SCHEMBL334927

SCHEMBL334927

O=C(NCCC(O)C(=O)O)OCc1ccccc1

nearest known ligand 0.64

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ SLC1A3 P43003 1/20 0.64
▸ SLC1A1 P43005 1/20 0.64
▸ LMNA P02545 1/20 0.63
▸ SMN1; SMN2 Q16637 1/20 0.63
▸ HTT P42858 1/20 0.60
▸ L3MBTL1 Q9Y468 2/20 0.56
▸ FOLH1 Q04609 4/20 0.54
▸ TGM2 P21980 1/20 0.53
▸ KEAP1 Q14145 2/20 0.52
▸ NFE2L2 Q16236 2/20 0.52
▸ MAPT P10636 1/20 0.51
▸ MMP2 P08253 1/20 0.51
▸ MMP9 P14780 1/20 0.51
▸ DPP8 Q6V1X1 1/20 0.49
▸ DPP7 Q9UHL4 1/20 0.49
▸ MEN1 O00255 1/20 0.49
▸ KMT2A Q03164 1/20 0.49

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
SCHEMBL735799 1.00 SLC1A3 (0.64) SLC1A3SLC1A1LMNASMN1; SMN2HTT
SCHEMBL334926 1.00 SLC1A3 (0.64) SLC1A3SLC1A1LMNASMN1; SMN2HTT
SCHEMBL11317170 0.91 HTT (0.65) SLC1A3SLC1A1LMNASMN1; SMN2HTT
SCHEMBL2139878 0.91 HTT (0.65) SLC1A3SLC1A1LMNASMN1; SMN2HTT
SCHEMBL2139876 0.91 HTT (0.65) SLC1A3SLC1A1LMNASMN1; SMN2HTT
SCHEMBL6827224 0.90 HTT (0.63) SLC1A3SLC1A1LMNASMN1; SMN2HTT
SCHEMBL318936 0.90 HTT (0.63) SLC1A3SLC1A1LMNASMN1; SMN2HTT
SCHEMBL318935 0.90 HTT (0.63) SLC1A3SLC1A1LMNASMN1; SMN2HTT
SCHEMBL6827355 0.89 TGM2 (0.62) SLC1A3SLC1A1LMNASMN1; SMN2HTT
SCHEMBL6827174 0.89 TGM2 (0.62) SLC1A3SLC1A1LMNASMN1; SMN2HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115716856-A Method for synthesizing aminoglycoside antibiotic arbekacin 山东厚德精诚药业有限公司 2023-02-28 — — CN claimed
US-5656735-A Process for the preparation of amikacin precursors BIOCHIMICA OPOS SPA (IT) 1997-08-12 — — US claimed
EP-0446670-B1 Method of preparation of amikacin precursors OPOS BIOCHIMICA SRL (IT) 1994-09-21 — — EP claimed
EP-0446670-A1 Method of preparation of amikacin precursors BIOCHIMICA OPOS SPA (IT) 1991-09-18 — — EP claimed
US-4268664-A Process for the preparation of 1-N-isoseryl- or 1-N-(L-4-amino-2-hydroxybutyryl)-3',4'-dideoxykanamycin B and intermediates thereof ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1981-05-19 — — US claimed
CN-120719568-A Environment-friendly newsprint and preparation method thereof 河北华泰纸业有限公司 2025-09-30 — — CN disclosed
CN-115716856-B Synthetic aminoglycoside method for antibiotic Abecamycin 北京耀诚惠仁科技有限公司 2025-04-25 — — CN disclosed
US-11932633-B2 KRas G12C inhibitors Mirati Therapeutics, Inc. (US) 2024-03-19 — — US disclosed
CN-115716856-A Method for synthesizing aminoglycoside antibiotic arbekacin 山东厚德精诚药业有限公司 2023-02-28 — — CN disclosed
US-20210380570-A1 KRAS G12C INHIBITORS Mirati Therapeutics, Inc. 2021-12-09 — — US disclosed
EP-3790551-A1 KRAS G12C INHIBITORS Mirati Therapeutics, Inc. (US) 2021-03-17 — — EP disclosed
WO-2019217307-A1 KRAS G12C INHIBITORS Mirati Therapeutics, Inc. (US) 2019-11-14 — — WO disclosed
US-4065616-A ANTIBIOTICS ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JA) 1977-12-27 — — US disclosed
US-4065615-A Deoxyaminoglycoside antibiotic derivatives TAKEDA CHEMICAL INDUSTRIES, LTD. (JA) 1977-12-27 — — US disclosed
US-4055715-A Method of producing 1-N-[L-(-)-α-hydroxy-γ-aminobutyryl]XK-62-2 ABBOTT LABORATORIES (US) 1977-10-25 — — US disclosed
US-4038478-A ANTIBACTERIAL AGENTS THE UPJOHN COMPANY (US) 1977-07-26 — — US disclosed
US-4001208-A DERIVATIVE OF AN AMINOGLYCOSIDIC ANTIBIOTIC ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYO KAI (JA) 1977-01-04 — — US disclosed
US-3996205-A BACTERICIDES THE UPJOHN COMPANY (US) 1976-12-07 — — US disclosed
US-3984393-A BACTERICIDES THE UPJOHN COMPANY (US) 1976-10-05 — — US disclosed
US-3940382-A BACTERICIDE ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JA) 1976-02-24 — — 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 (2 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-20210380570-A1 KRAS G12C INHIBITORS KRAS, NRAS, HRAS SLC1A3 3382/4885SLC1A1 3969/4885LMNA 2991/4885
US-11932633-B2 KRas G12C inhibitors KRAS, NRAS, HRAS SLC1A3 3382/4885SLC1A1 3969/4885LMNA 2991/4885

“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.

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