SCHEMBL991498

SCHEMBL991498

CC(C)CNc1nc2ccccc2[nH]1.CS(=O)(=O)O

nearest known ligand 0.53

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
ALOX12 P18054 1/20 0.53
RIPK1 Q13546 1/20 0.53
BCHE P06276 2/20 0.52
TRPC3 Q13507 1/20 0.52
TRPC4 Q9UBN4 1/20 0.52
TRPC5 Q9UL62 1/20 0.52
RAB9A P51151 3/20 0.51
SMN1; SMN2 Q16637 3/20 0.51
TP53 P04637 1/20 0.51
LMNA P02545 1/20 0.51
NPC1 O15118 2/20 0.50
HTT P42858 1/20 0.50
ALDH1A1 P00352 2/20 0.49
MAPK1 P28482 1/20 0.49
HSD17B10 Q99714 1/20 0.49
CYP3A4 P08684 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
PKM P14618 1/20 0.47
TSHR P16473 1/20 0.47
ALPL P05186 2/20 0.46

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
SCHEMBL989750 0.91 BCHE (0.60) RIPK1BCHETRPC3TRPC4TRPC5
SCHEMBL28983301 0.80 BCHE (0.57) BCHETRPC3TRPC4TRPC5RAB9A
SCHEMBL28983300 0.80 BCHE (0.57) BCHETRPC3TRPC4TRPC5RAB9A
SCHEMBL30175772 0.80 BCHE (0.57) BCHETRPC3TRPC4TRPC5RAB9A
SCHEMBL989354 0.77 ALOX12 (0.56) ALOX12SMN1; SMN2HTTALDH1A1MAPK1
SCHEMBL3541921 0.75 RAB9A (0.62) BCHETRPC3TRPC4TRPC5RAB9A
SCHEMBL14025138 0.74 BCHE (0.71) BCHETRPC3TRPC4TRPC5RAB9A
SCHEMBL30002927 0.74 ALDH1A1 (0.67) ALOX12BCHETRPC3TRPC4TRPC5
SCHEMBL4873251 0.74 ALDH1A1 (0.67) ALOX12BCHETRPC3TRPC4TRPC5
SCHEMBL14009913 0.74 ALDH1A1 (0.67) ALOX12RAB9ASMN1; SMN2LMNANPC1

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 ALOX12 4697/4885RIPK1 435/4885BCHE 4475/4885

“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.