Isoleucine

Isoleucine

SCHEMBL247126

CCC(C)C(N)C(=O)O.Cl

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
DPP4 known ✓ P27487 9/20 0.47
SLC7A5 Q01650 2/20 0.52
DPP8 Q6V1X1 6/20 0.47
DPP9 Q86TI2 6/20 0.47
DPP7 Q9UHL4 5/20 0.42
SLC1A3 P43003 1/20 0.41
SLC1A2 P43004 1/20 0.41
SLC1A1 P43005 1/20 0.41
ALDH1A1 P00352 1/20 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
Isoleucine SCHEMBL247127 1.00 SLC7A5 (0.52) SLC7A5DPP4DPP8DPP9DPP7
Isoleucine SCHEMBL31703777 1.00 SLC7A5 (0.52) SLC7A5DPP4DPP8DPP9DPP7
Isoleucine SCHEMBL16893956 1.00 SLC7A5 (0.52) SLC7A5DPP4DPP8DPP9DPP7
Isoleucine SCHEMBL3000366 1.00 SLC7A5 (0.52) SLC7A5DPP4DPP8DPP9DPP7
Isoleucine SCHEMBL6780686 1.00 SLC7A5 (0.52) SLC7A5DPP4DPP8DPP9DPP7
Isoleucine SCHEMBL16893955 1.00 SLC7A5 (0.52) SLC7A5DPP4DPP8DPP9DPP7
Isoleucine SCHEMBL1255582 0.97 SLC7A5 (0.55) SLC7A5DPP4DPP8DPP9DPP7
Isoleucine SCHEMBL20340795 0.97
Isoleucine SCHEMBL8868 0.97
Isoleucine SCHEMBL1255583 0.97 SLC7A5 (0.55) SLC7A5DPP4DPP8DPP9DPP7

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 105 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112409200-B Preparation method and application of isoleucine chelate metal 长沙兴嘉生物工程股份有限公司 2023-06-20 CN claimed
CN-112409200-A Preparation method and application of isoleucine chelated metal 长沙兴嘉生物工程股份有限公司 2021-02-26 CN claimed
US-10258579-B2 Process for the preparation of polysaccharide nanoparticles NANOVELOS SP. Z O.O. (PL) 2019-04-16 US claimed
EP-3082778-B1 STABLE LIQUID FILLED HARD CAPSULE COMPRISING BETA-HYDROXY-BETA-METHYLBUTYRIC ACID CAPSUGEL BELGIUM NV (BE) 2019-04-03 EP claimed
US-20150197483-A1 METHODS AND COMPOSITIONS FOR MAKING AN AMINO ACID TRIHYDROCHLORIDE WARSAW ORTHOPEDIC, INC. (US) 2015-07-16 US claimed
CN-103951572-A Separation and purification process for producing branched chain amino acid by using fermentation method WUXI JINGHAI AMINO ACID CO LTD 2014-07-30 CN claimed
US-6673942-B1 PREFERENTIAL CRYSTALLIZATION, PHYSICAL SEPARATION DEGUSSA AG (DE) 2004-01-06 US claimed
EP-1254092-A1 RESOLUTION OF DL-RACEMIC MIXTURES Degussa AG (DE) 2002-11-06 EP claimed
WO-2001058835-A1 RESOLUTION OF DL-RACEMIC MIXTURES DEGUSSA AG (DE) 2001-08-16 WO claimed
US-5480574-A 2-aminocarboxylic acid hydrochloride compositions for removal of hard-water deposits SINGERMAN GARY M (US) 1996-01-02 US claimed
JP-59062554-A None JP disclosed
CN-119818525-A Cytarabine amino acid ester composition and application thereof 沈阳信达泰康医药科技有限公司 2025-04-15 CN disclosed
CN-119265261-A Culture medium for producing tylosin through fermentation and preparation method thereof 宁夏泰益欣生物科技股份有限公司 2025-01-07 CN disclosed
WO-2024261477-A1 COMBINATION OF TLR4 ANTAGONIST, ORNITHINE AND PHENYLACETATE OR PHENYLBUTYRATE YAQRIT LIMITED (GB) 2024-12-26 WO disclosed
CN-112409200-B Preparation method and application of isoleucine chelate metal 长沙兴嘉生物工程股份有限公司 2023-06-20 CN disclosed
WO-1993006217-A1 EXPRESSION IN E. COLI OF ANTIBODY FRAGMENTS HAVING AT LEAST A CYSTEINE PRESENT AS A FREE THIOL, USE FOR THE PRODUCTION OF BIFUNCTIONAL F(ab')2 ANTIBODIES GENENTECH, INC. (US) 1993-04-01 WO disclosed
EP-0241094-A1 Process for the separation of L-leucine and L-isoleucine PFW (NEDERLAND) B.V. (NL) 1987-10-14 EP disclosed
JP-S5962554-A PURIFICATION OF ISOLEUCINE HYDROCHLORIDE TANABE SEIYAKU CO LTD 1984-04-10 JP disclosed
US-4263450-A PRECIPITATION AS HYDROCHLORIDE SOCIETE D'ASSISTANCE TECHNIQUE POUR PRODUITS NESTLE S.A. (CH) 1981-04-21 US disclosed
US-3959075-A CULTURING CORYNEFORM MUTANT KYOWA HAKKO KOGYO CO., LTD. (JA) 1976-05-25 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 (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-20150197483-A1 METHODS AND COMPOSITIONS FOR MAKING AN AMINO ACID TRIHYDROCHLORIDE ALKBH3, AADAT, ALKBH1 DPP4 2619/4885SLC7A5 1032/4885DPP8 2241/4885

“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.