SCHEMBL10147178

SCHEMBL10147178

CC(C)Cn1ccnc1Br

nearest known ligand 0.42

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
BRD4 O60885 1/20 0.42
POLB P06746 2/20 0.37
ADORA3 P0DMS8 1/20 0.36
ADORA2A P29274 1/20 0.36
ADORA2B P29275 1/20 0.36
ADORA1 P30542 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.34
ALDH1A1 P00352 1/20 0.33
KMT2A Q03164 1/20 0.33
GAA P10253 1/20 0.32
CCNE1 P24864 1/20 0.32
CDK2 P24941 1/20 0.32
KCNH2 Q12809 1/20 0.32
DYRK1A Q13627 1/20 0.32
TLR8 Q9NR97 1/20 0.32
TLR7 Q9NYK1 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
SCHEMBL13510864 0.82 ALDH1A1 (0.34) BRD4POLBSMN1; SMN2ALDH1A1KMT2A
SCHEMBL179780 0.77 KMT2A (0.52) BRD4POLBALDH1A1KMT2A
SCHEMBL4509139 0.76
SCHEMBL10147187 0.75 SMN1; SMN2 (0.53) BRD4POLBSMN1; SMN2KCNH2
SCHEMBL28221636 0.75 BRD4 (0.42) BRD4POLBSMN1; SMN2ALDH1A1KMT2A
SCHEMBL18814685 0.75 TLR8 (0.41) POLBALDH1A1KMT2ATLR8TLR7
SCHEMBL15969910 0.73 BRD4 (0.41) BRD4POLBSMN1; SMN2ALDH1A1KMT2A
SCHEMBL21646212 0.73 BRD4 (0.44) BRD4POLBSMN1; SMN2ALDH1A1KMT2A
Bromide SCHEMBL10795216 0.73 TLR8 (0.50) BRD4POLBADORA2ASMN1; SMN2CCNE1
SCHEMBL2638232 0.73 KCNH2 (0.42) BRD4POLBSMN1; SMN2ALDH1A1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025011533-A1 CARBOXYLIC ACID COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF 上海宇道生物技术有限公司 2025-01-16 WO disclosed
US-20240360120-A1 RAD51 INHIBITORS CYTEIR THERAPEUTICS, INC. 2024-10-31 US disclosed
EP-3938358-B1 RAD51 INHIBITORS CYTEIR THERAPEUTICS INC (US) 2024-10-02 EP disclosed
CN-114072390-B RAD51 inhibitors 赛泰尔治疗公司 2024-06-11 CN disclosed
US-11932636-B2 RAD51 inhibitors CYTEIR THERAPEUTICS, INC. (US) 2024-03-19 US disclosed
US-20220259198-A1 RAD51 INHIBITORS CYTEIR THERAPEUTICS, INC. 2022-08-18 US disclosed
CN-114072390-A RAD51 inhibitors 赛泰尔治疗公司 2022-02-18 CN disclosed
US-11247988-B2 RAD51 inhibitors CYTEIR THERAPEUTICS, INC. (US) 2022-02-15 US disclosed
US-11247988-B2 RAD51 inhibitors CYTEIR THERAPEUTICS, INC. (US) 2022-02-15 US disclosed
US-20200291014-A1 RAD51 INHIBITORS CYTEIR THERAPEUTICS, INC. 2020-09-17 US disclosed
US-9580392-B2 HIV replication inhibiting pyrimidines JANSSEN PHARMACEUTICA NV (BE) 2017-02-28 US disclosed
US-9192577-B2 Pharmaceutical compositions comprising a basic drug compound, a surfactant, and a physiologically tolerable water soluble acid JANSSEN PHARMACEUTICA NV (BE) 2015-11-24 US disclosed
US-20140343006-A1 HIV Replication Inhibiting Pyrimidines JANSSEN PHARMACEUTICA NV (NL) 2014-11-20 US disclosed
US-8828982-B2 Pyrimidine derivatives for the prevention of HIV infection JANSSEN PHARMACEUTICA N.V. (BE) 2014-09-09 US disclosed
US-20120076835-A1 HIV INHIBITING PYRIMIDINES DERIVATIVES GUILLEMONT JEROME EMILE GEORGES (FR) 2012-03-29 US disclosed
US-8080551-B2 HIV inhibiting pyrimidines derivatives JANSSEN PHARMACEUTICA N.V. (BE) 2011-12-20 US disclosed
US-8080551-B2 HIV inhibiting pyrimidines derivatives JANSSEN PHARMACEUTICA N.V. (BE) 2011-12-20 US disclosed
US-20100034810-A1 PYRIMIDINE DERIVATIVES FOR THE PREVENTION OF HIV INFECTION JANSSEN-CILAG (FR) 2010-02-11 US disclosed
US-20070021449-A1 Pyrimidine derivatives for the prevention of hiv infection HEERES JAN 2007-01-25 US disclosed
US-20070021449-A1 Pyrimidine derivatives for the prevention of hiv infection HEERES JAN 2007-01-25 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 (9 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-20140343006-A1 HIV Replication Inhibiting Pyrimidines RRM2B, CCNO, RRM2 BRD4 285/4885POLB 50/4885ADORA3 76/4885
US-11247988-B2 RAD51 inhibitors RAD51, MRE11, RAD54L BRD4 1500/4885POLB 86/4885ADORA3 4657/4885
US-20070021449-A1 Pyrimidine derivatives for the prevention of hiv infection ADORA2B, CYP1B1, DPYD BRD4 679/4885POLB 293/4885ADORA3 5/4885
US-20220259198-A1 RAD51 INHIBITORS RAD51, MRE11, RAD54L BRD4 1500/4885POLB 86/4885ADORA3 4657/4885
US-20120076835-A1 HIV INHIBITING PYRIMIDINES DERIVATIVES TYMS, PNP, DUT BRD4 1067/4885POLB 18/4885ADORA3 226/4885
US-20100034810-A1 PYRIMIDINE DERIVATIVES FOR THE PREVENTION OF HIV INFECTION NOX3, CBR3, CBR1 BRD4 1466/4885POLB 1486/4885ADORA3 19/4885
US-20200291014-A1 RAD51 INHIBITORS RAD51, MRE11, RAD54L BRD4 1500/4885POLB 86/4885ADORA3 4657/4885
US-20240360120-A1 RAD51 INHIBITORS RAD51, MRE11, RAD54L BRD4 1500/4885POLB 86/4885ADORA3 4657/4885
US-11932636-B2 RAD51 inhibitors RAD51, MRE11, RAD54L BRD4 1500/4885POLB 86/4885ADORA3 4657/4885

“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.