SCHEMBL3458769

SCHEMBL3458769

CC[n+]1ccc(-c2c3nc(c(-c4cc[n+](CC)cc4)c4ccc([nH]4)c(-c4ccc5ccc6cccc7ccc4c5c67)c4nc(c(-c5cc[n+](CC)cc5)c5ccc2[nH]5)C=C4)C=C3)cc1.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.50

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 13)

geneUniProtsupporting neighboursconfidence
▸ TERT O14746 5/20 0.50
▸ ENPP2 Q13822 1/20 0.48
▸ KDM4E B2RXH2 1/20 0.38
▸ ALDH1A1 P00352 1/20 0.38
▸ LMNA P02545 1/20 0.38
▸ MAPT P10636 1/20 0.38
▸ HTT P42858 1/20 0.38
▸ SMN1; SMN2 Q16637 1/20 0.38
▸ TDP1 Q9NUW8 1/20 0.38
▸ L3MBTL1 Q9Y468 1/20 0.38
▸ TOP1 P11387 3/20 0.32
▸ ABCG2 Q9UNQ0 1/20 0.32
▸ CYCS P99999 3/20 0.32

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
SCHEMBL3458767 0.92 TERT (0.59) TERTENPP2TOP1ABCG2CYCS
SCHEMBL3461640 0.83 TERT (0.73) TERTENPP2TOP1ABCG2CYCS
Tmpyp4 SCHEMBL7112191 0.76 TERT (0.80) TERTENPP2KDM4EALDH1A1LMNA
Tmpyp4 SCHEMBL3792658 0.76 TERT (0.80) TERTENPP2KDM4EALDH1A1LMNA
SCHEMBL2737183 0.75 ENPP2 (0.84) TERTENPP2KDM4EALDH1A1LMNA
Hydrochloric Acid SCHEMBL3459214 0.75 TERT (0.61) TERTENPP2TOP1CYCS
SCHEMBL224502 0.73 TERT (0.39) TERTENPP2ALDH1A1TDP1L3MBTL1
SCHEMBL28296392 0.72 TERT (0.38) TERTENPP2ALDH1A1TDP1L3MBTL1
SCHEMBL3459959 0.71 TOP1 (0.53) TERTENPP2TOP1CYCS
SCHEMBL15943766 0.71 ENPP2 (0.76) TERTENPP2KDM4EALDH1A1LMNA

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
EP-2230242-A1 Synthesis of new asymmetrically meso-substituted water-soluble porphyrins acting as cytostatic agents Johannes Kepler Universität (AT) 2010-09-22 — — EP claimed
EP-2230242-B1 Synthesis of new asymmetrically meso-substituted water-soluble porphyrins acting as cytostatic agents JOHANNES KEPLER UNI (AT) 2013-08-14 — — EP disclosed
EP-2230242-A1 Synthesis of new asymmetrically meso-substituted water-soluble porphyrins acting as cytostatic agents Johannes Kepler Universität (AT) 2010-09-22 — — EP disclosed
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