SCHEMBL2168386

SCHEMBL2168386

CS(=O)(=O)O.O=C(O)c1ccccc1F.OCC#CCO

nearest known ligand 0.45

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
HPGD P15428 1/20 0.45
PTPN1 P18031 1/20 0.45
ERCC5 P28715 1/20 0.45
FEN1 P39748 1/20 0.45
GAA P10253 2/20 0.45
CA12 O43570 2/20 0.44
CA9 Q16790 2/20 0.44
NPC1 O15118 1/20 0.44
RAB9A P51151 1/20 0.44
KAT6A Q92794 2/20 0.43
CES2 O00748 1/20 0.43
CES1 P23141 1/20 0.43
POLB P06746 2/20 0.43
ALB P02768 1/20 0.42
ALDH1A1 P00352 4/20 0.41
ALOX12 P18054 1/20 0.41
TP53 P04637 1/20 0.41
TSHR P16473 1/20 0.41
HTT P42858 1/20 0.41
L3MBTL1 Q9Y468 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
Ethylene Glycol SCHEMBL2168458 0.89 GAA (0.53) HPGDPTPN1ERCC5FEN1GAA
SCHEMBL2168384 0.82 NPC1 (0.46) GAANPC1ALDH1A1TP53TSHR
SCHEMBL2169189 0.82 CES2 (0.46) HPGDGAANPC1RAB9ACES2
Alcohol SCHEMBL27662236 0.78 GAA (0.55) PTPN1ERCC5FEN1GAACA12
Fluoromethane SCHEMBL28310900 0.77 CES2 (0.62) HPGDPTPN1ERCC5FEN1GAA
Methyl Alcohol SCHEMBL20994106 0.77 CES2 (0.62) HPGDPTPN1ERCC5FEN1GAA
SCHEMBL97828 0.77 CES2 (0.68) HPGDPTPN1ERCC5FEN1GAA
SCHEMBL30968201 0.77 CES2 (0.68) HPGDPTPN1ERCC5FEN1GAA
SCHEMBL29362443 0.77 CES2 (0.68) HPGDPTPN1ERCC5FEN1GAA
Hydrochloric Acid SCHEMBL23201659 0.75 CES2 (0.65) HPGDPTPN1ERCC5FEN1GAA

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 HPGD 1051/4885PTPN1 927/4885ERCC5 1151/4885

“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.