SCHEMBL11060098

SCHEMBL11060098

CCCCCCCCCCCCCCCCCCC(C)CC

nearest known ligand 0.52

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ACE2 Q9BYF1 1/20 0.52
OPRM1 P35372 1/20 0.50
TSHR P16473 1/20 0.47
THRB P10828 1/20 0.47
SPHK1 Q9NYA1 1/20 0.46
LMNA P02545 2/20 0.46
DNM1 Q05193 2/20 0.46
ADH1B P00325 1/20 0.43
ADH1C P00326 1/20 0.43
ADH1A P07327 1/20 0.43
ADH4 P08319 1/20 0.43
ADH7 P40394 1/20 0.43
GPR84 Q9NQS5 3/20 0.41
FDPS P14324 3/20 0.41
FFAR1 O14842 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
SCHEMBL10583127 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1
SCHEMBL4406595 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1
SCHEMBL5301671 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1
SCHEMBL671909 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1
SCHEMBL5294996 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1
SCHEMBL10579761 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1
SCHEMBL672720 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1
SCHEMBL450926 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1
SCHEMBL4406475 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1
SCHEMBL555207 1.00 ACE2 (0.52) ACE2OPRM1TSHRTHRBSPHK1

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250368594-A1 COMPOSITIONS AND METHODS TO SEPARATE CANNABINOIDS FROM IMPURITIES BY CRYSTALLIZATION NATURAL EXTRACTION SYS LLC (US) 2025-12-04 US claimed
US-12391637-B2 Methods to separate cannabinoids from impurities by crystallization Natural Extraction Systems, LLC (US) 2025-08-19 US claimed
US-20220396540-A1 METHODS TO SEPARATE CANNABINOIDS FROM IMPURITIES BY CRYSTALLIZATION Natural Extraction Systems, LLC (US) 2022-12-15 US claimed
WO-2021096886-A1 METHODS TO SEPARATE CANNABINOIDS FROM IMPURITIES BY CRYSTALLIZATION Natural Extraction Systems, LLC (US) 2021-05-20 WO claimed
US-20250368594-A1 COMPOSITIONS AND METHODS TO SEPARATE CANNABINOIDS FROM IMPURITIES BY CRYSTALLIZATION NATURAL EXTRACTION SYS LLC (US) 2025-12-04 US disclosed
US-12391637-B2 Methods to separate cannabinoids from impurities by crystallization Natural Extraction Systems, LLC (US) 2025-08-19 US disclosed
WO-2025096734-A1 MICROCAPSULES FMC CORPORATION (US) 2025-05-08 WO disclosed
US-11993562-B2 Methods for isolation and purification of cannabidiol (CBD) and terpenes from hemp RJ LEE GROUP, INC. (US) 2024-05-28 US disclosed
EP-3383380-B1 LIPID COMPOUNDS AND COMPOSITIONS AND THEIR OPTHALMIC USE BIOZEP AS (NO) 2023-01-04 EP disclosed
US-20220396540-A1 METHODS TO SEPARATE CANNABINOIDS FROM IMPURITIES BY CRYSTALLIZATION Natural Extraction Systems, LLC (US) 2022-12-15 US disclosed
US-20220324780-A1 METHODS FOR ISOLATION AND PURIFICATION OF CANNABIDIOL (CBD) AND TERPENES FROM HEMP RJ LEE GROUP, INC. 2022-10-13 US disclosed
CN-106650181-B Method for calculating density of hydrocarbon compound 中国石油化工股份有限公司 2021-08-06 CN disclosed
WO-2021096886-A1 METHODS TO SEPARATE CANNABINOIDS FROM IMPURITIES BY CRYSTALLIZATION Natural Extraction Systems, LLC (US) 2021-05-20 WO disclosed
CN-106407635-B A method of calculating hydrocarbon compound boiling point 中国石油化工股份有限公司 2019-03-08 CN disclosed
CN-106446485-A Method for calculating refractive index of hydrocarbon compounds 中国石油化工股份有限公司 2017-02-22 CN disclosed
CN-106407635-A Method for calculating boiling point of hydrocarbon compound 中国石油化工股份有限公司 2017-02-15 CN disclosed
CN-106383981-A Hydrocarbons compound physics property calculating method 中国石油化工股份有限公司 2017-02-08 CN disclosed
EP-3063190-A1 CONDUCTING POLYMER, 1-OCTADECENE, POLYMER WITH 2,5 FURANDIONE, METAL SALTS Laurino, Joseph P. (US) 2016-09-07 EP disclosed
WO-2015066015-A1 CONDUCTING POLYMER, 1-OCTADECENE, POLYMER WITH 2,5 FURANDIONE, METAL SALTS LAURINO JOSEPH P (US) 2015-05-07 WO disclosed
US-4425419-A Photosensitive composition HITACHI, LTD. (JP) 1984-01-10 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-20220324780-A1 METHODS FOR ISOLATION AND PURIFICATION OF CANNABIDIOL (CBD) AND TERPENES FROM HEMP CNR2, CNR1, CYP8B1 ACE2 3185/4885OPRM1 619/4885TSHR 4403/4885
US-11993562-B2 Methods for isolation and purification of cannabidiol (CBD) and terpenes from hemp CNR2, CNR1, CYP8B1 ACE2 3185/4885OPRM1 619/4885TSHR 4403/4885

“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.