SCHEMBL18461333

SCHEMBL18461333

O=C1c2ccccc2C(=O)N1CCO[SiH3]

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HPGD P15428 3/20 0.57
▸ NPSR1 Q6W5P4 1/20 0.57
▸ RAB9A P51151 8/20 0.56
▸ SMN1; SMN2 Q16637 3/20 0.56
▸ MAPT P10636 1/20 0.56
▸ NPC1 O15118 3/20 0.56
▸ TSHR P16473 2/20 0.56
▸ GLS O94925 1/20 0.55
▸ CASP3 P42574 1/20 0.53
▸ SENP8 Q96LD8 1/20 0.53
▸ SENP7 Q9BQF6 1/20 0.53
▸ SENP6 Q9GZR1 1/20 0.53
▸ ALDH1A1 P00352 2/20 0.51
▸ KMT2A Q03164 2/20 0.51
▸ TDP1 Q9NUW8 1/20 0.51
▸ GLA P06280 1/20 0.50
▸ BRCA1 P38398 1/20 0.50
▸ MAPK1 P28482 1/20 0.50
▸ L3MBTL1 Q9Y468 1/20 0.50
▸ CYP1A2 P05177 1/20 0.50

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
SCHEMBL2743018 0.83 HPGD (0.61) HPGDNPSR1RAB9ASMN1; SMN2MAPT
SCHEMBL25991266 0.83 HPGD (0.61) HPGDNPSR1RAB9ASMN1; SMN2MAPT
SCHEMBL8862746 0.82 GAA (0.60) HPGDNPSR1RAB9ASMN1; SMN2MAPT
SCHEMBL8862940 0.82 GAA (0.60) HPGDNPSR1RAB9ASMN1; SMN2MAPT
SCHEMBL7519591 0.82 GAA (0.60) HPGDNPSR1RAB9ASMN1; SMN2MAPT
SCHEMBL8862856 0.82 GAA (0.60) HPGDNPSR1RAB9ASMN1; SMN2MAPT
SCHEMBL6699936 0.80 GLS (0.71) RAB9ASMN1; SMN2MAPTNPC1GLS
SCHEMBL23791105 0.80 HPGD (0.57) HPGDNPSR1RAB9ASMN1; SMN2MAPT
SCHEMBL3642366 0.80 RAB9A (0.65) HPGDNPSR1RAB9ASMN1; SMN2MAPT
SCHEMBL12029182 0.80 HPGD (0.57) HPGDNPSR1RAB9ASMN1; SMN2MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210363164-A1 Hydroxide-Catalyzed Formation Of Silicon-Oxygen Bonds By Dehydrogenative Coupling Of Hydrosilanes And Alcohols CALIFORNIA INSTITUTE OF TECHNOLOGY 2021-11-25 — — US disclosed
US-10259831-B2 Hydroxide-catalyzed formation of silicon-oxygen bonds by dehydrogenative coupling of hydrosilanes and alcohols CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2019-04-16 — — US disclosed
US-20170029447-A1 HYDROXIDE-CATALYZED FORMATION OF SILICON-OXYGEN BONDS BY DEHYDROGENATIVE COUPLING OF HYDROSILANES AND ALCOHOLS CALIFORNIA INSTITUTE OF TECHNOLOGY 2017-02-02 — — 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-20210363164-A1 Hydroxide-Catalyzed Formation Of Silicon-Oxygen Bonds By Dehydrogenative Coupling Of Hydrosilanes And Alcohols SORD, ADH1A, ADH1C HPGD 407/4885NPSR1 2560/4885RAB9A 3113/4885
US-10259831-B2 Hydroxide-catalyzed formation of silicon-oxygen bonds by dehydrogenative coupling of hydrosilanes and alcohols SORD, ADH1A, ADH1C HPGD 407/4885NPSR1 2560/4885RAB9A 3113/4885
US-20170029447-A1 HYDROXIDE-CATALYZED FORMATION OF SILICON-OXYGEN BONDS BY DEHYDROGENATIVE COUPLING OF HYDROSILANES AND ALCOHOLS SORD, ADH1A, ADH1C HPGD 407/4885NPSR1 2560/4885RAB9A 3113/4885

“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.

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