SCHEMBL4247159

SCHEMBL4247159

CCC(N)(CC)CC#N.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.44

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
GLA P06280 1/20 0.43
ALDH1A1 P00352 7/20 0.39
MAPT P10636 3/20 0.39
TDP1 Q9NUW8 3/20 0.39
L3MBTL1 Q9Y468 2/20 0.39
KDM4E B2RXH2 1/20 0.39
LMNA P02545 1/20 0.39
HTT P42858 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
PRSS1 P07477 2/20 0.39
F2 P00734 1/20 0.39
PRSS2 P07478 1/20 0.39
PRSS3 P35030 1/20 0.39
CYP2D6 P10635 3/20 0.39
MAPK1 P28482 2/20 0.39
CYP1A2 P05177 3/20 0.39
CYP2C9 P11712 2/20 0.39
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
CA12 O43570 1/20 0.38

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
SCHEMBL8505195 0.85 ALDH1A1 (0.47) ALDH1A1MAPTTDP1L3MBTL1KDM4E
SCHEMBL4539902 0.85 ALDH1A1 (0.39) GLAALDH1A1MAPTTDP1L3MBTL1
SCHEMBL4797198 0.84 GLA (0.42) GLAALDH1A1MAPTTDP1L3MBTL1
SCHEMBL4246280 0.82 GLA (0.41) GLAALDH1A1MAPTTDP1L3MBTL1
Propionitrile SCHEMBL28654588 0.82 GLA (0.51) GLAALDH1A1MAPTTDP1L3MBTL1
SCHEMBL8745167 0.81 ALDH1A1 (0.43) ALDH1A1MAPTTDP1L3MBTL1KDM4E
SCHEMBL1437604 0.79 GLA (0.51) GLAALDH1A1MAPTTDP1L3MBTL1
SCHEMBL5480254 0.78 L3MBTL1 (0.44) GLAALDH1A1MAPTTDP1L3MBTL1
Propionitrile SCHEMBL6679473 0.78 GLA (0.51) GLAALDH1A1MAPTTDP1L3MBTL1
Tromethamine SCHEMBL29882687 0.77 ALDH1A1 (0.45) ALDH1A1MAPTTDP1L3MBTL1KDM4E

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 3 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090171111-A1 Method for Producing Sodium Chloride-Free Ammonium Nitriles CLARIANT FINANCE (BVI) LIMITED (VG) 2009-07-02 US disclosed
US-20090149668-A1 Method for Producing Sodium Chloride-Free Ammonium Nitriles CLARIANT INTERNATIONAL, LTD. (CH) 2009-06-11 US disclosed
US-20070245498-A1 Diethyl Methyl Ammonium Nitriles and Detergents and Cleaning Agents Containing Said Ammonium Nitriles REINHARDT GERD 2007-10-25 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 (2 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-20090171111-A1 Method for Producing Sodium Chloride-Free Ammonium Nitriles CBR3, MSRB3, CBR1 GLA 4729/4885ALDH1A1 2112/4885MAPT 4360/4885
US-20090149668-A1 Method for Producing Sodium Chloride-Free Ammonium Nitriles CBR3, CBR1, AKR1C3 GLA 4740/4885ALDH1A1 653/4885MAPT 4700/4885

“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.