SCHEMBL1654337

SCHEMBL1654337

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

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 1/20 0.43
NOS1 P29475 2/20 0.38
NOS3 P29474 1/20 0.38
NOS2 P35228 1/20 0.38
SLC1A1 P43005 2/20 0.35
HDAC3 O15379 1/20 0.35
HDAC1 Q13547 1/20 0.35
HDAC2 Q92769 1/20 0.35
HDAC8 Q9BY41 1/20 0.35
HDAC6 Q9UBN7 1/20 0.35
CYP1A2 P05177 2/20 0.33
GRM8 O00222 1/20 0.33
GRM6 O15303 1/20 0.33
GRIN2D O15399 1/20 0.33
GRIN3B O60391 1/20 0.33
GSR P00390 1/20 0.33
GRIK1 P39086 1/20 0.33
GRM5 P41594 1/20 0.33
GRIA1 P42261 1/20 0.33
GRIA2 P42262 1/20 0.33

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
SCHEMBL1841835 1.00 LTA4H (0.43) LTA4HNOS1NOS3NOS2SLC1A1
SCHEMBL18477 1.00 LTA4H (0.43) LTA4HNOS1NOS3NOS2SLC1A1
Hydrochloric Acid SCHEMBL4654220 0.98 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
SCHEMBL6893763 0.98 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
Hydrochloric Acid SCHEMBL18476 0.98 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
Water SCHEMBL27596082 0.98 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
Water SCHEMBL3912787 0.98 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
Hydrochloric Acid SCHEMBL1517836 0.98 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
SCHEMBL18744647 0.90 LTA4H (0.40) LTA4HNOS1NOS3NOS2SLC1A1
SCHEMBL23416460 0.89 LTA4H (0.39) LTA4HNOS1NOS3NOS2SLC1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110272468-B Preparation and application of prostate specific membrane antigen small molecule inhibitor and radionuclide complex thereof 上海益泰医药科技有限公司 2020-12-08 CN claimed
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
US-20250269043-A1 TARGETED BIFUNCTIONAL DEGRADERS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2025-08-28 US disclosed
CN-119562958-A Methods for preparing NAG-25 carbohydrate targeting moieties and intermediates thereof 安进公司 2025-03-04 CN disclosed
EP-4493221-A2 TARGETED BIFUNCTIONAL DEGRADERS Yale University (US) 2025-01-22 EP disclosed
CN-119212727-A Targeted bifunctional degradants 耶鲁大学 2024-12-27 CN disclosed
WO-2024224093-A1 DESMURAMYLPEPTIDE DIEESTERS AS NOD2 AGONISTS AND USE THEREOF Imhotex Limited (GB) 2024-10-31 WO disclosed
EP-4440701-A1 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION GILEAD SCIENCES, INC. (US) 2024-10-09 EP disclosed
WO-2024105205-A1 ANTIBODY-DRUG CONJUGATES (A2DCS) WITH ENZYMATICALLY CLEAVABLE GROUPS BAYER AKTIENGESELLSCHAFT (DE) 2024-05-23 WO disclosed
US-20100068769-A1 L-GLUTAMIC ACID-PRODUCING MICROORGANISM AND A METHOD FOR PRODUCING L-GLUTAMIC ACID NAKAMURA JUN 2010-03-18 US disclosed
EP-1831250-A2 L-GLUTAMIC ACID-PRODUCING MICROORGANISM AND A METHOD FOR PRODUCING L-GLUTAMIC ACID Ajinomoto Co., Inc. (JP) 2007-09-12 EP disclosed
WO-2006070944-A2 L-GLUTAMIC ACID-PRODUCING MICROORGANISM AND A METHOD FOR PRODUCING L-GLUTAMIC ACID AJINOMOTO CO., INC. (JP) 2006-07-06 WO disclosed
US-20060141588-A1 L-GLUTAMIC ACID-PRODUCING MICROORGANISM AND A METHOD FOR PRODUCING L-GLUTAMIC ACID AJINOMOTO CO., INC. (JP) 2006-06-29 US disclosed
US-5187167-A Antitumor agents IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1993-02-16 US disclosed
US-5108990-A GLUTAMIC ACID DERIVATIVES ROUSSEL UCLAF (FR) 1992-04-28 US disclosed
US-5081124-A Amino acid and polyamino acid derivatives, inhibitors of thymidylate synthetase IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1992-01-14 US disclosed
US-4992550-A Thymidylate synthetase inhibitors IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1991-02-12 US disclosed
US-4956461-A LEUKEMIA, ANTICARCINOGENIC AGENTS DANA FARBER CANCER INSTITUTE, INC. (US) 1990-09-11 US disclosed
WO-1990004593-A1 DESAMINO-AMINOPTERIN AND -METHOTREXATE DANA-FARBER CANCER INSTITUTE (US) 1990-05-03 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 (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-20250269043-A1 TARGETED BIFUNCTIONAL DEGRADERS SMURF2, SMURF1, MDM2 LTA4H 3924/4885NOS1 3482/4885NOS3 4005/4885
US-12404262-B2 Therapeutic compounds for HIV virus infection HAVCR2, MAVS, CD4 LTA4H 1204/4885NOS1 2449/4885NOS3 1219/4885
US-20260035357-A1 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION CCR10, CCR1, CCR3 LTA4H 3109/4885NOS1 1238/4885NOS3 539/4885

“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.