SCHEMBL4497365

SCHEMBL4497365

CCN(CC)CCCCNc1ncc(C(=O)Nc2c(C)cccc2C)c(Oc2cccc3c2OC(C)(C)C3)n1

nearest known ligand 0.41

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LCK P06239 2/20 0.41
JAK3 P52333 1/20 0.41
BTK Q06187 1/20 0.41
TNK2 Q07912 1/20 0.41
POLB P06746 2/20 0.40
MAPT P10636 1/20 0.40
PTBP1 P26599 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
KMT2A Q03164 3/20 0.40
NPC1 O15118 2/20 0.39
LMNA P02545 1/20 0.39
FGFR1 P11362 1/20 0.37
MEN1 O00255 1/20 0.37
TSHR P16473 1/20 0.37
HBB P68871 1/20 0.37
ALDH1A1 P00352 1/20 0.37
RAB9A P51151 1/20 0.36

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
SCHEMBL4491071 0.83 LCK (0.56) LCKJAK3BTKTNK2MAPT
SCHEMBL4493798 0.83 LCK (0.47) LCKJAK3BTKTNK2POLB
SCHEMBL4496982 0.79 POLB (0.49) LCKJAK3BTKTNK2POLB
SCHEMBL4484052 0.78 RAD52 (0.45) LCKJAK3BTKTNK2KMT2A
SCHEMBL4480855 0.77 LCK (0.43) LCKJAK3BTKTNK2MAPT
SCHEMBL4484237 0.76 LCK (0.55) LCKJAK3BTKTNK2FGFR1
SCHEMBL4500525 0.76 LCK (0.57) LCKJAK3BTKTNK2FGFR1
SCHEMBL4505318 0.75 LCK (0.60) LCKJAK3BTKTNK2FGFR1
SCHEMBL5686189 0.74 JAK3 (0.49) LCKJAK3BTKTNK2POLB
SCHEMBL4488306 0.74 APP (0.43) LCKJAK3BTKTNK2POLB

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1648464-A1 2-AMINO-4-HYDROXY-5-PYRIMIDINCARBOXAMID DERIVATIVES AND RELATED COMPOUNDS AS T-CELL ACTIVATION INHIBITORS FOR THE TREATMENT OF INFLAMMATIONS AMGEN INC. (US) 2006-04-26 EP claimed
US-20050209221-A1 Substituted heterocyclic compounds and methods of use AMGEN INC. 2005-09-22 US claimed
WO-2005009443-A1 2-AMINO-4-HYDROXY-5-PYRIMIDINECARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF T CELL ACTIVATION FOR THE TREATMENT OF INFLAMMATORY DISEASES AMGEN INC. (US) 2005-02-03 WO claimed
US-7504396-B2 Substituted heterocyclic compounds and methods of use AMGEN INC. (US) 2009-03-17 US disclosed
EP-1648464-A1 2-AMINO-4-HYDROXY-5-PYRIMIDINCARBOXAMID DERIVATIVES AND RELATED COMPOUNDS AS T-CELL ACTIVATION INHIBITORS FOR THE TREATMENT OF INFLAMMATIONS AMGEN INC. (US) 2006-04-26 EP disclosed
US-20050209221-A1 Substituted heterocyclic compounds and methods of use AMGEN INC. 2005-09-22 US disclosed
WO-2005009443-A1 2-AMINO-4-HYDROXY-5-PYRIMIDINECARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF T CELL ACTIVATION FOR THE TREATMENT OF INFLAMMATORY DISEASES AMGEN INC. (US) 2005-02-03 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 (1 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-20050209221-A1 Substituted heterocyclic compounds and methods of use ICOS, CD4, HLA-DRB1 LCK 33/4885JAK3 900/4885BTK 1420/4885

“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.