L-Tyrosine Ethylester

L-Tyrosine Ethylester

SCHEMBL595118

CCOC(=O)C(N)Cc1ccc(O)cc1.Cl

nearest known ligand 0.59

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 L-Tyrosine Ethylester. 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
SLC6A2 known ✓ P23975 1/20 0.50
HDAC8 known ✓ Q9BY41 2/20 0.48
ESR1 known ✓ P03372 3/20 0.47
ESR2 known ✓ Q92731 3/20 0.47
CA2 known ✓ P00918 1/20 0.47
SLC7A5 Q01650 1/20 0.59
TPH1 P17752 2/20 0.54
TAAR1 Q96RJ0 3/20 0.50
CA12 O43570 1/20 0.47
CA1 P00915 1/20 0.47
CA7 P43166 1/20 0.47
CA9 Q16790 1/20 0.47
CA14 Q9ULX7 1/20 0.47
ERAP2 Q6P179 1/20 0.43
LNPEP Q9UIQ6 1/20 0.43

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-Tyrosine Ethylester SCHEMBL595119 1.00 SLC7A5 (0.59) SLC7A5TPH1TAAR1SLC6A2HDAC8
L-Tyrosine Ethylester SCHEMBL9331146 1.00 SLC7A5 (0.59) SLC7A5TPH1TAAR1SLC6A2HDAC8
L-Tyrosine Ethylester SCHEMBL27732314 0.98 SLC7A5 (0.57) SLC7A5TPH1TAAR1SLC6A2HDAC8
L-Tyrosine Ethylester SCHEMBL9327871 0.98 SLC7A5 (0.61) SLC7A5TPH1TAAR1SLC6A2HDAC8
L-Tyrosine Ethylester SCHEMBL242946 0.98 SLC7A5 (0.61) SLC7A5TPH1TAAR1SLC6A2HDAC8
L-Tyrosine Ethylester SCHEMBL242947 0.98 SLC7A5 (0.61) SLC7A5TPH1TAAR1SLC6A2HDAC8
L-Tyrosine Ethylester SCHEMBL30772131 0.95 SLC7A5 (0.57) SLC7A5TPH1TAAR1SLC6A2HDAC8
L-Tyrosine Ethylester SCHEMBL1532619 0.95 SLC7A5 (0.57) SLC7A5TPH1TAAR1SLC6A2HDAC8
L-Tyrosine Ethylester SCHEMBL27074524 0.95 SLC7A5 (0.57) SLC7A5TPH1TAAR1SLC6A2HDAC8
L-Tyrosine Ethylester SCHEMBL3086510 0.95 SLC7A5 (0.57) SLC7A5TPH1TAAR1SLC6A2HDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118834232-A Trifunctional silane coupling agent, preparation method thereof, vulcanized rubber composition and vulcanized rubber 怡维怡橡胶研究院有限公司 2024-10-25 CN claimed
CN-116783212-A Compositions and methods for modulating cancer in non-human mammals 霍夫曼技术有限责任公司 2023-09-19 CN claimed
CN-115812503-A Method for reducing Chinese rose flower deformity 苏州市园艺站 2023-03-21 CN claimed
US-20220257625-A1 COMPOSITION AND METHODS FOR THE TREATMENT OF SKIN CONDITIONS BIODERM, INC. 2022-08-18 US claimed
WO-2021011664-A1 COMPOSITION AND METHODS FOR THE TREATMENT OF SKIN CONDITIONS BIODERM, INC. (US) 2021-01-21 WO claimed
EP-3749290-A1 METHODS FOR DOPAMINE MODULATION IN HUMAN NEUROLOGIC DISEASES Sackner-Bernstein, Jonathan (US) 2020-12-16 EP claimed
WO-2019147934-A1 METHODS FOR DOPAMINE MODULATION IN HUMAN NEUROLOGIC DISEASES SACKNER BERNSTEIN JONATHAN (US) 2019-08-01 WO claimed
CN-109481401-A Acetylsalicylic acid and its derivative water-base nano emulsion formulation and preparation method thereof and its application 华欧研创生物科技(深圳)有限公司 2019-03-19 CN claimed
EP-3429583-A1 PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF CANCER Tyme, Inc. (US) 2019-01-23 EP claimed
WO-2017160895-A1 PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF CANCER TYME, INC. (US) 2017-09-21 WO claimed
CN-102827169-B Novel porphyrin ligand and metal complex, preparation method and application for novel porphyrin ligand XI AN RUILIAN MODERN ELECTRONIC CHEMICALS CO LTD 2014-11-05 CN claimed
EP-1185260-B1 ASCORBIC ACID COMPOSITION FOR THE TREATMENT OF AGING OR DAMAGED SKIN BIODERM INC (US) 2014-10-15 EP claimed
US-6444699-B2 Method for treatment of aging or damage skin BIODERM, INC. 2002-09-03 US claimed
EP-1185260-A4 ASCORBIC ACID COMPOSITION AND METHOD FOR TREATMENT OF AGING OR DAMAGED SKIN BIODERM INC (US) 2002-07-24 EP claimed
WO-2000056327-A9 ASCORBIC ACID COMPOSITION AND METHOD FOR TREATMENT OF AGING OR DAMAGED SKIN BIODERM INC (US) 2002-03-28 WO claimed
US-20020031557-A1 Ascorbic acid composition and method for treatment of aging or damaged skin MEISNER LORRAINE FAXON (US) 2002-03-14 US claimed
EP-1185260-A1 ASCORBIC ACID COMPOSITION AND METHOD FOR TREATMENT OF AGING OR DAMAGED SKIN BIODERM, INC. (US) 2002-03-13 EP claimed
US-20010041193-A1 Method for treatment of aging or damaged skin BIODERM, INC. 2001-11-15 US claimed
US-6217914-B1 Ascorbic acid composition and method for treatment of aging or damaged skin BIODERM, INC. 2001-04-17 US claimed
WO-2000056327-A1 ASCORBIC ACID COMPOSITION AND METHOD FOR TREATMENT OF AGING OR DAMAGED SKIN BIODERM, INC. (US) 2000-09-28 WO claimed