SCHEMBL5487566

SCHEMBL5487566

Cc1ccccc1-c1cc2cc3nc(cc4ccc(cc5nc(cc1[nH]2)C=C5)[nH]4)C=C3

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NPC1 O15118 2/20 0.42
▸ ALDH1A1 P00352 2/20 0.42
▸ RAB9A P51151 2/20 0.42
▸ SMN1; SMN2 Q16637 2/20 0.42
▸ HPGD P15428 1/20 0.42
▸ HTT P42858 1/20 0.42
▸ NPSR1 Q6W5P4 1/20 0.42
▸ STAT3 P40763 1/20 0.40
▸ STAT1 P42224 1/20 0.40
▸ DCUN1D1 Q96GG9 2/20 0.36
▸ NPBWR1 P48145 1/20 0.36
▸ TRPA1 O75762 1/20 0.35
▸ MGAM O43451 4/20 0.35
▸ GAA P10253 4/20 0.35
▸ SI P14410 4/20 0.35
▸ MGAM2 Q2M2H8 4/20 0.35
▸ PTGES O14684 1/20 0.34
▸ HAVCR2 Q8TDQ0 1/20 0.32
▸ CYP19A1 P11511 1/20 0.32
▸ DHFR P00374 1/20 0.32

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
O-Xylene SCHEMBL28139724 0.87 ALDH1A1 (0.36) NPC1ALDH1A1RAB9ASMN1; SMN2HPGD
SCHEMBL28755100 0.85 STAT3 (0.40) NPC1ALDH1A1RAB9ASMN1; SMN2HPGD
SCHEMBL7260895 0.84 SMN1; SMN2 (0.43) NPC1ALDH1A1RAB9ASMN1; SMN2HPGD
SCHEMBL29489406 0.82 NPC1 (0.42) NPC1ALDH1A1RAB9ASMN1; SMN2HPGD
SCHEMBL5067202 0.82 NPC1 (0.42) NPC1ALDH1A1RAB9ASMN1; SMN2HPGD
SCHEMBL5013661 0.82 STAT3 (0.40) NPC1ALDH1A1RAB9AHPGDSTAT3
SCHEMBL2849617 0.82 F7 (0.40) NPC1ALDH1A1RAB9ASMN1; SMN2HPGD
SCHEMBL29062202 0.82 STAT3 (0.40) STAT3STAT1
SCHEMBL9764311 0.82 KDM4E (0.42) NPC1ALDH1A1RAB9ASMN1; SMN2HPGD
SCHEMBL27596488 0.82 STAT3 (0.40) STAT3STAT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117980004-A Porphyrin nanovesicles with fatty acid conjugates 大学健康网络 2024-05-03 — — CN claimed
CN-115403780-A Photosensitizer material, preparation method and application thereof in preparation of polymer 合肥工业大学 2022-11-29 — — CN claimed
CN-106474474-B Photo-thermal nano particle based on peptide and photosensitizer, preparation method and application thereof 中国科学院过程工程研究所 2020-02-14 — — CN claimed
CN-106659684-A Peptide-containing porphyrin lipid nanovesicles 大学健康网络 2017-05-10 — — CN claimed
CN-106474474-A A kind of photo-thermal nanoparticle based on peptide and photosensitizer, Preparation Method And The Use 中国科学院过程工程研究所 2017-03-08 — — CN claimed
CN-102573914-B Porphyrin nanovesicles 大学健康网络 2016-06-29 — — CN claimed
CN-104080929-A Giant porphyrin-phospholipid vesicles UNIV HEALTH NETWORK 2014-10-01 — — CN claimed
CN-103930137-A Porphyrin-phospholipid conjugate microbubbles and their use as contrast agents. UNIV HEALTH NETWORK 2014-07-16 — — CN claimed
CN-103857384-A Method for synthesizing porphyrin-phospholipid conjugates UNIV HEALTH NETWORK 2014-06-11 — — CN claimed
CN-102573914-A Porphyrin nanovesicles UNIV HEALTH NETWORK 2012-07-11 — — CN claimed
CN-115403780-B Photosensitizer material, preparation method and application thereof in preparation of polymer 合肥工业大学 2024-06-14 — — CN disclosed
CN-117980004-A Porphyrin nanovesicles with fatty acid conjugates 大学健康网络 2024-05-03 — — CN disclosed
CN-116744909-A Metal organic frameworks deliver small and biological macromolecules for cancer immunotherapy 芝加哥大学 2023-09-12 — — CN disclosed
CN-116249525-A Nanoparticles containing multiple cleavable prodrugs for cancer therapy 芝加哥大学 2023-06-09 — — CN disclosed
CN-111194232-B Nanoscale metal-organic layer and metal-organic nanosheet 芝加哥大学 2023-01-31 — — CN disclosed
WO-2007064841-A2 PORPHYRINIC COMPOUNDS FOR USE IN FLOW CYTOMETRY NORTH CAROLINA STATE UNIVERSITY (US) 2007-06-07 — — WO disclosed
EP-1763317-A1 SYNTHESIS OF PORPHYRINS DESIGNED FOR ATTACHMENT TO ELECTROACTIVE SURFACES VIA ONE OR MORE CARBON TETHERS North Carolina State University (US) 2007-03-21 — — EP disclosed
WO-2006016943-A1 SYNTHESIS OF PORPHYRINS DESIGNED FOR ATTACHMENT TO ELECTROACTIVE SURFACES VIA ONE OR MORE CARBON TETHERS NORTH CAROLINA STATE UNIVERSITY (US) 2006-02-16 — — WO disclosed
CN-1043143-C Beta, beta-dihydroxy meso-substituted chlorins, isobacteriochlorins, bacteriochlorins, and methods of making said compounds from beta, beta-unsubstituted tetrapyrrolic macrocycles UNIV BRITISH COLUMBIA (CA) 1999-04-28 — — CN disclosed
CN-1161697-A Beta, beta '-dihydroxy meso-substituted chlorins, isobacteriochlorins, bacteriochlorins, and methods of making said compounds from beta, beta' -unsubstituted tetrapyrrolic macrocycles UNIV BRITISH COLUMBIA (CA) 1997-10-08 — — CN disclosed
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