SCHEMBL679054

SCHEMBL679054

CS(=O)(=O)O.Cc1c(C(=O)Nc2ccc(Oc3cc4cn[nH]c4cc3-c3cccnc3)c(F)c2)c(=O)n(-c2ccc(F)cc2)n1C

nearest known ligand 0.61

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 10/20 0.50
ABL1 known ✓ P00519 1/20 0.50
KIT known ✓ P10721 1/20 0.50
MET P08581 20/20 0.61
AXL P30530 5/20 0.61
MERTK Q12866 3/20 0.61
FLT3 P36888 2/20 0.61
TYRO3 Q06418 1/20 0.61
IGF1R P08069 5/20 0.50
RET P07949 2/20 0.50
MST1R Q04912 2/20 0.50
AURKA O14965 1/20 0.50
JAK2 O60674 1/20 0.50
RPS6KA5 O75582 1/20 0.50
INSR P06213 1/20 0.50
LCK P06239 1/20 0.50
PIM1 P11309 1/20 0.50
FGFR1 P11362 1/20 0.50
SRC P12931 1/20 0.50
PRKACA P17612 1/20 0.50

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
SCHEMBL12190666 0.97 MET (0.64) METAXLMERTKFLT3TYRO3
SCHEMBL681088 0.93 MET (0.59) METAXLMERTKFLT3TYRO3
SCHEMBL681010 0.91 MET (0.56) METAXLMERTKFLT3TYRO3
SCHEMBL12190662 0.91 MET (0.62) METAXLMERTKFLT3TYRO3
SCHEMBL680471 0.90 MET (0.57) METAXLMERTKFLT3TYRO3
SCHEMBL12190699 0.89 MET (0.59) METAXLMERTKFLT3TYRO3
SCHEMBL679406 0.88 MET (0.60) METAXLMERTKFLT3TYRO3
SCHEMBL12190693 0.87 MET (0.60) METAXLMERTKFLT3TYRO3
SCHEMBL12190641 0.85 MET (0.63) METAXLMERTKFLT3TYRO3
SCHEMBL680804 0.84 MET (0.49) METAXLMERTKFLT3TYRO3

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.