Methyltestosterone

Methyltestosterone

SCHEMBL29416593

C[C@]12CCC(=O)C=C1CC[C@H]1[C@H]3CC[C@](C)(O)[C@@]3(C)CC[C@@H]12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AR

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ AR known ✓ P10275 3/20 0.72
▸ SHBG P04278 9/20 1.00
▸ NR3C1 P04150 5/20 1.00
▸ PGR P06401 4/20 1.00
▸ ALDH1A1 P00352 4/20 1.00
▸ ADRA1A P35348 1/20 1.00
▸ HTR2B P41595 1/20 1.00
▸ LMNA P02545 8/20 0.74
▸ SERPINA6 P08185 7/20 0.74
▸ SMN1; SMN2 Q16637 5/20 0.74
▸ BLM P54132 4/20 0.74
▸ CYP2C19 P33261 3/20 0.74
▸ MEN1 O00255 2/20 0.74
▸ KMT2A Q03164 2/20 0.74
▸ MAPT P10636 2/20 0.74
▸ ADORA3 P0DMS8 1/20 0.74
▸ MAPK3 P27361 1/20 0.74
▸ SLC6A3 Q01959 1/20 0.74
▸ TSHR P16473 5/20 0.72
▸ HIF1A Q16665 2/20 0.72

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
Methyltestosterone SCHEMBL18657 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A
Methyltestosterone SCHEMBL6472960 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A
Methyltestosterone SCHEMBL4442874 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A
Methyltestosterone SCHEMBL5021655 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A
Methyltestosterone SCHEMBL18891626 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A
Methyltestosterone SCHEMBL13575766 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A
Methyltestosterone SCHEMBL13965283 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A
Methyltestosterone SCHEMBL13768123 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A
Methyltestosterone SCHEMBL6152059 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A
Methyltestosterone SCHEMBL4575985 1.00 SHBG (1.00) SHBGNR3C1PGRALDH1A1ADRA1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120058450-A C (sp) in benzene ring2) Method for deuteration of the H bond 云南大学 2025-05-30 — — CN claimed
CN-110198949-B Process for the preparation of 9 beta, 10 alpha-progesterone (retroprogesterone) 工业化学有限公司 2022-05-10 — — CN claimed
CN-120058450-A C (sp) in benzene ring2) Method for deuteration of the H bond 云南大学 2025-05-30 — — CN disclosed
CN-116789726-A Steroid compound, preparation method and application thereof 珂阑(上海)医药科技有限公司 2023-09-22 — — CN disclosed
CN-116514892-A Steroid compound, preparation method and application thereof 珂阑(上海)医药科技有限公司 2023-08-01 — — CN disclosed
CN-116514893-A Steroid compound, preparation method and application thereof 珂阑(上海)医药科技有限公司 2023-08-01 — — CN disclosed
CN-107735101-B Antibiotic sensitivity restoring agent and photosensitizer 新墨西哥州科技研究基金会 2022-11-04 — — CN disclosed
CN-115160397-A Androstane derivative and preparation method and application thereof 天津红日药业股份有限公司 2022-10-11 — — CN disclosed
CN-112110880-B Androstane derivative and preparation method and application thereof 天津红日药业股份有限公司 2022-09-09 — — CN disclosed
CN-114466855-A Androstane derivatives with pure or significantly pure stimulant activity as SERCA2a for the treatment of heart failure 风树疗法公司 2022-05-10 — — CN disclosed
CN-110198949-B Process for the preparation of 9 beta, 10 alpha-progesterone (retroprogesterone) 工业化学有限公司 2022-05-10 — — CN disclosed
CN-114106077-A Abiraterone derivative and preparation and application thereof 广东中科药物研究有限公司 2022-03-01 — — CN disclosed
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