Serine

Serine

SCHEMBL348967

CC(C)C[C@H](N)C(=O)OC(=O)CN.N[C@@H](CO)C(=O)O

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
SLC7A5 Q01650 1/20 0.52
SLC1A3 P43003 4/20 0.42
SLC1A2 P43004 4/20 0.42
SLC1A1 P43005 5/20 0.37
LAP3 P28838 3/20 0.36
MME P08473 2/20 0.34
RNPEP Q9H4A4 2/20 0.32
ANPEP P15144 1/20 0.32
DNPEP Q9ULA0 1/20 0.32
CACNA2D1 P54289 2/20 0.32
CACNB3 P54284 1/20 0.32
CACNA1C Q13936 1/20 0.32
PGR P06401 1/20 0.32
ADRA1A P35348 1/20 0.32
HTR2B P41595 1/20 0.32
CACNA2D2 Q9NY47 1/20 0.32
GRIK1 P39086 1/20 0.32
GRIK2 Q13002 1/20 0.32

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
SCHEMBL1537346 0.88 SLC7A5 (0.48) SLC7A5SLC1A3SLC1A2SLC1A1LAP3
SCHEMBL1537226 0.88 SLC7A5 (0.48) SLC7A5SLC1A3SLC1A2SLC1A1LAP3
Serine SCHEMBL6666261 0.85 SLC7A5 (0.38) SLC7A5SLC1A3SLC1A2SLC1A1GRIK1
Serine SCHEMBL5320795 0.83 SLC7A5 (0.39) SLC7A5SLC1A3SLC1A2SLC1A1GRIK1
Serine SCHEMBL1064689 0.81 SLC1A1 (0.43) SLC7A5SLC1A3SLC1A2SLC1A1GRIK1
Serine SCHEMBL418634 0.81 PTGS1 (0.48) SLC1A1GRIK1GRIK2
Serine SCHEMBL3961258 0.81 SLC1A5 (0.36) SLC1A1GRIK1GRIK2
SCHEMBL16972731 0.80 SLC7A5 (0.64) SLC7A5SLC1A3SLC1A2SLC1A1RNPEP
Leucine SCHEMBL348968 0.80 SLC7A5 (0.69) SLC7A5SLC1A3SLC1A2SLC1A1LAP3
Leucine SCHEMBL27569034 0.80 SLC7A5 (0.69) SLC7A5SLC1A3SLC1A2SLC1A1LAP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1601330-A4 ANTITUMOR AGENTS COMPRISING A TARGETING PORTION AND AN IMMUNE RESPONSE TRIGGERING PORTION GHC RES DEV CORP (US) 2008-05-07 EP claimed
CN-1787838-A Antitumor agent comprising targeting moiety and immune response triggering moiety GREENVILLE HOSPITAL SYSTEM (US) 2006-06-14 CN claimed
EP-1601330-A2 ANTITUMOR AGENTS COMPRISING A TARGETING PORTION AND AN IMMUNE RESPONSE TRIGGERING PORTION Greenville Hospital System (US) 2005-12-07 EP claimed
US-20050025771-A1 Antitumor agents comprising a targeting portion and an immune response triggering portion GREENVILLE HOSPITAL SYSTEM 2005-02-03 US claimed
WO-2004078137-A2 ANTITUMOR AGENTS COMPRISING A TARGETING PORTION AND AN IMMUNE RESPONSE TRIGGERING PORTION GREENVILLE HOSPITAL SYSTEM (US) 2004-09-16 WO claimed
US-20230165952-A1 BETACORONAVIRUS PROPHYLAXIS AND THERAPY Nykode Therapeutics ASA (NO) 2023-06-01 US disclosed
EP-4143210-A1 BETACORONAVIRUS PROPHYLAXIS AND THERAPY Nykode Therapeutics ASA (NO) 2023-03-08 EP disclosed
WO-2021219897-A1 BETACORONAVIRUS PROPHYLAXIS AND THERAPY VACCIBODY AS (NO) 2021-11-04 WO disclosed
CN-106083932-B Novel preactivated oxazaphosphorin derivative, application and preparation method 法国古士塔柏罗斯学院 2019-08-06 CN disclosed
US-10125157-B2 Derivatives of oxazaphosphorines that are pre-activated, use and method of preparation INSTITUT GUSTAVE ROUSSY (FR) 2018-11-13 US disclosed
EP-2649084-B1 NOVEL DERIVATIVES OF OXAZAPHOSPHORINES THAT ARE PRE-ACTIVATED, USE AND METHOD OF PREPARATION ROUSSY INST GUSTAVE (FR) 2017-02-22 EP disclosed
US-20160333038-A1 NOVEL DERIVATIVES OF OXAZAPHOSPHORINES THAT ARE PRE-ACTIVATED, USE AND METHOD OF PREPARATION INSTITUT GUSTAVE ROUSSY (FR) 2016-11-17 US disclosed
WO-2001053342-A1 CHIMERIC PROSTATE-HOMING PEPTIDES WITH PRO-APOPTOTIC ACTIVITY THE BURNHAM INSTITUTE (US) 2001-07-26 WO disclosed
WO-1998010795-A9 TUMOR HOMING MOLECULES, CONJUGATES DERIVED THEREFROM, AND METHODS OF USING SAME BURNHAM INST (US) 2001-06-21 WO disclosed
US-6180084-B1 CONTACTING PURIFIED NGR RECEPTOR WITH ONE OR MORE MOLECULES AND DETERMINING SPECIFIC BINDING OF MOLECULE TO NGR RECEPTOR, WHERE PRESENCE OF SPECIFIC BINDING IDENTIFIES MOLECULE AS TUMOR HOMING MOLECULE THAT HOMES TO ANGIOGENIC VASCULATURE THE BURNHAM INSTITUTE 2001-01-30 US disclosed
WO-2000042973-A2 HOMING PRO-APOPTOTIC CONJUGATES AND METHODS OF USING SAME THE BURNHAM INSTITUTE (US) 2000-07-27 WO disclosed
EP-1015884-A1 METHODS OF IDENTIFYING MOLECULES THAT HOME TO ANGIOGENIC VASCULATURE IN TUMORS The Burnham Institute (US) 2000-07-05 EP disclosed
EP-0927045-A2 TUMOR HOMING MOLECULES, CONJUGATES DERIVED THEREFROM, AND METHODS OF USING SAME The Burnham Institute (US) 1999-07-07 EP disclosed
WO-1999013329-A1 METHODS OF IDENTIFYING MOLECULES THAT HOME TO ANGIOGENIC VASCULATURE IN TUMORS THE BURNHAM INSTITUTE (US) 1999-03-18 WO disclosed
WO-1998010795-A2 TUMOR HOMING MOLECULES, CONJUGATES DERIVED THEREFROM, AND METHODS OF USING SAME THE BURNHAM INSTITUTE (US) 1998-03-19 WO 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-20160333038-A1 NOVEL DERIVATIVES OF OXAZAPHOSPHORINES THAT ARE PRE-ACTIVATED, USE AND METHOD OF PREPARATION INPP5B, TYMP, ENTPD5 SLC7A5 3946/4885SLC1A3 3877/4885SLC1A2 4168/4885
US-10125157-B2 Derivatives of oxazaphosphorines that are pre-activated, use and method of preparation TYMP, INPP5B, ENTPD5 SLC7A5 3637/4885SLC1A3 3459/4885SLC1A2 3640/4885

“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.