SCHEMBL855007

SCHEMBL855007

CC(C)(C)OC(=O)C(N)CCCN

nearest known ligand 0.44

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
GSR P00390 1/20 0.44
NOS1 P29475 2/20 0.38
NOS3 P29474 1/20 0.38
NOS2 P35228 1/20 0.38
LTA4H P09960 1/20 0.38
CPB2 Q96IY4 3/20 0.38
DPP7 Q9UHL4 5/20 0.37
DPP4 P27487 2/20 0.37
DPP8 Q6V1X1 2/20 0.37
DPP9 Q86TI2 2/20 0.37
GNAI3 P08754 1/20 0.36
GNAO1 P09471 1/20 0.36
GNAI1 P63096 1/20 0.36
MEN1 O00255 1/20 0.35
GAA P10253 1/20 0.35
KMT2A Q03164 1/20 0.35
CYP1A2 P05177 1/20 0.34

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
SCHEMBL11415211 1.00 GSR (0.44) GSRNOS1NOS3NOS2LTA4H
SCHEMBL11415214 1.00 GSR (0.44) GSRNOS1NOS3NOS2LTA4H
Hydrochloric Acid SCHEMBL11272393 0.98 GSR (0.42) GSRNOS1NOS3NOS2LTA4H
SCHEMBL866977 0.94 GSR (0.52) GSRNOS1NOS3NOS2LTA4H
SCHEMBL855342 0.94 GSR (0.52) GSRNOS1NOS3NOS2LTA4H
SCHEMBL1309368 0.93 GSR (0.50) GSRNOS1LTA4HCPB2DPP7
Hydrochloric Acid SCHEMBL3088557 0.93 GSR (0.50) GSRNOS1NOS3NOS2LTA4H
SCHEMBL1309450 0.93 GSR (0.50) GSRNOS1LTA4HCPB2DPP7
SCHEMBL1310240 0.93 GSR (0.50) GSRNOS1LTA4HCPB2DPP7
SCHEMBL2131918 0.93 GSR (0.50) GSRNOS1LTA4HCPB2DPP7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122036671-A Tetramethyl rhodamine-marked agmatine fluorescent probe and preparation method and application thereof 中国人民解放军陆军特色医学中心 2026-05-15 CN claimed
CN-106632189-A Preparation method of N alpha- fluorenylmethoxycarbonyl-N Epsilon-7-methoxycoumarin-4-acetyl-lysine/ornithine 吉尔生化(上海)有限公司 2017-05-10 CN claimed
CN-122036671-A Tetramethyl rhodamine-marked agmatine fluorescent probe and preparation method and application thereof 中国人民解放军陆军特色医学中心 2026-05-15 CN disclosed
US-12569566-B2 Compositions containing, methods and uses of antibody-TLR agonist conjugates AMBRX, INC. (US) 2026-03-10 US disclosed
EP-4663632-A1 COMPOUNDS USEFUL FOR THE MODULATION OF THE ACTIVITY OF STING Sulis Therapeutics ApS (DK) 2025-12-17 EP disclosed
EP-4551210-A1 BIFACIAL PEPTIDE NUCLEIC ACID PROBES AND METHODS OF USING THEREOF Ohio State Innovation Foundation (US) 2025-05-14 EP disclosed
WO-2025073956-A1 STING ANTAGONIST COMPOUNDS SULIS THERAPEUTICS APS (DK) 2025-04-10 WO disclosed
EP-4534147-A1 STING ANTAGONIST COMPOUNDS Sulis Therapeutics ApS (DK) 2025-04-09 EP disclosed
CN-119350422-B Deubiquitinase targeting chimeric compound and preparation method and application thereof 中国药科大学 2025-04-04 CN disclosed
EP-4527828-A1 BIPHENYL COMPOUND, PHARMACEUTICAL COMPOSITION, METHOD FOR PREPARING SAME, AND USE THEREOF Longivitron (Suzhou) Biotechnology Co., Ltd (CN) 2025-03-26 EP disclosed
CN-119455003-A Compositions, methods and uses comprising antibody-TLR agonist conjugates AMBRX公司 2025-02-18 CN disclosed
US-4658015-A ANTAGONIST OF VASSOPRESSIN AND OXYTOCIN SMITHKLINE BECKMAN CORPORATION (US) 1987-04-14 US disclosed
US-4604378-A CYCLIC POLYPEPTIDES SMITHKLINE BECKMAN CORPORATION (US) 1986-08-05 US disclosed
EP-0182627-A2 Basic V1-vasopressin antagonists SMITHKLINE BECKMAN CORPORATION (US) 1986-05-28 EP disclosed
US-4543349-A Basic heptapeptide vasopressin antagonists SMITHKLINE BECKMAN CORPORATION (US) 1985-09-24 US disclosed
EP-0135379-A2 Basic hexa- and hepta-peptide vasopressin antagonists SMITHKLINE BECKMAN CORPORATION (US) 1985-03-27 EP disclosed
US-RE30496-E Tripeptide derivatives with central nervous system activity and preparation thereof AYERST, MCKENNA & HARRISON, LTD. (CA) 1981-01-27 US disclosed
US-4207315-A Process for treating proliferative skin diseases using certain diamino compounds UNIVERSITY PATENTS, INC. (US) 1980-06-10 US disclosed
US-4201788-A Process for alleviating proliferative skin diseases UNIVERSITY PATENTS, INC. (US) 1980-05-06 US disclosed
US-4018912-A Tripeptide derivatives with central nervous system activity and preparation thereof AYERST MCKENNA AND HARRISON LTD. (CA) 1977-04-19 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 (1 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-12569566-B2 Compositions containing, methods and uses of antibody-TLR agonist conjugates TLR3, TLR2, TLR1 GSR 4058/4885NOS1 64/4885NOS3 82/4885

“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.