SCHEMBL989354

SCHEMBL989354

CC(C)Cc1nc2ccccc2[nH]1.CS(=O)(=O)O.CS(=O)(=O)O

nearest known ligand 0.56

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
CHRM1 known ✓ P11229 1/20 0.49
ALOX12 P18054 1/20 0.56
PIN1 Q13526 2/20 0.54
DDAH1 O94760 1/20 0.53
SMN1; SMN2 Q16637 3/20 0.52
KDM4E B2RXH2 3/20 0.52
MAPT P10636 2/20 0.52
HSD17B10 Q99714 2/20 0.52
ALDH1A1 P00352 1/20 0.52
PKM P14618 1/20 0.51
HTT P42858 1/20 0.51
ALPL P05186 1/20 0.51
MAPK1 P28482 1/20 0.51
L3MBTL1 Q9Y468 2/20 0.50
GAA P10253 1/20 0.50
CYP1A2 P05177 1/20 0.50
CYP3A4 P08684 1/20 0.50
CYP2D6 P10635 1/20 0.50
CYP2C9 P11712 1/20 0.50
CYP2C19 P33261 1/20 0.50

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
SCHEMBL4113303 0.89 DDAH1 (0.65) DDAH1KDM4EMAPTPKMALPL
SCHEMBL27910228 0.85 DDAH1 (0.53) ALOX12PIN1DDAH1SMN1; SMN2KDM4E
SCHEMBL27973349 0.82 L3MBTL1 (0.53) ALOX12PIN1DDAH1SMN1; SMN2KDM4E
SCHEMBL133478 0.80 DDAH1 (0.61) DDAH1KDM4EPKMALPLMAPK1
SCHEMBL2680248 0.80 CYP3A4 (0.64) PIN1DDAH1PKMALPLMAPK1
SCHEMBL13050694 0.80 CYP3A4 (0.64) PIN1DDAH1PKMALPLMAPK1
SCHEMBL20646170 0.80 DDAH1 (0.61) DDAH1KDM4EPKMALPLMAPK1
Bendazol SCHEMBL28197265 0.79 GAA (0.77) DDAH1SMN1; SMN2ALDH1A1PKML3MBTL1
Ethylene SCHEMBL708237 0.79 L3MBTL1 (0.50) ALOX12PIN1DDAH1SMN1; SMN2KDM4E
SCHEMBL5069923 0.78 L3MBTL1 (0.59) DDAH1SMN1; SMN2KDM4EMAPTHSD17B10

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 CHRM1 4879/4885ALOX12 4697/4885PIN1 982/4885

“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.