SCHEMBL385554

SCHEMBL385554

O=C1CCCc2ccc(O)cc21

nearest known ligand 0.78

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
PBRM1 Q86U86 1/20 0.78
MAOB P27338 9/20 0.72
MAOA P21397 8/20 0.72
PRKCI P41743 1/20 0.72
HSD17B1 P14061 2/20 0.59
CYP2A6 P11509 1/20 0.53
MEN1 O00255 1/20 0.47
MAPK1 P28482 1/20 0.47
KMT2A Q03164 1/20 0.47
NPSR1 Q6W5P4 1/20 0.47
ESR1 P03372 1/20 0.43
UGT1A1 P22309 1/20 0.43
ESR2 Q92731 1/20 0.43
BAZ2B Q9UIF8 1/20 0.42
AKR1B1 P15121 1/20 0.42
CYP19A1 P11511 1/20 0.42
TYMS P04818 1/20 0.41
MAPK14 Q16539 1/20 0.41

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
SCHEMBL29983572 1.00 PBRM1 (0.78) PBRM1MAOBMAOAPRKCIHSD17B1
Hydrochloric Acid SCHEMBL6531236 0.96 PBRM1 (0.72) PBRM1MAOBMAOAPRKCIHSD17B1
SCHEMBL5145478 0.96 PBRM1 (0.78) PBRM1MAOBMAOAPRKCIHSD17B1
SCHEMBL28880 0.88 PBRM1 (1.00) PBRM1MAOBMAOAPRKCIHSD17B1
SCHEMBL30137886 0.88 PBRM1 (1.00) PBRM1MAOBMAOAPRKCIHSD17B1
SCHEMBL228128 0.84 MAOA (1.00) PBRM1MAOBMAOAPRKCIHSD17B1
SCHEMBL3825921 0.80 MAOA (0.92) PBRM1MAOBMAOAPRKCIHSD17B1
SCHEMBL29483386 0.80 MAOA (0.53) PBRM1MAOBMAOAPRKCIHSD17B1
SCHEMBL355820 0.80 MAOA (0.53) PBRM1MAOBMAOAPRKCIHSD17B1
SCHEMBL27323917 0.79 MAOB (0.77) PBRM1MAOBMAOAPRKCIHSD17B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115108928-B Nitrogen mustard-tetralone derivative, preparation method and application thereof 广东海洋大学 2024-06-11 CN claimed
CN-211384964-U Cooling device of reaction kettle for producing and preparing 7-hydroxy-1-tetralone 武汉海昕药物研究有限公司 2020-09-01 CN claimed
CN-106977377-B Preparation method of 7-hydroxy-1-tetralone 江西同和药业股份有限公司 2020-06-30 CN claimed
CN-109265431-B Synthesis process of 3-acetyl-10, 11-dihydro-5H-dibenzo [ C, G ] chromen-8 (9H) -one 江苏苏利精细化工股份有限公司 2020-05-26 CN claimed
CN-109265431-A 3- acetyl group -10,11- dihydro -5H- dibenzo [C, G] chromene -8(9H) -one synthesis technology 江苏苏利精细化工股份有限公司 2019-01-25 CN claimed
CN-108794316-A Preparation process of 7-hydroxy-3, 4-dihydro-2H-1-naphthalenone 海门市新港医药科技有限公司 2018-11-13 CN claimed
EP-2909166-A1 PROCESSES FOR THE PREPARATION OF AGOMELATINE USING NOVEL INTERMEDIATES Symed Labs Limited (IN) 2015-08-26 EP claimed
WO-2014064706-A1 PROCESSES FOR THE PREPARATION OF AGOMELATINE USING NOVEL INTERMEDIATES SYMED LABS LIMITED (IN) 2014-05-01 WO claimed
EP-2194035-B1 Hydroxytetralones SALTIGO GMBH (DE) 2011-11-02 EP claimed
EP-2194035-A2 Hydroxytetralones Saltigo GmbH (DE) 2010-06-09 EP claimed
CN-122074043-A Combination therapy with KRAS modulators 光达治疗公司 2026-05-22 CN disclosed
CN-122059824-A Synthesis method of ilalastyl chiral intermediate 上海格苓凯生物科技有限公司 2026-05-19 CN disclosed
CN-118026958-B 3, 4-Dihydro-1 (2H) -naphthalenone derivative, preparation method and application thereof 滨州医学院 2026-05-12 CN disclosed
US-12624052-B2 KRAS modulators and uses thereof QUANTA THERAPEUTICS, INC. (US) 2026-05-12 US disclosed
US-12509417-B2 Enantioselective process SYNGENTA CROP PROTECTION AG (CH) 2025-12-30 US disclosed
US-4001301-A ANTIINFLAMMATORY AGENTS, ANALGESICS, ANTIPYRETICS, ANTI-PRURITIC SYNTEX CORPORATION (PM) 1977-01-04 US disclosed
US-3998966-A Anti-inflammatory, analgesic, anti-pyretic and anti-pruritic 6-substituted 2-naphthyl acetic acid derivative-containing compositions and methods of use thereof SYNTEX CORPORATION (PM) 1976-12-21 US disclosed
US-3980699-A ANTIINFLAMMATORY, ANALGESICS, ANTIPYRETIC, ANTIPRURITIC SYNTEX CORPORATION (PM) 1976-09-14 US disclosed
US-3978116-A ANALGESIC, ANTIPYRETIC SYNTEX CORPORATION (PM) 1976-08-31 US disclosed
US-3978124-A ANALGESIC, ANTIPYRETIC SYNTEX CORPORATION (PM) 1976-08-31 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 (2 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-12509417-B2 Enantioselective process HCCS, AOC3, CYP8B1 PBRM1 1854/4885MAOB 278/4885MAOA 354/4885
US-12624052-B2 KRAS modulators and uses thereof KRAS, NRAS, HRAS PBRM1 367/4885MAOB 4747/4885MAOA 4851/4885

“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.