SCHEMBL2379614

SCHEMBL2379614

CCCC[Sn](CCCC)(CCCC)c1cc(OC)ccn1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CCR1 P32246 1/20 0.46
CCR5 P51681 1/20 0.46
CCR8 P51685 1/20 0.46
NOS3 P29474 4/20 0.43
NOS1 P29475 4/20 0.43
NOS2 P35228 4/20 0.43
DYRK1A Q13627 2/20 0.39
PLAU P00749 1/20 0.37
AHR P35869 1/20 0.36
HTR1A P08908 3/20 0.35
ADRA1D P25100 3/20 0.35
ADRA1A P35348 3/20 0.35
ADRA1B P35368 3/20 0.35
RIOK2 Q9BVS4 3/20 0.34
MAPT P10636 1/20 0.34
APOBEC3A P31941 1/20 0.34
NPC1 O15118 1/20 0.34
CYP1A2 P05177 1/20 0.34
CYP2C9 P11712 1/20 0.34
CYP2C19 P33261 1/20 0.34

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
SCHEMBL29693665 1.00 CCR1 (0.46) CCR1CCR5CCR8NOS3NOS1
SCHEMBL30225309 0.82 ATP1A1 (0.33) NPC1CYP1A2CYP2C9CYP2C19RAB9A
SCHEMBL30225298 0.81 HTT (0.37) MAPTCYP1A2CYP2C9CYP2C19RAB9A
SCHEMBL2377916 0.80 PARP15 (0.36) CYP2C9
SCHEMBL2380155 0.79 CFTR (0.38)
SCHEMBL29851063 0.78 KDM4E (0.43) CCR1CCR5CCR8NOS3NOS1
SCHEMBL1671463 0.78 KDM4E (0.43) CCR1CCR5CCR8NOS3NOS1
SCHEMBL23124290 0.77 TLR8 (0.36) CCR1CCR5CCR8NOS3NOS1
SCHEMBL29929888 0.77 ALDH1A1 (0.37) CCR1NOS1NOS2MAPTNPC1
SCHEMBL16584984 0.77 TLR8 (0.32) SMN1; 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 58 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4142732-B1 METHODS OF USE FOR PYRIMIDINES AS FERROPORTIN INHIBITORS GLOBAL BLOOD THERAPEUTICS INC (US) 2026-04-22 EP disclosed
US-12559502-B2 Thieno pyrimidines as ferroportin inhibitors Global Blood Therapeutics, Inc (US) 2026-02-24 US disclosed
US-20250109122-A1 CYCLOALKYL PYRIMIDINES AS FERROPORTIN INHIBITORS GLOBAL BLOOD THERAPEUTICS INC (US) 2025-04-03 US disclosed
WO-2025038863-A1 INDOLE AND PYRROLOYPYRIDINE DERIVATIVES AS GPR17 MODULATORS BIOGEN MA INC. (US) 2025-02-20 WO disclosed
US-12202817-B2 Cycloalkyl pyrimidines as ferroportin inhibitors GLOBAL BLOOD THERAPEUTICS, INC. (US) 2025-01-21 US disclosed
US-12084437-B2 Halo-substituted piperidines as orexin receptor modulators ASTRAZENECA AB (SE) 2024-09-10 US disclosed
US-20240140932-A1 CYCLOALKYL PYRIMIDINES AS FERROPORTIN INHIBITORS GLOBAL BLOOD THERAPEUTICS INC (US) 2024-05-02 US disclosed
US-11935803-B2 Resin composition, laminate, semiconductor wafer with resin composition layer, substrate for mounting semiconductor with resin composition layer and semiconductor device MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2024-03-19 US disclosed
US-20240025890-A1 HEPATITIS B CORE PROTEIN MODULATORS ASSEMBLY BIOSCIENCES INC (US) 2024-01-25 US disclosed
US-11814376-B2 Hepatitis b core protein modulators ASSEMBLY BIOSCIENCES, INC. (US) 2023-11-14 US disclosed
EP-2550273-A2 PYRROLOPYRAZINE KINASE INHIBITORS F. Hoffmann-La Roche AG (CH) 2013-01-30 EP disclosed
US-20110319426-A1 Substituted Isoindoles ASTRAZENECA AB (SE) 2011-12-29 US disclosed
US-8030500-B2 Substituted isoindoles for the treatment and/or prevention of Aβ- related pathologies ASTRAZENECA AB (SE) 2011-10-04 US disclosed
WO-2011117145-A2 PYRROLOPYRAZINE KINASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2011-09-29 WO disclosed
EP-2367814-A1 NEW COMPOUNDS 578 AstraZeneca AB (SE) 2011-09-28 EP disclosed
US-20110230462-A1 Pyrrolopyrazine Kinase Inhibitors HENDRICKS ROBERT THAN 2011-09-22 US disclosed
US-20100125082-A1 NEW COMPOUNDS 578 ASTRAZENECA AB (SE) 2010-05-20 US disclosed
WO-2010056194-A1 5H-PYRROLO [ 3, 4-B] PYRIDIN DERIVATIVES AND THEIR USE ASTRAZENECA AB (SE) 2010-05-20 WO disclosed
US-20100125081-A1 NEW COMPOUNDS 574 ASTRAZENECA AB (SE) 2010-05-20 US disclosed
WO-2010056196-A1 NEW COMPOUNDS 578 ASTRAZENECA AB (SE) 2010-05-20 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 (11 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-20110230462-A1 Pyrrolopyrazine Kinase Inhibitors SYK, ZAP70, BTK CCR1 3148/4885CCR5 1892/4885CCR8 4345/4885
US-12202817-B2 Cycloalkyl pyrimidines as ferroportin inhibitors HAMP, SLC40A1, FANCI CCR1 940/4885CCR5 496/4885CCR8 1412/4885
US-20100125082-A1 NEW COMPOUNDS 578 PSEN1, PSEN2, BACE1 CCR1 3931/4885CCR5 1200/4885CCR8 2580/4885
US-12559502-B2 Thieno pyrimidines as ferroportin inhibitors HAMP, TFRC, SLC40A1 CCR1 74/4885CCR5 140/4885CCR8 542/4885
US-20100125081-A1 NEW COMPOUNDS 574 PSEN1, PSEN2, BACE1 CCR1 4133/4885CCR5 1210/4885CCR8 4655/4885
US-20240025890-A1 HEPATITIS B CORE PROTEIN MODULATORS HAVCR2, FABP1, MAVS CCR1 2972/4885CCR5 1022/4885CCR8 2105/4885
US-12084437-B2 Halo-substituted piperidines as orexin receptor modulators HCRTR2, HCRTR1, OPRD1 CCR1 1085/4885CCR5 669/4885CCR8 2284/4885
US-20110319426-A1 Substituted Isoindoles PSEN2, PSEN1, SNCA CCR1 4371/4885CCR5 1219/4885CCR8 4690/4885
US-11814376-B2 Hepatitis b core protein modulators HAVCR2, FABP1, MAVS CCR1 2972/4885CCR5 1022/4885CCR8 2105/4885
US-20250109122-A1 CYCLOALKYL PYRIMIDINES AS FERROPORTIN INHIBITORS HAMP, SLC40A1, FANCI CCR1 940/4885CCR5 496/4885CCR8 1412/4885
US-20240140932-A1 CYCLOALKYL PYRIMIDINES AS FERROPORTIN INHIBITORS HAMP, SLC40A1, FANCI CCR1 940/4885CCR5 496/4885CCR8 1412/4885

“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.