SCHEMBL8418914

SCHEMBL8418914

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

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KIF11 P52732 6/20 0.50
GSR P00390 2/20 0.50
GRM8 O00222 1/20 0.50
GRM6 O15303 1/20 0.50
GRIN2D O15399 1/20 0.50
GRIN3B O60391 1/20 0.50
CYP1A2 P05177 1/20 0.50
GRIK1 P39086 1/20 0.50
GRM5 P41594 1/20 0.50
GRIA1 P42261 1/20 0.50
GRIA2 P42262 1/20 0.50
GRIA3 P42263 1/20 0.50
SLC1A3 P43003 1/20 0.50
SLC1A2 P43004 1/20 0.50
SLC1A1 P43005 1/20 0.50
GRIA4 P48058 1/20 0.50
GRIN1 Q05586 1/20 0.50
GRIN2A Q12879 1/20 0.50
GRIK2 Q13002 1/20 0.50
GRIK3 Q13003 1/20 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
SCHEMBL5697661 1.00 KIF11 (0.50) KIF11GSRGRM8GRM6GRIN2D
SCHEMBL14420362 1.00 KIF11 (0.50) KIF11GSRGRM8GRM6GRIN2D
Hydrochloric Acid SCHEMBL29213474 0.98 NOS2 (0.50) KIF11GSRGRM8GRM6GRIN2D
Hydrochloric Acid SCHEMBL319257 0.98 NOS2 (0.50) KIF11GSRGRM8GRM6GRIN2D
SCHEMBL10052913 0.88 GSR (0.56) GSRGRM8GRM6GRIN2DGRIN3B
SCHEMBL10052915 0.88 GSR (0.56) GSRGRM8GRM6GRIN2DGRIN3B
SCHEMBL16497780 0.88 GSR (0.56) GSRGRM8GRM6GRIN2DGRIN3B
Ammonia Solution, Strong SCHEMBL28728275 0.86 GSR (0.54) GSRGRM8GRM6GRIN2DGRIN3B
SCHEMBL17431026 0.85 GSR (0.57) GSRGRM8GRM6GRIN2DGRIN3B
SCHEMBL15222427 0.85 GSR (0.57) GSRGRM8GRM6GRIN2DGRIN3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119061087-A Synthesis method of (S) -2-amino-5, 5-dimethylhexanoic acid 四川同晟生物医药有限公司 2024-12-03 CN claimed
EP-4676914-A1 MODULATORS OF SORTILIN ACTIVITY Vesper Bio Aps (DK) 2026-01-14 EP disclosed
US-20250345446-A1 BIFUNCTIONAL MOLECULES THAT SELECTIVELY INDUCE DEGRADATION OF EXTRACELLULAR TARGETS IN LYSOSOMES DRAUPNIR BIO APS (DK) 2025-11-13 US disclosed
US-20250268854-A1 2-AMINO-5,5-DIMETHYLHEXANOIC ACID DERIVATIVES AS SORTILIN MODULATORS FOR USE IN THE TREATMENT OF DISEASE OF THE CENTRAL NERVOUS SYSTEM VESPER BIO APS (DK) 2025-08-28 US disclosed
CN-120077033-A Sortilin modulators 维斯珀生物应用有限公司 2025-05-30 CN disclosed
WO-2025087397-A1 LIGANDS FOR EXTRAHEPATIC DELIVERY OF siRNA RONA BIOSCIENCE, LIMITED (CN) 2025-05-01 WO disclosed
EP-4543858-A1 BIFUNCTIONAL MOLECULES THAT SELECTIVELY INDUCE DEGRADATION OF EXTRACELLULAR TARGETS IN LYSOSOMES Draupnir Bio ApS (DK) 2025-04-30 EP disclosed
EP-4486443-A1 AMINO ACID BASED CARBAMATES AND/OR UREAS FOR THE TREATMENT OF SORTILIN DEPENDENT DISEASES Vesper Bio Aps (DK) 2025-01-08 EP disclosed
CN-119061087-A Synthesis method of (S) -2-amino-5, 5-dimethylhexanoic acid 四川同晟生物医药有限公司 2024-12-03 CN disclosed
CN-119061087-A Synthesis method of (S) -2-amino-5, 5-dimethylhexanoic acid 四川同晟生物医药有限公司 2024-12-03 CN disclosed
WO-2017180535-A1 CHIRAL PEPTIDES CARNOT, LLC (US) 2017-10-19 WO disclosed
EP-2658857-B1 SUBSTITUTED PURINE NUCLEOSIDES, PHOSPHOROAMIDATE AND PHOSPHORODIAMIDATE DERIVATIVES FOR TREATMENT OF VIRAL INFECTIONS INHIBITEX INC (US) 2016-11-02 EP disclosed
US-9351989-B2 Substituted purine nucleosides, phosphoroamidate and phosphorodiamidate derivatives for treatment of viral infections INHIBITEX, INC. (US) 2016-05-31 US disclosed
US-20140140955-A1 SUBSTITUTED PURINE NUCLEOSIDES, PHOSPHOROAMIDATE AND PHOSPHORODIAMIDATE DERIVATIVES FOR TREATMENT OF VIRAL INFECTIONS UNIVERSITY COLLEGE OF CARDIFF CONSULTANTS LIMITED (GB) 2014-05-22 US disclosed
US-8540966-B2 Contrast agents endowed with high relaxivity BRACCO IMAGING S.P.A. (IT) 2013-09-24 US disclosed
US-8105567-B2 Multidentate AZA ligands able to complex metal ions and the use thereof in diagnostics and therapy BRACCO IMAGING SPA (IT) 2012-01-31 US disclosed
US-20110256067-A1 Contrast agents endowed with high relaxivity BRACCO IMAGING SPA (IT) 2011-10-20 US disclosed
EP-0692538-B1 Process for producing optically active L-amino acids DEGUSSA (DE) 1999-09-22 EP disclosed
EP-0692478-A1 Process for the preparation of optically active 4 substituted (S)-2-oxazolidinone, optically active (S)-aminoalcohols and utilization of there compounds Degussa Aktiengesellschaft (DE) 1996-01-17 EP disclosed
EP-0692538-A2 Process for producing optically active L-amino acids, novel optically active L-aminoacids with bulky side-chains and their use Degussa Aktiengesellschaft (DE) 1996-01-17 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 (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-20110256067-A1 Contrast agents endowed with high relaxivity SLC40A1, SLC67A1, SLC19A1 KIF11 2945/4885GSR 889/4885GRM8 3388/4885
US-20250268854-A1 2-AMINO-5,5-DIMETHYLHEXANOIC ACID DERIVATIVES AS SORTILIN MODULATORS FOR USE IN THE TREATMENT OF DISEASE OF THE CENTRAL NERVOUS SYSTEM SORT1, NMUR2, NMUR1 KIF11 1659/4885GSR 4825/4885GRM8 1797/4885
US-20250345446-A1 BIFUNCTIONAL MOLECULES THAT SELECTIVELY INDUCE DEGRADATION OF EXTRACELLULAR TARGETS IN LYSOSOMES SORT1, SCARB1, LAMP1 KIF11 3398/4885GSR 4540/4885GRM8 4061/4885
US-20140140955-A1 SUBSTITUTED PURINE NUCLEOSIDES, PHOSPHOROAMIDATE AND PHOSPHORODIAMIDATE DERIVATIVES FOR TREATMENT OF VIRAL INFECTIONS PNP, UMPS, UPP1 KIF11 4354/4885GSR 1735/4885GRM8 3885/4885

“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.