SCHEMBL4473876

SCHEMBL4473876

Cc1ccc2cccnc2c1N

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 1.00
CCR1 P32246 4/20 0.60
CCR8 P51685 4/20 0.60
MAPT P10636 4/20 0.60
CCR5 P51681 3/20 0.60
KDM4E B2RXH2 3/20 0.60
HTT P42858 3/20 0.60
MMP2 P08253 2/20 0.60
TSHR P16473 2/20 0.60
SMN1; SMN2 Q16637 2/20 0.60
TDP1 Q9NUW8 2/20 0.60
GMNN O75496 1/20 0.60
TP53 P04637 1/20 0.60
HSP90AA1 P07900 1/20 0.60
CYP3A4 P08684 1/20 0.60
CYP2D6 P10635 1/20 0.60
MMP9 P14780 1/20 0.60
ALOX15 P16050 1/20 0.60
NFKB1 P19838 1/20 0.60
MMP8 P22894 1/20 0.60

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
SCHEMBL8404537 0.81 LMNA (0.68) LMNACCR1CCR8MAPTCCR5
SCHEMBL29989596 0.78 LMNA (0.65) LMNACCR1CCR8MAPTCCR5
SCHEMBL9374479 0.78 LMNA (0.65) LMNACCR1CCR8MAPTCCR5
SCHEMBL18434875 0.78 LMNA (0.64) LMNACCR1CCR8MAPTCCR5
SCHEMBL23954442 0.78 LMNA (0.63) LMNACCR1CCR8MAPTCCR5
SCHEMBL623096 0.78 LMNA (0.63) LMNACCR1CCR8MAPTCCR5
SCHEMBL5546382 0.78 LMNA (0.63) LMNACCR1CCR8MAPTCCR5
SCHEMBL10911576 0.78 LMNA (0.63) LMNACCR1CCR8MAPTCCR5
SCHEMBL22026143 0.78 LMNA (0.63) LMNACCR1CCR8MAPTCCR5
SCHEMBL3070366 0.78 LMNA (0.63) LMNACCR1CCR8MAPTCCR5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102649786-B Preparation method for 2, 4-diamino-5-(8-dimethylamino-7-methyl-5-quinolyl Methyl)-2, 4-(1H and 3H) pyrimidine ZHENGZHOU FUYUAN ANIMAL PHARMACEUTICAL CO LTD 2014-08-27 CN claimed
CN-102649786-A Preparation method for 2, 4-diamino-5-(8-dimethylamino-7-methyl-5-quinolyl Methyl)-2, 4-(1H and 3H) pyrimidine ZHENGZHOU FUYUAN ANIMAL PHARMACEUTICAL CO LTD 2012-08-29 CN claimed
EP-4735453-A1 KRAS MODULATING COMPOUNDS GILEAD SCIENCES, INC. (US) 2026-05-06 EP disclosed
US-20250059208-A1 KRAS MODULATING COMPOUNDS GILEAD SCIENCES, INC. 2025-02-20 US disclosed
WO-2025006704-A1 KRAS MODULATING COMPOUNDS GILEAD SCIENCES, INC. (US) 2025-01-02 WO disclosed
CN-117865886-B N- (quinoline-8-yl) quinoline-8-sulfonamide compound and application thereof 中国药科大学 2024-05-10 CN disclosed
CN-117865886-A N- (quinoline-8-yl) quinoline-8-sulfonamide compound and application thereof 中国药科大学 2024-04-12 CN disclosed
US-20220081412-A1 QUINOLINYL-PYRAZINE-CARBOXAMIDE COMPOUNDS AND USES THEREOF THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2022-03-17 US disclosed
US-20210277003-A1 OGA INHIBITOR COMPOUNDS JANSSEN PHARMACEUTICA NV (BE) 2021-09-09 US disclosed
CN-104903321-B Three ring benzimidazoles are substituted as kinase inhibitor 赛尔维他股份公司 2017-10-24 CN disclosed
US-9745299-B2 Substituted tricyclic benzimidazoles as kinase inhibitors SELVITA SA (PL) 2017-08-29 US disclosed
US-7585859-B2 PDE4B inhibitors and uses therefor PLEXXIKON, INC. (US) 2009-09-08 US disclosed
US-7470794-B2 Preparation and use of ortho-sulfonamido aryl hydroxamic acids as matrix metalloproteinase inhibitors WYETH (US) 2008-12-30 US disclosed
EP-1993154-A1 Electron transporting materials and organic light-emitting devices therewith Yamagata Promotional Organization for Industrial Technology (JP) 2008-11-19 EP disclosed
US-20060041006-A1 PDE4B inhibitors and uses therefor PLEXXIKON, INC. 2006-02-23 US disclosed
US-4761475-A 2,4-diaminopyrimidines substituted with heterobicyclomethyl radicals at the 5 position useful as antibacterials SCHERING-PLOUGH ANIMAL HEALTH CORPORATION 1988-08-02 US disclosed
US-4587342-A 2,4-diamino-(substituted-benzopyran(quinolyl,isoquinoly)methyl)pyrimidines useful as antibacterials SCHERING-PLOUGH ANIMAL HEALTH CORPORATION 1986-05-06 US disclosed
EP-0051879-B1 SUBSTITUTED PYRIMIDINES, THEIR SYNTHESIS AND COMPOSITIONS CONTAINING THEM, THEIR USE IN MEDICINE AND INTERMEDIATES FOR MAKING THEM THE WELLCOME FOUNDATION LIMITED (GB) 1986-02-05 EP disclosed
EP-0051879-A2 Substituted pyrimidines, their synthesis and compositions containing them, their use in medicine and intermediates for making them THE WELLCOME FOUNDATION LIMITED (GB) 1982-05-19 EP disclosed
US-3956420-A CPOLYOLEFIN COMPOSITION FOR ELECTRICAL INSULATIONFERROCENE, 8-SUBSTITUTED QUINOLINE DAINICHI-NIPPON CABLES, LTD. (JA) 1976-05-11 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 (4 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-20220081412-A1 QUINOLINYL-PYRAZINE-CARBOXAMIDE COMPOUNDS AND USES THEREOF HMGB3, HCCS, ACACA LMNA 1772/4885CCR1 477/4885CCR8 1379/4885
US-20210277003-A1 OGA INHIBITOR COMPOUNDS OGA, OGT, GRN LMNA 848/4885CCR1 4729/4885CCR8 4812/4885
US-20060041006-A1 PDE4B inhibitors and uses therefor PDE4B, PDE7B, PDE4A LMNA 2349/4885CCR1 4273/4885CCR8 3580/4885
US-20250059208-A1 KRAS MODULATING COMPOUNDS KRAS, NRAS, HRAS LMNA 3815/4885CCR1 2969/4885CCR8 2748/4885

“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.