SCHEMBL2851338

SCHEMBL2851338

Cc1ccc(S(=O)(=O)O)cc1.N[C@@H](CC(=O)O)Cc1ccccc1

nearest known ligand 0.48

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
GAA P10253 2/20 0.47
CYP2D6 P10635 1/20 0.47
MAPK1 P28482 1/20 0.47
BCHE P06276 1/20 0.44
ACHE P22303 1/20 0.44
RECQL P46063 1/20 0.43
CA2 P00918 1/20 0.43
CA7 P43166 1/20 0.43
DPP4 P27487 1/20 0.42
KDM4E B2RXH2 1/20 0.42
EPHX1 P07099 1/20 0.42
KMT2A Q03164 1/20 0.42
CPA1 P15085 2/20 0.42
CPB1 P15086 1/20 0.42
CPA3 P15088 1/20 0.42
CPB2 Q96IY4 1/20 0.42
ALDH1A1 P00352 1/20 0.42
PKM P14618 1/20 0.41
MMP9 P14780 1/20 0.41
CYP1A2 P05177 2/20 0.41

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
L-Phenylalaninol SCHEMBL10520919 0.87 CYP2D6 (0.50) GAACYP2D6MAPK1BCHEACHE
Dl-Phenylalanine SCHEMBL28023088 0.83 SLC7A5 (0.63) GAACYP2D6MAPK1BCHEACHE
Phenylalanine SCHEMBL10429981 0.83 SLC7A5 (0.63) GAACYP2D6MAPK1BCHEACHE
SCHEMBL6534817 0.83 KDM4E (0.46) CYP2D6MAPK1RECQLCA2CA7
SCHEMBL2032514 0.82 ANPEP (0.50) EPHX1KMT2ACPA1CPB1CPA3
SCHEMBL2027694 0.82 ANPEP (0.50) EPHX1KMT2ACPA1CPB1CPA3
SCHEMBL2027696 0.82 ANPEP (0.50) EPHX1KMT2ACPA1CPB1CPA3
D-Phenylalanine SCHEMBL20267959 0.82 SLC7A5 (0.61) GAACYP2D6MAPK1BCHEACHE
Dl-Phenylalanine SCHEMBL20267856 0.82 SLC7A5 (0.61) GAACYP2D6MAPK1BCHEACHE
Dl-Phenylalanine SCHEMBL28341547 0.82 SLC7A5 (0.61) GAACYP2D6MAPK1BCHEACHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2100875-B1 Asymmetric reductive amination of keto acid derivatives for producing amino acid derivatives TAKASAGO PERFUMERY CO LTD (JP) 2016-11-16 EP disclosed
EP-1685092-B1 ASYMMETRIC REDUCTIVE AMINATION OF KETO ACID DERIVATIVES FOR PRODUCING AMINO ACID DERIVATIVES TAKASAGO PERFUMERY CO LTD (JP) 2010-01-13 EP disclosed
US-7626034-B2 Asymmetric reductive amination of keto acid derivatives for producing amino acid derivatives TAKASAGO INTERNATIONAL CORPORATION (JP) 2009-12-01 US disclosed
EP-2100875-A1 Asymmetric reductive amination of keto acid derivatives for producing amino acid derivatives Takasago International Corporation (JP) 2009-09-16 EP disclosed
US-20070142443-A1 Asymmetric reductive amination of keto acid derivatives for producing amino acid derivatives TAKASAGO INTERNATIONAL CORPORATION (JP) 2007-06-21 US disclosed
EP-1685092-A2 ASYMMETRIC REDUCTIVE AMINATION OF KETO ACID DERIVATIVES FOR PRODUCING AMINO ACID DERIVATIVES Takasago International Corporation (JP) 2006-08-02 EP disclosed
WO-2005028419-A2 ASYMMETRIC REDUCTIVE AMINATION OF KETO ACID DERIVATIVES FOR PRODUCING AMINO ACID DERIVATIVES TAKASAGO INTERNATIONAL CORPORATION (JP) 2005-03-31 WO 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-20070142443-A1 Asymmetric reductive amination of keto acid derivatives for producing amino acid derivatives AADAT, BCAT2, BCAT1 GAA 3505/4885CYP2D6 944/4885MAPK1 1309/4885

“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.