SCHEMBL112610

SCHEMBL112610

C[Si](C)(C)CCOCn1cnc2ccc(Br)cc21

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DGAT1 O75907 3/20 0.40
BRD4 O60885 5/20 0.39
IDO1 P14902 1/20 0.37
LMNA P02545 2/20 0.37
MCL1 Q07820 1/20 0.36
NPM1 P06748 1/20 0.36
ALK Q9UM73 1/20 0.36
CREBBP Q92793 1/20 0.36
SMN1; SMN2 Q16637 2/20 0.35
MTNR1A P48039 1/20 0.35
MTNR1B P49286 1/20 0.35
GLP1R P43220 1/20 0.35
FABP4 P15090 1/20 0.34
MEN1 O00255 1/20 0.34
KMT2A Q03164 1/20 0.34
NPC1 O15118 2/20 0.33
RAB9A P51151 2/20 0.33
MAPT P10636 1/20 0.33
NFKB1 P19838 1/20 0.33
NFKB2 Q00653 1/20 0.33

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
SCHEMBL1271910 0.89 NPC1 (0.41) DGAT1BRD4LMNAMCL1CREBBP
SCHEMBL22900564 0.84 MAPT (0.41) DGAT1BRD4LMNACREBBPSMN1; SMN2
SCHEMBL25510725 0.83 BRD4 (0.36) BRD4IDO1LMNAMCL1NPM1
SCHEMBL38657054 0.82 MCL1 (0.54) DGAT1BRD4LMNAMCL1CREBBP
SCHEMBL6041830 0.82 BRD4 (0.39) DGAT1BRD4LMNACREBBPSMN1; SMN2
SCHEMBL22524619 0.82 BRD4 (0.36) DGAT1BRD4LMNACREBBPSMN1; SMN2
SCHEMBL6041792 0.82 BRD4 (0.36) DGAT1BRD4LMNACREBBPSMN1; SMN2
SCHEMBL30040753 0.82 BRD4 (0.39) DGAT1BRD4LMNACREBBPSMN1; SMN2
SCHEMBL23242636 0.81 MTNR1A (0.36) DGAT1BRD4LMNACREBBPSMN1; SMN2
Hydrochloric Acid SCHEMBL30323076 0.81 BRD4 (0.36) DGAT1BRD4LMNACREBBPSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12459920-B2 Targeted protein degradation MONTE ROSA THERAPEUTICS AG (CH) 2025-11-04 US disclosed
CN-119775261-A Collagen 1 translation inhibitors and methods of use thereof 艾尼莫生物科技公司 2025-04-08 CN disclosed
WO-2025024521-A1 SUBSTITUTED PIPERIDINEDIONES FOR TARGETED PROTEIN DEGRADATION MONTE ROSA THERAPEUTICS, INC. (US) 2025-01-30 WO disclosed
CN-115427404-B Collagen 1 translation inhibitors and methods of use thereof 艾尼莫生物科技公司 2024-12-13 CN disclosed
EP-4430047-A1 PLATELET-DERIVED GROWTH FACTOR RECEPTOR (PDGFR) ALPHA INHIBITORS AND USES THEREOF Progentos Therapeutics, Inc. (US) 2024-09-18 EP disclosed
EP-4408837-A1 BENZIMIDAZOLE AND AZABENZIMIDAZOLE IL-17 INHIBITOR COMPOUNDS JANSSEN Pharmaceutica NV (BE) 2024-08-07 EP disclosed
EP-4408530-A1 BENZIMIDAZOLES AS MODULATORS OF IL-17 Janssen Pharmaceutica NV (BE) 2024-08-07 EP disclosed
CN-118139859-A Benzimidazole and azabenzimidazole IL-17 inhibitor compounds 詹森药业有限公司 2024-06-04 CN disclosed
CN-118119613-A Benzimidazoles as IL-17 modulators 詹森药业有限公司 2024-05-31 CN disclosed
US-20240083897-A1 GCN2 MODULATING COMPOUNDS AND USES THEREOF HIBERCELL, INC. 2024-03-14 US disclosed
CN-111793031-B Aromatic amine compound and application thereof in preparation of AR and BRD4 dual inhibitor and regulator 海创药业股份有限公司 2021-06-22 CN disclosed
CN-111793031-A Aromatic amine compound and application thereof in preparation of AR and BRD4 dual inhibitor and regulator 成都海创药业有限公司 2020-10-20 CN disclosed
WO-2020200209-A1 AROMATIC AMINE COMPOUND AND USE THEREOF IN PREPARATION OF AR AND BRD4 DUAL INHIBITORS AND REGULATORS 成都海创药业有限公司 2020-10-08 WO disclosed
WO-2020200209-A1 AROMATIC AMINE COMPOUND AND USE THEREOF IN PREPARATION OF AR AND BRD4 DUAL INHIBITORS AND REGULATORS 成都海创药业有限公司 2020-10-08 WO disclosed
EP-2424843-B1 IMIDAZOLE DERIVATIVES AND THEIR USE AS MODULATORS OF CYCLIN DEPENDENT KINASES NOVARTIS AG (CH) 2014-03-26 EP disclosed
US-8598217-B2 Imidazole derivatives and their use as modulators of cyclin dependent kinases ASTEX THERAPEUTICS LTD. (GB) 2013-12-03 US disclosed
US-20120101064-A1 IMIDAZOLE DERIVATIVES AND THEIR USE AS MODULATORS OF CYCLIN DEPENDENT KINASES ASTEX THERAPEUTICS LIMITED (GB) 2012-04-26 US disclosed
US-20120101064-A1 IMIDAZOLE DERIVATIVES AND THEIR USE AS MODULATORS OF CYCLIN DEPENDENT KINASES ASTEX THERAPEUTICS LIMITED (GB) 2012-04-26 US disclosed
EP-2424843-A1 IMIDAZOLE DERIVATIVES AND THEIR USE AS MODULATORS OF CYCLIN DEPENDENT KINASES Novartis AG (CH) 2012-03-07 EP disclosed
WO-2010125402-A1 IMIDAZOLE DERIVATIVES AND THEIR USE AS MODULATORS OF CYCLIN DEPENDENT KINASES NOVARTIS AG (CH) 2010-11-04 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 (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-12459920-B2 Targeted protein degradation NEK7, NEK1, RIPK1 DGAT1 3679/4885BRD4 1945/4885IDO1 1477/4885
US-20240083897-A1 GCN2 MODULATING COMPOUNDS AND USES THEREOF EIF2AK4, GCN1, CLN6 DGAT1 565/4885BRD4 2126/4885IDO1 4654/4885
US-20120101064-A1 IMIDAZOLE DERIVATIVES AND THEIR USE AS MODULATORS OF CYCLIN DEPENDENT KINASES CDK3, CCNI, CDK1 DGAT1 4775/4885BRD4 610/4885IDO1 766/4885

“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.