SCHEMBL704384

SCHEMBL704384

C[Si](C)(Br)c1ccccc1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 1/20 0.44
ESR2 Q92731 1/20 0.44
MAPT P10636 1/20 0.39
NR1H2 P55055 2/20 0.35
NR1H3 Q13133 2/20 0.35
ALDH1A1 P00352 3/20 0.35
TSHR P16473 3/20 0.35
LMNA P02545 2/20 0.35
TDP1 Q9NUW8 2/20 0.35
ALOX12 P18054 1/20 0.35
ACHE P22303 1/20 0.35
TP53 P04637 2/20 0.32
MAPK1 P28482 2/20 0.32
MEN1 O00255 1/20 0.32
HTT P42858 1/20 0.32
KMT2A Q03164 1/20 0.32
L3MBTL1 Q9Y468 1/20 0.32
NPC1 O15118 3/20 0.32
RAB9A P51151 3/20 0.32
SMN1; SMN2 Q16637 2/20 0.32

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
SCHEMBL706038 0.83 ESR1 (0.32) ESR1ESR2HPGD
SCHEMBL190639 0.81 ESR1 (0.44) ESR1ESR2MAPTNR1H2NR1H3
SCHEMBL704609 0.81 ESR1 (0.44) ESR1ESR2MAPTNR1H2NR1H3
SCHEMBL18108503 0.78 ESR1 (0.38) ESR1ESR2MAPTNR1H2NR1H3
SCHEMBL18108340 0.77 ESR1 (0.41) ESR1ESR2MAPTNR1H2NR1H3
SCHEMBL18108302 0.77 ESR1 (0.41) ESR1ESR2MAPTNR1H2NR1H3
SCHEMBL707750 0.75 ESR1 (0.44) ESR1ESR2MAPTNR1H2NR1H3
SCHEMBL63526 0.73 ESR1 (0.70) ESR1ESR2MAPTNR1H2NR1H3
SCHEMBL439492 0.73 ESR1 (0.48) ESR1ESR2MAPTNR1H2NR1H3
SCHEMBL239179 0.73 ESR1 (0.48) ESR1ESR2MAPTNR1H2NR1H3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3092264-A1 METHOD FOR CAPPING MQ-TYPE SILICONE RESINS Dow Corning Corporation (US) 2016-11-16 EP claimed
US-20160326320-A1 Method For Capping Mq-Type Silicone Resins DOW COMING CORPORATION (US) 2016-11-10 US claimed
WO-2015105931-A1 METHOD FOR CAPPING MQ-TYPE SILICONE RESINS DOW CORNING CORPORATION (US) 2015-07-16 WO claimed
EP-4737444-A1 PROCESSES AND INTERMEDIATES FOR PREPARING MCL1 INHIBITORS Gilead Sciences, Inc. (US) 2026-05-06 EP disclosed
US-12410146-B2 Processes and intermediates for preparing MCL1 inhibitors GILEAD SCIENCES, INC. (US) 2025-09-09 US disclosed
US-20250179004-A1 PROCESSES AND INTERMEDIATES FOR PREPARING MCL1 INHIBITORS GILEAD SCIENCES, INC. 2025-06-05 US disclosed
CN-114787139-B Methods and intermediates for preparing MCL1 inhibitors 吉利德科学公司 2025-03-11 CN disclosed
US-12202782-B2 Processes and intermediates for preparing MCL1 inhibitors GILEAD SCIENCES, INC. (US) 2025-01-21 US disclosed
EP-4484435-A2 PROCESSES AND INTERMEDIATES FOR PREPARING MCL1 INHIBITORS Gilead Sciences, Inc. (US) 2025-01-01 EP disclosed
EP-4065567-B1 PROCESSES AND INTERMEDIATES FOR PREPARING MCL1 INHIBITORS GILEAD SCIENCES INC (US) 2024-09-11 EP disclosed
WO-2024081372-A1 PROCESSES FOR THE PREPARATION OF THE AGENT-LINKER CONJUGATE CL2A-SN-38 AND THE IMMUNOCONJUGATES SACITUZUMAB GOVITECAN AND LABETUZUMAB GOVETICAN GILEAD SCIENCES, INC. (US) 2024-04-18 WO disclosed
US-4182709-A Manufacture of semi-synthetic penicillin antibiotics GLAXO GROUP LIMITED (GB) 1980-01-08 US disclosed
US-4160863-A ANTIBIOTIC BRISTOL-MYERS COMPANY (US) 1979-07-10 US disclosed
US-4113591-A BROMINATION IN PRESENCE OF ULTRAVIOLET RADIATION, VISIBLE LIGHT, OR GAMMA RAYS GLAXO LABORATORIES LIMITED (GB) 1978-09-12 US disclosed
US-4066657-A ANTIBACTERIAL AGENTS FOR ANIMAL FEED SUPPLEMENTS PFIZER INC. (US) 1978-01-03 US disclosed
US-4036846-A ANTIBACTERIAL PFIZER INC. (US) 1977-07-19 US disclosed
US-4031077-A Antibacterial 3-phosphono penams PFIZER INC. (US) 1977-06-21 US disclosed
US-3994939-A BACTERICIDES PFIZER INC. (US) 1976-11-30 US disclosed
US-3943123-A ANTIBIOTIC KONINKLIJKE NEDERLANDSCHE GIST-EN SPIRITUSFABRIEK N.V. (NL) 1976-03-09 US disclosed
US-3935342-A POLYMERIZATION WITH AN UNSATURATED SILYL MONOMER MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DT) 1976-01-27 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-12410146-B2 Processes and intermediates for preparing MCL1 inhibitors MCL1, BAK1, BCL3 ESR1 4558/4885ESR2 4681/4885MAPT 3023/4885
US-12202782-B2 Processes and intermediates for preparing MCL1 inhibitors MCL1, BCL3, XIAP ESR1 4273/4885ESR2 4077/4885MAPT 3861/4885
US-20250179004-A1 PROCESSES AND INTERMEDIATES FOR PREPARING MCL1 INHIBITORS MCL1, BCL3, XIAP ESR1 4273/4885ESR2 4077/4885MAPT 3861/4885

“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.