SCHEMBL354949

SCHEMBL354949

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

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC15A1 P46059 1/20 0.61
ALDH1A1 P00352 4/20 0.56
SLC1A3 P43003 2/20 0.51
SLC1A2 P43004 2/20 0.51
SLC1A1 P43005 2/20 0.51
KMT2A Q03164 2/20 0.51
MEN1 O00255 1/20 0.51
CYP1A2 P05177 1/20 0.51
CYP2D6 P10635 1/20 0.51
CYP2C9 P11712 1/20 0.51
CYP2C19 P33261 1/20 0.51
MAPK1 P28482 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
SLC6A2 P23975 1/20 0.50
SLC6A3 Q01959 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
CTSB P07858 1/20 0.48
LTA4H P09960 2/20 0.48
LAP3 P28838 1/20 0.48
LMNA P02545 2/20 0.46

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
SCHEMBL542444 1.00 SLC15A1 (0.61) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1
SCHEMBL2137609 1.00 SLC15A1 (0.61) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1
Hydrochloric Acid SCHEMBL2135391 0.98 SLC15A1 (0.59) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1
Hydrochloric Acid SCHEMBL7275901 0.98 SLC15A1 (0.59) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1
Hydrochloric Acid SCHEMBL542587 0.98 SLC15A1 (0.59) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1
Hydrochloric Acid SCHEMBL2137602 0.98 SLC15A1 (0.59) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1
Hydrochloric Acid SCHEMBL7275897 0.98 SLC15A1 (0.59) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1
Valine SCHEMBL28244846 0.95 SLC15A1 (0.60) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1
Valine SCHEMBL28244847 0.95 SLC15A1 (0.60) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1
Lactic Acid SCHEMBL28307486 0.94 SLC15A1 (0.59) SLC15A1ALDH1A1SLC1A3SLC1A2SLC1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118852338-A Oral micromolecular salvianic acid derivatives, and preparation method and application thereof 首都医科大学 2024-10-29 CN claimed
CN-118852337-A Antitumor drug and preparation method thereof 广西中医药大学 2024-10-29 CN claimed
CN-112812149-B Amino acid derivative, preparation method and application thereof, anti-tumor micelle and preparation method thereof 首都医科大学 2022-04-29 CN claimed
CN-111689877-B High-selectivity mercury ion detection fluorescent probe and synthetic method and application thereof 商丘师范学院 2022-03-25 CN claimed
CN-107698660-B imidazopyridine-6-formyl-Lys (Lys) -oligopeptides, their synthesis, activity and uses 首都医科大学 2021-06-08 CN claimed
CN-111689877-A High-selectivity mercury ion detection fluorescent probe and synthetic method and application thereof 商丘师范学院 2020-09-22 CN claimed
CN-106349332-B imidazopyridinyl-KRGDV, its synthesis, antithrombotic activity and use 首都医科大学 2019-12-10 CN claimed
EP-3275864-B1 COMPOUND OF 3-HYDROXYL PYRIDINE, PREPARATION METHOD THEREOF AND PHARMACEUTICAL USE THEREOF SHENYANG SUNSHINE PHARMACEUTICAL CO LTD (CN) 2019-08-14 EP claimed
US-10149841-B2 Compound of 3-hydroxyl pyridine, preparation method thereof and pharmaceutical use thereof SHENYANG SUNSHINE PHARMACEUTICAL CO. LTD. (CN) 2018-12-11 US claimed
US-20180117021-A1 COMPOUND OF 3-HYDROXYL PYRIDINE, PREPARATION METHOD THEREOF AND PHARMACEUTICAL USE THEREOF SHENYANG SUNSHINE PHARMACEUTICAL CO., LTD. (CN) 2018-05-03 US claimed
US-20090192318-A1 Method of preparation of N-(1-oxopentyl)-N-[[2'-(1H-tetrazol-5-y1) [1,1'-biphenyl]-4-y1]methyl]-L-valine (valsartan) ZENTIVA, A.S. (CZ) 2009-07-30 US claimed
WO-2008135762-A1 PROCESS FOR PREPARING VALSARTAN CIPLA LIMITED (IN) 2008-11-13 WO claimed
WO-2008012852-A1 INTERMEDIATE COMPOUNDS FOR THE PREPARATION OF ANGIOTENSIN II ANTAGONISTS S.I.M.S. S.r.l. - SOCIETÀ ITALIANA MEDICINALI SCANDICCI (IT) 2008-01-31 WO claimed
US-20060281801-A1 Process for the preparation of valsartan and its intermediates IPCA LABORATORIES LIMITED (IN) 2006-12-14 US claimed
EP-1714963-A1 Process for the Preparation of Valsartan and its Intermediates IPCA Laboratories Limited (IN) 2006-10-25 EP claimed
EP-1622882-B1 A METHOD OF PREPARATION OF N -(1-OXOPENTYL)- N-¬¬ 2-(1TETRAZOL-5-y1) ¬1,1 -BIPHENYL|-4-y1 METHYL| -L-VALINE (VALSARTAN) ZENTIVA AS (CZ) 2006-07-12 EP claimed
EP-1622882-A1 A METHOD OF PREPARATION OF N -(1-OXOPENTYL)- N-[[ 2-(1TETRAZOL-5-y1) [1,1 -BIPHENYL]-4-y1 METHYL] -L-VALINE (VALSARTAN) ZENTIVA, A.S. (CZ) 2006-02-08 EP claimed
WO-2004101534-A1 A METHOD OF PREPARATION OF N-(1-OXOPENTYL)-N-[[2'-(1H-TETRAZOL-5-y1) [1,1'-BIPHENYL] -4-y1]METHYL]-L-VALINE (VALSARTAN) ZENTIVA, A. S. (CZ) 2004-11-25 WO claimed
US-5602161-A ELASTASE INHIBITORS; PREVENTING AND TREATING EMPHYSEMA, ENDOTOXIN-INDUCED LUNG DISORDERS WAKAMOTO PHARMACEUTICAL CO., LTD. (JP) 1997-02-11 US claimed
EP-0676396-A1 Tetrazolylphenyl pivalate derivatives and medicinal composition containing the same as effective component Wakamoto Pharmaceutical Co., Ltd. (JP) 1995-10-11 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-20060281801-A1 Process for the preparation of valsartan and its intermediates ACE, REN, AGT SLC15A1 1529/4885ALDH1A1 934/4885SLC1A3 2463/4885
US-20090192318-A1 Method of preparation of N-(1-oxopentyl)-N-[[2'-(1H-tetrazol-5-y1) [1,1'-biphenyl]-4-y1]methyl]-L-valine (valsartan) TTR, REN, VARS1 SLC15A1 2056/4885ALDH1A1 2118/4885SLC1A3 1376/4885
US-20180117021-A1 COMPOUND OF 3-HYDROXYL PYRIDINE, PREPARATION METHOD THEREOF AND PHARMACEUTICAL USE THEREOF EGLN3, EGLN2, P4HA1 SLC15A1 3223/4885ALDH1A1 243/4885SLC1A3 3012/4885
US-10149841-B2 Compound of 3-hydroxyl pyridine, preparation method thereof and pharmaceutical use thereof EGLN3, EGLN2, P4HA1 SLC15A1 3223/4885ALDH1A1 243/4885SLC1A3 3012/4885

“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.