Known targets — ChEMBL curated mechanism
ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Anthracene. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | KDM4E | B2RXH2 | 5/20 | 0.52 |
| ▸ | ALDH1A1 | P00352 | 5/20 | 0.52 |
| ▸ | HPGD | P15428 | 4/20 | 0.52 |
| ▸ | MEN1 | O00255 | 4/20 | 0.52 |
| ▸ | KMT2A | Q03164 | 4/20 | 0.52 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.52 |
| ▸ | CYP1A2 | P05177 | 2/20 | 0.52 |
| ▸ | CYP2C19 | P33261 | 2/20 | 0.52 |
| ▸ | GLA | P06280 | 1/20 | 0.52 |
| ▸ | IDO1 | P14902 | 1/20 | 0.48 |
| ▸ | CES2 | O00748 | 2/20 | 0.48 |
| ▸ | CES1 | P23141 | 2/20 | 0.48 |
| ▸ | POLB | P06746 | 1/20 | 0.46 |
| ▸ | CASP6 | P55212 | 1/20 | 0.46 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.45 |
| ▸ | GAA | P10253 | 1/20 | 0.45 |
| ▸ | NAPRT | Q6XQN6 | 1/20 | 0.44 |
| ▸ | MYC | P01106 | 1/20 | 0.44 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.44 |
| ▸ | MAPT | P10636 | 3/20 | 0.43 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Anthracene SCHEMBL28769838 | 1.00 | KDM4E (0.52) | KDM4EALDH1A1HPGDMEN1KMT2A | |
| Benz(B)Anthracene SCHEMBL31229359 | 0.97 | ALDH1A1 (0.50) | KDM4EALDH1A1HPGDMEN1KMT2A | |
| Anthracene SCHEMBL28851488 | 0.91 | CES2 (0.50) | KDM4EALDH1A1HPGDMEN1KMT2A | |
| Anthracene SCHEMBL27577677 | 0.88 | CES2 (0.48) | KDM4EALDH1A1HPGDMEN1KMT2A | |
| Anthracene SCHEMBL3911533 | 0.88 | ALDH1A1 (0.56) | KDM4EALDH1A1HPGDMEN1KMT2A | |
| Naphthalene SCHEMBL3759523 | 0.88 | CYP2A6 (0.53) | KDM4EALDH1A1HPGDMEN1KMT2A | |
| Naphthalene SCHEMBL263645 | 0.88 | CYP2A6 (0.53) | KDM4EALDH1A1HPGDMEN1KMT2A | |
| Naphthalene SCHEMBL28769152 | 0.88 | CYP2A6 (0.53) | KDM4EALDH1A1HPGDMEN1KMT2A | |
| Anthracene SCHEMBL29605772 | 0.88 | ALDH1A1 (0.56) | KDM4EALDH1A1HPGDMEN1KMT2A | |
| Anthracene SCHEMBL29071655 | 0.88 | ALDH1A1 (0.56) | KDM4EALDH1A1HPGDMEN1KMT2A |
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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118782816-A | Preparation method of oxygen reduction catalyst of fuel cell | 昆明理工大学 | 2024-10-15 | — | — | CN | claimed |
| CN-103450714-B | A kind of conductive graphite flake and preparation method thereof | TORAY ADVANCED MATERIALS RESEARCH LABORATORIES (CHINA) CO., LTD. (CN) | 2015-11-25 | — | — | CN | claimed |
| CN-103450714-A | Conductive graphite flake and preparation method thereof | TORAY ADVANCED MATERIALS RES LAB CHINA CO LTD | 2013-12-18 | — | — | CN | claimed |
| JP-5021165-A | — | — | None | — | — | JP | disclosed |
| CN-118782816-A | Preparation method of oxygen reduction catalyst of fuel cell | 昆明理工大学 | 2024-10-15 | — | — | CN | disclosed |
| CN-118202810-A | Organic electroluminescent element and electronic device | 出光兴产株式会社 | 2024-06-14 | — | — | CN | disclosed |
| CN-113376965-B | Coloring composition and compound | 住友化学株式会社 | 2024-05-28 | — | — | CN | disclosed |
| CN-113376962-B | Coloring composition and compound | 住友化学株式会社 | 2024-05-28 | — | — | CN | disclosed |
| CN-113376963-B | Coloring composition and compound | 住友化学株式会社 | 2024-05-28 | — | — | CN | disclosed |
| CN-118077328-A | Organic electroluminescent element and electronic device | 出光兴产株式会社 | 2024-05-24 | — | — | CN | disclosed |
| CN-118044353-A | Organic electroluminescent element and electronic device | 出光兴产株式会社 | 2024-05-14 | — | — | CN | disclosed |
| CN-101982447-A | Application of O-acylation amino acid and salts thereof as catalysts for asymmetric organic synthesis reaction | CHONGQING YIPAIYIN CHEMICAL INDUSTRY PRODUCTS CO LTD | 2011-03-02 | — | — | CN | disclosed |
| CN-101972672-A | S-acylation L-cysteine and application of salt thereof as catalyst for asymmetrical organic synthesis reaction | CHONGQING YIPAIYIN CHEMICAL PRODUCTS CO LTD | 2011-02-16 | — | — | CN | disclosed |
| CN-100438914-C | Composition for intraorally rapidly disintegrating tablet | FUJI CHEM IND CO LTD (JP) | 2008-12-03 | — | — | CN | disclosed |
| CN-1856328-A | Composition for intraorally rapidly disintegrating tablet | FUJI CHEM IND CO LTD (JP) | 2006-11-01 | — | — | CN | disclosed |
| CN-1856298-A | Tablets rapidly disintegrating in oral cavity | FUJI CHEM IND CO LTD (JP) | 2006-11-01 | — | — | CN | disclosed |
| EP-0705221-A4 | METHOD AND APPARATUS FOR PHOTOCHEMICALLY OXIDIZING GASEOUS ORGANIC COMPOUNDS | PROCESS TECHNOLOGIES INC (US) | 1997-01-22 | — | — | EP | disclosed |
| EP-0705221-A1 | METHOD AND APPARATUS FOR PHOTOCHEMICALLY OXIDIZING GASEOUS ORGANIC COMPOUNDS | PROCESS TECHNOLOGIES, INCORPORATED (US) | 1996-04-10 | — | — | EP | disclosed |
| WO-1994029221-A1 | METHOD AND APPARATUS FOR PHOTOCHEMICALLY OXIDIZING GASEOUS ORGANIC COMPOUNDS | PROCESS TECHNOLOGIES, INC. (US) | 1994-12-22 | — | — | WO | disclosed |
| JP-H0521165-A | ELECTRIC FIELD LIGHT EMITTING ELEMENT | RICOH CO LTD | 1993-01-29 | — | — | JP | disclosed |