Weight | 1346.377 g/mol |
---|---|
Formula | C62H89CoN13O15P |
Hydrogen Acceptors | 20 |
Hydrogen Donors | 9 |
Aromatic Rings | 2 |
Rotatable Bonds | 26 |
Cyanokit (13422-51-0)
Hydroxocobalamin · Hydroxycobalamin · Hydroxo-Cobalamin
Score:
#1224 in Biology
,
#1407 in Chemistry
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- Decreased activities of ubiquinol:ferricytochrome c oxidoreductase (complex III) and ferrocytochrome c:oxygen oxidoreductase (complex IV) in liver mitochondria from rats with hydroxycobalamin[c-lactam]-induced methylmalonic aciduria. (Journal of Biological Chemistry, 1991)
- Prospective Study of Hydroxocobalamin for Acute Cyanide Poisoning in Smoke Inhalation (Annals of Emergency Medicine, 2007)
- Prevention of Nitroprusside-Induced Cyanide Toxicity with Hydroxocobalamin (The New England Journal of Medicine, 1978)
- HYDROXOCOBALAMIN AS A CYANIDE ANTIDOTE: SAFETY, EFFICACY AND PHARMACOKINETICS IN HEAVILY SMOKING NORMAL VOLUNTEERS (Clinical Toxicology, 1993)
- Sodium Thiosulfate or Hydroxocobalamin for the Empiric Treatment of Cyanide Poisoning (Annals of Emergency Medicine, 2007)
- Differential effects of hydroxocobalamin on NO-mediated relaxations in rat aorta and anococcygeus muscle (British Journal of Pharmacology, 1993)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Hydroxocobalamin
- Hydroxycobalamin
- Hydroxo-Cobalamin
-
SMILESCC1=CC2=C(C=C1C)N(C=N2)C3C(C(C(O3)CO)OP(=O)([O-])OC(C)CNC(=O)CCC4(C(C5C6(C(C(C(=N6)C(=C7C(C(C(=N7)C=C8C(C(C(=N8)C(=C4[N-]5)C)CCC(=O)N)(C)C)CCC(=O)N)(C)CC(=O)N)C)CCC(=O)N)(C)CC(=O)N)C)CC(=O)N)C)O.[OH-].[Co+3]
-
InChIKeyYOZNUFWCRFCGIH-UHFFFAOYSA-K
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