Alanine

Alanine

SCHEMBL723059

CC(N)C(=O)O.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.51

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Alanine. 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
SLC1A3 P43003 1/20 0.51
SLC1A2 P43004 1/20 0.51
SLC1A1 P43005 1/20 0.51
CYP2D6 P10635 2/20 0.51
MAPK1 P28482 1/20 0.51
MMP9 P14780 3/20 0.46
MMP1 P03956 2/20 0.46
MMP2 P08253 2/20 0.46
MMP13 P45452 2/20 0.46
MMP3 P08254 1/20 0.46
MMP7 P09237 1/20 0.46
SNCA P37840 1/20 0.46
ALDH1A1 P00352 3/20 0.45
TSHR P16473 2/20 0.45
CA1 P00915 2/20 0.45
CA2 P00918 2/20 0.45
CA12 O43570 1/20 0.45
CA3 P07451 1/20 0.45
CA6 P23280 1/20 0.45
CA5A P35218 1/20 0.45

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
D-Alanine SCHEMBL3725637 1.00 SLC1A3 (0.51) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1
Alanine SCHEMBL3254315 1.00 SLC1A3 (0.51) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1
SCHEMBL30513488 0.89 CYP2D6 (0.50) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1
Isopropylamine SCHEMBL2350740 0.88 CYP2D6 (0.53) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1
Valine SCHEMBL2295611 0.88 SLC1A3 (0.55) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1
Valine SCHEMBL5159688 0.88 SLC1A3 (0.55) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1
Lactic Acid SCHEMBL2447119 0.87 CYP2D6 (0.49) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1
SCHEMBL1274859 0.86 CYP2D6 (0.51) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1
Threonine SCHEMBL18075540 0.86 SLC1A3 (0.54) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1
Alanine SCHEMBL10627958 0.85 TSHR (0.64) SLC1A3SLC1A2SLC1A1CYP2D6MAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110678174-A Prodrugs of treprostinil 联合治疗学有限公司 2020-01-10 CN disclosed
EP-3294296-A1 COMPOSITIONS AND METHODS FOR ASSESSING EYE VASCULATURE Medibeacon Inc. (US) 2018-03-21 EP disclosed
WO-2016183351-A1 COMPOSITIONS AND METHODS FOR ASSESSING EYE VASCULATURE MEDIBEACON INC. (US) 2016-11-17 WO disclosed
US-8759318-B2 Phosphoramidate derivatives of guanosine nucleoside compounds for treatment of viral infections INHIBITEX, INC. (US) 2014-06-24 US disclosed
US-20120052046-A1 Phosphoramidate Derivatives of Guanosine Nucleoside Compunds for Treatment of Viral Infections UNIVERSITY COLLEGE CARDIFF CONSULTANTS LIMITED (GB) 2012-03-01 US disclosed
EP-2385951-A2 PHOSPHORAMIDATE DERIVATIVES OF GUANOSINE NUCLEOSIDE COMPOUNDS FOR TREATMENT OF VIRAL INFECTIONS University College Cardiff Consultants, Ltd. (GB) 2011-11-16 EP disclosed
US-20110254856-A1 MOBILE TERMINAL AND METHOD OF CONTROLLING OPERATION OF THE MOBILE TERMINAL LG ELECTRONICS INC. (KR) 2011-10-20 US disclosed
WO-2010081082-A2 PHOSPHORAMIDATE DERIVATIVES OF GUANOSINE NUCLEOSIDE COMPOUNDS FOR TREATMENT OF VIRAL INFECTIONS UNIVERSITY COLLEGE OF CARDIFF CONSULTANTS LIMITED (GB) 2010-07-15 WO disclosed
CN-1631539-A Amino acid salt ion liquid and its preparation UNIV BEIJING (CN) 2005-06-29 CN 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-20120052046-A1 Phosphoramidate Derivatives of Guanosine Nucleoside Compunds for Treatment of Viral Infections PNP, SAMHD1, MTAP SLC1A3 2260/4885SLC1A2 2880/4885SLC1A1 1973/4885

“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.