1A1LMNAMEN1

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115427464-A Lewis base catalyst and process therefor 埃克森美孚化学专利公司 2022-12-02 CN disclosed
CN-113423742-A Bis (arylphenolate) lewis base catalysts and processes thereof 埃克森美孚化学专利公司 2021-09-21 CN disclosed
CN-113423744-A Lewis base catalyst and process therefor 埃克森美孚化学专利公司 2021-09-21 CN disclosed
CN-112351987-A Non-coordinating anionic activators containing cations with large alkyl groups 埃克森美孚化学专利公司 2021-02-09 CN disclosed
CN-112020491-A Non-coordinating anionic activators containing cations with branched alkyl groups 埃克森美孚化学专利公司 2020-12-01 CN disclosed
US-10730904-B2 Method for liquid-phase synthesis of nucleic acid TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2020-08-04 US disclosed
EP-2921499-B1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACIDS TAKEDA PHARMACEUTICALS CO (JP) 2020-01-22 EP disclosed
US-20190135852-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2019-05-09 US disclosed
US-20150315229-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2015-11-05 US disclosed
EP-2921499-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID Takeda Pharmaceutical Company Limited (JP) 2015-09-23 EP 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-20150315229-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID POLM, POLRMT, RNMT TSHR 495/4885THRB 936/4885ALDH1A1 2399/4885
US-20190135852-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID RNGTT, POLR2H, POLR2E TSHR 551/4885THRB 1506/4885ALDH1A1 1956/4885
US-10730904-B2 Method for liquid-phase synthesis of nucleic acid RNGTT, POLR2H, POLR2E TSHR 411/4885THRB 1249/4885ALDH1A1 1416/4885

“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.