Leucine

Leucine

SCHEMBL3362640

CC(C)C[C@H](N)C(=O)[O-].CC(C)C[C@H](N)C(=O)[O-].[Ca+2]

nearest known ligand 0.58

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Known targets — ChEMBL curated mechanism

GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHMGCRMMP1MMP13MMP7MMP8PTGS1PTGS2ileSpolrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Leucine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
SLC7A5 Q01650 1/20 0.58
SLC1A3 P43003 3/20 0.45
SLC1A2 P43004 3/20 0.45
ANPEP P15144 6/20 0.42
RNPEP Q9H4A4 3/20 0.42
DNPEP Q9ULA0 1/20 0.42
LAP3 P28838 4/20 0.39
ERAP1 Q9NZ08 1/20 0.39
ALDH1A1 P00352 1/20 0.39
TSHR P16473 1/20 0.39
MAPK1 P28482 1/20 0.39
CA2 P00918 1/20 0.39
SLC1A1 P43005 2/20 0.38
CA1 P00915 2/20 0.37
LARS1 Q9P2J5 1/20 0.36

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
Leucine SCHEMBL30109857 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP
Leucine SCHEMBL8802761 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP
Leucine SCHEMBL3285972 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP
Leucine SCHEMBL9303138 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP
Leucine SCHEMBL2286761 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP
Leucine SCHEMBL9581376 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP
Leucine SCHEMBL9453845 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP
Leucine SCHEMBL7781917 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP
Leucine SCHEMBL10619258 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP
Leucine SCHEMBL15111234 0.95 SLC7A5 (0.58) SLC7A5SLC1A3SLC1A2ANPEPRNPEP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4643658-A1 DIETARY PRODUCT FOR HYPOPROTEIC DIET LABORATORIOS ERN S.A. (ES) 2025-11-05 EP disclosed
CN-117603042-A Preparation method and application of ketoleucine salt derivative 河北天成药业股份有限公司 2024-02-27 CN disclosed
CN-114246856-A Composition containing amino acid derivative 南京恒生制药有限公司 2022-03-29 CN disclosed
CN-103922949-A Calcium leucine chelate powder and processing method thereof UNIV JILIN 2014-07-16 CN disclosed
US-20100041622-A1 Compositions containing aminoalkanes and aminoalkane derivatives VIRUN, INC. 2010-02-18 US disclosed
WO-2010019255-A1 COMPOSITIONS CONTAINING AMINOALKANES AND AMINOALKANE DERIVATIVES VIRUN, INC. (US) 2010-02-18 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-20100041622-A1 Compositions containing aminoalkanes and aminoalkane derivatives TAAR5, PDE3A, PDE2A SLC7A5 564/4885SLC1A3 177/4885SLC1A2 121/4885

“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.