SCHEMBL989450

SCHEMBL989450

CS(=O)(=O)O.CS(=O)(=O)O.Cn1cnc2ccccc21

nearest known ligand 0.47

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 16)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.47
ALDH3A1 P30838 3/20 0.46
HTT P42858 2/20 0.46
ALDH1A1 P00352 1/20 0.46
MAPT P10636 1/20 0.46
POLB P06746 1/20 0.46
NOD1 Q9Y239 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
EGLN3 Q9H6Z9 1/20 0.45
KMT2A Q03164 1/20 0.44
GRM5 P41594 1/20 0.44
ASAH1 Q13510 2/20 0.43
FGFR1 P11362 1/20 0.43
KDM4E B2RXH2 1/20 0.43
NPC1 O15118 1/20 0.43
TSHR P16473 1/20 0.42

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
Sulfuric Acid SCHEMBL4285301 0.95 TDP1 (0.48) TDP1ALDH3A1HTTALDH1A1MAPT
Trifluoromethanesulfonic Acid SCHEMBL2411761 0.87 ALDH3A1 (0.42) TDP1ALDH3A1HTTALDH1A1MAPT
SCHEMBL5399 0.87 TDP1 (0.59) TDP1HTTPOLBL3MBTL1EGLN3
SCHEMBL29359161 0.87 TDP1 (0.59) TDP1HTTPOLBL3MBTL1EGLN3
Iodide SCHEMBL15375366 0.85 TDP1 (0.57) TDP1HTTPOLBL3MBTL1EGLN3
SCHEMBL28652434 0.85 TDP1 (0.57) TDP1HTTPOLBL3MBTL1EGLN3
Bromide SCHEMBL6955674 0.85 TDP1 (0.57) TDP1HTTPOLBL3MBTL1EGLN3
Hydrochloric Acid SCHEMBL3713895 0.85 TDP1 (0.57) TDP1HTTPOLBL3MBTL1EGLN3
Hydrochloric Acid SCHEMBL7206595 0.85 TDP1 (0.57) TDP1HTTPOLBL3MBTL1EGLN3
Bromide SCHEMBL10432264 0.85 TDP1 (0.57) TDP1HTTPOLBL3MBTL1EGLN3

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-7863310-B2 Kinase inhibitors ELI LILLY AND COMPANY (US) 2011-01-04 US disclosed
US-20080227839-A1 Kinase Inhibitors ELI LILLY AND COMPANY 2008-09-18 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-20080227839-A1 Kinase Inhibitors ABL1, MAP3K20, MAP3K19 TDP1 1481/4885ALDH3A1 3687/4885HTT 4547/4885

“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.