SCHEMBL304099

SCHEMBL304099

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

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NOS1 P29475 2/20 0.45
NOS3 P29474 1/20 0.45
NOS2 P35228 1/20 0.45
LMNA P02545 2/20 0.36
KMT2A Q03164 1/20 0.36
CA12 O43570 1/20 0.33
CA14 Q9ULX7 1/20 0.33
CYP2D6 P10635 2/20 0.33
CA1 P00915 1/20 0.32
CA2 P00918 1/20 0.32
CA7 P43166 1/20 0.32
DGAT1 O75907 1/20 0.32
SLC7A5 Q01650 1/20 0.32
CYP3A4 P08684 2/20 0.31
CYP1A2 P05177 1/20 0.31
CYP2C9 P11712 1/20 0.31
NFKB1 P19838 1/20 0.31
CYP2C19 P33261 1/20 0.31
POLB P06746 1/20 0.31
NPSR1 Q6W5P4 1/20 0.31

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
SCHEMBL19858386 1.00 NOS1 (0.45) NOS1NOS3NOS2LMNAKMT2A
SCHEMBL31606685 1.00 NOS1 (0.45) NOS1NOS3NOS2LMNAKMT2A
SCHEMBL9952902 1.00 NOS1 (0.45) NOS1NOS3NOS2LMNAKMT2A
SCHEMBL28179952 1.00 NOS1 (0.45) NOS1NOS3NOS2LMNAKMT2A
SCHEMBL27183262 1.00 NOS1 (0.45) NOS1NOS3NOS2LMNAKMT2A
SCHEMBL304098 1.00 NOS1 (0.45) NOS1NOS3NOS2LMNAKMT2A
Hydrochloric Acid SCHEMBL19858050 0.98 NOS1 (0.44) NOS1NOS3NOS2LMNAKMT2A
Hydrochloric Acid SCHEMBL2409207 0.98 NOS1 (0.44) NOS1NOS3NOS2LMNAKMT2A
Hydrochloric Acid SCHEMBL1825341 0.98 NOS1 (0.44) NOS1NOS3NOS2LMNAKMT2A
Hydrochloric Acid SCHEMBL1825344 0.98 NOS1 (0.44) NOS1NOS3NOS2LMNAKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118239879-A Method for preparing 3-substituted oxindole, dihydroisoindigo and tetra-substituted ethane based on primary amine and application of primary amine 泰山学院 2024-06-25 CN claimed
CN-110790674-A Method for continuously producing O-tert-butyl-L-threonine tert-butyl ester 熊飞龙 2020-02-14 CN claimed
CN-109134314-A A kind of preparation method of polypeptide raw material N- fluorenylmethoxycarb-nyl -nyl O-tert-butyl threonine 吉尔生化(上海)有限公司 2019-01-04 CN claimed
CN-106414435-A Amino-substituted isothiazoles 拜耳制药股份公司 2017-02-15 CN claimed
CN-1026979-C One-step synthesis of tert-butyl threonine UNIV JILIN (CN) 1994-12-14 CN claimed
CN-1041757-A The single stage method of tert-butyl threonine is synthetic UNIV JILIN (CN) 1990-05-02 CN claimed
US-4401757-A CONVERTING ANIMAL INSULIN TO DES-B30-INSULIN, REACTING WITH THREONINE SHIONOGI & CO., LTD. (JP) 1983-08-30 US claimed
US-4400465-A FROM ANIMAL INSULIN BY EXCHANGING THE B30 ALANINE WITH THREONINE SHIONOGI & CO., LTD. (JP) 1983-08-23 US claimed
EP-0017938-B1 PROCESS FOR PREPARING A B30-THREONINE INSULIN SHIONOGI & CO., LTD. (JP) 1983-08-03 EP claimed
US-4320196-A ENZYMATIC CATALYZED REACTION WITH THREONINE DERIVATIVE SHIONOGI & CO., LTD. (JP) 1982-03-16 US claimed
US-4320197-A THREONINE DERIVATIVE SHIONOGI & CO., LTD. (JP) 1982-03-16 US claimed
EP-0017938-A1 Process for preparing a B30-threonine insulin SHIONOGI & CO., LTD. (JP) 1980-10-29 EP claimed
US-20260103498-A1 METHOD FOR PREPARING LIRAGLUTIDE BACHEM HOLDING AG (CH) 2026-04-16 US disclosed
US-20260035357-A1 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION GILEAD SCIENCE INC (US) 2026-02-05 US disclosed
US-12404262-B2 Therapeutic compounds for HIV virus infection GILEAD SCIENCES, INC. (US) 2025-09-02 US disclosed
CN-120136962-A Fibroblast activation protein targeting compound, nuclide marker thereof, pharmaceutical composition containing same and application 潍坊市人民医院(潍坊市公共卫生临床中心、潍坊市职业病医院) 2025-06-13 CN disclosed
EP-0056951-A1 Process for the preparation of human insulin or its derivatives from pig insulin or its derivatives HOECHST AKTIENGESELLSCHAFT (DE) 1982-08-04 EP disclosed
US-4320197-A THREONINE DERIVATIVE SHIONOGI & CO., LTD. (JP) 1982-03-16 US disclosed
US-4320196-A ENZYMATIC CATALYZED REACTION WITH THREONINE DERIVATIVE SHIONOGI & CO., LTD. (JP) 1982-03-16 US disclosed
EP-0017938-A1 Process for preparing a B30-threonine insulin SHIONOGI & CO., LTD. (JP) 1980-10-29 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 (3 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-20260103498-A1 METHOD FOR PREPARING LIRAGLUTIDE GLP1R, IAPP, VIP NOS1 828/4885NOS3 1174/4885NOS2 2202/4885
US-12404262-B2 Therapeutic compounds for HIV virus infection HAVCR2, MAVS, CD4 NOS1 2449/4885NOS3 1219/4885NOS2 1844/4885
US-20260035357-A1 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION CCR10, CCR1, CCR3 NOS1 1238/4885NOS3 539/4885NOS2 2648/4885

“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.