SCHEMBL632286

SCHEMBL632286

CCC(N)c1ccccc1O

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 2/20 0.63
▸ GABRA1 P14867 1/20 0.52
▸ GABRB2 P47870 1/20 0.52
▸ POLB P06746 2/20 0.42
▸ LMNA P02545 2/20 0.40
▸ ALOX15 P16050 2/20 0.38
▸ KDM4E B2RXH2 1/20 0.38
▸ NPC1 O15118 1/20 0.38
▸ CA12 O43570 1/20 0.38
▸ GMNN O75496 1/20 0.38
▸ ALDH1A1 P00352 1/20 0.38
▸ EGFR P00533 1/20 0.38
▸ CA2 P00918 1/20 0.38
▸ FYN P06241 1/20 0.38
▸ CA3 P07451 1/20 0.38
▸ CYP3A4 P08684 1/20 0.38
▸ MAPT P10636 1/20 0.38
▸ MMP9 P14780 1/20 0.38
▸ HPGD P15428 1/20 0.38
▸ NFKB1 P19838 1/20 0.38

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
SCHEMBL17092611 1.00 TSHR (0.63) TSHRGABRA1GABRB2POLBLMNA
Hydrochloric Acid SCHEMBL9461595 0.98 TSHR (0.61) TSHRGABRA1GABRB2POLBLMNA
SCHEMBL3678678 0.84 TSHR (0.44) TSHRLMNAALDH1A1SLC6A4
SCHEMBL940014 0.83 TSHR (0.53) TSHRGABRA1GABRB2POLBLMNA
SCHEMBL5934663 0.82 TSHR (0.50) TSHRGABRA1GABRB2POLBLMNA
Hydrochloric Acid SCHEMBL326013 0.82 TSHR (0.52) TSHRGABRA1GABRB2POLBLMNA
SCHEMBL5792353 0.80 TSHR (0.50) TSHRGABRA1GABRB2POLBLMNA
SCHEMBL12610425 0.80 TSHR (0.65) TSHRGABRA1GABRB2POLBLMNA
SCHEMBL2990957 0.80 TSHR (0.65) TSHRGABRA1GABRB2POLBLMNA
SCHEMBL9750794 0.80 TSHR (0.48) TSHRGABRA1GABRB2POLBLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12383515-B2 Compositions and methods of use of γ-ketoaldehyde scavengers for treating, preventing or improving nonalcoholic fatty liver disease (NAFLD), NASH, ALD or conditions related to the liver MTI BIOTECH, INC. (US) 2025-08-12 — — US claimed
CN-119212681-A Method for preparing 3-D printed pharmaceutical products 百时美施贵宝公司 2024-12-27 — — CN claimed
CN-118290290-A Preparation method and application of continuous flow for synthesizing ethylsalicylamine 天津大学 2024-07-05 — — CN claimed
CN-117597115-A Coated solid pharmaceutical preparation SS制药株式会社 2024-02-23 — — CN claimed
CN-122055143-A Solid compositions containing bromhexine 第一三共健康事业株式会社 2026-05-15 — — CN disclosed
CN-119486761-A Hyaluronic acid derivative pharmaceutical composition and pharmaceutical composition 旭化成株式会社 2025-02-18 — — CN disclosed
CN-119278035-A Solid preparation and method for producing the same 第一三共健康事业株式会社 2025-01-07 — — CN disclosed
CN-119212681-A Method for preparing 3-D printed pharmaceutical products 百时美施贵宝公司 2024-12-27 — — CN disclosed
CN-118660695-A Pharmaceutical kit for parenteral combination administration G2G生物公司 2024-09-17 — — CN disclosed
CN-118562694-A Microorganism expressing exogenous protein and use thereof 丽必微股份有限公司 2024-08-30 — — CN disclosed
CN-118512598-A Aqueous composition containing hypromellose acetate succinate and method for producing solid preparation 信越化学工业株式会社 2024-08-20 — — CN disclosed
CN-118401124-A Tablet containing lactic acid bacteria 麒麟控股株式会社 2024-07-26 — — CN disclosed
US-5200561-A PROCESS FOR PRODUCING OPTICALLY ACTIVE AMINES SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1993-04-06 — — US disclosed
EP-0311385-B1 OPTICALLY ACTIVE HYDROXYBENZYLAMINE DERIVATIVE, OPTICALLY ACTIVE AMINE-BORON COMPOUND CONTAINING SAID DERIVATIVE, AND PROCESS FOR PRODUCING OPTICALLY ACTIVE COMPOUND BY USING SAID COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1993-02-03 — — EP disclosed
US-5120853-A Reacting optically active amine-boron complex with oxime or ketone to produce opotically active amine or alcohol compounds SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1992-06-09 — — US disclosed
EP-0485069-A1 Process for producing optically active amines SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1992-05-13 — — EP disclosed
US-5011989-A Asymmetric reducing agents SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1991-04-30 — — US disclosed
EP-0311385-A2 Optically active hydroxybenzylamine derivative, optically active amine-boron compound containing said derivative, and process for producing optically active compound by using said compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1989-04-12 — — EP disclosed
US-4108868-A 3-(Hydroxyhydrocarbylsecondaryamino)thiophene 1,1-dioxides and polyurethanes chain extended therewith UNIROYAL, INC. (US) 1978-08-22 — — US disclosed
US-3983139-A 3-(Hydroxyhydrocarbylsecondaryamino)thiophene 1,1-dioxides and polyurethanes chain extended therewith UNIROYAL INC. (US) 1976-09-28 — — 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-12383515-B2 Compositions and methods of use of γ-ketoaldehyde scavengers for treating, preventing or improving nonalcoholic fatty liver disease (NAFLD), NASH, ALD or conditions related to the liver AKR7A2, CPT1A, FABP1 TSHR 4558/4885GABRA1 2090/4885GABRB2 1064/4885

“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.

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