SCHEMBL680268

SCHEMBL680268

CS(=O)(=O)O.O=C(Nc1ccc(Oc2cc3cn[nH]c3cc2N2CCOCC2)c(F)c1)c1cccn(-c2ccc(F)cc2)c1=O

nearest known ligand 0.55

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 13)

geneUniProtsupporting neighboursconfidence
ABL1 known ✓ P00519 1/20 0.52
KIT known ✓ P10721 1/20 0.52
KDR known ✓ P35968 1/20 0.52
AXL P30530 14/20 0.55
MET P08581 11/20 0.53
RIPK3 Q9Y572 2/20 0.53
TYRO3 Q06418 3/20 0.53
MERTK Q12866 3/20 0.53
LCK P06239 1/20 0.52
FLT3 P36888 1/20 0.52
RIPK1 Q13546 1/20 0.52
CYP3A4 P08684 1/20 0.51
CYP2C9 P11712 1/20 0.51

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
SCHEMBL680709 0.97 AXL (0.58) AXLMETRIPK3TYRO3MERTK
SCHEMBL680639 0.89 AXL (0.52) AXLMETTYRO3MERTKABL1
SCHEMBL681013 0.89 AXL (0.53) AXLMETRIPK3TYRO3MERTK
SCHEMBL681063 0.89 AXL (0.54) AXLMETRIPK3TYRO3MERTK
SCHEMBL681026 0.89 AXL (0.53) AXLMETRIPK3TYRO3MERTK
SCHEMBL12190687 0.87 AXL (0.51) AXLMETTYRO3MERTK
SCHEMBL680685 0.87 AXL (0.56) AXLMETRIPK3TYRO3MERTK
SCHEMBL680684 0.87 AXL (0.56) AXLMETRIPK3TYRO3MERTK
SCHEMBL12190677 0.86 AXL (0.54) AXLMETTYRO3MERTKABL1
SCHEMBL680780 0.86 AXL (0.64) AXLMETTYRO3MERTKKDR

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 ABL1 16/4885KIT 567/4885KDR 180/4885

“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.