SCHEMBL120494

SCHEMBL120494

N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OC=O

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.67
KDM4E B2RXH2 2/20 0.67
MEN1 O00255 2/20 0.67
LMNA P02545 2/20 0.67
KMT2A Q03164 2/20 0.67
MPO P05164 1/20 0.67
TSHR P16473 1/20 0.67
BLM P54132 1/20 0.67
PMP22 Q01453 1/20 0.67
HIF1A Q16665 1/20 0.67
TACR1 P25103 2/20 0.61
HTR2A P28223 2/20 0.54
ADRB1 P08588 1/20 0.54
HTR1A P08908 1/20 0.54
ADRA2A P08913 1/20 0.54
SLC6A2 P23975 1/20 0.54
HTR1D P28221 1/20 0.54
HTR1B P28222 1/20 0.54
HTR2C P28335 1/20 0.54
HTR1E P28566 1/20 0.54

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
SCHEMBL28548119 1.00 MAPT (0.67) MAPTKDM4EMEN1LMNAKMT2A
Hydrochloric Acid SCHEMBL27358254 0.99 MAPT (0.65) MAPTKDM4EMEN1LMNAKMT2A
SCHEMBL29151371 0.88 MAPT (0.61) MAPTKDM4EMEN1LMNAKMT2A
SCHEMBL23723484 0.88 MAPT (0.76) MAPTKDM4EMEN1LMNAKMT2A
SCHEMBL29472033 0.88 MAPT (0.76) MAPTKDM4EMEN1LMNAKMT2A
SCHEMBL289044 0.86 MAPT (0.74) MAPTKDM4EMEN1LMNAKMT2A
SCHEMBL475351 0.86 MAPT (0.74) MAPTKDM4EMEN1LMNAKMT2A
SCHEMBL27495642 0.86 KDM4E (0.66) MAPTKDM4EMEN1LMNAKMT2A
SCHEMBL626831 0.85 MAPT (0.72) MAPTKDM4EMEN1LMNAKMT2A
SCHEMBL28780405 0.85 MAPT (0.72) MAPTKDM4EMEN1LMNAKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118834265-A Polypeptide with complement inhibition activity, fusion protein and medical application thereof 北京拓界生物医药科技有限公司 2024-10-25 CN disclosed
US-20240218018-A1 Compstatin Analogs with Increased Solubility and Improved Pharmacokinetic Properties THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2024-07-04 US disclosed
US-11884747-B2 Compstatin analogs with increased solubility and improved pharmacokinetic properties THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2024-01-30 US disclosed
CN-110229216-B Compstatin peptides with improved pharmacokinetic properties 宾夕法尼亚州大学理事会 2023-06-16 CN disclosed
EP-4011905-A2 COMPSTATIN ANALOGS WITH INCREASED SOLUBILITY AND IMPROVED PHARMACOKINETIC PROPERTIES The Trustees Of The University Of Pennsylvania (US) 2022-06-15 EP disclosed
EP-3645550-B1 COMPSTATIN ANALOGS WITH INCREASED SOLUBILITY AND IMPROVED PHARMACOKINETIC PROPERTIES UNIV PENNSYLVANIA (US) 2021-11-03 EP disclosed
CN-112334477-A Compstatin analogs with increased solubility and improved pharmacokinetic properties 宾夕法尼亚大学理事会 2021-02-05 CN disclosed
US-20210032291-A1 Compstatin Analogs With Improved Pharmacokinetic Properties THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2021-02-04 US disclosed
CN-112041330-A Compstatin analogs and medical uses thereof 西兰制药第三特殊目的公司 2020-12-04 CN disclosed
US-10800812-B2 Compstatin analogs with increased solubility and improved pharmacokinetic properties THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2020-10-13 US disclosed
EP-0405537-A1 N-substituted cycloalkyl and polycycloalkyl alpha-substituted Trp-Phe- and phenethylamine derivatives WARNER-LAMBERT COMPANY (US) 1991-01-02 EP disclosed
EP-0403600-A1 DEPROTECTION OF PROTECTED PEPTIDES THE ROCKEFELLER UNIVERSITY (US) 1990-12-27 EP disclosed
WO-1990013563-A1 SYNTHETIC PSEUDOMONAS AERUGINOSA PILIN PEPTIDE AND RELATED VACCINES AND DIAGNOSTICS THE GOVERNORS OF THE UNIVERSITY OF ALBERTA (CA) 1990-11-15 WO disclosed
WO-1990002138-A1 DEPROTECTION OF PROTECTED PEPTIDES THE ROCKEFELLER UNIVERSITY (US) 1990-03-08 WO disclosed
EP-0349354-A1 Peptides PF10 to PF19 from a retro virus HIV, method for the synthesis of these peptides and their use, particularly in diagnostics INSTITUT PASTEUR (FR) 1990-01-03 EP disclosed
WO-1989009227-A2 PF10 TO PF19 PEPTIDES OF AN HIV RETROVIRUS, PROCESS FOR SYNTHETIZING SAID PEPTIDES AND THEIR USE, IN PARTICULAR FOR DIAGNOSIS INSTITUT PASTEUR (FR) 1989-10-05 WO disclosed
EP-0284383-A1 Synthetic antigens for the detection of aids-related disease caused by LAV-2 GENETIC SYSTEMS CORPORATION (US) 1988-09-28 EP disclosed
WO-1988005051-A1 SYNTHETIC PEPTIDES WHICH INDUCE CELLULAR IMMUNITY OF THE AIDS VIRUS AND AIDS VIRAL PROTEINS UNITED STATES OF AMERICA, REPRESENTED BY THE UNITE (US) 1988-07-14 WO disclosed
EP-0273716-A2 Synthetic peptides which induce cellular immunity to the aids virus and aids viral proteins THE UNITED STATES OF AMERICA as represented by the Secretary United States Department of Commerce (US) 1988-07-06 EP disclosed
US-4507230-A DETACHING RESINS FROM PEPTIDES RESEARCH CORPORATION (US) 1985-03-26 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-20210032291-A1 Compstatin Analogs With Improved Pharmacokinetic Properties VIP, C1QBP, C9 MAPT 3025/4885KDM4E 4593/4885MEN1 223/4885

“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.