SCHEMBL2166786

SCHEMBL2166786

CS(=O)(=O)O.O=C(OCCO)c1c(F)cc(F)cc1F

nearest known ligand 0.40

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
KMT2A Q03164 2/20 0.38
GAA P10253 1/20 0.38
TTR P02766 1/20 0.38
MAPK14 Q16539 1/20 0.36
ALDH1A1 P00352 3/20 0.35
PFKFB3 Q16875 1/20 0.34
CA1 P00915 1/20 0.34
CA2 P00918 1/20 0.34
PTGS2 P35354 2/20 0.34
ESR1 P03372 1/20 0.33
PTGS1 P23219 1/20 0.32
TDP2 O95551 1/20 0.32
KDM4E B2RXH2 1/20 0.32
GLA P06280 1/20 0.32
HPGD P15428 1/20 0.32
CASP1 P29466 1/20 0.32
CASP7 P55210 1/20 0.32
HSD17B10 Q99714 1/20 0.32
TP53 P04637 1/20 0.32
MAPT P10636 1/20 0.32

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
SCHEMBL2166055 0.84 KMT2A (0.51) KMT2AGAAALDH1A1CA1CA2
SCHEMBL18776013 0.81 KMT2A (0.37) KMT2AGAATTRCA1CA2
SCHEMBL2166185 0.81 ALDH1A1 (0.50) KMT2AGAAMAPK14ALDH1A1PFKFB3
SCHEMBL2167360 0.80 ESR1 (0.47) GAAALDH1A1CA1CA2ESR1
SCHEMBL2166940 0.80 KMT2A (0.35) KMT2AGAATTRALDH1A1
SCHEMBL31590871 0.78 ALDH1A1 (0.47) KMT2AGAAALDH1A1ESR1KDM4E
Ethylene Glycol SCHEMBL2166792 0.77 PLK1 (0.39) KMT2AGAATTRALDH1A1
SCHEMBL2165914 0.76 KMT2A (0.50) KMT2AALDH1A1CA1CA2ESR1
SCHEMBL31590766 0.76 ESR1 (0.58) ESR1TP53
SCHEMBL2167868 0.75 ADRB2 (0.51) KMT2AALDH1A1CA1CA2ESR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8383274-B2 Nonaqueous electrolyte solution for lithium battery, lithium battery using same, and formyloxy group-containing compound used therein UBE INDUSTRIES, LTD. (JP) 2013-02-26 US disclosed
US-20110183199-A1 NONAQUEOUS ELECTROLYTE SOLUTION FOR LITHIUM BATTERY, LITHIUM BATTERY USING SAME, AND FORMYLOXY GROUP-CONTAINING COMPOUND USED THEREIN UBE INDUSTRIES, LTD. (JP) 2011-07-28 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-20110183199-A1 NONAQUEOUS ELECTROLYTE SOLUTION FOR LITHIUM BATTERY, LITHIUM BATTERY USING SAME, AND FORMYLOXY GROUP-CONTAINING COMPOUND USED THEREIN HCN2, KCNN2, KCNB1 KMT2A 2361/4885GAA 4111/4885TTR 2250/4885

“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.