SCHEMBL1452142

SCHEMBL1452142

CC1=Cc2ccccc2C1[Ge](C)(C)C1C(C)=Cc2ccccc21

nearest known ligand 0.33

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.31
TSHR P16473 1/20 0.31
ALOX12 P18054 1/20 0.31
ACHE P22303 1/20 0.31

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
SCHEMBL8149969 0.79 LMNA (0.35) LMNATSHRALOX12ACHE
Fluoride Ion SCHEMBL27948797 0.74 LMNA (0.31) LMNATSHRALOX12ACHE
SCHEMBL28743130 0.74 LMNA (0.31) LMNATSHRALOX12ACHE
Hydrochloric Acid SCHEMBL4089359 0.74 CYP11B1 (0.33) LMNATSHRALOX12ACHE
Iodide SCHEMBL27477264 0.74 LMNA (0.31) LMNATSHRALOX12ACHE
Bromide SCHEMBL27933161 0.74 HTR2A (0.33) LMNATSHRALOX12ACHE
SCHEMBL29458545 0.73 DRD2 (0.41) LMNATSHRALOX12ACHE
SCHEMBL251288 0.73 DRD2 (0.41) LMNATSHRALOX12ACHE
SCHEMBL813995 0.73 LMNA (0.33) LMNATSHRALOX12ACHE
SCHEMBL5090888 0.73 LMNA (0.33) LMNATSHRALOX12ACHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7910783-B2 Preparation of substituted bridged indenyl and related ligands EXXONMOBIL CHEMICAL PATENTS INC. (US) 2011-03-22 US disclosed
EP-1971621-A1 PREPARATION OF SUBSTITUTED BRIDGED INDENYL AND RELATED LIGANDS ExxonMobil Chemical Patents Inc. (US) 2008-09-24 EP disclosed
WO-2007070045-A1 PREPARATION OF SUBSTITUTED BRIDGED INDENYL AND RELATED LIGANDS EXXONMOBIL CHEMICAL PATENTS, INC. (US) 2007-06-21 WO disclosed
US-20070135596-A1 Preparation of substituted bridged indenyl and related ligands EXXONMOBIL CHEMICAL PATENTS INC. 2007-06-14 US disclosed
WO-1996019488-A1 A METHOD OF PREPARING HIGH PURITY RACEMIC METALLOCENE ALKYLS AND USE THEREOF EXXON CHEMICAL PATENTS INC. (US) 1996-06-27 WO 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 (1 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-20070135596-A1 Preparation of substituted bridged indenyl and related ligands SP1, TTL, TTLL12 LMNA 1155/4885TSHR 47/4885ALOX12 4483/4885

“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.