Cytisinicline

Cytisinicline

SCHEMBL472026

O=c1cccc2n1CC1CNCC2C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHRNA4CHRNB2

The experimentally established mechanism targets of Cytisinicline. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CHRNB2 known ✓ P17787 12/20 1.00
CHRNA4 known ✓ P43681 12/20 1.00
CHRNB4 P30926 9/20 1.00
CHRNA3 P32297 9/20 1.00
CHRNA7 P36544 4/20 1.00
CHRNA1 P02708 4/20 1.00
CHRNG P07510 4/20 1.00
CHRNB1 P11230 4/20 1.00
CHRND Q07001 4/20 1.00
KDM4E B2RXH2 2/20 1.00
CYP3A4 P08684 2/20 1.00
MEN1 O00255 1/20 1.00
LMNA P02545 1/20 1.00
CYP1A2 P05177 1/20 1.00
MAPT P10636 1/20 1.00
KMT2A Q03164 1/20 1.00

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
Cytisinicline SCHEMBL13595657 1.00 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7
Cytisinicline SCHEMBL8309064 1.00 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7
Cytisinicline SCHEMBL1500421 1.00 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7
Cytisinicline SCHEMBL14870500 1.00 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7
Cytisinicline SCHEMBL161398 1.00 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7
Cytisinicline SCHEMBL19877933 0.98 CHRNB2 (0.97) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7
Cytisinicline SCHEMBL29903945 0.98 CHRNB2 (0.97) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7
Cytisinicline SCHEMBL1500403 0.93 CHRNB2 (0.86) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7
Cytisinicline SCHEMBL20680760 0.91 CHRNB2 (0.82) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7
Cytisinicline SCHEMBL20680750 0.89 CHRNB2 (0.80) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115078513-A Method for detecting black sugar in ethanol-containing beverage 贵州茅台酒股份有限公司 2022-09-20 CN claimed
CN-106479315-A The preparation method of water-saving closet sewage draining valve inwall protective coating 合肥海宝节能科技有限公司 2017-03-08 CN claimed
CN-106439550-A LED flashlight with spectacle frame 合肥学院 2017-02-22 CN claimed
CN-106349885-A Protective coating for inner wall of drainage valve of water-saving toilet bowl 合肥海宝节能科技有限公司 2017-01-25 CN claimed
EP-4529924-B1 TRANSDERMAL THERAPEUTIC SYSTEM COMPRISING CYTISINE LTS LOHMANN THERAPIE SYSTEME AG (DE) 2026-02-18 EP disclosed
WO-2025077770-A1 FUSED RING COMPOUND AND USE THEREOF IN KRAS INHIBITOR 成都海博为药业有限公司 2025-04-17 WO disclosed
EP-4529924-A1 TRANSDERMAL THERAPEUTIC SYSTEM COMPRISING CYTISINE LTS Lohmann Therapie-Systeme AG (DE) 2025-04-02 EP disclosed
US-11911380-B2 Compositions and use of varenicline for treating dry eye Oyster Point Pharma, Inc. (US) 2024-02-27 US disclosed
US-20230226052-A1 DRY EYE TREATMENTS OYSTER POINT PHARMA INC (US) 2023-07-20 US disclosed
US-20230226053-A1 DRY EYE TREATMENTS OYSTER POINT PHARMA INC (US) 2023-07-20 US disclosed
US-20230226054-A1 DRY EYE TREATMENTS OYSTER POINT PHARMA INC (US) 2023-07-20 US disclosed
US-20230203038-A1 4-SUBSTITUED CYTISINE ANALOGUES THE UNIVERSITY OF BRISTOL (GB) 2023-06-29 US disclosed
US-20030065173-A1 Pyridone-fused azabicyclic- or cytisine derivatives, their preparation and their use in addiction therapy O'NEILL BRIAN T (US) 2003-04-03 US disclosed
EP-0870768-B1 Azaindole-ethylamine derivatives as nicotinic acetylcholine receptor binding agents PFIZER (US) 2002-05-15 EP disclosed
EP-1178045-A1 Azaindole-ethylamine derivatives as nicotine acetylchlorine receptor binding agents PFIZER INC. (US) 2002-02-06 EP disclosed
US-6235734-B1 TOBACCO ADDICTION PFIZER INC 2001-05-22 US disclosed
US-6235734-B1 TOBACCO ADDICTION PFIZER INC 2001-05-22 US disclosed
CN-1295076-A Sophorine extracting process JIANGXI TRADITIONAL CHIENSE ME (CN) 2001-05-16 CN disclosed
US-5977131-A Azaindole-ethylamine derivatives as nicotinic acetylcholine receptor binding agents PFIZER INC. (US) 1999-11-02 US disclosed
EP-0870768-A1 Azaindole-ethylamine derivatives as nicotinic acetylcholine receptor binding agents PFIZER INC. (US) 1998-10-14 EP 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 (6 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-20030065173-A1 Pyridone-fused azabicyclic- or cytisine derivatives, their preparation and their use in addiction therapy CHRNA5, CHRNA4, CHRNA10 CHRNB2 12/4885CHRNA4 2/4885CHRNB4 4/4885
US-20230226054-A1 DRY EYE TREATMENTS PDE6D, CRYAB, ALDH1A2 CHRNB2 1787/4885CHRNA4 2137/4885CHRNB4 1806/4885
US-20230203038-A1 4-SUBSTITUED CYTISINE ANALOGUES CES2, CDA, PCYT1A CHRNB2 48/4885CHRNA4 7/4885CHRNB4 21/4885
US-11911380-B2 Compositions and use of varenicline for treating dry eye CHRNA7, ACHE, HTR7 CHRNB2 30/4885CHRNA4 34/4885CHRNB4 38/4885
US-20230226053-A1 DRY EYE TREATMENTS PDE6D, CRYAB, ALDH1A2 CHRNB2 1787/4885CHRNA4 2137/4885CHRNB4 1806/4885
US-20230226052-A1 DRY EYE TREATMENTS PDE6D, CRYAB, ALDH1A2 CHRNB2 1787/4885CHRNA4 2137/4885CHRNB4 1806/4885

“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.