SCHEMBL6401282

SCHEMBL6401282

CS(=O)(=O)O.N=C(NNC(=O)c1cc2cc(Cl)ccc2[nH]1)c1ccccc1F

nearest known ligand 0.54

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
BCAT1 P54687 4/20 0.54
NHERF1 O14745 2/20 0.53
GUSB P08236 2/20 0.52
KDM4E B2RXH2 1/20 0.48
MEN1 O00255 3/20 0.48
KMT2A Q03164 3/20 0.48
RXFP1 Q9HBX9 1/20 0.48
RAB9A P51151 2/20 0.46
ALDH1A1 P00352 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
PYGL P06737 2/20 0.46
KAT6A Q92794 1/20 0.45
NPC1 O15118 1/20 0.45

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
SCHEMBL6400560 0.95 NHERF1 (0.58) BCAT1NHERF1GUSBKDM4EMEN1
Hydrochloric Acid SCHEMBL6400667 0.94 NHERF1 (0.57) BCAT1NHERF1GUSBKDM4EMEN1
SCHEMBL6401772 0.90 BCAT1 (0.61) BCAT1NHERF1GUSBKDM4EMEN1
SCHEMBL6398780 0.89 MEN1 (0.53) BCAT1NHERF1GUSBMEN1KMT2A
SCHEMBL6404129 0.89 BCAT1 (0.54) BCAT1NHERF1GUSBMEN1KMT2A
SCHEMBL6398781 0.86 BCAT1 (0.52) BCAT1NHERF1KDM4EMEN1KMT2A
SCHEMBL6405416 0.85 BCAT1 (0.58) BCAT1NHERF1GUSBMEN1KMT2A
SCHEMBL6407474 0.84 BCAT1 (0.50) BCAT1NHERF1GUSBMEN1KMT2A
SCHEMBL6406739 0.84 BCAT1 (0.62) BCAT1NHERF1GUSBKDM4EMEN1
SCHEMBL6401150 0.84 NHERF1 (0.61) BCAT1NHERF1GUSBKDM4EMEN1

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-20050054696-A1 Indole compounds and medicinal use thereof JAPAN TOBACCO INC. (JP) 2005-03-10 US claimed
EP-1452526-A1 INDOLE COMPOUND AND MEDICINAL USE THEREOF JAPAN TOBACCO INC. (JP) 2004-09-01 EP claimed
US-20050054696-A1 Indole compounds and medicinal use thereof JAPAN TOBACCO INC. (JP) 2005-03-10 US disclosed
EP-1452526-A1 INDOLE COMPOUND AND MEDICINAL USE THEREOF JAPAN TOBACCO INC. (JP) 2004-09-01 EP 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-20050054696-A1 Indole compounds and medicinal use thereof IDO1, GPR119, SLC5A1 BCAT1 854/4885NHERF1 332/4885GUSB 171/4885

“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.