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Results: 10

1.

Estradiol, (-)-Isomer

MedGen UID:
214583
Concept ID:
C0917767
Pharmacologic Substance
2.

Estradiol, (+-)-Isomer

MedGen UID:
210081
Concept ID:
C1135742
Pharmacologic Substance
3.

MedGen UID:
183050
Concept ID:
C0919376
4.

MedGen UID:
182502
Concept ID:
C0919387
5.

CN-55,945-27

MedGen UID:
45107
Concept ID:
C0028184
Pharmacologic Substance
6.

Enclomiphene

The trans or (E)-isomer of clomiphene. [from MeSH]

MedGen UID:
39183
Concept ID:
C0086213
Pharmacologic Substance
7.

Nitromifene

A non-steroidal estrogen antagonist (as the 1:1 citrate) most commonly used as a research tool in animal studies. [from MeSH]

MedGen UID:
14384
Concept ID:
C0028183
Pharmacologic Substance
8.

Nafoxidine

An estrogen antagonist that has been used in the treatment of breast cancer. [from MeSH]

MedGen UID:
10254
Concept ID:
C0027328
Pharmacologic Substance
9.

Zuclomiphene

The cis or (Z)-isomer of clomiphene. [from MeSH]

MedGen UID:
39754
Concept ID:
C0087182
Pharmacologic Substance
10.

triphenylethylene

the core chemical structure of a number of related anti-estrogen compounds. The triphenylethylene antiestrogens, which include idoxifene, toremifene, chlorotrianisene, raloxifene and tamoxifen, act at the level of the estrogen receptor, triggering inhibition or stimulation of estrogen-dependent gene transcription and cellular physiology. Triphenylethylenes were initially developed for the treatment of estrogen-dependent breast cancers. Selective estrogen receptor modulators (SERMs) such as raloxifene and tamoxifen represent triphenylethylene derivatives that affect transcriptional regulation through modulation of specific alpha and beta estrogen receptors that are differentially expressed in various normal and neoplastic tissues. (NCI04) [from NCI]

MedGen UID:
35545
Concept ID:
C0077252
Pharmacologic Substance

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