SCHEMBL680454

SCHEMBL680454

CS(=O)(=O)O.Cc1cc(C)n(-c2ccc(F)cc2)c(=O)c1C(=O)Nc1ccc(Oc2cc3cn[nH]c3cc2N)c(F)c1

nearest known ligand 0.51

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR known ✓ P35968 4/20 0.47
ABL1 known ✓ P00519 1/20 0.41
KIT known ✓ P10721 1/20 0.41
MET P08581 17/20 0.51
AXL P30530 15/20 0.51
MERTK Q12866 7/20 0.47
MST1R Q04912 3/20 0.47
PLK4 O00444 2/20 0.47
NTRK1 P04629 2/20 0.47
RET P07949 2/20 0.47
FLT3 P36888 2/20 0.47
DDR1 Q08345 2/20 0.47
DDR2 Q16832 2/20 0.47
CAMK4 Q16566 1/20 0.47
MKNK1 Q9BUB5 1/20 0.47
MKNK2 Q9HBH9 1/20 0.47
TYRO3 Q06418 7/20 0.44
LCK P06239 1/20 0.41
PDGFRA P16234 1/20 0.41
PRKACA P17612 1/20 0.41

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
SCHEMBL12190713 0.97 MET (0.51) METAXLMERTKKDRMST1R
SCHEMBL681126 0.88 MET (0.50) METAXLMERTKKDRMST1R
SCHEMBL679069 0.87 AXL (0.48) METAXLMERTKKDRMST1R
SCHEMBL680235 0.87 AXL (0.61) METAXLMERTKKDRMST1R
SCHEMBL2496790 0.87 AXL (0.49) METAXLMERTKKDRMST1R
SCHEMBL680824 0.85 AXL (0.43) METAXLMERTKKDRMST1R
SCHEMBL12190681 0.84 MET (0.52) METAXLMERTKKDRMST1R
SCHEMBL1548016 0.84 MET (0.53) METAXLMERTKKDRMST1R
SCHEMBL681095 0.84 AXL (0.61) METAXLMERTKKDRMST1R
SCHEMBL680287 0.83 AXL (0.52) METAXLMERTKKDRMST1R

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-RE43878-E1 Amidophenoxyindazoles useful as inhibitors of c-Met ELI LILLY AND COMPANY (US) 2012-12-25 US disclosed
EP-2310382-B1 AMIDOPHENOXYINDAZOLES USEFUL AS INHIBITORS OF C-MET LILLY CO ELI (US) 2012-02-22 EP disclosed
US-8030302-B2 Amidophenoxyindazoles useful as inhibitors of c-Met ELI LILLY AND COMPANY (US) 2011-10-04 US disclosed
US-20100022529-A1 AMIDOPHENOXYINDAZOLES USEFUL AS INHIBITORS OF C-MET ELI LILLY AND COMPANY 2010-01-28 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 (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-20100022529-A1 AMIDOPHENOXYINDAZOLES USEFUL AS INHIBITORS OF C-MET MET, MYCBP, MYC KDR 180/4885ABL1 16/4885KIT 567/4885

“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.