SCHEMBL3099705

SCHEMBL3099705

N[C@H](Cc1ccccc1)C(=O)OCc1ccccc1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC7A5 Q01650 2/20 0.63
ALPI P09923 1/20 0.63
PKM P14618 1/20 0.63
PTGS1 P23219 1/20 0.63
XIAP P98170 1/20 0.63
SLC15A1 P46059 2/20 0.60
ALDH1A1 P00352 3/20 0.58
LTA4H P09960 2/20 0.56
LAP3 P28838 1/20 0.56
KMT2A Q03164 2/20 0.52
MAPK1 P28482 1/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
SLC6A2 P23975 1/20 0.52
SLC6A3 Q01959 1/20 0.52
TDP1 Q9NUW8 1/20 0.52
IDO1 P14902 1/20 0.51
CTRB1 P17538 2/20 0.50
SLC1A3 P43003 2/20 0.50
SLC1A2 P43004 2/20 0.50
SLC1A1 P43005 2/20 0.50

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
SCHEMBL73707 1.00 SLC7A5 (0.63) SLC7A5ALPIPKMPTGS1XIAP
SCHEMBL73708 1.00 SLC7A5 (0.63) SLC7A5ALPIPKMPTGS1XIAP
Hydrochloric Acid SCHEMBL1168587 0.98 SLC7A5 (0.61) SLC7A5ALPIPKMPTGS1XIAP
Hydrochloric Acid SCHEMBL353729 0.98 SLC7A5 (0.61) SLC7A5ALPIPKMPTGS1XIAP
Hydrochloric Acid SCHEMBL6364440 0.98 SLC7A5 (0.61) SLC7A5ALPIPKMPTGS1XIAP
Carbamic Acid SCHEMBL13836019 0.96 SLC7A5 (0.59) SLC7A5ALPIPKMPTGS1XIAP
SCHEMBL121369 0.93 SLC7A5 (0.62) SLC7A5ALPIPKMPTGS1XIAP
SCHEMBL630209 0.93 SLC7A5 (0.62) SLC7A5ALPIPKMPTGS1XIAP
SCHEMBL16080193 0.93 SLC7A5 (0.62) SLC7A5ALPIPKMPTGS1XIAP
SCHEMBL26023571 0.93 SLC7A5 (0.62) SLC7A5ALPIPKMPTGS1XIAP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118007135-A Corrosion inhibition method for inhibiting metal corrosion in sulfur-containing medium 福建理工大学 2024-05-10 CN claimed
CN-105085321-B A kind of preparation method of N methoxycarbonyl groups L Terleus 浙江九洲药业股份有限公司 2017-11-24 CN claimed
CN-105085321-A Preparation method of N- methoxycarbonyl group-L-tertiary leucine ZHEJIANG JIUZHOU PHARM CO LTD 2015-11-25 CN claimed
CN-103159647-A Preparation method of N-methoxycarbonyl-L-tert-leucine ZHEJIANG JIUZHOU PHARM CO LTD 2013-06-19 CN claimed
US-20240374689-A1 HIGHLY ACTIVE POLYPEPTIDES AND METHODS OF MAKING AND USING THE SAME LONGEVITY BIOTECH, INC. 2024-11-14 US disclosed
CN-118007135-A Corrosion inhibition method for inhibiting metal corrosion in sulfur-containing medium 福建理工大学 2024-05-10 CN disclosed
CN-116655732-A Tetrapeptide compound TP-2, preparation method and application 兰州大学 2023-08-29 CN disclosed
CN-109517032-B Tetrapeptide compound and preparation method and application thereof 兰州大学 2023-07-28 CN disclosed
CN-110229217-B Cyclic peptide, pharmaceutical or cosmetic composition comprising the same, and preparation method thereof 丝芙芮生医科技有限公司 2022-04-05 CN disclosed
CN-108727468-B Cyclic peptide, pharmaceutical or cosmetic composition comprising the same, and preparation method thereof 陈建添 2021-12-03 CN disclosed
EP-3628677-B1 METHOD FOR PREPARING A CYCLOPEPTIDE UNIV NAT TSING HUA (TW) 2021-11-10 EP disclosed
EP-3628677-B1 METHOD FOR PREPARING A CYCLOPEPTIDE UNIV NAT TSING HUA (TW) 2021-11-10 EP disclosed
EP-0689545-A1 MACROCYCLIC AMIDE AND UREA IMMUNOMODULATORS ABBOTT LABORATORIES (US) 1996-01-03 EP disclosed
EP-0642516-A1 MACROCYCLIC IMMUNOMODULATORS ABBOTT LABORATORIES (US) 1995-03-15 EP disclosed
WO-1994021642-A1 MACROCYCLIC AMIDE AND UREA IMMUNOMODULATORS ABBOTT LABORATORIES (US) 1994-09-29 WO disclosed
EP-0642516-A4 MACROCYCLIC IMMUNOMODULATORS. ABBOTT LAB (US) 1994-06-15 EP disclosed
US-5242903-A Enzyme inhibitors BAYER AKTIENGESELLSCHAFT (DE) 1993-09-07 US disclosed
WO-1993004680-A1 MACROCYCLIC IMMUNOMODULATORS ABBOTT LABORATORIES (US) 1993-03-18 WO disclosed
US-5095006-A Enzyme inhibitors BAYER AKTIENGESELLSCHAFT (DE) 1992-03-10 US disclosed
EP-0412350-A2 Renininhibitors, procedure for their preparation and use as medicaments BAYER AG (DE) 1991-02-13 EP 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-20240374689-A1 HIGHLY ACTIVE POLYPEPTIDES AND METHODS OF MAKING AND USING THE SAME SCTR, GIPR, APLNR SLC7A5 570/4885ALPI 3115/4885PKM 2245/4885

“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.