Squalamine

Squalamine

SCHEMBL12836

CC(C)[C@@H](CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@H]4C[C@@H](NCCCNCCCCN)CC[C@]4(C)[C@H]3CC[C@]12C)OS(=O)(=O)O

nearest known ligand 0.97

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC9A3

The experimentally established mechanism targets of Squalamine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 2/20 0.97
NR1H4 Q96RI1 8/20 0.53
SLC10A1 Q14973 3/20 0.51
GPBAR1 Q8TDU6 9/20 0.51
SLC10A2 Q12908 2/20 0.48
ABCC4 O15439 1/20 0.48
ABCB11 O95342 1/20 0.48
PLA2G1B P04054 1/20 0.48
ENPP2 Q13822 1/20 0.48

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
Squalamine SCHEMBL14441307 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2
Squalamine SCHEMBL17359656 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2
Squalamine SCHEMBL16072074 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2
Squalamine SCHEMBL13294189 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2
Squalamine SCHEMBL14430016 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2
Squalamine SCHEMBL18838926 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2
Squalamine SCHEMBL22356672 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2
Squalamine SCHEMBL21248627 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2
Squalamine SCHEMBL20850040 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2
Squalamine SCHEMBL13014098 1.00 PTPN1 (0.97) PTPN1NR1H4SLC10A1GPBAR1SLC10A2

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

Appears in 24123 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260116861-A1 ISOXAZOLE HYDROXAMIC ACIDS AS HISTONE DEACETYLASE 6 INHIBITORS THE GEORGE WASHINGTON UNIVERSITY, A CONGRESSIONALLY CHARTERED NOT-FOR-PROFIT CORPORATION (US) 2026-04-30 US claimed
EP-4724079-A2 METHODS AND COMPOSITIONS FOR THE TREATMENT OF AGE-RELATED MACULAR DEGENERATION Stealth BioTherapeutics Inc. (US) 2026-04-15 EP claimed
EP-4719387-A2 COMPLEMENT ANTIBODY-DRUG CONJUGATES ADS Therapeutics LLC (US) 2026-04-08 EP claimed
US-12577255-B2 MDM2-based modulators of proteolysis and associated methods of use ARVINAS OPERATIONS, INC. (US) 2026-03-17 US claimed
EP-4704832-A2 BIFUNCTIONAL SMALL MOLECULES TO TARGET THE SELECTIVE DEGRADATION OF CIRCULATING PROTEINS Biohaven Therapeutics Ltd. (VG) 2026-03-11 EP claimed
US-20260048096-A1 METHODS AND COMPOSITIONS FOR PRESERVING THE RETINAL OUTER NUCLEAR LAYER (ONL), PHOTORECEPTORS, AND RETINAL THICKNESS STEALTH BIOTHERAPEUTICS INC. (US) 2026-02-19 US claimed
US-20260022117-A1 COMPOUNDS AND METHODS FOR THE ENHANCED DEGRADATION OF TARGETED PROTEINS ARVINAS OPERATIONS INC (US) 2026-01-22 US claimed
US-12522572-B2 Isoxazole hydroxamic acids as histone deacetylase 6 inhibitors THE GEORGE WASHINGTON UNIVERSITY, A CONGRESSIONALLY CHARTERED NOT-FOR-PROFIT CORPORATION (US) 2026-01-13 US claimed
US-12485178-B2 Bifunctional small molecules to target the selective degradation of circulating proteins YALE UNIVERSITY (US) 2025-12-02 US claimed
US-20250332274-A1 BIFUNCTIONAL SMALL MOLECULES TO TARGET THE SELECTIVE DEGRADATION OF CIRCULATING PROTEINS UNIV YALE (US) 2025-10-30 US claimed
WO-1997026888-A1 USE OF SQUALAMINE AND ITS ANALOGUES IN OPHTHALMIC COMPOSITIONS ALCON LABORATORIES, INC. (US) 1997-07-31 WO claimed
WO-1997009973-A2 PERIPHERALLY ACTIVE ANTI-HYPERALGESIC OPIATES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1997-03-20 WO claimed
US-5607691-A IONTOPHORESIS AFFYMAX TECHNOLOGIES N.V. (GB) 1997-03-04 US claimed
EP-0749437-A1 STEROID DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND THEIR PHARMACEUTICAL USES MAGAININ PHARMACEUTICALS INC. (US) 1996-12-27 EP claimed
WO-1996040151-A1 USE OF SQUALAMINE FOR THE MANUFACTURE OF A MEDICAMENT FOR INHIBITING NHE MAGAININ PHARMACEUTICALS INC. (US) 1996-12-19 WO claimed
WO-1996008270-A9 METHOD FOR INHIBITING SEXUALLY TRANSMITTED DISEASES USING MAGAINING ANTIMICROBIALS OR SQUALAMINE COMPOUNDS 1996-06-27 WO claimed
WO-1996008270-A2 METHOD FOR INHIBITING SEXUALLY TRANSMITTED DISEASES USING MAGAINING ANTIMICROBIALS OR SQUALAMINE COMPOUNDS MAGAININ PHARMACEUTICALS INC. (US) 1996-03-21 WO claimed
WO-1995024415-A1 STEROID DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND THEIR PHARMACEUTICAL USES MAGAININ PHARMACEUTICALS INC. (US) 1995-09-14 WO claimed
EP-0647133-A1 COMPOSITIONS AND METHODS FOR ENHANCED DRUG DELIVERY AFFYMAX TECHNOLOGIES N.V. (AN) 1995-04-12 EP claimed
WO-1993025197-A1 COMPOSITIONS AND METHODS FOR ENHANCED DRUG DELIVERY AFFYMAX TECHNOLOGIES N.V. (AN) 1993-12-23 WO claimed